高效液相色谱法测定制剂和环境水样中扑热息痛的含量

N. Ahmad, F. Omar
{"title":"高效液相色谱法测定制剂和环境水样中扑热息痛的含量","authors":"N. Ahmad, F. Omar","doi":"10.7598/cst2019.1486","DOIUrl":null,"url":null,"abstract":"A simple, precise, rapid, and accurate reversed – phase high performance liquid chromatography method has been developed for the determination of paracetamol in pure from, pharmaceutical formulations and environmental water samples. Chromatography was carried out on supelco L1 (C18) reversedphase column (25cm × 4.6mm), 5 microns, using a mixture of acetonitril : buffer pH3.0 (40: 60v/v) as a mobile phase at a flow rate of 1.5 ml.min -1 . Detection was performed at 243nm at ambient temperature. The retention time was found 2.2 minutes. The calibration curve was linear (r= 0.999) over a concentration range from 10 to 100 μg/ml. Limit of detection (LOD) and limit of quantitation (LOQ) were found 3ng/ml and 9 ng/ml respectively. The method was validated for its linearity, precision and accuracy. The proposed method was successfully applied for the determination of paracetamol in pure form, pharmaceutical formulations and in environmental water samples. KEYWORD: HPLC, Paracetamol, Pharmaceutical Formulations, Environmental Water Samples.","PeriodicalId":10087,"journal":{"name":"Chemical science transactions","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":"{\"title\":\"HPLC Method for Determination of Paracetamol in Pharmaceutical Formulations and Environmental Water Samples\",\"authors\":\"N. Ahmad, F. Omar\",\"doi\":\"10.7598/cst2019.1486\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A simple, precise, rapid, and accurate reversed – phase high performance liquid chromatography method has been developed for the determination of paracetamol in pure from, pharmaceutical formulations and environmental water samples. Chromatography was carried out on supelco L1 (C18) reversedphase column (25cm × 4.6mm), 5 microns, using a mixture of acetonitril : buffer pH3.0 (40: 60v/v) as a mobile phase at a flow rate of 1.5 ml.min -1 . Detection was performed at 243nm at ambient temperature. The retention time was found 2.2 minutes. The calibration curve was linear (r= 0.999) over a concentration range from 10 to 100 μg/ml. Limit of detection (LOD) and limit of quantitation (LOQ) were found 3ng/ml and 9 ng/ml respectively. The method was validated for its linearity, precision and accuracy. The proposed method was successfully applied for the determination of paracetamol in pure form, pharmaceutical formulations and in environmental water samples. KEYWORD: HPLC, Paracetamol, Pharmaceutical Formulations, Environmental Water Samples.\",\"PeriodicalId\":10087,\"journal\":{\"name\":\"Chemical science transactions\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"7\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical science transactions\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.7598/cst2019.1486\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical science transactions","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7598/cst2019.1486","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7

摘要

建立了一种简单、精确、快速、准确的反相高效液相色谱法测定纯品、制剂和环境水样中扑热息痛的含量。色谱柱为supelco L1 (C18)反相柱(25cm × 4.6mm), 5微米,以乙腈:缓冲液pH3.0 (40: 60v/v)为流动相,流速为1.5 ml.min -1。室温下243nm波长检测。停留时间为2.2 min。在10 ~ 100 μg/ml范围内,标度曲线呈线性关系(r= 0.999)。检测限(LOD)为3ng/ml,定量限(LOQ)为9ng /ml。验证了该方法的线性度、精密度和准确度。该方法成功地应用于纯品、制剂和环境水样中扑热息痛的测定。关键词:高效液相色谱法,扑热息痛,药物制剂,环境水样
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
HPLC Method for Determination of Paracetamol in Pharmaceutical Formulations and Environmental Water Samples
A simple, precise, rapid, and accurate reversed – phase high performance liquid chromatography method has been developed for the determination of paracetamol in pure from, pharmaceutical formulations and environmental water samples. Chromatography was carried out on supelco L1 (C18) reversedphase column (25cm × 4.6mm), 5 microns, using a mixture of acetonitril : buffer pH3.0 (40: 60v/v) as a mobile phase at a flow rate of 1.5 ml.min -1 . Detection was performed at 243nm at ambient temperature. The retention time was found 2.2 minutes. The calibration curve was linear (r= 0.999) over a concentration range from 10 to 100 μg/ml. Limit of detection (LOD) and limit of quantitation (LOQ) were found 3ng/ml and 9 ng/ml respectively. The method was validated for its linearity, precision and accuracy. The proposed method was successfully applied for the determination of paracetamol in pure form, pharmaceutical formulations and in environmental water samples. KEYWORD: HPLC, Paracetamol, Pharmaceutical Formulations, Environmental Water Samples.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Optimization of Synthesis Temperature and Study the Structural and Optical Properties of ZnS Nanoparticles via Simple Chemical Precipitation Method Green Synthesis of Silver Nanoparticles Using Secondary Metabolites as Reducing and Stabilizing Agent in Presence of Microwave Synthesis and Characterization of 3-Amino-5-methylpyrazolinium Picrate (AMPP) /βCD Complex and the Contribution in Different Biological Uses Kinetics of Water Desorption in Select Marine Ferromanganese Crust materials by Stepped Isothermal Evolved Gas Analysis Electrochemical Determination of Cardiovascular Drug Ranolazine Employing Nafion-Carbon Nanotubes Composite Glassy Carbon Electrode
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1