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基于辛酸癸酸聚乙二醇甘油酯的两亲性药物微乳给药载体的表征

Characterization of caprylocaproyl macrogolglycerides based microemulsion drug delivery vehicles for an amphiphilic drug.

作者信息

Djordjevic Ljiljana, Primorac Marija, Stupar Mirjana, Krajisnik Danina

机构信息

Department of Pharmaceutical Technology and Cosmetology, Faculty of Pharmacy, Vojvode Stepe 450, P.O. Box 146, 11221 Belgrade, Serbia and Montenegro.

出版信息

Int J Pharm. 2004 Mar 1;271(1-2):11-9. doi: 10.1016/j.ijpharm.2003.10.037.

Abstract

Microemulsion systems composed of water, isopropyl myristate, PEG-8 caprylic/capric glycerides (Labrasol), and polyglyceryl-6 dioleate (Plurol Oleique), were investigated as potential drug delivery vehicles for an amphiphilic model drug (diclofenac diethylamine). Pseudo-ternary phase diagram of the investigated system, at constant surfactant/cosurfactant mass ratio (Km 4:1) was constructed at room temperature by titration, and the oil-to-surfactant/cosurfactant mass ratios (O/SC) that exhibit the maximum in the solubilization of water were found. This allowed the investigation of the continuous structural inversion from water-in-oil to oil-in-water microemulsions on dilution with water phase. Furthermore, electrical conductivity (sigma) of the system at Km 1:4, and O/SC 0.250 was studied, and the percolation phenomenon was observed. Conductivity and apparent viscosity (eta') measurement results well described colloidal microstructure of the selected formulations, including gradual changes during their formation. Moreover, sigma, eta', and pH values of six selected microemulsion vehicles which differ in water phase volume fraction (phi(w)) at the selected Km and O/SC values, were measured. In order to investigate the influence of the amphiphilic drug on the vehicle microstructures, each system was formulated with 1.16% (w/w) diclofenac diethylamine. Electrical conductivity, and eta' of the investigated systems were strongly affected by drug incorporation. The obtained results suggest that diclofenac diethylamine interacts with the specific microstructure of the investigated vehicles, and that the different drug release kinetics from these microemulsions may be expected. The investigated microemulsions should be very interesting as new drug carrier systems for dermal application of diclofenac diethylamine.

摘要

研究了由水、肉豆蔻酸异丙酯、聚乙二醇8辛酸/癸酸甘油酯(Labrasol)和聚甘油-6二油酸酯(Plurol Oleique)组成的微乳液体系,作为两亲性模型药物(双氯芬酸二乙胺)的潜在药物递送载体。通过滴定法在室温下构建了所研究体系在恒定表面活性剂/助表面活性剂质量比(Km 4:1)下的拟三元相图,并找到了水增溶量最大时的油与表面活性剂/助表面活性剂质量比(O/SC)。这使得能够研究用水相稀释时从油包水微乳液到水包油微乳液的连续结构转变。此外,研究了Km为1:4且O/SC为0.250时体系的电导率(σ),并观察到了渗滤现象。电导率和表观粘度(η')的测量结果很好地描述了所选制剂的胶体微观结构,包括其形成过程中的逐渐变化。此外,还测量了在选定的Km和O/SC值下,水相体积分数(φ(w))不同的六种选定微乳液载体的σ、η'和pH值。为了研究两亲性药物对载体微观结构的影响,每个体系都含有1.16%(w/w)的双氯芬酸二乙胺。所研究体系的电导率和η'受药物加入的强烈影响。所得结果表明,双氯芬酸二乙胺与所研究载体的特定微观结构相互作用,并且可以预期这些微乳液具有不同的药物释放动力学。所研究的微乳液作为双氯芬酸二乙胺皮肤给药的新型药物载体系统应该会非常有趣。

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