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首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >FORMULATION AND EVALUATION OF SEABUCKTHORN LEAF EXTRACT LOADED ETHOSOMAL GEL.
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FORMULATION AND EVALUATION OF SEABUCKTHORN LEAF EXTRACT LOADED ETHOSOMAL GEL.

机译:沙棘叶提取物乙醇凝胶的配制与评价。

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Objective: The objective of present research work is develop an ethosome as a carrier system for 75% ethanolic SBT leaf extract, its incorporation in to gel formulations and to characterize the prepared is to develop ethosomes and gel formulations using various parameters including estimation of total phenol content in terms of Gallic Acid Equivalents (GAE). Seabuckthorn (Hippophae rhamnoids. SBT) is a cold desert medicinal plant, and has high antioxidant content, especially phenol content. There are many reports revealing pharmacological potential of SBT extracts, however, only few literature reports highlight the conversion of these extract in to suitable dosage. Methods: Twelve batches (F1 – F12) of ethosomes were prepared using Soyaphosphatidylcholine (SPC) (1-3%) and ethanol (10-40%). Carbopol 934P was used to prepare ethosomal gel. The range of entrapment efficiency (EE) of ethosomes was 51.05%-91.09%, polydispersity index (PDI) ranges between 0.041-0.392 and vesicle size from 96.98 nm to 395 nm. Four ethosomal batches were selected on the basis of EE and PDI to be used for further incorporation in to 4 gel formulations (G1, G2, G3 & G4, respectively). Prepared gels were then evaluated for their physicochemical properties, drug content and diffusion characteristics. Results: The pH of the gel formulations was found to be in the range of 6.2 to 6.6. Viscosities of the gels were ranging between 4900 - 4550 centipoises. The drug content of the gels ranged between 46.47% - 82.47%. The cumulative release of ethosomal gel was maximum in G4 formulation (94.34%) and minimum in G1 (70.75%). These ethosomes, when converted in to gels, were found to show good physicochemical properties, drug content and diffusion pattern. Conclusion: The present study revealed ethosomal gel as an efficient carrier for herbal extract.
机译:目的:本研究工作的目的是开发一种作为75%乙醇SBT叶提取物的载体的乙醇体,将其掺入凝胶制剂中并表征所制备的物质是使用各种参数(包括估计总苯酚)开发乙醇体和凝胶制剂没食子酸当量(GAE)的含量。沙棘(沙棘)是一种寒冷的沙漠药用植物,具有很高的抗氧化剂含量,尤其是苯酚含量。有许多报道揭示了SBT提取物的药理潜力,但是,只有很少的文献报道强调这些提取物转化为合适的剂量。方法:使用大豆磷脂酰胆碱(SPC)(1-3%)和乙醇(10-40%)制备十二批次(F1-F12)的脂质体。使用Carbopol 934P制备酶体凝胶。核糖体的包封率(EE)为51.05%-91.09%,多分散指数(PDI)为0.041-0.392,囊泡大小为96.98 nm至395 nm。根据EE和PDI选择了四个酶体批次,分别用于进一步掺入4种凝胶制剂(分别为G1,G2,G3和G4)。然后评估制备的凝胶的理化性质,药物含量和扩散特性。结果:发现凝胶制剂的pH在6.2至6.6的范围内。凝胶的粘度在4900-4550厘泊之间。凝胶中的药物含量为46.47%-82.47%。内体凝胶的累积释放在G4制剂中最大(94.34%),在G1制剂中最小(70.75%)。当这些脂质体转变成凝胶时,发现它们显示出良好的理化性质,药物含量和扩散模式。结论:本研究揭示了酶体凝胶是草药提取物的有效载体。

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