{"title":"Formulation, Development and Evaluation of Topiramate Loaded\nNiosomes for the Treatment of Epilepsy","authors":"","doi":"10.46243/jst.2020.v5.i5.pp119-129","DOIUrl":null,"url":null,"abstract":"Topiramate (TPM) is an anti-epileptic drug used in the treatment of epilepsy and seizures. The study was\ndesigned with three aims. First, to enhance the solubility and bioavailability of BCS class III drug TPM; second, to\nease administration of the formulation to the epileptic patient, during an attack, and third, to decrease the dose of\ndrug for enduring treatment. Formulation of TPM niosomes was optimized by changing the concentration of Tween,\nLabrafil and cholesterol using response surface design. Further the TPM niosomes were prepared by using ether\ninjection method. The formulation was then evaluated for vesicle size, entrapment efficiency and in-vitro drug\nrelease study. FTIR and DSC studies were performed for pure drug and optimized batch. The vesicle size of the\noptimized batch was found to be 0. 35 nm. The %entrapment efficiency and %drug release of optimized batch was\nfound to be 94.64% and 92.027% respectively. From the present study it can be concluded that the developed\nniosomes of TPM has shown great potential in treatment of epilepsy.","PeriodicalId":23534,"journal":{"name":"Volume 5, Issue 4","volume":"5 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Volume 5, Issue 4","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46243/jst.2020.v5.i5.pp119-129","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Topiramate (TPM) is an anti-epileptic drug used in the treatment of epilepsy and seizures. The study was
designed with three aims. First, to enhance the solubility and bioavailability of BCS class III drug TPM; second, to
ease administration of the formulation to the epileptic patient, during an attack, and third, to decrease the dose of
drug for enduring treatment. Formulation of TPM niosomes was optimized by changing the concentration of Tween,
Labrafil and cholesterol using response surface design. Further the TPM niosomes were prepared by using ether
injection method. The formulation was then evaluated for vesicle size, entrapment efficiency and in-vitro drug
release study. FTIR and DSC studies were performed for pure drug and optimized batch. The vesicle size of the
optimized batch was found to be 0. 35 nm. The %entrapment efficiency and %drug release of optimized batch was
found to be 94.64% and 92.027% respectively. From the present study it can be concluded that the developed
niosomes of TPM has shown great potential in treatment of epilepsy.