H. Shafi, N. Din, Muhammad Imran, M. Sarwar, M. Tahir, S. Khursheed
{"title":"PDA反相液相色谱法同时测定非生物和生物基质中的右美沙芬和氯苯那敏","authors":"H. Shafi, N. Din, Muhammad Imran, M. Sarwar, M. Tahir, S. Khursheed","doi":"10.4172/2153-2435.1000590","DOIUrl":null,"url":null,"abstract":"A simple, precise and sensitive reversed-phase HPLC method using Photo-diode array detector for simultaneous determination of dextromethorphan (DXM) and chlorpheniramine (CLP) in various matrices had been developed and validated. The separation was achieved within 8 minutes on a C-18 column (15 cm x 4.6 mm x 5 μm) using methanol/ pH 3.0 potassium dihydrogen phosphate buffer (60:40, v/v) mobile phase in an isocratic elution mode with flow rate 0.8 mL/min and UV-detection at 230 nm. External standard was employed for quantification. The current method demonstrated good linearity ranged 1-200 μg/mL for CLP (retention time 3.83 ± 0.10 min) with r2 of 0.9994 and 2-1000 μg/mL for DXM (retention time 5.02 ± 0.10 min) with R2 of 0.9993. The limits of detection and quantification were 0.25 μg/mL and 1.0 μg/mL for CLP and 0.50 μg/mL and 1.5 μg/mL for DXM. No interference from matrices was observed and samples remained stable in the HPLC injector for 12 h. The developed method was accurate that employed a simple liquid/liquid extraction procedure with recovery ranged 90.0%-101.9% for both analytes. Intra and inter-day precision were less than 2.5%. The method was proved robust and reproducible that is applicable to pharmaceutical (active raw materials, syrups) and biological (blood) matrices.","PeriodicalId":19833,"journal":{"name":"Pharmaceutica Analytica Acta","volume":"239 1","pages":"1-6"},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":"{\"title\":\"Validated Reversed-Phase Liquid Chromatographic Method for Simultaneous Determination of Dextromethorphan and Chlorpheniramine in Non-biological and Biological Matrices Using PDA Detector\",\"authors\":\"H. Shafi, N. Din, Muhammad Imran, M. Sarwar, M. Tahir, S. Khursheed\",\"doi\":\"10.4172/2153-2435.1000590\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A simple, precise and sensitive reversed-phase HPLC method using Photo-diode array detector for simultaneous determination of dextromethorphan (DXM) and chlorpheniramine (CLP) in various matrices had been developed and validated. The separation was achieved within 8 minutes on a C-18 column (15 cm x 4.6 mm x 5 μm) using methanol/ pH 3.0 potassium dihydrogen phosphate buffer (60:40, v/v) mobile phase in an isocratic elution mode with flow rate 0.8 mL/min and UV-detection at 230 nm. External standard was employed for quantification. The current method demonstrated good linearity ranged 1-200 μg/mL for CLP (retention time 3.83 ± 0.10 min) with r2 of 0.9994 and 2-1000 μg/mL for DXM (retention time 5.02 ± 0.10 min) with R2 of 0.9993. The limits of detection and quantification were 0.25 μg/mL and 1.0 μg/mL for CLP and 0.50 μg/mL and 1.5 μg/mL for DXM. No interference from matrices was observed and samples remained stable in the HPLC injector for 12 h. The developed method was accurate that employed a simple liquid/liquid extraction procedure with recovery ranged 90.0%-101.9% for both analytes. Intra and inter-day precision were less than 2.5%. The method was proved robust and reproducible that is applicable to pharmaceutical (active raw materials, syrups) and biological (blood) matrices.\",\"PeriodicalId\":19833,\"journal\":{\"name\":\"Pharmaceutica Analytica Acta\",\"volume\":\"239 1\",\"pages\":\"1-6\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pharmaceutica Analytica Acta\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4172/2153-2435.1000590\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmaceutica Analytica Acta","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2153-2435.1000590","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Validated Reversed-Phase Liquid Chromatographic Method for Simultaneous Determination of Dextromethorphan and Chlorpheniramine in Non-biological and Biological Matrices Using PDA Detector
A simple, precise and sensitive reversed-phase HPLC method using Photo-diode array detector for simultaneous determination of dextromethorphan (DXM) and chlorpheniramine (CLP) in various matrices had been developed and validated. The separation was achieved within 8 minutes on a C-18 column (15 cm x 4.6 mm x 5 μm) using methanol/ pH 3.0 potassium dihydrogen phosphate buffer (60:40, v/v) mobile phase in an isocratic elution mode with flow rate 0.8 mL/min and UV-detection at 230 nm. External standard was employed for quantification. The current method demonstrated good linearity ranged 1-200 μg/mL for CLP (retention time 3.83 ± 0.10 min) with r2 of 0.9994 and 2-1000 μg/mL for DXM (retention time 5.02 ± 0.10 min) with R2 of 0.9993. The limits of detection and quantification were 0.25 μg/mL and 1.0 μg/mL for CLP and 0.50 μg/mL and 1.5 μg/mL for DXM. No interference from matrices was observed and samples remained stable in the HPLC injector for 12 h. The developed method was accurate that employed a simple liquid/liquid extraction procedure with recovery ranged 90.0%-101.9% for both analytes. Intra and inter-day precision were less than 2.5%. The method was proved robust and reproducible that is applicable to pharmaceutical (active raw materials, syrups) and biological (blood) matrices.