Scholarly article on topic 'Current progress on bio-based polymers and their future trends'

Current progress on bio-based polymers and their future trends Academic research paper on "Agricultural biotechnology"

Share paper
Academic journal
Prog Biomater
OECD Field of science

Academic research paper on topic "Current progress on bio-based polymers and their future trends"

O Progress in Biomaterials

a SpringerOpen Journal


Current progress on bio-based polymers and their future trends

Ramesh P Babu1,2*, Kevin O'Connor3 and Ramakrishna Seeram4,5,6


This article reviews the recent trends, developments, and future applications of bio-based polymers produced from renewable resources. Bio-based polymers are attracting increased attention due to environmental concerns and the realization that global petroleum resources are finite. Bio-based polymers not only replace existing polymers in a number of applications but also provide new combinations of properties for new applications. A range of bio-based polymers are presented in this review, focusing on general methods of production, properties, and commercial applications. The review examines the technological and future challenges discussed in bringing these materials to a wide range of applications, together with potential solutions, as well as discusses the major industry players who are bringing these materials to the market.

Keywords: Bio-based polymers, Renewable resources, Biotechnologies, Sustainable materials



Bio-based polymers are materials which are produced from renewable resources. The terms bio-based polymers and biodegradable polymers are used extensively in the literature, but there is a key difference between the two types of polymers. Biodegradable polymers are defined as materials whose physical and chemical properties undergo deterioration and completely degrade when exposed to microorganisms, carbon dioxide (aerobic) processes, methane (anaerobic processes), and water (aerobic and anaerobic processes). Bio-based polymers can be biodegradable (e.g., polylactic acid) or nondegradable (e.g., biopolyhethylene). Similarly, while many bio-based polymers are biodegradable (e.g., starch and polyhydroxyalkanoates), not all biodegradable polymers are bio-based (e.g., polycaprolactone).

Bio-based polymers still hold a tiny fraction of the total global plastic market. Currently, biopolymers share less than 1% of the total market. At the current growth rate, it is expected that biopolymers will account for just over 1% of polymers by 2015 (Doug 2010).

The worldwide interest in bio-based polymers has accelerated in recent years due to the desire and need to

* Correspondence:

Centre for Research Adoptive Nanostructures and Nano Devices, Trinity College, Dublin 2, Ireland

2Schoolof Physics, Trinity College Dublin, Dublin 2, Ireland Fulllist of author information is available at the end of the article

find non-fossil fuel-based polymers. As indicated by ISI Web of Sciences and Thomas Innovations, there is a tremendous increase in the number of publication citations on bio-based polymers and applications in recent years, as shown in Figure 1 (Chen and Martin 2012).

Bio-based polymers offer important contributions by reducing the dependence on fossil fuels and through the related positive environmental impacts such as reduced carbon dioxide emissions. The legislative landscape is also changing where bio-based products are being favored through initiatives such as the Lead Market Initiative (European Union) and BioPreferred (USA). As a result, there is a worldwide demand for replacing petroleum-derived raw materials with renewable resource-based raw materials for the production of polymers.

The first generation of bio-based polymers focused on deriving polymers from agricultural feedstocks such as corn, potatoes, and other carbohydrate feedstocks. However, the focus has shifted in recent years due to a desire to move away from food-based resources and significant breakthroughs in biotechnology. Bio-based polymers similar to conventional polymers are produced by bacterial fermentation processes by synthesizing the building blocks (monomers) from renewable resources, including lignocellulosic biomass (starch and cellulose), fatty acids, and organic waste. Natural bio-based polymers are the other class of bio-based polymers which


©2013 Babu et al. licensee Springer. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

4000 3500 3000 2500

_q 2000

Z 1500

1000 500 0

ntmfflSCOOlOrNffliUllSNlOOIOrN mOtOtOtOtrnOtOOOOOOOOOOi-i-T-



a: (Source: ISI web of sciences)


o o o o o o o ooooooooooooo


b: (Source: Thomas Innovations)

Figure 1 Citation trends of (a) publications and (b) patents on bio-based polymers in recent years.

are found naturally, such as proteins, nucleic acids, and polysaccharides (collagen, chitosan, etc.). These bio-based polymers have shown enormous growth in recent years in terms of technological developments and their commercial applications. There are three principal ways to produce bio-based polymers using renewable resources:

(1) Using natural bio-based polymers with partial modification to meet the requirements (e.g., starch)

(2) Producing bio-based monomers by fermentation/ conventional chemistry followed by polymerization (e.g., polylactic acid, polybutylene succinate, and polyethylene)

(3) Producing bio-based polymers directly by bacteria (e.g., polyhydroxyalkanoates).

In this paper, an overview of bio-based polymers made from renewable resources and natural polymers derived

from plant and animal origins is presented. The review will focus on the preparation, properties, applications, and future trends for bio-based polymers. This paper discusses the use of renewable resources such as ligno-cellulosic biomass to create monomers and polymers that can replace petroleum-based polymers, such as polyester, polylactic acids, and other natural bio-based polymers, which are presented in Figure 2.

Polylactic acid

Polylactic acid (PLA) has been known since 1845 but not commercialized until early 1990. PLA belongs to the family of aliphatic polyesters with the basic constitutional unit lactic acid. The monomer lactic acid is the hydroxyl carboxylic acid which can be obtained via bacterial fermentation from corn (starch) or sugars obtained from renewable resources. Although other renewable resources can be used, corn has the advantage of providing a high-quality feedstock for fermentation which results in a high-purity lactic acid, which is required for an efficient synthetic process. L-lactic acid or D-lactic acid is obtained depending on the microbial strain used during the fermentation process.

PLA can be synthesized from lactic acid by direct poly-condensation reaction or ring-opening polymerization of lactide monomer. However, it is difficult to obtain high molecular weight PLA via polycondensation reaction because of water formation during the reaction. Nature Works LLC (previously Cargill Dow LLC) has developed a low-cost continuous process for the production of PLA (Erwin et al. 2007). In this process, low molecular weight pre-polymer lactide dimers are formed during a condensation process. In the second step, the pre-polymers are converted into high molecular weight PLA via ring-opening polymerization with selected catalysts. Depending on the ratio and stereochemical nature of the monomer (L or D), various types of PLA and PLA copolymers can be obtained. The final properties of PLA produced are highly dependent on the ratio of the D and L forms of the lactic acid which are listed in Table 1 for various blend ratios (Garlotta 2001).

PLA is a commercially interesting polymer as it shares some similarities with hydrocarbon polymers such as polyethylene terephthalate (PET). It has many unique characteristics, including good transparency, glossy appearance, high rigidity, and ability to tolerate various types of processing conditions.

PLA is a thermoplastic polymer which has the potential to replace traditional polymers such as PET, PS, and PC for packaging to electronic and automotive applications (Majid et al. 2010). While PLA has similar mechanical properties to traditional polymers, the thermal properties are not attractive due to low Tg of 60°C. This problem can be overcome by changing the stereochemistry of the polymer and blending with other polymers and processing aids to improve the mechanical properties, e.g., varying the ratio of L and D isomer ratio strongly influences the crystallinity of the final polymer. However, much more work is required to improve the properties of PLA to suit various applications.

Currently, Nature Works LLC, USA, is the major supplier of PLA sold under the brand name Ingeo, with a production capacity of 100,000 ton/year. There are other manufactures of PLA based in the USA, Europe, China, and Japan developing various grades of PLA suitable for different industrial sectors such as automobile, electronics, medical devices, and commodity applications, which are mentioned in Table 2) (Doug 2010; Ravenstijn 2010).

PLA is widely used in many day-to-day applications. It has been mainly used in food packing (including food trays, tableware such as plates and cutlery, water bottles, candy wraps, cups, etc.). Although PLA has one of the highest heat resistances and mechanical strengths of all bio-based polymers, it is still not suitable for use in electronic devices and other engineering applications. NEC Corporation (Japan) recently produced a PLA with carbon and kenaf fibers with improved thermal and flame retardancy properties. Fujitsu (Japan) developed a polycarbonate blend with PLA to make computer housings. In recent years, PLA has been employed as a membrane material for use in automotive and chemical industry.

Production of Biobased Polymers

Polymers from Agro resources (By extraction and separation)

Polysaccharides and Lipids (Starch, Cellulose, Alginates)

From micro-organisms (by fermentation)

Polyhydroxyalkanoates (mcl-PHA, PHB, PHB-co-V)

From biotechnology via conventional synthesis

Poly lactides , PBS, PBS, PE,PTT,PPP

Figure 2 Most common categories of bio-based polymers produced by various processes. From Luc and Eric (2012).

Table 1 Variation in glass transition and melting temperature of PLA with various ratios of L-monomer composition

Copolymer ratio Glass transition (Tg), °C Melting temperature (Tm), °C

100:0 (L/DL)-PLA 63 178

95:5 (L/DL)-PLA 59 164

90:10 (L/DL)-PLA 56 150

85:15 (L/DL)-PLA 56 140

80:20 (L/DL)-PLA 56 125

The ease of melt processing has led to the production of PLA fibers, which are increasingly accepted in a wide variety of textiles from dresses to sportswear, furnishing to drapes, and soft nonwoven baby wipes to tough landscape textiles. These textiles can outperform traditional textiles made from synthetic counterparts. Bioresorbable scaffolds produced with PLA and various PLA blends are used in implants for growing living cells. The US Food and Drug Administration (FDA) has approved the use of PLA for certain human clinical applications (Dorozhkin 2009; Garlotta 2001). In addition, PLA-based materials have been used for bone support splints. Applications of PLA-based polymers in various fields are listed in Table 3.

Polyhyd roxyalkanoates

Polyhydroxyalkanoates (PHAs) are a family of polyesters produced by bacterial fermentation with the potential to replace conventional hydrocarbon-based polymers. PHAs occur naturally in a variety of organisms, but microorganisms can be employed to tailor their production in cells. Polyhydroxybutyrate (PHB), the simplest PHA, was discovered in 1926 by Maurice Lemoigne as a constituent of the bacterium Bacillus megaterium (Lemoigne 1923).

PHA can be produced by varieties of bacteria using several renewable waste feedstocks. A generic process to produce PHA by bacterial fermentation involves fermentation, isolation, and purification from fermentation broth. A large fermentation vessel is filled with mineral medium and inoculated with a seed culture that contains bacteria. The feedstocks include cellulosics, vegetable oils, organic waste, municipal solid waste, and fatty acids depending on the specific PHA required. The carbon source is fed into the vessel until it is consumed and cell growth and PHA accumulation is complete. In general, a minimum of 48 h is required for fermentation time. To isolate and purify PHA, cells are concentrated, dried, and extracted with solvents such as acetone or chloroform. The residual cell debris is removed from the solvent containing dissolved PHA by solid-liquid separation process. The PHA is then precipitated by the addition of an alcohol (e.g., methanol) and recovered by a precipitation process (Kathiraser et al. 2007).

More than 150 PHA monomers have been identified as the constituents of PHAs (Steinbüchel and Valentin 1995). Such diversity allows the production of bio-based polymers with a wide range of properties, tailored for specific applications. Poly-3-hydroxybutyrate was the first bacterial PHA identified. It has received the greatest attention in terms of pathway characterization and industrial-scale production. It possesses similar thermal and mechanical properties to those of polystyrene and polypropylene (Savenkova et al. 2000). However, due to its slow crystallization, narrow processing temperature range, and tendency to 'creep! it is not attractive for many applications, requiring development in order to overcome these shortcomings (Reis et al. 2008). Several companies have developed PHA copolymers with typically 80% to 95% (R)-3-hydroxybutyric acid monomer and 5% to 20% of a second monomer in order to improve the properties of PHAs. Some specific examples of PHAs include the following:

Table 2 Global suppliers of PLA

Company Location Brand Production/planned capacity

name (kton/year)

Nature Works USA Ingeo 140 (by 2013)

Futerro Belgium Futerro 1.5 (by 2010)

Tate & Lyle Netherlands Hycail 0.2 (by 2012)

Purac Netherlands Purasorb 0.05

Hiusan Biosciences China Hisun 5

Jiangsu Jiulding China 5

Teijin Japan Biofront 1

Toyobo Japan Vylocol 0.2

Synbra Netherlands Biofoam 50

Table 3 Application of PLA and their blends in various fields

Polymer Applications Reference

PLGA/PGA Ovine pulmonary valve replacement Williams et al. 1999; Sodian et al. 1999, 2000; Cheng et al. 2009

PLA/chitosan PLA/PLGA/ chitosan PLA Drug carrier/drug release Jeevitha and Kanchana 2013; Jayanth and Vinod 2012; Nagarwalet al. 2010; Chandy et al. 2000; Valantin et al. 2003

PLGA and copolymers Degradable sutures Rajev 2000

PLA/HA composites Porous scaffolds for cellular applications Jung-Ju et al. 2012

PLA-CaP and PLGA-CaP Bone fixation devices, plates, pins, screws, and wires, orthopedic applications Huan et al. 2012

PDLLA Coatings on metalimplants Schmidmaier et al. 2001

PLA/PLGA Use in cell-based gene therapy for cardiovascular diseases, muscle tissues, bone and cartilage regeneration, and other treatments of cardiovascular and neurological conditions Coutu et al. 2009; Kellomaki et al. 2000; Papenburg et al. 2009

PLA and PLA blends Packaging films, commodity containers, electrical appliances, mobile phone housings, floor mats, automotive spare parts Rafaelet al. 2010

PLA Textile applications Gupta et al. 2007; Avinc and Akbar 2009

PLGA, polylactic aeid-co-glyeolie acid; CaP, calcium phosphates; HA, hydroxyapatite.

• Poly(3HB): Poly(3-hydroxybutyrate)

• Poly(3HB-co-3HV): Poly(3-hydroxybutyrate-co-3-hydroxyvalerate), PHBV

• Poly(3-HB-co-4HB): Poly(3-hydroxybutyrate-co-4-hydroxybutyrate)

• Poly(3HB-co-3HH): Poly(3-hydroxyoctanoate-co-hydroxyhexanoate)

• Poly(3HO-co-3HH): Poly(3-hydroxyoctanoate-co-hydroxyhexanoate)

• Poly (4-HB): Poly(4-hydroxybutyrate).

The copolymer poly(3HB-co-3HV) has a much lower crystallinity, decreased stiffness and brittleness, and increased tensile strength and toughness compared to poly (3HB) while remaining biodegradable. It also has a higher melt viscosity, which is a desirable property for extrusion and blow molding (Hanggi 1995).

The first commercial plant for PHBV was built in the USA in a joint venture between Metabolix and Archer Daniels Midland. However, the joint venture between these two companies ended in 2012. Currently, Tianan Biologic Material Co. in China is the largest producer of PHB and PHB copolymers. Tianan's PHBV contains about 5% valerate which improves the flexibility of the polymer. Tainjin Green Biosciences, China, invested along with DSM to build a production plant with 10-kton/year capacity to produce PHAs for packing and biomedical applications (DSM press release 2008). The current global manufacturers of PHB-based polymers are listed in Table 4 (Doug 2010; Ravenstijn 2010).

PHA polymers are thermoplastic, and their thermal and mechanical properties depend on their composition.

The Tg of the polymers varies from -40°C to 5°C, and the melting temperatures range from 50°C to 180°C, depending on their chemical composition (McChalicher and Srienc 2007). PHB is similar in its material properties to polypropylene, with a good resistance to moisture and aroma barrier properties. Polyhydroxybutyric acid synthesized from pure PHB is relatively brittle and stiff. PHB copolymers, which may include other fatty acids such as beta-hydroxyvaleric acid, may be elastic (McChalicher and Srienc 2007).

PHAs can be processed in existing polymer-processing equipment and can be converted into injection-molded components: film and sheet, fibers, laminates, and coated articles; nonwoven fabrics, synthetic paper products, disposable items, feminine hygiene products, adhe-sives, waxes, paints, binders, and foams. Metabolix has received FDA clearance for use of PHAs in food contact applications. These materials are suitable for a wide range of food packing applications including caps and closures, disposable items such as forks, spoons, knives, tubs, trays, and hot cup lids, and products such as housewares, cosmetics, and medical packaging (Philip et al. 2007).

PHA and its copolymers are widely used as biomedical implant materials. Various applications of PHA and their polymer blends are listed in Table 5. These include sutures, suture fasteners, meniscus repair devices, rivets, bone plates, surgical mesh, repair patches, cardiovascular patches, tissue repair patches, and stem cell growth. Changing the PHA composition allows the manufacturer to tune the properties such as biocompatibility and polymer degradation time within desirable time frames

Table 4 Global suppliers of various types of PHAs



Brand name

Production/planned capacity (kton/year)

Bio-on Kaneka Meredian Metabolix

Mitsubishi Gas Chemicals PHB Industrial S/A Shenzen O'Bioer TEPHA

Tianan Biological Materials Tianjin Green Biosciences Tianjin Northern Food Yikeman Shandong







Green Bio

10 (by 2013)

under specific conditions. PHAs can also be used in drug delivery due to their biocompatibility and controlled degradability. Only a few examples of PHAs have been evaluated for this type of applications, and it remains an important area for exploitation (Tang et al. 2008).

Polybutylene succinate

Polybutylene succinate (PBS) is an aliphatic polyester with similar properties to those of PET. PBS is produced by condensation of succinic acid and 1,4-butanediol. PBS can be produced by either monomers derived from petroleum-based systems or the bacterial fermentation route. There are several processes for producing succinic acid from fossil fuels. Among them, electrochemical synthesis is a common process with high yield and low cost. However, the fermentation production of succinic acid has numerous advantages compared to the chemical process. Fermentation process uses renewable resources and consumes less energy compared to chemical process. Several companies (solely or in partnership) are now scaling bio-succinate production processes which have traditionally suffered from poor productivity and high downstream processing costs. Mitsubishi Chemical (Japan) has developed biomass-derived succinic

acid in collaboration with Ajinomoto to commercialize bio-based PBS. DSM and Roquette are developing a commercially feasible fermentation process for the production of succinic acid 1,4-butanediol and subsequent production of PBS. Myriant and Bioamber have developed a fermentation technology to produce monomers. There are several companies around the world developing technologies for the production of PBS, as listed in Table 6, including North America and China (Doug 2010; Ravenstijn 2010).

Conventional processes for the production of 1,4-butanediol use fossil fuel feedstocks such as acetylene and formaldehyde. The bio-based process involves the use of glucose from renewable resources to produce succinic acid followed by a chemical reduction to produce bu-tanediol. PBS is produced by transesterification, direct polymerization, and condensation polymerization reactions. PBS copolymers can be produced by adding a third monomer such as sebacic acid, adipic acid, and succinic acid which is also produced by renewable resources (Bechthold et al. 2008).

PBS is a semicrystalline polyester with a melting point higher than that of PLA. Its mechanical and thermal properties depend on the crystal structure and the degree of crystallinity (Nicolas et al. 2011). PBS displays similar

Table 5 Application of PHAs and their blends in various fields

PHA polymer type Applications


P(3HB), P(3HB-co-3HHX) and blends


Scaffolds, nerve regeneration, soft tissue, artificialesophagus, drug delivery, skin regeneration, food additive

Cardiac tissue engineering, drug delivery, cosmetics, drug molecules

P(4HB) and P(3HO) Heart valve scaffolds, food additive

P(3HB-co-4HB), P(3HB-co-3HV)

PHB, MirelP103

Drug delivery, scaffolds, artificial heart values, patches to repair gastrointestinal tracts, sutures

Commodity applications, shampoo and cosmetic bottles, cups and food containers

Yang et al. 2002; Chen and Qiong 2005; Bayram and Denbas 2008; Tang et al. 2008; Clarinvaland Halleux 2005

Sodian et al. 2000; Wang et al. 2003; de Roo et al. 2002; Zhao et al. 2003; Ruth et al. 2007

Clarinvaland Halleux 2005; Valappilet al. 2006

Turesin et al. 2001; Williams et al. 1999; Chen et al. 2008; Freier et al. 2002; Kunze et al. 2006; Volova et al. 2003

Philip et al. 2007; Amass et al.

; Walle etal. 200'

Table 6 Global producers of PBS

Company Location Brand name/polymer type Production/planned capacity (kton/year)

BASF Germany PBS

Dupont de Nemours USA PBST

Hexing Chemical China PBS 3

Ube Japan NA NA


IRE Chemical Korea Enpol, PBS, PBSA 3.5

Kingfa China PBSA 1

Mitsubishi Gas Chemical Japan PBS, PES, PBSLa 3

Showa Japan Bionelle PBS, PBSA, PBS 3

SK Chemicals Korea Skygreen NA

DSM Netherlands NA NA

NA, not available; PBSA, poly(butylene succinate adipate).

crystallization behavior and mechanical properties to those of polyolefin such as polyethylene. It has a good tensile and impact strength with moderate rigidity and hardness. The Tg is approximately -32°C, and the melting temperature is approximately 115°C. In comparison with PLA, PBS is tougher in nature but with a lower rigidity and Young's modulus. By changing the monomer composition, mechanical properties can be tuned to suit the required application (Liu et al. 2009a, b).

PBS and their blends have found commercial applications in agriculture, fishery, forestry, construction, and other industrial fields which are listed in Table 7. For example, PBS has been employed as mulch film, packaging, and flushable hygiene products and also used as a non-migrant plasticizer for polyvinyl chloride (PVC). In addition, it is used in foaming and food packaging application. The relatively poor mechanical flexibility of PBS limits the applications of 100% PBS-based products. However, this can be overcome by blending PBS with PLA or starch to improve the mechanical properties significantly, providing properties similar to that of polyolefin (Eslmai and Kamal 2013; Zhao et al. 2010).


Polyethylene (PE) is an important engineering polymer traditionally produced from fossil resources. PE is

produced by polymerization of ethylene under pressure, temperature, in the presence of a catalyst. Traditionally, ethylene is produced through steam cracking of naphtha or heavy oils or ethanol dehydration. With increases in oil prices, microbial PE or green PE is now being manufactured from dehydration of ethanol produced by microbial fermentation. The concept of producing PE from bioethanol is not a particularly new one. In the 1980s, Braskem made bio-PE and bio-PVC from bioethanol. However, low oil prices and the limitations of the biotechnology processes made the technology unattractive at that time (de Guzman 2010).

Currently, bio-PE produced on an industrial scale from bioethanol is derived from sugarcane. Bioethanol is also derived from biorenewable feedstocks, including sugar beet, starch crops such as maize, wood, wheat, corn, and other plant wastes through microbial strain and biological fermentation process. In a typical process, extracted sugarcane juice with high sucrose content is anaerobically fermented to produce ethanol. At the end of the fermentation process, ethanol is distilled in order to remove water and to yield azeotropic mixture of hydrous ethanol. Ethanol is then dehydrated at high temperatures over a solid catalyst to produce ethylene and, subsequently, polyethylene (Guangwen et al. 2007; Luiz et al. 2010).

Table 7 Applications of PBS and their blends

Polymer type Applications Reference

PBS/PLA blend Packaging films, dishware, fibers, medical Weraporn et al. 2011; Liu et al. 2009 a, b; Bhatia et al. 2007; Lee and Wang

materials 2006

PBS and blends Drug encapsulation systems Cornelia et al. 2011

PBS/starch Barrier films Jian-Bing et al. 2011

PBS and Industrialapplications Jun and Bao-Hua 2010 a, b


PBS ionomers Orthopedic applications Jung et al. 2009

Bio-based polyethylene has exactly the same chemical, physical, and mechanical properties as petrochemical polyethylene. Braskem (Brazil) is the largest producer of bio-PE with 52% market share, and this is the first certified bio-PE in the world. Similarly, Braskem is developing other bio-based polymers such as bio-polyvinyl chloride, bio-polypropylene, and their copolymers with similar industrial technologies. The current Braskem bio-based PE grades are mainly targeted towards food packing, cosmetics, personal care, automotive parts, and toys. Dow Chemical (USA) in cooperation with Crystalsev is the second largest producer of bio-PE with 12% market share. Solvay (Belgium), another producer of bio-PE, has 10% share in the current market. However, Solvay is a leader in the production of bio-PVC with similar industrial technologies. China Petrochemical Corporation also plans to set up production facilities in China to produce bio-PE from bioethanol (Haung et al. 2008).

Bio-PE can replace all the applications of current fossil-based PE. It is widely used in engineering, agriculture, packaging, and many day-to-day commodity applications because of its low price and good performance. Table 8 shows applications of bio-PE in different fields where it can replace conventional PE.

Bio-based natural polymers

This group consists of naturally occurring polymers such as cellulose, starch, chitin, and various polysaccharides and proteins. These materials and their derivatives offer a wide range of properties and applications. In this section, some of the natural bio-based polymers and their applications in various fields are discussed.


Starch is a unique bio-based polymer because it occurs in nature as discrete granules. Starch is the end product of photosynthesis in plants - a natural carbohydrate-based polymer that is abundantly available in nature from various sources including wheat, rice, corn, and potato. Essentially, starch consists of the linear polysaccharide amylose and the highly branched polysaccharide amylopec-tin. In particular, thermoplastic starch is of growing interest within the industry. The thermal and mechanical properties of starch can vary greatly and depend upon such factors as the amount of plasticizer present. The Tg varies between -50°C and 110°C, and the modulus is similar to polyole-fins (Jane 1995). Several challenges exist in producing

commercially viable starch plastics. Starch's molecular structure is complex and partly nonlinear, leading to issues with ductility. Starch and starch thermoplastics suffer from the phenomenon of retrogradation - a natural increase in crystallinity over time, leading to increased brittleness. Plasticizers need to be found to create starch plastics with mechanical properties comparable to polyolefin-derived packaging. Plasticized starch blends and composites and/or chemical modifications may overcome these issues, creating biodegradable polymers with sufficient mechanical strength, flexibility, and water barrier properties for commercial packaging and consumer products (Maurizio et al. 2005).

Novamont is one of the leading companies in processing starch-based products (Li et al. 2009). The company produces various types of starch-based products using proprietary blend formulations. There are other companies around the world producing starch-based products in a similar scale for various applications, which are listed in Table 9 (Doug 2010; Ravenstijn 2010).

Applications of thermoplastic starch polymers include films, such as for shopping, bread, and fishing bait bags, overwraps, flushable sanitary product, packing materials, and special mulch films. Potential future applications could include foam loose-fill packaging and injection-molded products such as 'take-away' food containers. Starch and modified starches have a broad range of applications both in the food and non-food sectors. In Europe in 2002, the total consumption of starch and starch derivatives was approximately 7.9 million tons, of which 54% was used for food applications and 46% in non-food applications (Frost & Sullivan report 2009).

The largest users of starch in the European Union (30%) are the paper, cardboard, and corrugating industries (Frost & Sullivan report 2009). Other important fields of starch application are textiles, cosmetics, pharmaceuticals, construction, and paints, which are listed in Table 10. In the medium and long term, starch will play an increasing role in the field of 'renewable raw materials' for the production of biodegradable plastics, packaging material, and molded products.


Cellulose is the predominant constituent in cell walls of all plants. Cellulose is a complex polysaccharide with crystalline morphology. Cellulose differs from starch where glucose units are linked by |3-1,4-glycosidic bonds,

Table 8 Application of bio-PE polymer and their blends

Polymer type Applications Reference

Bio-PE Plastics bags, milk and water bottles, food packaging films, toys Vona et al. 1965; Aamer et al. 2008

Bio-PE and blends Agriculturalmulch films Kasirajan and Ngouajio 2012

Table 9 Global suppliers of starch-based products

Company Location

Novamont Italy

Japan Corn Starch Japan

Biotec Germany

Rodenberg Netherlands

BIOP Germany

Plantic Australia

Wuhan Huali Environment Protection Sci. &Tech China

Biograde China


Livan Canada

Brand name Production/planned capacity (kton/year)

Mater-Bi 120

Ever Corn NA

Bioplast NA Solanyl50

Biopar 5

Plantic 7.5

PSM 15

Cardia 3

Plaststarch NA

Livan 10

whereas the bonds in starch are predominantly a-1,4 linkages. The most important raw material sources for the production of cellulosic plastics are cotton fibers and wood. Plant fiber is dissolved in alkali and carbon disul-fide to create viscose, which is then reconverted to cellulose in cellophane form following a sulfuric acid and sodium sulfate bath. There are currently two processes used to separate cellulose from the other wood constituents (Yan et al. 2009). These methods, sulfite and pre-hydrolysis kraft pulping, use high pressure and chemicals to separate cellulose from lignin and hemicellulose, attaining greater than 97% cellulose purity. The main derivatives of cellulose for industrial purposes are cellulose acetate, cellulose esters (molding, extrusion, and films), and regenerated cellulose for fibers.

Cellulose is a hard polymer and has a high tensile strength of 62 to 500 MPa and elongation of 4% (Bisanda and Ansell 1992; Eichhorn et al. 2001). In order to overcome the inherent processing problems of cellulose, it is necessary to modify, plasticize, and blend with other polymers. The mechanical and thermal properties vary from blend to blend depending on the composition. The Tg of cellulosic derivatives ranged between 53°C and 180°C (Picker and Hoag 2002).

Eastman Chemical is a major producer of cellulosic polymers. FKuR launched a biopolymer business in the

year 2000 and has a capacity of 2,800 metric ton/year of various cellulosic compounds for different applications (Doug 2010). The major producers of cellulose-based compounds are listed in Table 11 (Doug 2010; Ravenstijn 2010).

There are three main groups of cellulosic polymers that are produced by chemical modification of cellulose for various applications. Cellulose esters, namely cellulose nitrate and cellulose acetate, are mainly developed for film and fiber applications. Cellulose ethers, such as carboxymethyl cellulose and hydroxyethyl cellulose, are widely used in construction, food, personal care, pharmaceuticals, paint, and other pharmaceutical applications (Kamel et al. 2008). Finally, regenerated cellulose is the largest bio-based polymer produced globally for fiber and film applications. Regenerated cellulose fibers are used in textiles, hygienic disposables, and home furnishing fabrics because of its thermal stability and modulus (Kevin et al. 2001).

Chemically pure cellulose can be produced using a certain type of bacteria. Bacterial cellulose is characterized by its purity and high strength. It can be used to produce articles with relatively high strength. Currently, applications for bacterial cellulose outside food and biomedical fields are rather limited because of its high price. The other applications include acoustic diaphragms, mining, paints, oil gas recovery, and adhesives.

Table 10 Application of starch and their blends in various fields

Polymer type Applications Reference

Starch Orthopedic implant devices as bone fillers Ashammakhi and Rokkanen 1997

Starch/ethylene vinylalcohol/HA starch/polycaprolactone blends Bone replacement/fixation implants, orthopedic applications Mainilet al. 1997; Mendes et al. 2001; Marques and Reis 2005

Starch/cellulose acetate blends with methylmethacrylate and acrylic acid Bone cements Espigares et al. 2002

Modified starch Food applications Jaspreet et al. 2007; Fuentes et al. 2010

Starch derivatives Drug delivery Asha and Martins 2012

Thermoplastic starch Packaging, containers, mulch films, textile sizing agents, adhesives Zhao et al. 2008; Maurizio et al. 2005; Ozdemir and Floros 2004; Dave et al. 1999; Guo et al. 2005; Kumbar et al. 2001; Li et al. 2011

Table 11 Global suppliers of cellulosic products

Company Location Brand name

Innovia films UK Nature Flex

Eastman Chemical USA Tenite

FKuR Germany Biograde

Sateri China Sateri

However, the low yields and high costs of bacterial cellulose represent barriers to large-scale industrial applications (Prashant et al. 2009). Table 12 summarizes the applications of cellulose and their compounds in different fields.

Chitin and chitosan

Chitin and chitosan are the most abundant natural amino polysaccharide and valuable bio-based natural polymers derived from shells of prawns and crabs. Currently, chitin and chitosan are produced commercially by chemical extraction process from crab, shrimp, and prawn wastes (Roberts 1997). The chemical extraction of chitin is quite an aggressive process based on demineralization by acid and deproteination by the action of alkali followed by dea-cetylated into chitosan (Roberts 1997). Chitin can also be produced by using enzyme hydrolysis or fermentation process, but these processes are not economically feasible on an industrial scale (Win and Stevens 2001). Currently, there are few industrial-scale plants of chitin and chitosan worldwide located in the USA, Canada, Scandinavia, and Asia (Ravi Kumar 2000).

Chitosan displays interesting characteristics including biodegradability, biocompatibility, chemical inertness, high mechanical strength, good film-forming properties, and low cost (Marguerite 2006; Virginia et al. 2011; Liu et al. 2012). Chitosan is being used in a vast array of widely varying products and applications ranging from pharmaceutical and cosmetic products to water treatment and plant protection. For each application, different properties of chito-san are required, which changes with the degree of acetylation and molecular weight. Chitosan is compatible with many biologically active components incorporated in

cosmetic product composition (Ravi Kumar 2000). Due to its low toxicity, biocompatibility, and bioactivity, chitosan has become a very attractive material in such diverse applications as biomaterials in medical devices and as a pharmaceutical ingredient (Bae and Moo-Moo 2010; Ramya et al. 2012). Chitosan has application in shampoos, rinses, and permanent hair-coloring agents. Chitosan and its derivatives also have applications in the skin care industry. Chito-san can function as a moisturizer for the skin, and because of its lower costs, it might compete with hyaluronic acid in this application (Bansal et al. 2011; Valerie and Vinod 1998; Hafdani and Sadeghinia 2011).


Pullulan is a linear water-soluble polysaccharide mainly consisting of maltotriose units connected by a-1,6 glyco-sidic units. Pullulan was first reported by Bauer (1938) and is obtained from the fermentation broth of Aureobasidium pullulans. Pullulan is produced by a simple fermentation process using a number of feedstocks containing simple sugars (Bernier 1958; Catley 1971; Sena et al. 2006). Pullulan can be chemically modified to produce a polymer that is either less soluble or completely insoluble in water. The unique properties of this polysaccharide are due to its characteristic glycosidic linking. Pullulan is easily chemically modified to reduce the water solubility or to develop pH sensitivity, by introducing functional reactive groups, etc. Due to its high water solubility and low viscosity, pullulan has numerous commercial applications including use as a food additive, a flocculant, a blood plasma substitute, an adhesive, and a film (Zajic and LeDuy 1973; Singh et al. 2008; Cheng et al. 2011). Pullulan can be formed into molding articles which can resemble conventional polymers such as polystyrene in their transparency, strength, and toughness (Leathers 2003).

Pullulan is extensively used in the food industry. It is a slow-digesting macromolecule which is tasteless as well as odorless, hence its application as a low-calorie food additive providing bulk and texture. Pullulan possesses oxygen barrier property and good moisture retention,

Table 12 Application of cellulose and their compounds in various fields

Polymer type Applications Reference

Cellulose esters Membranes for separation Kumano and Fujiwara 2008

Carboxylated methylcellulose Drug formulations, as binder for drugs, film-coating agent for drugs, ointment base Chambin et al. 2004; Obae and Imada 1999; Westermark et al. 1999; Hirosawa et al. 2000

Cellulose acetate fibers Wound dressings Orawan et al. 2008; Abdelrahman and Newton 2011

Hydroxyethylcellulose Spray for clothes polluted with pollen Hori et al. 2005

Modified celluloses, cellulose whiskers, microfibrous cellulose Barrier films, water preservation in food packing Amit and Ragauskas 2009

Cellulose nanofibers Textile applications Zeeshan et al. 2013

Cellulose particles Chromatographic applications, chiralseparations Levison 1993; Arshady 1991a, b

and also, it inhibits fungal growth. These properties make it an excellent material for food preservation, and it is used extensively in the food industry (Conca and Yang 1993). In recent years, pullulan has also been studied for biomedical applications in various aspects, including targeted drug and gene delivery, tissue engineering, wound healing, and even in diagnostic imaging medium (Rekha and Chrndra 2007). Other emerging markets for pullulan include oral care products (Barkalow et al. 2002) and formulations of capsules for dietary supplements and pharmaceuticals (Leathers 2003), leading to increased demand for this unique biopolymer.

Collagen and gelatin

Collagen is the major insoluble fibrous protein in the extracellular matrix and in connective tissue. In fact, it is the single most abundant protein in the animal kingdom. There are at least 27 types of collagens, and the structures all serve the same purpose: to help tissues withstand stretching. The most abundant sources of collagen are pig skin, bovine hide, and pork and cattle bones. However, the industrial use of collagen is obtained from nonmammalian species (Gomez-Guille et al. 2011). Gelatin is obtained through the hydrolysis of collagen. The degree of conversion of collagen into gelatin depends on the pretreatment, function of temperature, pH, and extraction time (Johnston-Banks 1990).

Collagen is one of the most useful biomaterials due to its biocompatibility, biodegradability, and weak antigenicity (Maeda et al. 1999). The main application of collagen films in ophthalmology is as drug delivery systems for slow release of incorporated drugs (Rubin et al. 1973). It was also used for tissue engineering including skin replacement, bone substitutes, and artificial blood vessels and valves (Lee et al. 2001).

The classical food, photographic, cosmetic, and pharmaceutical applications of gelatin is based mainly on its gel-forming properties. Recently in the food industry, an increasing number of new applications have been found for gelatin in products in line with the growing trend to replace synthetic agents with more natural ones (Gomez-Guille et al. 2011). These include emulsifiers, foaming agents, colloid stabilizers, biodegradable film-forming materials, and microencapsulating agents.


Alginate is a linear polysaccharide that is abundant in nature as it is synthesized by brown seaweeds and by soil bacteria (Draget et al. 1997). Sodium alginate is the most commonly used alginate form in the industry since it is the first by-product of algal purification (Draget 2000). Sodium alginate consists of a-l-guluronic acid residues (G blocks)

and p-d-mannuronic acid residues (M blocks), as well as segments of alternating guluronic and mannuronic acids.

Although alginates are a heterogeneous family of polymers with varying content of G and M blocks depending on the source of extraction, alginates with high G content have far more industrial importance (Siddhesh and Edgar 2012). The acid or alkali treatment processes used to make sodium alginate from brown seaweeds are relatively simple. The difficulties in processing arise mainly from the separation of sodium alginate from slimy residues (Black and Woodward 1954). It is estimated that the annual production of alginates is approximately 38,000 tons worldwide (Helgerud et al. 2009).

Alginates have various industrial uses as viscosifiers, stabilizers, and gel-forming, film-forming, or water-binding agents (Helga and Svein 1998). These applications range from textile printing and manufacturing of ceramics to production of welding rods and water treatment (Teli and Chiplunkar 1986; Qin et al. 2007; Xie et al. 2001). The polymer is soluble in cold water and forms thermostable gels. These properties are utilized in the food industry in products such as custard creams and restructured food. The polymer is also used as a stabilizer and thickener in a variety of beverages, ice creams, emulsions, and sauces (Iain et al. 2009).

Alginates are widely used as a gelling agent in pharmaceutical and food applications. Studies into their positive effects on human health have broadened recently with the recognition that they have a number of potentially beneficial physiological effects in the gastrointestinal tract (Peter et al. 2011; Mandel et al. 2000). Alginate-containing wound dressings are commonly used, especially in making hydrophilic gels over wounds which can produce comfortable, localized hydrophilic environments in healing wounds (Onsoyen 1996). Alginates are used in controlled drug delivery, where the rate of drug release depends on the type and molecular weight of alginates used (Alexnader et al. 2006; Goh et al. 2012). Additionally, dental impressions made with alginates are easy to handle for both dentist and patient as they fast set at room temperature and are cost-effective (Onsoyen 1996). Recent studies show that alginates can be effective in treating obesity, and currently, various functional algi-nates are being evaluated in human clinical trials (Georg et al. 2012).

Current status and future trends

The use of bio-based feedstocks in the chemical sector is not a novel concept. They have been industrially feasible on a large scale for more than a decade. However, the price of oil was so cost-effective, and the development of oil-based products created so many opportunities that bio-based products were not prioritized at the time. Several factors, such as the limitations and

uncertainty in supplies of fossil fuels, environmental considerations, and technological developments, accelerated the advancement of bio-based polymers and products. It took more than a century to evolve the fossil fuel-based chemical industry; however, the bio-based polymer industry is already catching up with fossil fuel-based chemical industry, which has augmented in the last 20 years. Thanks to advancements in white biotechnology, the production of bio-based polymers and other chemicals from renewable resources has become a reality. The first-generation technologies mainly focused on food resources such as corn, starch, rice, etc. to produce bio-based polymers. As the food-versus-fuel debate ascended, the focus of technologies diverted to cellulose-based feedstocks, focusing on waste from wood and paper, food industries, and even stems and leaves and solid municipal waste streams. More and more of these technologies are already in the pipeline to align with the abovementioned waste streams; however, it may take another 20 years to develop the full spectrum of chemicals based on these technologies (Michael et al. 2011).

Challenges that need to be addressed in the coming years include management of raw materials, performance of bio-based materials, and their cost for production. Economy of scale will be one of the main challenges for production of bio-based monomers and bio-based polymers from renewable sources. Building large-scale plants can be difficult due to the lack of experience in new technologies and estimation of supply/demand balance. In order to make these technologies economically viable, it is very important to develop (1) logistics for biomass feedstocks, (2) new manufacturing routes by replacing existing methods with high yields, (3) new microbial strains/enzymes, and (4) efficient downstream processing methods for recovery of bio-based products.

The current bio-based industry focus is mainly on making bio-versions of existing monomers and polymers. Performance of these products is well known, and it is relatively easy to replace the existing product with similar performance of bio-versions. All the polymers mentioned above often display similar properties of current fossil-based polymers. Recently, many efforts are seen towards introducing new bio-based polymers with higher performance and value. For example, Nature Works LLC has introduced new grades of PLA with higher thermal and mechanical properties. New PLA-tri block copolymers have been reported to behave like thermoplastic elastomer. Many developments are currently underway to develop various polyamides, polyesters, polyhydroxyaloknates, etc. with a high differentiation in their final properties for use in automotive, electronics, and biomedical applications.

The disadvantage of some of the new bio-based polymers is that they cannot be processed in all current

processing equipment. There is vast knowledge on additive-based chemistry developed for improving the performance and processing of fossil fuel-based polymers, and this knowledge can be used to develop new additive chemistry to improve the performance and properties of bio-based polymers (Ray and Bousmina 2005). For bio-based polymers like PLA and PHA, additives are being developed to improve their performance, by blending with other polymers or making new copolymers. However, the additive market for bio-based polymers is still very small, which makes it difficult to justify major development efforts according to some key additive supplier companies.

The use of nanoparticles as additives to enhance polymer performance has long been established for petroleum-based polymers. Various nano-reinforcements currently being developed include carbon nanotubes, graphene, nanoclays, 2-D layered materials, and cellulose nanowhiskers. Combining these nanofillers with bio-based polymers could enhance a large number of physical properties, including barrier, flame resistance, thermal stability, solvent uptake, and rate of biodegradability, relative to unmodified polymer resin. These improvements are generally attained at low filler content, and this nano-reinforcement is a very attractive route to generate new functional biomaterials for various applications.

Even though new bio-based polymers are produced on an industrial scale, there are still several factors which need to be determined for the long-term viability of bio-based polymers. It is expected that there will be feedstock competition as global demand for food and energy increases over time. Currently, renewable feedstocks used for manufacturing bio-based monomers and polymers often compete with requirements for food-based products. The expansion of first-generation bio-based fuel production will place unsustainable demands on biomass resources and is as much a threat to the sus-tainability of biochemical and biopolymer production as it is to food production (Michael et al. 2011). Indeed the European commission has altered its targets downwards for first-generation biofuels since October 2012, indicating its preference for non-food sources of sugar for biofuel production ( 2012). Several initiatives are underway to use cellulose-based feedstocks for the production of usable sugars for biofuels, biochemicals, and biopolymers (Jong et al. 2010).


Bio-based polymers are closer to the reality of replacing conventional polymers than ever before. Nowadays, bio-based polymers are commonly found in many applications from commodity to hi-tech applications due to advancement in biotechnologies and public awareness. However, despite these advancements, there are still some drawbacks which prevent the wider commercialization of bio-based

polymers in many applications. This is mainly due to performance and price when compared with their conventional counterparts, which remains a significant challenge for bio-based polymers.

Competing interests

The authors declare that they have no competing interests. Authors' contributions

RPB contributed in writing the whole manuscript. KOC contributed in providing the information on applications and policy information of bio-based polymers. SR contributed in providing the outline for the manuscript. Allauthors read and approved the finalmanuscript.


RPB would like to acknowledge the financialsupport from the EnvironmentalProtection Agency, Ireland, under grant no. 2008-ET-LS-1-S2.

Author details

1Centre for Research Adoptive Nanostructures and Nano Devices, Trinity College, Dublin 2, Ireland. 2Schoolof Physics, Trinity College Dublin, Dublin 2, Ireland. 3Schoolof Biomolecular and BiomedicalSciences, Centre for Synthesis and ChemicalBiology, UCD Conway Institute, and Earth Institute, University College Dublin, Belfield, Dublin 4, Ireland. 4NUSNNI, National University of Singapore, 2 Engineering Drive 3, Singapore 117581, Singapore. institute of Materials Research and Engineering, Singapore 117602, Singapore. 6Jinan University, Guangzhou, China.

Received: 21 December 2012 Accepted: 21 February 2013 Published: 18 March 2013


Aamer AS, Fariha H, Abdul H, Safia A (2008) Biological degradation of plastics: a

comprehensive review. Biotechnol Adv 26:246-265 Abdelrahman T, Newton H (2011) Wound dressings: principles and practice. Surgery 29:491-495

Alexnader DA, Kong HJ, Mooney DJ (2006) Alginate hydrogels as biomaterials.

Macromolecular Biosciences 6:623-633 Amass W, Amass A, Tighe B (1998) A review of biodegradable polymers: uses, current developments in the synthesis and characterization of biodegradable polyesters, blends of biodegradable polymers and recent advances in biodegradation studies. Polymer International 47:89-144 Amit S, Ragauskas AJ (2009) Water transmission barrier properties of

biodegradable films based on cellulosic whiskers and xylan. Carbohydr Polym 78(2):357-360 Arshady R (1991a) Beaded polymer supports and gels: 2. Physicochemical criteria

and functionalization. J Chromatogr 586:199-219 Arshady R (1991b) Beaded polymer supports and gels: 1. Manufacturing

techniques. J Chromatogr 586:181 -197 Asha R, Martins E (2012) Recent applications of starch derivatives in nanodrug

delivery. Carbohydr Polym 87(2):987-994 Ashammakhi N, Rokkanen P (1997) Absorbable polyglycolide devices in trauma

and bone surgery. Biomaterials 18(1):3-9 Avinc A, Akbar K (2009) Overview of poly (lactic acid) fibres. Part I: production, properties, performance, environmental impact, and end-use applications of poly (lactic acid) fibres. Fiber Chemistry 41(6):391 -401 Bae KP, Moo-Moo K (2010) Applications of chitin and its derivatives in biological

medicine. Int J Mol Sci 11:5152-5164 Bansal V, Pramod KS, Nitin S, Omprakask P, Malviya R (2011) Applications of

chitosan and chitosan derivatives for drug delivery. Adva Biol Res 5:28-37 Barkalow DG, Chapedelaine AH, Dzija MJ (2002) Improved pullulan free edible film compositions and methods of making same. PCT International Application WO 02/43657, US 01/43397, 21 Nov Bauer R (1938) Physiology of Dematium pullulans de Bary. Zentralbl Bacteriol

Parasitenkd Infektionskr Hyg Abt2 98:133-167 Bayram C, Denbas EB (2008) Preparation and characterization of triamcinolone acetonide-loaded poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBHx) microspheres. J Bioactive and Compatible Polymer 23:334-347

Bechthold I, Bretz K, Kabasci S, Kopitzky R, Springer A (2008) Succinic acid: a new platform chemical from biobased polymers from renewable resources. Chemical Engg Technol 31:647-654 Bernier B (1958) The production of polysaccharides by fungi active in the decomposition of wood and forest litter. Can J Microbiol 4:195-204 Bhatia A, Gupta RK, Bhattacharaya SN, Choi HJ (2007) Compatibility of

biodegradable PLA and PBS blends for packaging applications. Korea Aust Rheol J 19:125-131

Bisanda ETN, Ansell MP (1992) Properties of sisal-CNSL composites. J Mater Sci 27:1690-1700

Black WAP, Woodward FN (1954) Alginates from common British brown marine algae. In Natural plant hydrocolloids. Adv Chem Ser Am Chem Soc 11:83-91 Catley BJ (1971) Utilization of carbon sources by Pullularia pullulans for the elaboration of extracellular polysaccharides. Appl Microbiol 22:641-649 Chambin DC, Debray C, Rochat-Gonthier MH, Le MM, Pourcelot M (2004) Effects of different cellulose derivatives on drug release mechanism studied at a pre-formulation stage. J Controll Release 95(1):101 -108 Chandy T, Das GS, Rao GH (2000) 5-Fluorouracil-loaded chitosan coated polylactic acid microspheres as biodegradable drug carriers for cerebral tumours. J Microencapsul 5:625-631 Chen GQ, Qiong W (2005) The application of polyhydroxyalkanoates as tissue

engineering materials. Biomaterials 26:6565-6578 Chen GQ, Martin KP (2012) Plastics derived from biological sources: present and

future: a technical and environmental review. Chem Rev 112:2082-2099 Chen QZ, Harding SE, Ali NN, Lyon AR, Boccaccini AR (2008) Biomaterials in cardiac tissue engineering: ten years of research survey. Materials Sci Eng: Reports 59:1-37

Cheng KC, Demirci A, Catchmark JM (2011) Pullulan: biosynthesis, production,

and applications. Appl Microbiol Biotechnol 92:29-44 Cheng Y, Deng S, Chen P, Ruan R (2009) Polylactic acid (PLA) synthesis and

modifications: a review. Front Chem China 4:259-264 Clarinval AM, Halleux J (2005) Classification of biodegradable polymers. In: Smith R (ed)

Biodegradable polymers for industrial applications. Woodhead, Cambridge Conca KR, Yang TCS (1993) Edible food barrier coatings. In: Ching C, Kaplan DL, Thomas EL (ed) Biodegradable polymers and packaging. Technomic, Lancaster, pp 357-369 Cornelia TB, Erkan TB, Elisabete DP, Rui LR, Nuno MN (2011) Performance of biodegradable microcapsules of poly(butylene succinate), poly(butylene succinate-co-adipate) and poly(butylene terephthalate-co-adipate) as drug encapsulation systems. Colloids Surf B Biointerfaces 84:498-507 Coutu DL, Yousefi AM, Galipeau J (2009) Three-dimensional porous scaffolds at the crossroads of tissue engineering and cell-based gene therapy. J Cell Biochem 108:537-546 Dave AM, Mehta MH, Aminabhavi TM, Kulkarni AR, Soppimath KS (1999) A review on controlled release of nitrogen fertilizers through polymeric membrane devices. Polymer- Plastics Technol Eng 38:675-71 1 de Roo G, Kellerhals MB, Ren Q, Witholt B, Kessler B (2002) Production of chiral R-3-hydroxyalkanoic acids and R-3-hydroxyalkanoic acid methylesters via hydrolytic degradation of polyhydroxyalkanoate synthesized by pseudomonads. Biotechnol Bioeng 77:717-722

de Guzman D (2010) Bioplastic development increases with new applications. http:// Accessed October 2010 Dorozhkin SV (2009) Calcium orthophosphate-based biocomposites and hybrid

biomaterials. J Mater Sci 44:2343-2387 Doug S (2010) Bioplastics: technologies and global markets. BCC research reports PLS050A. Draget KI (2000) Alginates. In: Philips O, Williams A (ed) Handbook of

hydrocolloids. Woodhead, Philadelphia, p 379 Draget KI, Skjäk-Braek G, Smidsrod O (1997) Alginate based new materials. Int J

Biol Macromol 21:47-55 DSM press release (2008) DSM invests in development of bio-based materials. no_id=73274&seccion=mercado&id_categoria=80002. Accessed March 2008 Eichhorn SJ, Baillie CA, Zaferiropouls N, Mwaikambo LY, Ansell MP, Dufresne A, Entwistle KM, Herrera-Franco PJ, Escamilla GC, Groom L, Hughes M, Hill C, Rials TG, Wild PM (2001) Review: current international research into cellulosic fibres and composites. J Material Sc 36:2107-2131

Erwin TH, David AG, Jeffrey JK, Robert JW, Ryan PO (2007) The eco-profiles for current and near-future NatureWorks® polylactide (PLA) production. Industrial Biotechnology 3:58-81 Eslmai H, Kamal RM (2013) Elongational rheology of biodegradable poly(lactic acid)/poly[(butylene succinate)-co-adipate] binary blends and poly(lactic acid)/poly[(butylene succinate)-co-adipate]/clay ternary nanocomposites. J Appl Polym Sci 127:2290-2306 Espigares I, Elvira C, Mano JF, Vlazquez B, Roman JS, Reis RL (2002) New partially degradable and bioactive acrylic bone cements based on starch blends and ceramic fillers. Biomaterials 23(8):1883-1895 (2012) EU calls time on first-generation biofuels. http://www. Accessed Oct 2012 Frost & Sullivan report (2009) Global bio-based plastic market, M4AI-39. Chapter 5. ctxixpLink=FcmCtx9&searchQuery=Global+bio-based+plastic+market%2C +2009&bdata=aHR0cDovL3d3dy5mcm9zdC5jb20vc3JjaC9jYXRhbG9nLXNlYX JjaC5kbz9wdWJsaWNhdGlvblllYXJzPTIwMDkmcXVlcnlUZXh0PUdsb2 JhbCtiaW8tYmFzZWQrcGxhc3RpYyttYXJrZXQlMkMrMjAw0SZmaWx0ZXJT d2l0Y2g9ZmFsc2UmcGFnZVNpemU9MTJAfkBTZWFyY2ggUmVzdWx0c0B% 2BQDEzNjMxMDQzNjA1NjA%3D&ctxixpLabel=FcmCtx10&id=M4A1-01-00-00-00. Accessed 22 Dec 2009 Freier T, Kunze C, Nischan C (2002) In vitro and in vivo degradation studies for development of a biodegradable patch based on poly(3-hydroxybutyrate). Biomaterials 23:2649-2657 Fuentes Z, Riquelme MJN, Sánchez-Zapata E, Pérez JAÁ (2010) Resistant starch as

functional ingredient: a review. Food Res Int 43:931 -942 Garlotta D (2001) A literature review of poly (lactic acid). J Polyms and the Envir 9(2):63-84

Georg JM, Kristensen M, Astrup A (2012) Effect of alginate supplementation on weight loss in obese subjects completing a 12-week energy restricted diet: a randomized controlled trail. Am J Clin Nutr 96:5-13 Goh GH, Heng PWS, Chan LW (2012) Alginates as a useful natural polymer for

microencapsulation and therapeutic applications. Carbohydr Polym 88:1-12 Gomez-Guille MC, Gimenez B, Lopez CME, Montero MP (2011) Functional bioactive properties of collagen and gelatin from alternative sources: a review. Food Hydrocolloids 25:1813-1827 Guangwen C, Shulian L, Fengjun J, Quan Y (2007) Catalytic dehydration of bioethanol to ethylene over Ti02/y-Al203 catalyst in microchannel reactors. Catal today 125:111-119 Guo M, Liu M, Zhan F, Wu L (2005) Preparation and properties of a slow-release membrane-encapsulated urea fertilizer with superabsorbent and moisture preservation. Ind Eng Chem Res 44:4206-4211 Gupta B, Revagade N, Hilborn J (2007) Poly(lactic acid) fiber: an overview. Prog

Polym Sci 34:455-482 Hafdani FN, Sadeghinia N (2011) A review on applications of chitosan as a natural antimicrobial. World Academy of Sci Engg Technol 50:252-256 Hanggi JU (1995) Requirements on bacterial polyesters as future substitute for

conventional plastics for consumer goods. FEMS Microbioly Rev 16:213-220 Haung YM, Li H, Huang XJ, Hu YC, Hu Y (2008) Advances of bio-ethylene. Chin J

Bioprocess Eng 6:1 -6 Helga E, Svein V (1998) Biosynthesis and applications of alginates. Polym

Degradation and Stability 59:85-91 Helgerud T, Gaserod O, Fjreide T, Andresen PO, Larsen CK (2009) Alginates. In: Imeson A (ed) Food stabilisers, thickeners and gelling agents. Wiley Blackwell, Oxford, pp 50-72

Hirosawa E, Danjo K, Sunada H (2000) Influence of granulating method on physical and mechanical properties, compression behavior, and compactibility of lactose and microcrystalline cellulose granules. Drug Dev Ind Pharm 26:583-593 Hori K, Nojiri H, Nonomura M, Okuda F, Yanagida H, et al. (2005) Allergen

inactivator. US Patent 197319, 20 Nov 2005 Huan Z, Joseph GL, Sarit BB (2012) Fabrication aspects of PLA-CaP/PLGA-CaP

composites for orthopedic applications: a review. Acta Biomater 8(6):1999-2016 Iain AB, Seal CJ, Wilcox M, Dettmar PW, Pearson PJ (2009) Applications of alginates in food. In: Brend HAR (ed) Alginates: biology and applications. Microbiology monographs 13. Springer, Hiedelberg, pp 211-228 Jane J (1995) Starch properties, modifications and applications. J Macromolecular Sci 32:751 -757

Jaspreet S, Lovedeep K, McCarthy OJ (2007) Factors influencing the physico-chemical, morphological, thermal and rheological properties of some

chemically modified starches for food applications—a review. Food Hydrocolloids 21:1-22 Jayanth P, Vinod L (2012) Biodegradable nanoparticles for drug and gene

delivery to cells and tissue. Adv Drug Deliv Rev 64:61 -71 Jeevitha D, Kanchana A (2013) Chitosan/PLA nanoparticles as a novel carrier for the delivery of anthraquinone: synthesis, characterization and in vitro cytotoxicity evaluation. Colloids Surf B Biointerfaces 101(1):126-134 Jian-Bing Z, Ling J, Yi-Dong L, Madhusudhan S, Tao L, Yu-Zhong W (2011) Bio-based blends of starch and poly(butylene succinate) with improved miscibility, mechanical properties, and reduced water absorption. Carbohydr Polym 83:762-768

Johnston-Banks FA (1990) Gelatin. In: Harris P (ed) Food gels. Elsevier, London, pp 233-289

Jong ED, Higson A, Walsh P, Maria W (2010) Bio-based chemicals: value added products from biorefineries. IEA Bioenergy Task 42 Biorefinery:1-34. http:// eID=dam_frontend_push&docID=2051. Accessed 15 Feb 2012 Jun X, Bao-Hua G (2010a) Microbial succinic acid, its polymer poly(butylene

succinate), and applications. Microbiology Monographs 14:347-388 Jun X, Bao-Hua G (2010b) Poly(butylene succinate) and its copolymers: research,

development and industrialization. Biotechnol J 5:1149-1163 Jung S, Lim E, Jong HK (2009) New application of poly(butylene succinate) (PBS) based ionomer as biopolymer: a role of ion group for hydroxyapatite (HAp) crystal formation. J Mater Sci 44:6398-6403 Jung-Ju K, Guang-Zhen J, Hye-Sun Y, Seong-Jun C, Hae-Won K, Ivan BW (2012) Providing osteogenesis conditions to mesenchymal stem cells using bioactive nanocomposite bone scaffolds. Mater Sci Eng C 32:2545-2551 Kamel S, Ali N, Jahangir K, Shah SM, El-Gendy (2008) Pharmaceutical significance

of cellulose: a review. Express polymer Letters 2:758-778 Kasirajan S, Ngouajio M (2012) Polyethylene and biodegradable mulches for

agricultural applications: a review. Agronomy Sustainable Dev 32(2):501-529 Kathiraser Y, Aroua MK, Ramachandran KB, Tan IKP (2007) Chemical

characterization of medium-chain-length polyhydroxyalkanoates (PHAs) recovered by enzymatic treatment and ultrafiltration. J Chem Tech Biotech 82:847-855

Kellomaki M, Niiranen H, Puumanen K, Ashammakhi N, Waris T, Tormala P (2000) Bioabsorbable scaffolds for guided bone regeneration and generation. Biomaterials 21:2495-2505 Kevin JE, Charles MB, John DS, Paul AR, Brian DS, Michael CS, Debra T (2001) Advances in cellulose eater performance and applications. Progress in Polymer Sci 26:1605-1688 Kumano A, Fujiwara N (2008) Cellulose triacetate membranes for reverse osmosis. In: Normam AGF, Li N, Winston Ho WS, Matsuura T (ed) Advanced membrane technology and application. Wiley, New Jersey, pp 21-43 Kumbar SG, Kulkarni AR, Dave AM, Aminabha TM (2001) Encapsulation efficiency and release kinetics of solid and liquid pesticides through urea formaldehyde cross-linked starch, guar gum, and starch + guar gum matrices. J Appli Polym Sci 82:2863-2866

Kunze C, Edgar Bernd H, Androsch R (2006) In vitro and in vivo studies on blends of isotactic and atactic poly (3-hydroxybutyrate) for development of a dura substitute material. Biomaterials 27:192-201 Leathers TD (2003) Biotechnological production and applications of pullulan.

Appl Microbiol Biotechnol 62:468-473 Lee SH, Wang S (2006) Biodegradable polymers/bamboo fiber composite with

bio-based coupling agent. Compos Part A37:80-91 Lee HC, Anuj S, Lee Y (2001) Biomedical applications of collagen. International J

of Pharmaceutics 221:1 -22 Lemoigne M (1923) Production d'acide p-oxybutyrique par certaines bact'eries

du groupe du Bacillus subtilis. CR. Hebd. Seances Acad. Sci 176:1761 Levison PR (1993) Cellulosics as ion-exchange materials. In: Kennedy JF, Phillips GO, Williams PA (ed) Cellulosics: materials for selective separations and other technologies. Ellis Horwood, Chichester, pp 25-36 Li G, Yong H, Chen C (2011) Discussion on application prospect of starch-based

adhesives on architectural gel materials. Adv Materials Res 250:800-803 Li S, Juliane H, Martin KP (2009) Product overview and market projection of

emerging biobased products. PRo-BIP 1:1 -245 Liu L, Yu J, Cheng L, Qu W (2009a) Mechanical properties of poly(butylene succinate) (PBS) biocomposites reinforced with surface modified jute fibre. Composites Part A: Appl Sci Manufacturing 40:669-674 Liu LF, Yu JY, Cheng LD, Yang XJ (2009b) Biodegradability of PBS composite reinforced with jute. Polym Degrade Stab 94:90-94

Liu M, Zhang Y, Wu C, Xiong S, Zhou C (2012) Chitosan/halloysite nanotubes bionanocomposites: structure, mechanical properties and biocompatibility. Int J Biological Macromol 51:566-575 Luc A, Eric P (2012) Biodegradable polymers. In: Environmental silicate nano-

biocomposites. Green energy and technology. Springer, Hiedelberg, pp 13-39 Luiz A, De Castro R, Morschbacker (2010) A method for the production of one or

more olefins, an olefin, and a polymer. US 2010/0069691A1, 18 Mar 201C Maeda M, Tani S, Sano A, Fujioka K (1999) Microstructure and release

characteristics of the minipellet, a collagen based drug delivery system for controlled release of protein drugs. J Controlled Rel 62:313-324 Mainil V, Rahn B, Gogolewski S (1997) Long-term in vivo degradation and bone reaction to various polylactides: 1. One-year results. Biomaterials 18:257-266 McChalicher CW, Srienc F (2007) Investigating the structure-property relationship

of bacterial PHA block copolymers. J Biotechnology 132:296-302 Ravi Kumar MNV (2000) A review of chitin and chitosan applications. Reactive

Functional Polym 46:1 -27 Majid J, Elmira AT, Muhammad I, Muriel J, St'ephane D (2010) Poly-lactic acid: production, applications, nanocomposites, and release studies. Comprehensive Rev Food Sci Safety 9(5):552-571 Mandel KG, Daggy BP, Brodie DA, Jacoby HI (2000) Review article: alginate-raft formulations in the treatment of heartburn and acid reflux. Aliment Pharmacol Ther 14:669-690 Marguerite R (2006) Chitin and chitosan: properties and applications. Progress in

Polym Sci 31:603-632 Marques AP, Reis RL (2005) Hydroxyapatite reinforcement of different starch-based polymers affect osteoblast-like cells adhesion/spreading and proliferation. Mater Sci Engg 25(2):215-229 Maurizio A, Jan JDV, Maria EE, Sabine F, Paolo V, Maria GV (2005) Biodegradable starch/clay nanocomposite films for food packaging applications. Food Chem 93(3):467-474 Mendes RL, Reis YP, Bovell AM, Cunha CA, Blitterswijk V, de Bruijn JD (2001)

Biocompatibility testing of novel starch-based materials with potential application in orthopedic surgery: a preliminary study. Biomaterials 22:2057-2064 Michael C, Dirk C, Harald K, Jan R, Joachim V (2011) Policy paper on bio-based economy in the EU: level playing field for bio-based chemistry and materials.. Accessed December 2012 Nagarwal RC, Singh PN, Kant S, Maiti P, Pandit JK (2010) Chitosan coated PLA nanoparticles for ophthalmic delivery: characterization, in-vitro and in-vivo study in rabbit eye. J Biomed Nanotechnol 6:648-656 Nicolas J, Floriane F, Francoise F, Alan R, Jean PP, Patrick F, Rene SL (2011) Synthesis and properties of poly(butylene succinate): efficiency of different transesterfication catalysts. J Polym Sci Part A: Polym Chem 49:5301-5312 Obae HI, Imada K (1999) Morphological effect of microcrystalline cellulose

particles on tablet tensile strength. Int J Pharm 182:155-164 Onsoyen E (1996) Commercial applications of alginates. Carbohydrates in Europe 14:26-31

Orawan S, Uracha R, Pitt S (2008) Electrospun cellulose acetate fiber mats containing asiaticoside or Centella asiatica crude extract and the release characteristics of asiaticoside. Polymer 49(19):4239-4247 Ozdemir M, Floros JD (2004) Active food packaging technologies. Crit Rev Food Sci Nutr 44:185-193

Papenburg BJ, Liu J, Higuera G, Barradas AMC, Boer J, Blitterswijk VCA, Wessling M, Stamatialis D (2009) Development and analysis of multi-layer scaffolds for tissue engineering. Biomaterials 30:6228-6239 Peter WD, Vicki S, Richardson JC (2011) The key role alginates play in health.

Food Hydrocolloids 25:263-266 Philip S, KeshavarzT, Roy I (2007) Polyhydroxyalkanoates: biodegradable

polymers with a range of applications. J Chemical Tech Biotech 2(3):233-247 Picker KM, Hoag SW (2002) Characterization of the thermal properties of microcrystalline cellulose by modulated temperature differential scanning calorimetry. J Pharmaceutical Sci 91:342-349 Prashant RC, Ishwar BB, Shrikant AS, Rekha SS (2009) Microbial cellulose: fermentive

production and applications. Food Technol Biotechnol 47:107-124 Qin Y, Cai L, Feng D, Shi B, Liu J, Zhang W, Shen Y (2007) Combined use of chitosan and alginate in the treatment of waste water. J Appl Polym Sci 104:3181 -3587 Rafael A, Loong TL, Susan EM, Selke HT (2010) Poly(lactic acid): synthesis, structures,

properties, processing and applications. Chapter 28:457-467 Rajev AJ (2000) The manufacturing techniques of various drug loaded biodegradable poly(lactide-co-glycolide) (PLGA) devices. Biomaterials 21:2475-2490

Ramya R, Venkatesan, Jayachanndran Kim S, Sudha PN (2012) Biomedical

applications of chitosan: an overview. J Biomaterial Tissue Engg 2:100-111 Ravenstijn JTJ (2010) The state-of-the art on bioplastics: products, markets, trends

and technologies. Polymedia, Lüdenscheid Ray SS, Bousmina M (2005) Biodegradable polymers and their layered silicate nanocomposites: in greening the 21st century materials world. Progress Material Sci 50:962-1079 Reis KC, Pereira J, Smith AC, Carvalho CWP, Wellner N, Yakimets I (2008) Characterization of polyhydroxybutyrate-hydroxyvalerate (PHB-HV)/maize starch blend films. J Food Engg 89:361-369 Rekha MR, Chrndra PS (2007) Pullulan as a promising biomaterial for biomedical

applications: a perspective. Trends in Biomaterials and Artificial Organs 20:21-45 Roberts GAF (1997) Chitosan production routes and their role in determining the structure and properties of the product. In: Domard M, Roberts AF, Värum KM (ed) Advances in Chitin Science, vol. 2, National Taiwan Ocean University, Taiwan. Jacques Andre, Lyon, pp 22-31. 1998 Rubin AL, Stenzel KH, Miyata T, White MJ, Dune M (1973) Collagen as a vehicle for drug delivery: preliminary report. J of Clinical Pharmacology 13:309-312 Ruth KG, Hartmann R, Egli T, Zinn M, Ren Q (2007) Efficient production of (R)-3-hydroxycarboxylic acids by biotechnological conversion of polyhydroxyalkanoates and their purification. Biomacromolecules 8:279-286 Savenkova L, Gercberga Z, Nikolaeva V, Dzene A, Bibers I, Kalina M (2000)

Mechanical properties and biodegradation characteristics of PHB-based films. Process Biochem 35:537-579 Schmidmaier G, Wildemann A, Stemberger A, Has MR (2001) Biodegradable poly (D, L-lactide) coating of implants for continuous release of growth factors. J Biomed Mater Res 58:449-455 Sena RF, Costelli MC, Gibson LH, Coughlin RW (2006) Enhanced production of pullulan by two strains of A. pullulans with different concentrations of soybean oil in sucrose solution in batch fermentations. Brazilian J Chem Eng 2:507-515

Siddhesh NP, Edgar KJ (2012) Alginate derivatization: a review chemistry,

properties and applications. Biomaterials 33:3279-3305 Singh RS, Saini GK, Kennedy JF (2008) Pullulan: microbial sources, production and

applications. Carbohydr Polym 73:515-531 Sodian R, Hoerstrup SP, Sperling JS, Daebritz S, Martin DP, Moran AM, Kim BS, Schoen FJ, Vacanti JP, Mayer JE (2000) Early in vivo experience with tissue engineered trileaflet heart valves. Circulation 102:22-29 Sodian R, Sperling JS, Martin DP (1999) Tissue engineering of a trileaflet heart valve-

early in vitro experiences with a combined polymer. Tissue Engg 5:489-494 Steinbüchel A, Valentin HE (1995) Diversity of bacterial polyhydroxyalkanoic acids.

FEMS Microbiol Lett 128:219-228 Tang H, Ishii D, Mahara A, Murakami S, Yamaoka T, Sudesh K, Samian R, Fujita M, Maeda M, Iwata T (2008) Scaffolds from electrospun polyhydroxyalkanoate copolymers: fabrication, characterization, bio absorption and tissue response. Biomaterials 29:1307-1317 Teli MD, Chiplunkar V (1986) Role of thickeners in final performance of reactive

prints. Textile Dyer Printer 19:13-19 Türesin F, Gürsel I, Hasirci V (2001) Biodegradable polyhydroxyalkanoate implants for osteomyelitis therapy: in vitro antibiotic release. J Biomaterials Sci 12 (2):195-207. Polymer Edition Valantin MA, Aubron-Olivier C, Ghosn J, Laglenne E, Pauchard M, Schoen H (2003) Polylactic acid implants to correct facial lipoatrophy in HIV-infected patients: results of the open-label study. Vega Aids 17:2471 -2477 Valappil S, Misra S, Boccaccini A, Roy I (2006) Biomedical applications of

polyhydroxyalkanoates, an overview of animal testing an in vivo responses. Expert Rev Med Devices 3:853-868 Valerie D, Vinod DV (1998) Pharmaceutical applications of chitosan.

Pharmaceutical Sci Technol Today 1:246-253 Virginia E, Marie G, Eric P, Luc A (2011) Structure and properties of glycerol plasticized

chitosan obtained by mechanical kneading. Carbohydrate Polym 83:947-952 Volova T, Shishatskaya E, Sevastianov V, Efremov S, Mogilnaya O (2003) Results of

biomedical investigations of PHB and PHB/PHV fibers. Biochem Eng J 16:125-133 Vona IA, Costanza JR, Cantor HA, Robert WJ (1965) Manufacture of plastics, vol 1. Wiley,

New York, pp 141-142 Walle GAM, de Koning GJM, Weusthuis RA, Eggink G (2001) Properties, modifications and applications of biopolyesters. Adv Biochem Eng Biotechnol 71:264-291 Wang Z, Itoh Y, Hosaka Y, Kobayashi I, Nakano Y, Maeda I, Umeda F, Yamakawa J, Kawase M, Yagi K (2003) Novel transdermal drug delivery system with

polyhydroxyalkanoate and starburst polyamidoamine dendrimer. J Biosci and Bioengg 95(5):541 -543 Weraporn PA, Sorapong P, Narongchai OC, Ubon I, Puritud J, Sommai PA (2011) Preparation of polymer blends between poly (L-lactic acid), poly (butylene succinate-co-adipate) and poly (butylene adipate-co-terephthalate) for blown film industrial application. Energy Procedia. 9:581-588 Westermark S, Juppo AM, Kervinen L, Yliruusi J (1999) Microcrystalline cellulose and its microstructure in pharmaceutical processing. Eur J Pharm Biopharm 48:199-206

Williams SF, Martin DP, Horowitz DM, Peoples OP (1999) PHA applications: addressing the price performance issue I. Tissue engineering. Int J Biol Macromolecules 25:111-121 Win NN, Stevens WF (2001) Shrimp chitin as substrate for fungal chitin

deacetylase. Appl Microbiol Biotechnol 57:334-341 Xie ZP, Huang Y, Chen YL, Jia Y (2001) A new gel casting of ceramics by reaction of sodium alginate and calcium iodate at increased temperature. J Mat Sci Lett 20:1255-1257

Yan YF, Krishnaiah D, Rajin M, Bono A (2009) Cellulose extraction from palm

kernel cake using liquid phase oxidation. J Engg Sci Tech 4:57-68 Yang F, Li X, Li G, Zhao N, Zhang X (2002) Study on chitosan and PHBHHx used

as nerve regeneration conduit material. J Biomedical Engg 19:25-29 Zajic JE, LeDuy A (1973) Flocculant and chemical properties of a polysaccharide

from Pullularia pullulans. Appl Microbiol 25:628-635 Zeeshan K, Gopiraman M, Yuichi H, Kai W, Kim IS (2013) Cationic-cellulose

nanofibers: preparation and dyeability with anionic reactive dyes for apparel application. Carbohydrate 91:434-443 Zhao RX, Torley P, Halley PJ (2008) Emerging biodegradable materials: starch-

and protein-based bio-nanocomposites. J Mat Sci 43:3058-3071 Zhao K, Tian G, Zheng Z, Chen JC, Chen GQ (2003) Production of D-(-)-3-hydroxyalkanoic acid by recombinant Escherichia coli. FEMS Microbiol Lett 218:59-64

Zhao P, Liu W, Wu Q, Ren J (2010) Preparation, mechanical, and thermal properties of biodegradable polyesters/poly(lactic acid) blends. J of Nanomaterials 2010:1-8


Cite this article as: Babu et al.: Current progress on bio-based polymers and their future trends. Progress in Biomaterials 2013 2:8.

Submit your manuscript to a SpringerOpen journal and benefit from:

7 Convenient online submission 7 Rigorous peer review 7 Immediate publication on acceptance 7 Open access: articles freely available online 7 High visibility within the field 7 Retaining the copyright to your article

Submit your next manuscript at 7