Polymers for biodegradable medical devices. 1. The potential of polyesters as controlled macromolecular release systems
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[1] J. Feijen,et al. Biodegradable hollow fibres for the controlled release of drugs. , 1988, Biomaterials.
[2] J. Feijen,et al. Biodegradable hollow fibres for the controlled release of hormones , 1987 .
[3] G. Zaikov. QUANTITATIVE ASPECTS OF POLYMER DEGRADATION IN THE LIVING BODY , 1985 .
[4] L. M. Sanders,et al. Controlled delivery of an LHRH analogue from biodegradable injectable microspheres , 1985 .
[5] J. Heller. Controlled drug release from poly(ortho esters) — A surface eroding polymer☆ , 1985 .
[6] Robert Langer,et al. Controlled release of macromolecules: Biological studies☆ , 1985 .
[7] J. Remon,et al. Synthesis and characterization of some modified polysaccharides containing drug moieties , 1985 .
[8] Thomas O. Dappert,et al. The effect of hydrocortisone acetate loaded poly(DL-lactide) films on the inflammatory response , 1985 .
[9] R. Langer,et al. An explanation for the controlled release of macromolecules from polymers , 1985 .
[10] E. Edelman,et al. Controlled Release and Magnetically Modulated Systems for Macromolecular Drugs , 1985, Annals of the New York Academy of Sciences.
[11] W. Bailey,et al. Synthesis of Biodegradable Addition Polymers a , 1985, Annals of the New York Academy of Sciences.
[12] J. Dutkiewicz,et al. A New Simple Controlled Release Delivery System a , 1985, Annals of the New York Academy of Sciences.
[13] J. Heller. Controlled Drug Release from Poly(ortho esters) , 1985, Annals of the New York Academy of Sciences.
[14] James M. Anderson,et al. In Vitro and In Vivo Studies of Drug‐Releasing Poly(amino acids) , 1985, Annals of the New York Academy of Sciences.
[15] D. Williams,et al. The degradation of a synthetic polyester by a lysomal enzyme , 1985 .
[16] C. Chu. Degradation phenomena of two linear aliphatic polyester fibres used in medicine and surgery , 1985 .
[17] F. Moatamed,et al. The intracellular degradation of poly(ε-caprolactone) , 1985 .
[18] J. Heller,et al. In vitro and in vivo release of levonorgestrel from poly(ortho esters): I. Linear polymers , 1985 .
[19] R. Langer,et al. Polymers for the controlled release of macromolecules: effect of molecular weight of ethylene-vinyl acetate copolymer. , 1985, Journal of biomedical materials research.
[20] F. Hutchinson,et al. Biodegradable polymers for the sustained release of peptides. , 1985, Biochemical Society transactions.
[21] M. Takada,et al. Controlled drug release by ultrasound irradiation. , 1985, Chemical & pharmaceutical bulletin.
[22] Ping I. Lee. Kinetics of Drug Release from Glassy Polymers: Effect of Initially Nonuniform Drug Distribution , 1985 .
[23] P A Holmes,et al. Applications of PHB - a microbially produced biodegradable thermoplastic , 1985 .
[24] R. V. Petersen. Biodegradable Drug Delivery Systems Based on Polypeptides , 1985 .
[25] J. W. Gibson,et al. Fibrous Delivery Systems for Antimicrobial Agents , 1985 .
[26] C. Schuerch. Biomedical Applications of Polysaccharides , 1985 .
[27] The role of polymer matrix structure and interparticle interactions in diffusion-limited drug release. , 1985, Biophysical journal.
[28] J. C. Price,et al. Microencapsulation and dissolution properties of a neuroleptic in a biodegradable polymer, poly(d,l-lactide). , 1985, Journal of pharmaceutical sciences.
[29] Robert Langer,et al. NEW APPROACH TO THE DEVELOPMENT OF BIOERODIBLE POLYMERS FOR CONTROLLED RELEASE APPLICATIONS EMPLOYING NATURALLY OCCURRING AMINO ACIDS. , 1984 .
[30] J. Benoit,et al. Characterization of drug-loaded poly(d,l-lactide) microspheres. , 1984, Journal of pharmaceutical sciences.
[31] P. I. Lee,et al. Novel approach to zero-order drug delivery via immobilized nonuniform drug distribution in glassy hydrogels. , 1984, Journal of pharmaceutical sciences.
[32] A. Schindler,et al. The enzymatic surface erosion of aliphatic polyesters , 1984 .
[33] K. Himmelstein,et al. Controlled release from erod1ble poly(ortho ester) drug delivery systems , 1984 .
[34] D. Lewis,et al. Controlled release of a luteinizing hormone-releasing hormone analogue from poly(d,l-lactide-co-glycolide) microspheres. , 1984, Journal of pharmaceutical sciences.
[35] K. Himmelstein,et al. Drug delivery from catalysed erodible polymeric matrices of poly(ortho ester)s. , 1984, Biomaterials.
[36] A. Schindler,et al. Capronor--a biodegradable delivery system for levonorgestrel. , 1984 .
[37] J. Heller,et al. Controlled release of contraceptive agents from poly(ortho esters). , 1984 .
[38] W. Kortsatko,et al. Poly-D(-)-3-hydroxybuttersäure-eimbiologisch abbaubarer Arzneistoffträger zur Liberationsverzögerung. III: Gewelsverträflichkeitsstudien parental applizierbarer poly-D(−)-3-hydroxybuttersäure-tabletten in gewebekultur und in vivo , 1984 .
[39] A. Melveger,et al. Morphological and structural changes in a copolymer of glycolide and lactide occurring as a result of hydrolysis , 1984 .
[40] P. Holmes,et al. The thermal degradation of poly(-(d)-β-hydroxybutyric acid): Part 2—Changes in molecular weight , 1984 .
[41] P. Holmes,et al. The thermal degradation of poly(-(d)-β-hydroxybutyric acid): Part 1—Identification and quantitative analysis of products , 1984 .
[42] P. Holmes,et al. The thermal degradation of poly(-(d)-β-hydroxybutyric acid): Part 3—The reaction mechanism , 1984 .
[43] E. Edelman,et al. Polymer Based Drug Delivery:Magnetically Modulated and Bioerodible Systems , 1984 .
[44] J. P. Bell,et al. Mechanism of the Biodegradation of Polycaprolactone , 1984 .
[45] M. Vert,et al. Poly(β-Malic Acid) as a Source of Polyvalent Drug Carriers: Possible Effects of Hydrophobic Substituents in Aqueous Media , 1984 .
[46] J. Heller,et al. Biodegradable polymers in controlled drug delivery. , 1984, Critical reviews in therapeutic drug carrier systems.
[47] R. Langer,et al. In vivo and in vitro release of macromolecules from polymeric drug delivery systems. , 1983, Journal of pharmaceutical sciences.
[48] M. Tuttle,et al. Controlled release of water-soluble macromolecules from bioerodible hydrogels. , 1983, Biomaterials.
[49] C. Chu,et al. An In vitro Evaluation of the Stability of Mechanical Properties of Surgical Suture Materials In Various pH Conditions , 1983, Annals of surgery.
[50] N. Peppas,et al. Mechanisms of solute release from porous hydrophilic polymers , 1983 .
[51] J. Heller. Synthesis of Biodegradable Polymers for Biomedical Utilization , 1983 .
[52] Beck Lr,et al. Poly(lactic acid) and poly(lactic acid-co-glycolic acid) contraceptive delivery systems. , 1983 .
[53] Robert Langer,et al. Chemical and Physical Structure of Polymers as Carriers for Controlled Release of Bioactive Agents: A Review , 1983 .
[54] R. Langer,et al. Zero-order controlled-release polymer matrices for micro- and macromolecules. , 1983, Journal of pharmaceutical sciences.
[55] C. Chu,et al. Scanning electron microscopic study of the hydrolytic degradation of poly(glycolic acid) suture. , 1982, Journal of biomedical materials research.
[56] D. Williams,et al. Biodegradation of surgical polymers , 1982 .
[57] C. Chu. The effect of pH on the in vitro degradation of poly(glycolide lactide) copolymer absorbable sutures. , 1982, Journal of biomedical materials research.
[58] C. Chu. A Comparison of the Effect of pH on the Biodegradation of Two Synthetic Absorbable Sutures , 1982, Annals of surgery.
[59] G. Geelhoed,et al. Absorbable ligating clips. , 1982, Surgery, gynecology & obstetrics.
[60] A. Schindler,et al. Aliphatic polyesters. I. The degradation of poly(ϵ‐caprolactone) in vivo , 1981 .
[61] C. Chu,et al. The in-vitro degradation of poly(glycolic acid) sutures--effect of pH. , 1981, Journal of biomedical materials research.
[62] G L Kimmel,et al. Aliphatic polyesters II. The degradation of poly (DL-lactide), poly (epsilon-caprolactone), and their copolymers in vivo. , 1981, Biomaterials.
[63] N. Peppas,et al. Present and future applications of biomaterials in controlled drug delivery systems. , 1981, Biomaterials.
[64] A. Melveger,et al. Polydioxanone (PDS), a novel monofilament synthetic absorbable suture. , 1981, Surgery, gynecology & obstetrics.
[65] C. Chu. Hydrolytic degradation of polyglycolic acid: Tensile strength and crystallinity study , 1981 .
[66] A. M. Reed,et al. Biodegradable polymers for use in surgery — poly(glycolic)/poly(Iactic acid) homo and copolymers: 2. In vitro degradation , 1981 .
[67] H. Brem,et al. Biocompatibility of polymeric delivery systems for macromolecules. , 1981, Journal of biomedical materials research.
[68] D. Williams,et al. The Effects of Lipids on the Mechanical Properties of Polyglycolic Acid Sutures , 1981 .
[69] R. Langer,et al. Experimental Approaches for Achieving Both Zero-Order and Modulated Controlled Release from Polymer Matrix Systems , 1981 .
[70] Donnie F. Williams. Enzymic Hydrolysis of Polylactic Acid , 1981 .
[71] A. Schindler,et al. Biodegradable drug delivery systems based on aliphatic polyesters: application to contraceptives and narcotic antagonists. , 1981, NIDA research monograph.
[72] C. Chu. An in-vitro study of the effect of buffer on the degradation of poly(glycolic acid) sutures. , 1981, Journal of biomedical materials research.
[73] I. B. Rozanova,et al. Polycaproamide degradation in rabbits and in several model media. , 1980, Biomaterials.
[74] D. Wise,et al. Long‐term controlled delivery of levonorgestrel in rats by means of small biodegradable cylinders , 1980, The Journal of pharmacy and pharmacology.
[75] D. Williams,et al. The effect of bacteria on absorbable sutures. , 1980, Journal of biomedical materials research.
[76] R. Langer,et al. Polymers for sustained macromolecule release: procedures to fabricate reproducible delivery systems and control release kinetics. , 1980, Journal of pharmaceutical sciences.
[77] The design of controlled drug delivery systems based on biodegradable polymers. , 1980 .
[78] Robert Langer,et al. INVITED REVIEW POLYMERIC DELIVERY SYSTEMS FOR CONTROLLED DRUG RELEASE , 1980 .
[79] H. Bossche,et al. The use of mebendazole and levamisole in sustained release formulations. , 1980 .
[80] G. Griffin. Synthetic polymers and the living environment , 1980 .
[81] J. Heller. Controlled release of biologically active compounds from bioerodible polymers. , 1980, Biomaterials.
[82] Ross R. Muth,et al. Biodegradable polymers for use in surgery—polyglycolic/poly(actic acid) homo- and copolymers: 1 , 1979 .
[83] A. Schindler,et al. Sustained drug delivery systems II: Factors affecting release rates from poly(epsilon-caprolactone) and related biodegradable polyesters. , 1979, Journal of pharmaceutical sciences.
[84] Df Williams. Some Observations on the Role of Cellular Enzymes in the In-Vivo Degradation of Polymers , 1979 .
[85] D. Wise,et al. Sustained release of a dual antimalarial system , 1979, The Journal of pharmacy and pharmacology.
[86] H. Gabelnick,et al. Biodegradable systems for the sustained release of fertility-regulating agents. , 1979, Journal of steroid biochemistry.
[87] J M Brady,et al. Degradation rates of oral resorbable implants (polylactates and polyglycolates): rate modification with changes in PLA/PGA copolymer ratios. , 1977, Journal of biomedical materials research.
[88] G. Kimmel,et al. Biodegradable Polymers for Sustained Drug Delivery , 1977 .
[89] G. Kimmel,et al. Biodegradable polymers and sustained delivery of contraceptive drugs. , 1977 .
[90] Salthouse Tn,et al. Polyglactin 910 suture absorption and the role of cellular enzymes. , 1976 .
[91] D. Wise,et al. An injectable sustained release fertility control system. , 1976, Contraception.
[92] T. N. Salthouse. Cellular enzyme activity at the polymer-tissue interface: a review. , 1976, Journal of biomedical materials research.
[93] Richard L. Kronenthal,et al. BIODEGRADABLE POLYMERS IN MEDICINE AND SURGERY , 1975 .
[94] B. F. Matlaga,et al. An approach to the numerical quantitation of acute tissue response to biomaterials. , 1975, Biomaterials, medical devices, and artificial organs.
[95] Ferdinand Rodriguez,et al. Microbial degradation of polyesters: Polycaprolactone degraded by P. pullulans† , 1974 .
[96] J. Merrick,et al. Extracellular Enzyme Secretion by Pseudomonas lemoignei , 1974, Journal of bacteriology.
[97] J M Brady,et al. Resorption rate, route, route of elimination, and ultrastructure of the implant site of polylactic acid in the abdominal wall of the rat. , 1973, Journal of biomedical materials research.
[98] E. J. Frazza,et al. A new absorbable suture. , 1971, Journal of biomedical materials research.
[99] G. Higgins,et al. Polyglycolic acid sutures. Laboratory and clinical evaluation of a new absorbable suture material. , 1970, Archives of surgery.