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胰岛素壳聚糖胶态纳米粒的制备及体外释药性能 被引量:8

Preparation and in vitro Release of Chitosan Colloidal Nanoparticles for Insulin
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摘要 采用离子趋向凝胶化法制备了胰岛素壳聚糖胶态微粒,并考察了外观、粒径和体外释药性能。所得产品呈球形,表面光滑圆整,平均粒径为276nm,多分散系数为0.08。体外释药呈pH依赖性,释药速度受载药量及泊洛沙姆188含量的影响。 Insulin-loaded chitosan colloidal nanoparticles were prepared using ionotropic gelation technique. Theshape, size and in vitro release of the prepared nanoparticles were examined. The results showed that the nanoparticles werespherical and smooth with a mean particle size of 276nm and a polydisperse coefficient of 0.08. The in vitro release ofinsulin from the colloidal nanoparticles was pH-dependent, the drug loading and the poloxamer188 content had an influenceon the release speed.
出处 《中国医药工业杂志》 CAS CSCD 北大核心 2004年第11期655-657,共3页 Chinese Journal of Pharmaceuticals
关键词 胰岛素 壳聚糖 胶态纳米粒 体外释药 insulin chitosan colloidal nanoparticles in vitro release
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  • 1Li SX, Zou LJ, Zhang TM. Insulin [A]. Wang FS, Ling PX. Biochemistry Drug Research (生化药物研究) [M]. Beijing: People's Medical Publishing House, 1997.442-447.
  • 2Carino GP, Jacob JS, Mathiowitz E. Nanosphere based oral insulin delivery [J]. J Controlled Release, 2000,65(1):261-269.
  • 3Rocio FU, Pilar C, Carmen RL, et al. Enhancement of nasal absorption of Insulin using chitosan nanoparticles [J]. Pharm Res, 1999,16(10):1576-1581.
  • 4Kawashima Y, Yamamoto H, Takeuchi H, et al. Pulmonary delivery of insulin with nebulized DL-lactide/glycolide copolymer (PLGA) nanospheres to prolong hypoglycemic effect [J]. J Controlled Release, 1999,62(1-2):279-287.
  • 5Ma LM, Zhang Q, Li YZ, et al. Preparation and drug efficacy of insulin-loaded polyester nanoparticles [J]. Chin Pharm J (中国药学杂志), 2001,36(1):38-42.
  • 6Yu SJ, Lei HP. Experiment method of hypoglycemic drugs [A]. Xu SY, Bian RL, Chen X. Methodology of Pharmacological Experiments (药理实验方法学) [M]. Beijing: People's Medical Publishing House, 1982.982-996.
  • 7Maria MG, Dolores B, Maria EM, et al. Formulation of L-asparaginase-loaded PLGA nanoparticles: influence of polymer properties on enzyme loading, activity and in vitro release [J]. J Controlled Release, 1998,52(1):53-62.
  • 8Huang YY, Chung TW, Tzeng TW. A method using biodegradable polylactides/polyethylene glycol for drug release with reduced initial burst [J]. Int J Pharm, 1999,182(1):93-100.

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