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Self-emulsifying drug delivery systems as a tool to improve solubility and bioavailability of resveratrol

机译:自乳化药物输送系统可作为提高白藜芦醇溶解度和生物利用度的工具

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摘要

Resveratrol is a nonflavonoid polyphenolic compound which has a broad range of desirable biological actions which include antioxidant, anti-inflammatory, antidiabetic, cardioprotective, and antitumor activities. However, there is concern that the bioavailability of resveratrol may limit some of its clinical utility. So, the aim of this study was to enhance the dissolution rate and oral hypoglycemic and hypolipidemic effect of resveratrol. This was achieved using self-emulsifying drug delivery system. The solubility of resveratrol was determined in various oils, surfactants, and cosurfactants. Phase diagram was plotted to identify the efficient self-emulsification regions using olive oil, Tween 80, and propylene glycol. The prepared self-emulsifying drug delivery system formulations were tested for thermodynamic stability, emulsification efficiency, droplet size, zeta potential, and in vitro drug release. Self-emulsification time averaged 17–99 seconds without precipitation and the mean droplet sizes ranged from 285 to 823 nm with overall zeta potential of −2.24 to −15.4 mv. All formulations improved drug dissolution in relation to unprocessed drug with a trend of decreased dissolution parameters with increasing oil content. The optimized formula, F19, with dissolution efficiency of 94% compared to only 42% of pure drug was used to study the in vivo hypoglycemic and hypolipidemic effects of resveratrol in diabetic-induced albino rats and comparing these effects with that of pure resveratrol in different doses. Treatment with the optimized formula, F19, at 10 mg/kg had significant hypoglycemic and hypolipidemic effects in diabetic-induced albino rats which were nearly similar to the high dose (20 mg/kg) of unprocessed resveratrol. From the study, it was concluded that formulation F19 has good emulsification property with uniform globule size, satisfactory in vitro drug release profile, and significant in vivo hypoglycemic effects which identify future opportunities for resveratrol delivery.
机译:白藜芦醇是一种非类黄酮多酚化合物,具有广泛的所需生物作用,包括抗氧化剂,抗炎剂,抗糖尿病药,心脏保护药和抗肿瘤药。但是,人们担心白藜芦醇的生物利用度可能会限制其某些临床用途。因此,本研究的目的是提高白藜芦醇的溶出度以及口服降血糖和降血脂作用。这是使用自乳化药物递送系统实现的。测定了白藜芦醇在各种油,表面活性剂和助表面活性剂中的溶解度。绘制相图以鉴定使用橄榄油,吐温80和丙二醇的有效自乳化区域。测试了制备的自乳化药物递送系统制剂的热力学稳定性,乳化效率,液滴大小,ζ电势和体外药物释放。自乳化时间平均为17-99秒,无沉淀,平均液滴尺寸范围为285至823 nm,总Zeta电位为-2.24至-15.4 mv。与未加工的药物相比,所有制剂均改善了药物溶出度,且溶出参数随油含量的增加而降低。优化的配方F19的溶解效率为94%,而纯药物的溶解效率仅为42%,用于研究白藜芦醇在糖尿病引起的白化病大鼠中的体内降血糖和降血脂作用,并将这些作用与纯白藜芦醇在不同情况下的作用进行比较剂量。在糖尿病诱发的白化病大鼠中,用最优化的配方F19进行的10 mg / kg的治疗具有明显的降血糖和降血脂作用,这与未加工白藜芦醇的高剂量(20 mg / kg)几乎相似。从研究中得出的结论是,制剂F19具有良好的乳化性能,具有均匀的小球尺寸,令人满意的体外药物释放曲线以及显着的体内降血糖作用,这确定了白藜芦醇输送的未来机会。

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