ABA-triblock copolymers from biodegradable polyester A-blocks and hydrophilic poly(ethylene oxide) B-blocks as a candidate for in situ forming hydrogel delivery systems for proteins.
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[1] J. M. Harris,et al. Introduction to Biotechnical and Biomedical Applications of Poly(Ethylene Glycol) , 1992 .
[2] G. Winter,et al. Biodegradable recombinant human erythropoietin loaded microspheres prepared from linear and star-branched block copolymers: influence of encapsulation technique and polymer composition on particle characteristics. , 1999, Journal of controlled release : official journal of the Controlled Release Society.
[3] H. Ravivarapu,et al. Sustained suppression of pituitary-gonadal axis with an injectable, in situ forming implant of leuprolide acetate. , 2000, Journal of pharmaceutical sciences.
[4] Michel Vert,et al. STRUCTURE – PROPERTY RELATIONSHIP IN THE CASE OF THE DEGRADATION OF MASSIVE ALIPHATIC POLY – (-HYDROXY ACIDS) IN AQUEOUS MEDIA, PART 1: DEGRADATION OF LACTIDE - GLYCOLIDE COPOLYMERS: PLA 37.5 GA 25 AND PLA 75 GA 25 , 1990 .
[5] L. Youxin,et al. Biodegradable block copolymer matrices for long-acting contraceptives with constant release. , 1992 .
[6] H. Hopfenberg,et al. Swelling‐controlled, constant rate delivery systems , 1978 .
[7] Xiaohong Li,et al. In Vitro Protein Release and Degradation of Poly-dl-lactide-poly(ethylene glycol) Microspheres with Entrapped Human Serum Albumin: Quantitative Evaluation of the Factors Involved in Protein Release Phases , 2004, Pharmaceutical Research.
[8] Kazutoshi Nozaki,et al. A biodegradable polymer as a cytokine delivery system for inducing bone formation , 2001, Nature Biotechnology.
[9] A. Skoulios,et al. Synthèse et caractérisation de copolymères séquencés polyoxyéthylène/poly-ε-caprolactone† , 1972 .
[10] M Morlock,et al. Erythropoietin loaded microspheres prepared from biodegradable LPLG-PEO-LPLG triblock copolymers: protein stabilization and in-vitro release properties. , 1998, Journal of controlled release : official journal of the Controlled Release Society.
[11] J. Feijen,et al. Freeze-Drying and Lyopreservation of Diblock and Triblock Poly(Lactic Acid)–Poly(Ethylene Oxide) (PLA–PEO) Copolymer Nanoparticles , 2000, Pharmaceutical development and technology.
[12] J. Kovarova,et al. Microdomain structure in polylactide-block-poly(ethylene oxide) copolymer films. , 2000, Biomaterials.
[13] M. Lück,et al. Plasma protein adsorption on biodegradable microspheres consisting of poly(D,L-lactide-co-glycolide), poly(L-lactide) or ABA triblock copolymers containing poly(oxyethylene). Influence of production method and polymer composition. , 1998, Journal of controlled release : official journal of the Controlled Release Society.
[14] Y. Lee,et al. Hydrogels of poly(ethylene glycol)-co-poly(lactones) diacrylate macromers and β-chitin , 1997 .
[15] Gerhard Winter,et al. Microencapsulation of rh-erythropoietin, using biodegradable poly(d,l-lactide-co-glycolide): protein stability and the effects of stabilizing excipients , 1997 .
[16] Hsin-Jiant Liu,et al. Structural analysis and degradation behavior in polyethylene glycol/poly(L‐lactide) copolymers , 1994 .
[17] D. Cohn,et al. Morphological study of biodegradable PEO/PLA block copolymers. , 1987, Journal of biomedical materials research.
[18] C. Xiong,et al. Optimization of preparative conditions for poly-DL-lactide- polyethylene glycol microspheres with entrapped Vibrio cholera antigens. , 1999, Journal of controlled release : official journal of the Controlled Release Society.
[19] K. Sakurai,et al. PREPARATION AND CHARACTERIZATION OF POLYLACTIDE-POLY(ETHYLENE GLYCOL)-POLYLACTIDE TRIBLOCK POLYMERS AND A PRELIMINARY IN VIVO EXAMINATION OF THE BLOOD CIRCULATION TIME FOR THE NANOPARTICLES MADE THEREFROM , 1999 .
[20] C. Xiong,et al. Studies on the block copolymerization of D,L‐lactide and poly(ethyle glycol) with aluminium complex catalyst , 1995 .
[21] T. Kissel,et al. Monitoring Microviscosity and Microacidity of the Albumin Microenvironment Inside Degrading Microparticles from Poly(lactide-co-glycolide) (PLG) or ABA-triblock Polymers Containing Hydrophobic Poly(lactide-co-glycolide) A Blocks and Hydrophilic Poly(ethyleneoxide) B Blocks , 1998, Pharmaceutical Research.
[22] K. Sakurai,et al. Evaluation of long-circulating nanoparticles using biodegradable ABA triblock copolymers containing of poly(l-lactic acid) A-blocks attached to central poly(oxyethylene) B-blocks in vivo , 1998 .
[23] S. Schwendeman,et al. Stabilization of proteins encapsulated in injectable poly (lactide-co-glycolide) , 2000, Nature Biotechnology.
[24] K. Sakurai,et al. Preparation of nanoparticles consisted of poly(L-lactide)-poly(ethylene glycol)-poly(L-lactide) and their evaluation in vitro. , 1999, International journal of pharmaceutics.
[25] K. Takaoka,et al. Biodegradable Poly-d,l-Lactic Acid-Polyethylene Glycol Block Copolymers as a BMP Delivery System for Inducing Bone , 2001, The Journal of bone and joint surgery. American volume.
[26] C. Xiong,et al. Investigation on process parameters involved in preparation of poly-DL-lactide-poly(ethylene glycol) microspheres containing Leptospira Interrogans antigens. , 1999, International journal of pharmaceutics.
[27] M. Paci,et al. Polyether-polyester block copolymers by non-catalysed polymerization of ɛ-caprolactone with poly(ethylene glycol) , 1989 .
[28] Kristi S. Anseth,et al. Predicting Controlled-Release Behavior of Degradable PLA-b-PEG-b-PLA Hydrogels , 2001 .
[29] D. Cohn,et al. Compositional and structural analysis of PELA biodegradable block copolymers degrading under in vitro conditions. , 1989, Biomaterials.
[30] J. Feijen,et al. A versatile and highly efficient catalyst system for the preparation of polyesters based on lanthanide tris(2,6-di-tert-butylphenolate)s and various alcohols , 1996 .
[31] Suming Li,et al. Biodegradation of PLA/GA polymers: increasing complexity. , 1994, Biomaterials.
[32] T. Park,et al. Protein delivery from poly(lactic-co-glycolic acid) biodegradable microspheres: release kinetics and stability issues. , 1998, Journal of microencapsulation.
[33] J. Anderson,et al. In vivo biocompatibility study of ABA triblock copolymers consisting of poly(L-lactic-co-glycolic acid) A blocks attached to central poly(oxyethylene) B blocks. , 1996, Journal of biomedical materials research.
[34] Mattheus F. A. Goosen,et al. Mechanism of lactide polymerization in the presence of stannous octoate: The effect of hydroxy and carboxylic acid substances , 1994 .
[35] Kai Griebenow,et al. Protein Spray-Freeze Drying. Effect of Atomization Conditions on Particle Size and Stability , 2000, Pharmaceutical Research.
[36] K. Takaoka,et al. Polylactic acid-polyethylene glycol block copolymer. A new biodegradable synthetic carrier for bone morphogenetic protein. , 1993, Clinical orthopaedics and related research.
[37] T. Kissel,et al. Microencapsulation of antigens using biodegradable polyesters: facts and phantasies. , 1997, Behring Institute Mitteilungen.
[38] Robert Langer,et al. Visual Evidence of Acidic Environment Within Degrading Poly(lactic-co-glycolic acid) (PLGA) Microspheres , 2004, Pharmaceutical Research.
[39] I. Rashkov,et al. Hydrolytic degradation of PLA/PEO/PLA triblock copolymers prepared in the presence of Zn metal or CaH2 , 1998 .
[40] K. Shakesheff,et al. Polymeric systems for controlled drug release. , 1999, Chemical reviews.
[41] Mitch Jacoby. CUSTOM-MADE BIOMATERIALS: Applying engineering, materials, and chemistry principles, researchers produce safe, smart, and effective implantable devices , 2001 .
[42] Suming Li,et al. Hydrolytic degradation of devices based on poly(DL-lactic acid) size-dependence. , 1995, Biomaterials.
[43] Cees W. M. Bastiaansen,et al. ABA Type Copolymers of Lactide with Poly(ethylene glycol). Kinetic, Mechanistic, and Model Studies , 1995 .
[44] F. Bates,et al. Polymer-Polymer Phase Behavior , 1991, Science.
[45] H. Kricheldorf,et al. Polylactones, 22 ABA triblock copolymers of L-lactide and poly(ethylene glycol)† , 1993 .
[46] A. Klibanov,et al. Protein stability in controlled-release systems , 2000, Nature Biotechnology.
[47] D. Attwood,et al. The Release of 5-Fluorouracil from a Swellable Matrix of a Triblock Copolymer of ε-Caprolactone and Ethylene Oxide , 1995, Pharmaceutical Research.
[48] T. Kissel,et al. The degradation, swelling and erosion properties of biodegradable implants prepared by extrusion or compression moulding of poly(lactide-co-glycolide) and ABA triblock copolymers. , 2000, Biomaterials.
[49] E. Chiellini,et al. Frontiers in biomedical polymer applications , 1998 .
[50] T. Kissel,et al. Biocompatibility testing of ABA triblock copolymers consisting of poly(L-lactic-co-glycolic acid) A blocks attached to a central poly(ethylene oxide) B block under in vitro conditions using different L929 mouse fibroblasts cell culture models. , 1998, Journal of controlled release : official journal of the Controlled Release Society.
[51] J. W. Gibson,et al. New long-acting injectable microcapsule contraceptive system. , 1979, American journal of obstetrics and gynecology.
[52] K. Takaoka,et al. New synthetic absorbable polymers as BMP carriers: plastic properties of poly-D,L-lactic acid-polyethylene glycol block copolymers. , 1999, Journal of biomedical materials research.
[53] Michel Vert,et al. Synthesis, Characterization, and Hydrolytic Degradation of PLA/PEO/PLA Triblock Copolymers with Short Poly(l-lactic acid) Chains , 1996 .
[54] A Apicella,et al. Poly(ethylene oxide) (PEO) and different molecular weight PEO blends monolithic devices for drug release. , 1993, Biomaterials.
[55] R. A. Jain,et al. The manufacturing techniques of various drug loaded biodegradable poly(lactide-co-glycolide) (PLGA) devices. , 2000, Biomaterials.
[56] T. Kissel,et al. In-vitro degradation and bovine serum albumin release of the ABA triblock copolymers consisting of poly (L(+) lactic acid), or poly(L(+) lactic acid-co-glycolic acid) A-blocks attached to central polyoxyethylene B-blocks , 1994 .
[57] S. Li,et al. Protein release from physically crosslinked hydrogels of the PLA/PEO/PLA triblock copolymer-type. , 2001, Biomaterials.
[58] N. B. Graham,et al. Hydrogels for controlled drug delivery. , 1984, Biomaterials.
[59] Depu Chen,et al. Lithium chloride as catalyst for the ring-opening polymerization of lactide in the presence of hydroxyl-containing compounds , 1999 .
[60] T. Kissel,et al. Biodegradable microspheres containing influenza A vaccine: immune response in mice. , 1999, Vaccine.
[61] D. Cohn,et al. Biodegradable PELA block copolymers: in vitro degradation and tissue reaction. , 1988, Biomaterials, artificial cells, and artificial organs.
[62] Lisbeth Illum,et al. Long circulating microparticulate drug carriers , 1995 .
[63] T. Kissel,et al. Parenteral protein delivery systems using biodegradable polyesters of ABA block structure, containing hydrophobic poly(lactide-co-glycolide) A blocks and hydrophilic poly(ethylene oxide) B blocks , 1996 .
[64] J. Feijen,et al. Kinetics and mechanism of L-lactide polymerization using two different yttrium alkoxides as initiators , 1996 .
[65] K. Takaoka,et al. Evaluation of polylactic acid homopolymers as carriers for bone morphogenetic protein. , 1992, Clinical orthopaedics and related research.
[66] T. Kissel,et al. Synthesis, characteristics and in vitro degradation of star-block copolymers consisting of l-lactide, glycolide and branched multi-arm poly(ethylene oxide) , 1998 .
[67] Michel Vert,et al. MORE ABOUT THE DEGRADATION OF LA/GA – DERIVED MATRICES IN AQUEOUS MEDIA , 1991 .
[68] Yi-you Huang,et al. Drug release from PLA/PEG microparticulates , 1997 .
[69] P. Giusti,et al. Block copolymers of L-lactide and poly(ethylene glycol) for biomedical applications , 1994 .
[70] I. Lancranjan,et al. Parenteral depot-systems on the basis of biodegradable polyesters , 1991 .
[71] M. Sefton. Biomaterials and Clinical Applications , 1988 .
[72] Wim E. Hennink,et al. Protein Instability in Poly(Lactic-co-Glycolic Acid) Microparticles , 2000, Pharmaceutical Research.
[73] H. Janeczek,et al. Polymerization of lactones, 17. Synthesis of ethylene glycol‐L‐lactide block copolymers , 1993 .
[74] T. Kissel,et al. Morphological characterization of microspheres, films and implants prepared from poly(lactide-co-glycolide) and ABA triblock copolymers: is the erosion controlled by degradation, swelling or diffusion? , 2001, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[75] B. Gander,et al. Improving Stability and Release Kinetics of Microencapsulated Tetanus Toxoid by Co-Encapsulation of Additives , 1998, Pharmaceutical Research.
[76] David Shiaw-Guang Hu,et al. Effect of soft segment on degradation kinetics in polyethylene glycol/poly(l-lactide) block copolymers , 1993 .
[77] J L Cleland,et al. The development of stable protein formulations: a close look at protein aggregation, deamidation, and oxidation. , 1993, Critical reviews in therapeutic drug carrier systems.
[78] J. Feijen,et al. Stereocomplex formation in ABA triblock copolymers of poly(lactide) (A) and poly(ethylene glycol) (B) , 1995 .
[79] A. M. Reed,et al. Biodegradable polymers for use in surgery—poly(ethylene oxide) poly(ethylene terephthalate) (PEO/PET) copolymers: 1 , 1979 .
[80] S. Schwendeman,et al. Stabilization of Proteins Encapsulated in Cylindrical Poly(lactide-co-glycolide) Implants: Mechanism of Stabilization by Basic Additives , 2000, Pharmaceutical Research.
[81] T. Kissel,et al. Branched biodegradable polyesters for parenteral drug delivery systems. , 2000, Journal of controlled release : official journal of the Controlled Release Society.
[82] H. S. Kim,et al. Thermal behaviour of poly(ε-caprolactone)-poly(ethylene glycol)-poly(ε-caprolactone) tri-block copolymers , 2001 .
[83] M. Sarbolouki,et al. Synthesis and Characterization of Novel ABA Triblock Copolymers from L-Lactide, Glycolide, and PEG , 1999 .
[84] K. Zhu,et al. Poly-DL-lactic acid: polyethylene glycol block copolymers. The influence of polyethylene glycol on the degradation of poly-DL-lactic acid. , 1994, Journal of biomaterials science. Polymer edition.
[85] R. Müller,et al. The controlled intravenous delivery of drugs using PEG-coated sterically stabilized nanospheres. , 1995, Advanced drug delivery reviews.
[86] R. Barsacchi,et al. The biodegradation of poly (ester-ether-ester) block copolymers in a cellular environmentin vitro , 1994 .
[87] W. Hunter,et al. Development of biodegradable polymeric paste formulations for taxol: An in vitro and in vivo study , 1996 .
[88] T. Kissel,et al. Synthesis and properties of biodegradable ABA triblock copolymers consisting of poly(l-lactic acid) or poly (l-lactic-co-glycolic acid) A-blocks attached to central poly ( oxyethylene ) B-blocks , 1993 .
[89] James M. Anderson,et al. Biocompatibility of ABA triblock copolymer microparticles consisting of poly(l-lactic-co-glycolic-acid) A-blocks attached to central poly(oxyethylene) B-blocks in rats after intramuscular injection , 1997 .
[90] T. Kissel,et al. Degradation and protein release properties of microspheres prepared from biodegradable poly(lactide-co-glycolide) and ABA triblock copolymers: influence of buffer media on polymer erosion and bovine serum albumin release. , 1999, Journal of controlled release : official journal of the Controlled Release Society.
[91] P. Giusti,et al. Poly(ester-ether-ester) block copolymers as biomaterials , 1994 .
[92] C. Xiong,et al. Synthesis and characterization of block copolymers from D, L‐lactide and poly(ethylene glycol) with stannous chloride , 1990 .
[93] M. Paci,et al. Synthesis and characterization of polymers from β-propiolactone and poly(ethylene glycol)s , 1987 .
[94] C. Cristallini,et al. Degradation products of poly(ester-ether-ester) block copolymers do not alter endothelial metabolism in vitro , 1995 .
[95] J. M. Harris,et al. Poly(Ethylene Glycol) Chemistry , 1992 .
[96] J. Feijen,et al. Cellular Uptake of PEO Surface-Modified Nanoparticles: Evaluation of Nanoparticles Made of PLA: PEO Diblock and Triblock Copolymers , 2000, Journal of drug targeting.
[97] T. Kissel,et al. Factors influencing the release of peptides and proteins from biodegradable parenteral depot systems , 1992 .
[98] M. Davies,et al. XPS and SSIMS Analysis Revealing Surface Segregation and Short-Range Order in Solid Films of Block Copolymers of PEO and PLGA , 1997 .
[99] Michel Vert,et al. Structure-property relationships in the case of the degradation of massive poly(α-hydroxy acids) in aqueous media , 1990 .
[100] Michel Vert,et al. Structure-property relationships in the case of the degradation of massive aliphatic poly-(α-hydroxy acids) in aqueous media , 1990 .
[101] H. Okada,et al. One- and three-month release injectable microspheres of the LH-RH superagonist leuprorelin acetate. , 1997, Advanced drug delivery reviews.