Degradable Synthetic Biopolymers in Medicine

Drumright RE, Gruber PR, Henton DE. Polylactic Acid Technology. Advanced Materials; 2000;12(23): 1841–1846. doi.org/10.1002/1521-4095(200012)12:23<1841::AID-ADMA1841>3.0.CO;2-E

Van de Velde K, Kiekens P. Biopolymers: overview of several properties and consequences on their applications, Department of Textiles, Ghent University; 2002;21: 433–442. doi.org/10.1016/S0142-9418(01)00107-6

Hartmann MH. High Molecular Weight Polylactic Acid Polymers. In: Kaplan, D.L. (eds) Biopolymers from Renewable Resources. Macromolecular Systems — Materials Approach. Springer, Berlin, Heidelberg, 1998.

Nijenhuis AJ, Du YJ, Van Aert HAM, Bastiaansen C. ABA Type Copolymers of Lactide with Poly(ethylene glycol). Kinetic, Mechanistic, and Model Studies. Macromolecules; 1995;28(7): 2124-2132. doi.org/10.1021/ma00111a004

Lasprilla AJR, Martinez GAR, Lunelli BH, Jardini AL, Filho RM. Poly-lactic acid synthesis for application in biomedical devices. A review. Biotechnology Advances; 2012;30(1):321–328. doi.org/10.1016/j.biotechadv.2011.06.019

Fukushima K, Kimura Y. Stereocomplexed polylactides (Neo-PLA) as high-performance bio-based polymers: their formation, properties, and application. Polymer International; 2006;55(6):626–642. https://doi.org/10.1002/pi.2010

Tracy MA, Ward KL. Firouzabadian, L.; Wang, Y.; Dong, N.; Qian, R.; Zhang, Y. Factors affecting the degradation rate of poly (lactide-co-glycolide) microspheres in vivo and in vitro. Biomaterials; 1999;20(11): 1057–1062. https://doi.org/10.1016/S0142-9612(99)00002-2

Liu L, Li S, Garreau H, Vert M. Selective Enzymatic Degradations of Poly(l-lactide) and poly(E-caprolactone) blend films. Biomacromolecules; 2000;1(3): 350–359. doi.org/10.1021/bm000046k

Soni S, Gupta H, Kumar N, Nishad D, Mittal G, Bhatnagar A. Biodegradable biomaterials; 2010;3(1): 30–40.

Nakafuku C, Yoshimura H. Melting parameters of poly(glycolic acid). Polymer (Guildf); 2004;45(11): 3583–3585. doi.org/10.1016/j.polymer.2004.03.041

Polyglycolic Acid (PGA) Market Research Report - Global Forecast till 2030. https://www.marketresearchfuture.com/reports/ polyglycolic-acid-market-5749 (Accessed: August 2023)

Jahno VD. Síntese e caracterização do Poli (L-Ácido Láctico) para uso como biomaterial, 2005.

Nair LS, Laurencin CT. Biodegradable polymers as biomaterials. Progress in Polymer Science; 2007;32(8-9):762–98. doi.org/10.1016/j.progpolymsci.2007.05.017

Hayashi T. Biodegradable polymers for biomedical uses. Progress in Polymer Science; 1994;19(4): 663–702. doi.org/10.1016/0079-6700(94)90030-2

Sinha VR, Bansal K, Kaushik R, Kumria R, Trehan A. Poly-ϵ-caprolactone microspheres and nanospheres: an overview. International Joyrnal of Pharmaceutics; 2004;278(1): 1–23. doi.org/10.1016/j.ijpharm.2004.01.044

Woodruff MA, Hutmacher DW. The return of a forgotten polymer—Polycaprolactone in the 21st century. Progress in Polymer Science; 2010;35(10): 1217–1256. doi.org/10.1016/j.progpolymsci.2010.04.002

Lohmeijer BGG, Pratt RC, Leibfarth F, Logan JW, Long DA, Dove AP, Nederberg F, Choi Wade C, Waymouth RM, Hedrick JL. Guanidine and amidine organocatalysts for ring-opening polymerization of cyclic esters. Macromolecules; 2006;39(25): 8574–8583. doi.org/10.1021/ma0619381

Yuan M, Xiong C, Deng X. Ring‐opening polymerization of ε‐caprolactone initiated by cyclopentadienyl sodium. Journal of Applied Polymer Science; 1998;67(7): 1273–1276. doi.org/10.1002/(SICI)1097-4628(19980214)67:7<1273::AID-APP17>3.0.CO;2-2

Kowalski A, Duda A, Penczek S. Kinetics and Mechanism of Cyclic Esters Polymerization Initiated with Tin(II) Octoate. 3.† Polymerization of l,l-Dilactide. Macromolecular Rapid Communications; 2000;33(20) 77359-7370. doi.org/10.1021/ma000125o

Yamashita M, Takemoto Y, Ihara E,Yasuda H., Organolanthanide-Initiated Living Polymerizations of ε-Caprolactone, δ-Valerolactone, and β-Propiolactone. Macromolecules; 1996;29(5), 1798-1806. doi.org/10.1021/ma951400n

Williams MD, Rahn JA, Sherman DH. Production of a polyhydroxyalkanoate biopolymer in insect cells with a modified eucaryotic fatty acid sythase. Applied and Environmental Microbiology; 1996;62(7): 2540-2546. doi.org/10.1128/aem.62.7.2540-2546.1996

Patnaik P. "Intelligent" descriptions of microbial kinetics in finitely dispersed bioreactors: neural and cybernetic modelsfor PHB biosynthesis by Ralstonia eutropha. Microbial Cell Factories; 2007;6: 23-25. doi.org/10.1186/1475-2859-6-23

Lee C, Song B, Jegal J, Kimura Y. Cell adhesion and surface chemistry of biodegradable aliphatic polyesters: discovery of particularly low cell adhesion behavior on poly (3-RS.-hydroxybutyrate. Macromolecular Research; 2003;21: 305–1313. doi.org/10.1007/s13233-013-1181-8

Simon F, Martin DP. Applications of PHAs in medicine and pharmacy. In: Y. Doi, A. Steinbuchel (eds) Biopolymers, 4th edn. Wiley-VCH, Weinham; 2002;91–103.

Yagmurlu MF, Korkusuz F, Gursel I, Korkusuz P, Ors U, Hasirci V. Sulbactamcefoperazone polyhydroxybutyrate-co-hydroxyvalerate (PHBV) local antibiotic delivery system: in vivo effectiveness and biocompatibility in the treatment of implant-related experimental osteomyelitis. Journal of Biomedical Materials Research; 1999; 46(4): 494–503. doi.org/10.1002/(SICI)1097-4636(19990915)46:4<494::AID-JBM7>3.0.CO;2-E

Xu J, Guo BH. Poly(butylene succinate) and its copolymers: Research, development and industrialization. Biotechnology Journal; 2010;5(11): 1149–1163. doi.org/10.1002/biot.201000136

Ishioka R, Kitakuni E, Ichikawa Y. Aliphatic polyesters: “Bionolle”. In: Doi,Y., Steinbüchel,A. (Eds.), Biopolymers, Polyesters III Applications and Commercial Products; 2002;4:275–297. doi.org/10.1002/3527600035.bpol4010

Platnieks O, Gaidukovs S, Thakur VK, Barkane A, Beluns S. Bio-based poly (butylene succinate): Recent progress, challenges and future opportunities. European Polymer Journal; 2021;161:110855. doi.org/10.1016/j.eurpolymj.2021.110855.

Mtibe A, Muniyasamy S, Mokhena TC, Ofosu O, Ojijo V, John M. Recent insight into the biomedical applications of polybutylene succinate and polybutylene succinate-based materials. Express Polymer Letters; 2023;17(1): 2–28. doi.org/10.3144/expresspolymlett.2023.2

Cicero L, Licciardi M, Cirincione R, Puleio R, Giammona G, Giglia G, Sardo P, Vigni GE, Cioffi A, Sanfilippo A, Cassata G. Polybutylene succinate artificial scaffold for peripheral nerve regeneration. Journal of Biomedical Materials Research Part B Applied Biomaterials; 2022;110(1): 125–134. doi.org/10.1002/jbm.b.34896

Mtibe A, Motloung MP, Bandyopadhyay J, Ray SS. Synthetic biopolymers and their composites: Advantages and limitations – An Overview. Macromolecular Rapid Communications; 2021;42(15): 2100130. doi.org/10.1002/marc.202100130

Das R, Kundu D. Structural and Transport Properties of Norbornene-Functionalized Poly(vinyl alcohol) “Click” Hydrogel: A Molecular Dynamics Study. ACS Sustainable Chemistry & Engineering; 2023;11(29): 10812-10824. doi.org/10.1021/acssuschemeng.3c01948

Hassan CM, Peppas NA. Structure and Applications of Poly(vinyl alcohol) Hydrogels Produced by Conventional Crosslinking or by Freezing/Thawing Methods. In: Biopolymers · PVA Hydrogels, Anionic Polymerisation Nanocomposites. Advances in Polymer Science; 2000;153:37-65. doi.org/10.1007/3-540-46414-X_2

Wan WK, Campbell G, Zhang ZF, Hui AJ, Boughner DR. Optimizing the tensile properties of polyvinyl alcohol hydrogel for the construction of a bioprosthetic heart valve stent. Journal of Biomedical Materials Research; 2002;63(6): 854-61. doi.org/10.1002/jbm.10333

Peppas NA, Benner RE. Proposed method of intracordal injection and gelation of poly (vinyl alcohol) solution in vocal cords: polymer considerations. Biomaterials; 1980;1(3):158-62. doi.org/10.1016/0142-9612(80)90039-3

Paul W, Sharma CP. Polyacrylonitrile-reinforced poly(vinyl alcohol) membranes: Mechanical and dialysis performance. Journal of Applied Polymer Science; 1995;57(12): 1447–1454. doi.org/10.1002/app.1995.070571204

https://www.rxlist.com/ (access date:08.16.2023)

McNeil C, Basan S. Thermal degradation of blends of PVC with poly(ethylene adipate). Polymer Degradation and Stability; 1993;41(3): 311-17. doi.org/10.1016/0141-3910(93)90077-V

Monvisade P, Loungvanidprapa P. Synthesis of poly(ethylene adipate) and poly(ethylene adipate-co-terephthalate) via ring-opening polymerization. European Polymer Journal; 2007;43(8): 3408-3414. doi.org/10.1016/j.eurpolymj.2007.05.009

Chen L, Xu J, Xue W, Zeng Z. Mechanism and kinetics of esterification of adipic acid and ethylene glycol by tetrabutyl titanate catalyst. Korean Journal of Chemical Engineering; 2017;35(1): 82–88. doi.org/10.1007/s11814-017-0276-x

Jin HJ, Lee BY, Kim MN,Yoon JS. Properties and biodegradation of poly(ethylene adipate) and poly(butylene succinate) containing styrene glycol units. European Polymer Journal; 2000;36(12): 2693–2698. https://doi.org/10.1016/S0014-3057(00)00057-4

Atanase LI, Salhi S, Cucoveica O, Ponjavic M, Nikodinovic-Runic J, Delaite C. Biodegradability Assessment of Polyester Copolymers Based on Poly(ethylene adipate) and Poly(ε-caprolactone). Polymers; 2022;14(18): 3736. https://doi.org/10.3390/polym14183736

Atkins TW. Biodegradation of poly(ethylene adipate) microcapsules in physiological media. Biomaterials; 1998;19(1–3): 61-67. https://doi.org/10.1016/S0142-9612(97)00156-7

Anthierens T, Billiet L, Devlieghere F, Du Prez F. Poly(butylene adipate) functionalized with quaternary phosphonium groups as potential antimicrobial packaging material. Innovative Food Science & Emerging Technologies, 2012;15: 81–85. https://doi.org/10.1016/j.ifset.2012.02.010

Bikiaris D, Karavelidis V, Karavas E. Novel Biodegradable Polyesters. Synthesis and Application as Drug Carriers for the Preparation of Raloxifene HCl Loaded Nanoparticles. Molecules; 2009;14(7): 2410-2430. https://doi.org/10.3390/molecules14072410

Rahimpour A, Madaeni SS, Mehdipour-Ataei S. Synthesis of a novel poly (amide-imide)(PAI) and preparation and characterization of PAI blended polyethersulfone (PES) membranes. Journal of Membrane Science; 2008;311(1–2):349–359. https://doi.org/10.1016/j.memsci.2007.12.038

https://omnexus.specialchem.com/selection-guide/polyethersulfone-pesthermoplastic/key-applications (access date: 09.02.2023)

Burg KJL, Shalaby SW. PES and PEEK. Encyclopedia of Materials: Science and Technology; 2001;6837–6839. 10.1016/B0-08-043152-6/01212-2

Lelah MD, Cooper JL. Polyurethanes in Medicine. Boca Raton, FL: CRC Press, ISBN: 0849363071,1987.

Tatai L, Moore TG, Adhikari R, Malherbe F, Jayasekara R, Griffiths I, Gunatillake PA. Thermoplastic biodegradable polyurethanes: The effect of chain extender structure on properties and in-vitro degradation. Biomaterials; 2007;28(36): 5407–5417. doi.org/10.1016/j.biomaterials.2007.08.035

Cohn D, Lando G, Sosnik A, Garty S, Levi A. PEOPPO-PEO-based poly(ether ester urethane)s as degradable reverse thermo-responsive multiblock copolymers. Biomaterials; 2006;27(9): 1718. https://doi.org/10.1016/j.biomaterials.2005.10.035

Loomis K, McNeeley K, Bellamkonda V. Nanoparticles with targeting, triggered release, and imaging functionality for cancer applications. Soft Matter; 2011;7(3): 839–856. DOI: 10.1039/c0sm00534g

Guelcher SA. Biodegradable Polyurethanes: Synthesis and Applications in Regenerative Medicine. Tissue Engineering Part B: Reviews, 2008;14(1): 3–17. doi.org/10.1089/teb.2007.0133

Santerre JP, Woodhouse K, Laroche G, Labow RS. Understanding the biodegradation of polyurethanes: From classical implants to tissue engineering materials. Biomaterials; 2005;26: 7457–7470. https://doi.org/10.1016/j.biomaterials.2005.05.079

Ding M, Li J, Tan H, Fu Q. Self-assembly of biodegradable polyurethanes for controlled delivery applications. Soft Matter; 2012;8(20): 5414. DOI: 10.1039/c2sm07402h

Kurakula M, Rao GSNK. Type of Article: REVIEW Pharmaceutical Assessment of Polyvinylpyrrolidone (PVP): As Excipient from Conventional to Controlled Delivery Systems with a Spotlight on COVID-19 Inhibition. Journal of Drug Delivery Science and Technology; 2020;60: 102046. https://doi.org/10.1016/j.jddst.2020.102046

Christensen M, Johansen P, Hau C. Storage of polyvinylpyrrolidone (PVP) in tissues following long-term treatment with a PVP-containing vasopressin preparation. Acta Medica Scandinavica; 1978;204(1-6): 295–298. https://doi.org/10.1111/j.0954-6820.1978.tb08442.x

Bühler V. Polyvinylpyrrolidone – Excipients for Pharmaceuticals: Povidone, Crospovidone and Copovidone, Illustrate, Springer-Verlag, Berlin Heidelberg, New York, 2005;67.