Mehta S K, Kaur Gurpreet, Bhasin K K
Department of Chemistry and Center of Advanced Studies in Chemistry, Panjab University, Chandigarh 160014, India.
Colloids Surf B Biointerfaces. 2007 Oct 15;60(1):95-104. doi: 10.1016/j.colsurfb.2007.06.012. Epub 2007 Jun 16.
The purpose of present study was to formulate microemulsion composed of oleic acid+phosphate buffer (PB)+Tween 80+ethanol and to investigate its potential as drug delivery system for an antitubercular drug rifampicin. The pseudo-ternary phase diagram has been delineated at constant surfactant/cosurfactant ratio (K(m) 0.55). Conductivity (sigma) and viscosity (keta) studies with variation in Phi (weight fraction of aqueous phase) and omega (molar concentration ratio) show the occurrence of structural changes from water-in-oil (w/o) microemulsion to oil-in-water (o/w). Along with the solubility and partition studies of rifampicin in microemulsion components, the changes in the microstructure of the microemulsion after incorporation of drug have been evaluated using pH, sigma and keta studies. The results have shown that the microemulsion remained stable after the incorporation of rifampicin (in terms of optical texture and phase separation). In addition, the particle size analysis indicates that the microemulsion changes into o/w emulsion at infinite dilution. Dissolution studies infer that a controlled release of rifampicin is expected from o/w emulsion droplet.
本研究的目的是制备由油酸+磷酸盐缓冲液(PB)+吐温80+乙醇组成的微乳,并研究其作为抗结核药物利福平给药系统的潜力。在恒定的表面活性剂/助表面活性剂比例(K(m) 0.55)下绘制了拟三元相图。随着Φ(水相重量分数)和ω(摩尔浓度比)的变化进行电导率(σ)和粘度(η)研究,结果表明存在从油包水(w/o)微乳到水包油(o/w)的结构变化。除了利福平在微乳组分中的溶解度和分配研究外,还通过pH、σ和η研究评估了药物加入后微乳微观结构的变化。结果表明,加入利福平后微乳保持稳定(在光学质地和相分离方面)。此外,粒度分析表明,微乳在无限稀释时转变为o/w乳液。溶出度研究推断,预计o/w乳液滴会实现利福平的控释。