A controlled release system for proteins based on poly(ether ester) block-copolymers: polymer network characterization.
暂无分享,去创建一个
[1] J. Feijen,et al. Zero-order release of lysozyme from poly(ethylene glycol)/poly(butylene terephthalate) matrices. , 2000, Journal of controlled release : official journal of the Controlled Release Society.
[2] Y. Lee,et al. Albumin release from bioerodible hydrogels based on semi-interpenetrating polymer networks composed of poly(ϵ-caprolactone) and poly(ethylene glycol) macromer , 1997 .
[3] J. E. Mark,et al. Physical Properties of Polymers: Index , 2004 .
[4] C. V. van Blitterswijk,et al. Application of porous PEO/PBT copolymers for bone replacement. , 1996, Journal of biomedical materials research.
[5] N. Peppas,et al. Transport of ionizable drugs and proteins in crosslinked poly(acrylic acid) and poly(acrylic acid-co-2-hydroxyethyl methacrylate) hydrogels. I. Polymer characterization , 1996 .
[6] A. Coombes,et al. Improving the delivery capacity of microparticle systems using blends of poly(DL-lactide co-glycolide) and poly(ethylene glycol) , 1995 .
[7] C. Blitterswijk,et al. Preventing postoperative intraperitoneal adhesion formation with Polyactive™, a degradable copolymer acting as a barrier , 1995 .
[8] C. V. van Blitterswijk,et al. Degradative behaviour of polymeric matrices in (sub)dermal and muscle tissue of the rat: a quantitative study. , 1994, Biomaterials.
[9] C. V. van Blitterswijk,et al. Biocompatibility of a biodegradable matrix used as a skin substitute: an in vivo evaluation. , 1994, Journal of biomedical materials research.
[10] C. V. van Blitterswijk,et al. Interface reactions to PEO/PBT copolymers (Polyactive) after implantation in cortical bone. , 1994, Journal of biomedical materials research.
[11] N. Peppas,et al. Hydrophilic/hydrophobic, block and graft copolymeric hydrogels: synthesis, characterization, and solute partition and penetration , 1993 .
[12] Y. Bae,et al. Hydrogel delivery systems based on polymer blends, block co-polymers or interpenetrating networks , 1993 .
[13] Kinam Park,et al. Biodegradable Hydrogels for Drug Delivery , 1993 .
[14] A. Hiltner,et al. An FTIR–ATR investigation of in vivo poly(ether urethane) degradation , 1992 .
[15] S. Fakirov,et al. Effect of the block length on the deformation behavior of polyetheresters as revealed by small-angle X-ray scattering , 1992 .
[16] J. J. Grote,et al. New alloplastic tympanic membrane material. , 1991, The American journal of otology.
[17] T. Okano,et al. Heterogeneous interpenetrating polymer networks for drug delivery , 1991 .
[18] S. Fakirov,et al. Structure of segmented poly (ether ester)s as revealed by synchrotron radiation , 1990 .
[19] J. J. Grote,et al. Biocompatibility of a polyether urethane, polypropylene oxide, and a polyether polyester copolymer. A qualitative and quantitative study of three alloplastic tympanic membrane materials in the rat middle ear. , 1990, Journal of biomedical materials research.
[20] S. Fakirov,et al. Poly(ether/ester)s based on poly(butylene terephthalate) and poly(ethylene glycol), 1. Poly(ether/ester)s with various polyether: polyester ratios , 1990 .
[21] S. Fakirov,et al. Poly(ether/ester)s based on poly(butylene terephthalate) and poly(ethylene glycol), 2. Effect of polyether segment length , 1990 .
[22] K. Zhu,et al. Preparation , Characterization , and Properties of Polylactide ( PLA )-Poly ( ethylene Glycol ) ( PEG ) Copolymers : A Potential Drug Carrier , 2017 .
[23] N. Peppas,et al. Correlation between mesh size and equilibrium degree of swelling of polymeric networks. , 1989, Journal of biomedical materials research.
[24] N. Peppas. Hydrogels in Medicine and Pharmacy , 1987 .
[25] K. Kataoka,et al. Drug release from monolithic devices of segmented polyether‐poly(urethane‐urea)s having both hydrophobic and hydrophilic soft segments , 1986 .
[26] N. A. Peppas,et al. Microcrystalline and three-dimensional network structure of plasticized poly(vinyl chloride) , 1982 .
[27] G. Wilkes,et al. Structure–property relationships of a new series of segmented polyether–polyester copolymers , 1981 .
[28] A. M. Reed,et al. Biodegradable polymers for use in surgery — poly(ethylene oxide)/poly(ethylene terephthalate) (PEO/PET) copolymers: 2. In vitro degradation , 1981 .
[29] A. M. Reed,et al. Biodegradable polymers for use in surgery—poly(ethylene oxide) poly(ethylene terephthalate) (PEO/PET) copolymers: 1 , 1979 .
[30] A. Tobolsky,et al. Synthesis, characterization, and permeation properties of polyether‐based polyurethanes , 1972 .
[31] K. A. Smith,et al. Permeability studies with cellulosic membranes. , 1971, Journal of biomedical materials research.
[32] Charles Tanford,et al. Physical Chemistry of Macromolecules , 1961 .
[33] A. Mikos,et al. Diffusion-controlled delivery of proteins from hydrogels and other hydrophilic systems. , 1997, Pharmaceutical biotechnology.
[34] P. Ferruti,et al. Degradation behaviour of block copolymers containing poly(lactic-glycolic acid) and poly(ethylene glycol) segments. , 1996, Biomaterials.
[35] C A van Blitterswijk,et al. Cell-seeding and in vitro biocompatibility evaluation of polymeric matrices of PEO/PBT copolymers and PLLA. , 1993, Biomaterials.
[36] T. Park,et al. Poly(L-lactic acid)/pluronic blends : characterization of phase separation behavior, degradation, and morphology and use as protein-releasing matrices , 1992 .
[37] J. Feijen,et al. Albumin-heparin microspheres as carriers for cytostatic agents , 1990 .
[38] P. Flory. Principles of polymer chemistry , 1953 .
[39] D. J. Montgomery,et al. The physics of rubber elasticity , 1949 .