Benita S, Levy M Y
Pharmacy Department, School of Pharmacy, Hebrew University of Jerusalem, Israel.
J Pharm Sci. 1993 Nov;82(11):1069-79. doi: 10.1002/jps.2600821102.
Submicron injectable emulsions have been gaining more and more attention in the last few years, mainly as a vehicle for the intravenous administration of lipophilic drugs rather than as an improved delivery system for drug targeting. Submicron emulsions are available, clinically well accepted, and successfully marketed. Novel original emulsion formulations are being extensively investigated and already exhibit improved pharmacological activity; this fact underlines the promising therapeutic properties of these colloidal drug carriers as vehicles for potent lipophilic drugs. It is therefore essential to carry out a comprehensive physicochemical characterization of these submicron emulsions. It is the objective of the present review to emphasize the need for physicochemical studies in the design of new submicron emulsion drug delivery systems and to describe the different approaches available for carrying out such a complete examination of the emulsion colloidal drug carrier system.
在过去几年中,亚微米可注射乳剂越来越受到关注,主要作为亲脂性药物静脉给药的载体,而非用于药物靶向的改进递送系统。亚微米乳剂已可获得,在临床上被广泛接受并成功上市。新型原创乳剂配方正在被广泛研究,并且已经展现出改善的药理活性;这一事实凸显了这些胶体药物载体作为强效亲脂性药物载体所具有的有前景的治疗特性。因此,对这些亚微米乳剂进行全面的物理化学表征至关重要。本综述的目的是强调在设计新的亚微米乳剂药物递送系统时进行物理化学研究的必要性,并描述用于对乳剂胶体药物载体系统进行如此全面检查的不同方法。