发明名称 Fascile synthesis of biocompatible polymer capsule nanoparticles for drug encapsulation
摘要 The present invention relates to a method for preparing a capsule nanoparticle used in encapsulating hydrophobic medicines, comprising the following steps: (A) providing a biocompatible polymer and an organic solution containing a hydrophobic medicine; (B) stirring the organic solution at 3-10° C., and titrating with an alcohol solution, so as to make the biocompatible polymer encapsulate hydrophobic medicine to form a capsule nanoparticle; (C) ultrasonic vibrating the capsule nanoparticle at 3-10° C.; (D) filtering the capsule nanoparticle to an average size controllable in the range of 60-450 nm; and (E) lyophilizing the encapsulated particles.
申请公布号 US9592205(B2) 申请公布日期 2017.03.14
申请号 US201213624038 申请日期 2012.09.21
申请人 NATIONAL CHENG KUNG UNIVERSITY 发明人 Shieh Dar-Bin
分类号 A61K9/50;A61K9/51;A61K31/337;B82Y5/00 主分类号 A61K9/50
代理机构 Bacon & Thomas, PLLC 代理人 Bacon & Thomas, PLLC
主权项 1. A method for preparing capsules encapsulating hydrophobic medicines, comprising the steps of: (A) providing an organic solution having a biocompatible polymer and a hydrophobic medicine; (B) stirring the organic solution at a low temperature of 3 to 10° C., and titrating with an alcohol solution, to make the biocompatible polymer encapsulate the hydrophobic medicine to form a capsule nanoparticle; (C) ultrasonic vibrating the capsule nanoparticle at a low temperature of 3 to 10° C.; (D) filtering the capsule nanoparticle, to make an average capsule nanoparticle diameter of the capsule nanoparticle at 60-450 nm; and (E) lyophilizing the capsule nanoparticle; Wherein the biocompatible polymer is selected from the group consisting (poly-(D,L-lactide-co-glycolide)), PLA, and PEG-PLA; and wherein the steps (A) to (E) are performed without surfactant.
地址 TW