Technique to encapsulate a low molecular weight hydrophilic drug in biodegradable polymer particles in a liquid–liquid system
暂无分享,去创建一个
[1] Saehun Mun,et al. Preparation and characterization of water/oil/water emulsions stabilized by polyglycerol polyricinoleate and whey protein isolate. , 2010, Journal of food science.
[2] H. Kawakami,et al. Control of drug loading efficiency and drug release behavior in preparation of hydrophilic-drug-containing monodisperse PLGA microspheres , 2010, Journal of materials science. Materials in medicine.
[3] D. Chirio,et al. Preparation of solid lipid nanoparticles from W/O/W emulsions: Preliminary studies on insulin encapsulation , 2009, Journal of microencapsulation.
[4] H. Kawakami,et al. Study of types and mixture ratio of organic solvent used to dissolve polymers for preparation of drug-containing PLGA microspheres , 2009 .
[5] J. Duszczyk,et al. Size effect of PLGA spheres on drug loading efficiency and release profiles , 2009, Journal of materials science. Materials in medicine.
[6] H. Kawakami,et al. Preparation and properties of PLGA microspheres containing hydrophilic drugs by the SPG (shirasu porous glass) membrane emulsification technique. , 2008, Colloids and surfaces. B, Biointerfaces.
[7] Kiyoshi Kanamura,et al. Effect of polyethylene glycol on preparation of rifampicin-loaded PLGA microspheres with membrane emulsification technique. , 2008, Colloids and surfaces. B, Biointerfaces.
[8] K. Makino,et al. Factors affecting the loading efficiency of water-soluble drugs in PLGA microspheres. , 2008, Colloids and surfaces. B, Biointerfaces.
[9] K. Makino,et al. Incorporation of water-soluble drugs in PLGA microspheres. , 2007, Colloids and surfaces. B, Biointerfaces.
[10] Sha Huang,et al. Preparation of insulin-loaded PLA/PLGA microcapsules by a novel membrane emulsification method and its release in vitro. , 2006, Colloids and surfaces. B, Biointerfaces.
[11] T. Yotsuyanagi,et al. Properties of poly(lactic-co-glycolic acid) nanospheres containing protease inhibitors: camostat mesilate and nafamostat mesilate. , 2006, International journal of pharmaceutics.
[12] G. Ma,et al. Preparation of uniform-sized PLA microcapsules by combining Shirasu porous glass membrane emulsification technique and multiple emulsion-solvent evaporation method. , 2005, Journal of controlled release : official journal of the Controlled Release Society.
[13] A. Durand,et al. Influence of polymeric surfactants on the properties of drug-loaded PLA nanospheres , 2003 .
[14] K. Zhu,et al. Preparation and characterization of hCG-loaded polylactide or poly(lactide-co-glycolide) microspheres using a modified water-in-oil-in-water (w/o/w) emulsion solvent evaporation technique. , 2001, Journal of microencapsulation.
[15] T. Hino,et al. Drug release from w/o/w emulsions prepared with different chitosan salts and concomitant creaming up. , 2000, Journal of controlled release : official journal of the Controlled Release Society.
[16] Toguchi Hajime,et al. Factors influencing the profiles of TRH release from copoly(d,l-lactic/glycolic acid) microspheres , 1991 .
[17] T Yashiki,et al. A new technique to efficiently entrap leuprolide acetate into microcapsules of polylactic acid or copoly(lactic/glycolic) acid. , 1988, Chemical & pharmaceutical bulletin.
[18] T. Uchida,et al. Preparation and characterization of polylactic acid microspheres containing water-soluble dyes using a novel w/o/w emulsion solvent evaporation method. , 1996, Journal of microencapsulation.