Gareth C. Gilvary, A. Almajaan, Shu Li, Zoe Senta Loys, Yiwei Tian, Jeremiah Kelleher, A. Madi, A. Healy, David S. Jones, G. Andrews
{"title":"Hot-melt co-extrusion technology as a manufacturing platform for anti-hypertensive fixed-dose combinations","authors":"Gareth C. Gilvary, A. Almajaan, Shu Li, Zoe Senta Loys, Yiwei Tian, Jeremiah Kelleher, A. Madi, A. Healy, David S. Jones, G. Andrews","doi":"10.5920/BJPHARM.596","DOIUrl":null,"url":null,"abstract":"This work focused on the development of a concentric multi-layered fixed-dose combination via an advanced manufacturing technique, hot-melt co-extrusion. The dosage form was designed to offer differing release behaviour; immediate and sustained release from the coat and core, respectively. Hydrochlorothiazide and losartan potassium were incorporated as anti-hypertensive drugs. Solid-state characterisation revealed that both were transformed into their amorphous forms. In-vitro dissolution testing showed desired release performances offering both immediate and modified release.","PeriodicalId":9253,"journal":{"name":"British Journal of Pharmacy","volume":"240 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"British Journal of Pharmacy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5920/BJPHARM.596","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
Abstract
This work focused on the development of a concentric multi-layered fixed-dose combination via an advanced manufacturing technique, hot-melt co-extrusion. The dosage form was designed to offer differing release behaviour; immediate and sustained release from the coat and core, respectively. Hydrochlorothiazide and losartan potassium were incorporated as anti-hypertensive drugs. Solid-state characterisation revealed that both were transformed into their amorphous forms. In-vitro dissolution testing showed desired release performances offering both immediate and modified release.