{"title":"稳定性指示液相色谱法测定片剂中盐酸丁丙诺啡和盐酸纳洛酮的含量:开发和验证考虑","authors":"","doi":"10.24214/ajbpr/8/2/0819","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":210528,"journal":{"name":"Asian Journal of Biochemical and Pharmaceutical Research","volume":"45 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Stability Indicating Liquid Chromatographic Method Development for Estimation of Buprenorphine Hydrochloride and Naloxone Hydrochloride in Tablet Formulation: Development and Validation Consideration\",\"authors\":\"\",\"doi\":\"10.24214/ajbpr/8/2/0819\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\",\"PeriodicalId\":210528,\"journal\":{\"name\":\"Asian Journal of Biochemical and Pharmaceutical Research\",\"volume\":\"45 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-06-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Asian Journal of Biochemical and Pharmaceutical Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.24214/ajbpr/8/2/0819\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Biochemical and Pharmaceutical Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.24214/ajbpr/8/2/0819","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Stability Indicating Liquid Chromatographic Method Development for Estimation of Buprenorphine Hydrochloride and Naloxone Hydrochloride in Tablet Formulation: Development and Validation Consideration