Date Abhijit A, Nagarsenker M S
Department of Pharmaceutics, Bombay College of Pharmacy, Kalina, Santacruz (E.), Mumbai 400098, India.
Int J Pharm. 2008 May 1;355(1-2):19-30. doi: 10.1016/j.ijpharm.2008.01.004. Epub 2008 Jan 12.
Parenteral delivery of the hydrophobic drugs is a very challenging task. The conventional approaches such as use of co-solvents, oily vehicles and modern approaches such as mixed micelles, liposomes, complexation with cyclodextrins and emulsions have several limitations. Microemulsions have evolved as a novel vehicle for parenteral delivery of the hydrophobic drugs. Their interesting features such as spontaneity of formation, ease of manufacture, high solubilization capacity and self-preserving property make them the vehicle of choice. The review focuses on the excipients available for formulation of the parenteral microemulsions and describes the investigations reported for the various classes of therapeutic agents.
疏水性药物的肠胃外给药是一项极具挑战性的任务。传统方法如使用助溶剂、油性载体,以及现代方法如混合胶束、脂质体、与环糊精络合和乳剂等都有若干局限性。微乳剂已发展成为疏水性药物肠胃外给药的新型载体。它们具有诸如形成的自发性、易于制造、高增溶能力和自我保存特性等有趣特征,使其成为首选载体。本文综述聚焦于可用于肠胃外微乳剂制剂的辅料,并描述了针对各类治疗剂所报道的研究。