Raghunandan, V. Pai, Lakshmi Crs, D. V. Gowda, M. S. Khan, S. Bhat
{"title":"抗高脂血药胃留置浮片的研制与评价","authors":"Raghunandan, V. Pai, Lakshmi Crs, D. V. Gowda, M. S. Khan, S. Bhat","doi":"10.5138/IJDD.V4I2.572","DOIUrl":null,"url":null,"abstract":"The aim of the present study was to develop Gastro retentive effervescent floating tablets (GREFT) containing 20 mg of simvastatin were developed by direct compression method using HPMC K4M, HPMC K15M, HPMC K100M with different drug to polymer ratio. Tablets were evaluated for their physical characteristics, viz ., hardness, friability, drug content and floating properties. Further, tablets were studied for in vitro drug release characteristics for 12 h. The tablets exhibited controlled and prolonged drug release, with optimum hardness, consistent uniformity in weight and low friability. The formulation with F2 (HPMC K100M 1:3 ratio) showed 85.83 % drug release at the end of 12 h and exhibited optimum floating lag time. A decrease in release rate of the drug was observed on increasing polymer ratio and also by increasing viscosity grades of the polymer (HPMC). Drug release from effervescent floating matrix tablets was sustained over 12 h with buoyant properties. DSC study revealed that there is no drug excipient interaction. Based on the release kinetics, all formulations best fitted the Higuchi, first-order model and non-Fickian as the mechanism of drug release. Optimized formulation (F9) was selected based on the similarity factor ( f 2) (71.32) and invitro dissolution was used in radiographic studies by incorporating BaSO4. In vivo X-ray studies in human volunteers showed that the mean gastric residence time was 5.4 ± 0.32 h.","PeriodicalId":13912,"journal":{"name":"International Journal of Drug Delivery","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2012-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Development and evaluation of gastro retentive floating tablets of anti hyperlipidemic drug\",\"authors\":\"Raghunandan, V. Pai, Lakshmi Crs, D. V. Gowda, M. S. Khan, S. Bhat\",\"doi\":\"10.5138/IJDD.V4I2.572\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The aim of the present study was to develop Gastro retentive effervescent floating tablets (GREFT) containing 20 mg of simvastatin were developed by direct compression method using HPMC K4M, HPMC K15M, HPMC K100M with different drug to polymer ratio. Tablets were evaluated for their physical characteristics, viz ., hardness, friability, drug content and floating properties. Further, tablets were studied for in vitro drug release characteristics for 12 h. The tablets exhibited controlled and prolonged drug release, with optimum hardness, consistent uniformity in weight and low friability. The formulation with F2 (HPMC K100M 1:3 ratio) showed 85.83 % drug release at the end of 12 h and exhibited optimum floating lag time. A decrease in release rate of the drug was observed on increasing polymer ratio and also by increasing viscosity grades of the polymer (HPMC). Drug release from effervescent floating matrix tablets was sustained over 12 h with buoyant properties. DSC study revealed that there is no drug excipient interaction. Based on the release kinetics, all formulations best fitted the Higuchi, first-order model and non-Fickian as the mechanism of drug release. Optimized formulation (F9) was selected based on the similarity factor ( f 2) (71.32) and invitro dissolution was used in radiographic studies by incorporating BaSO4. In vivo X-ray studies in human volunteers showed that the mean gastric residence time was 5.4 ± 0.32 h.\",\"PeriodicalId\":13912,\"journal\":{\"name\":\"International Journal of Drug Delivery\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-11-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Drug Delivery\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5138/IJDD.V4I2.572\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Drug Delivery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5138/IJDD.V4I2.572","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Development and evaluation of gastro retentive floating tablets of anti hyperlipidemic drug
The aim of the present study was to develop Gastro retentive effervescent floating tablets (GREFT) containing 20 mg of simvastatin were developed by direct compression method using HPMC K4M, HPMC K15M, HPMC K100M with different drug to polymer ratio. Tablets were evaluated for their physical characteristics, viz ., hardness, friability, drug content and floating properties. Further, tablets were studied for in vitro drug release characteristics for 12 h. The tablets exhibited controlled and prolonged drug release, with optimum hardness, consistent uniformity in weight and low friability. The formulation with F2 (HPMC K100M 1:3 ratio) showed 85.83 % drug release at the end of 12 h and exhibited optimum floating lag time. A decrease in release rate of the drug was observed on increasing polymer ratio and also by increasing viscosity grades of the polymer (HPMC). Drug release from effervescent floating matrix tablets was sustained over 12 h with buoyant properties. DSC study revealed that there is no drug excipient interaction. Based on the release kinetics, all formulations best fitted the Higuchi, first-order model and non-Fickian as the mechanism of drug release. Optimized formulation (F9) was selected based on the similarity factor ( f 2) (71.32) and invitro dissolution was used in radiographic studies by incorporating BaSO4. In vivo X-ray studies in human volunteers showed that the mean gastric residence time was 5.4 ± 0.32 h.