• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

用于测定原料药及药物剂型中坦索罗辛的经验证的分光光度法。

Validated spectrophtometric method for determination of tamsulosin in bulk and pharmaceutical dosage forms.

作者信息

Amanlou Massoud, Ghazi Moghadam Amin, Barazandeh Tehrani Maliheh, Souri Effat

出版信息

Iran J Pharm Res. 2014 Winter;13(1):81-6.

PMID:24734058
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3985241/
Abstract

In this study a sensitive, simple and accurate spectrophotometric method was suggested for determination of tamsulosin in bulk powder and pharmaceutical dosage form based on the formation of an ion-pair complex between the drug and bromocresol green in a buffer solution at pH 3.5. The formed yellow color complex was extracted with chloroform and measured at 415 nm. The optimum reaction conditions such as pH, reagent amount, extracting solvent and the stoichiometry of the ion-pair complex were investigated. Under the optimized conditions, the Beer's law was obeyed in the concentration range of 1-160 g/mL with acceptable correlation coefficient (r(2) > 0.9997) and precision (CV < 3%) and accuracy (error < 2%). The proposed method was successfully used for the determination of tamsulosin in pharmaceutical capsule with nosignificant interferences of excipients.

摘要

本研究提出了一种灵敏、简便且准确的分光光度法,用于测定原料药粉末和药物剂型中的坦索罗辛。该方法基于在pH 3.5的缓冲溶液中,药物与溴甲酚绿形成离子对络合物。所形成的黄色络合物用氯仿萃取,并在415 nm处进行测定。研究了最佳反应条件,如pH、试剂量、萃取溶剂和离子对络合物的化学计量关系。在优化条件下,在1 - 160 μg/mL的浓度范围内符合比尔定律,具有可接受的相关系数(r² > 0.9997)、精密度(CV < 3%)和准确度(误差 < 2%)。所提出的方法成功用于测定药物胶囊中的坦索罗辛,辅料无明显干扰。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b7a/3985241/b6e787df6be0/ijpr-13-081-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b7a/3985241/93ce376382a0/ijpr-13-081-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b7a/3985241/c97f7db7cecb/ijpr-13-081-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b7a/3985241/b45edf881eb0/ijpr-13-081-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b7a/3985241/b6e787df6be0/ijpr-13-081-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b7a/3985241/93ce376382a0/ijpr-13-081-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b7a/3985241/c97f7db7cecb/ijpr-13-081-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b7a/3985241/b45edf881eb0/ijpr-13-081-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b7a/3985241/b6e787df6be0/ijpr-13-081-g004.jpg

相似文献

1
Validated spectrophtometric method for determination of tamsulosin in bulk and pharmaceutical dosage forms.用于测定原料药及药物剂型中坦索罗辛的经验证的分光光度法。
Iran J Pharm Res. 2014 Winter;13(1):81-6.
2
Extractive spectrophotometric methods for the determination of oxomemazine hydrochloride in bulk and pharmaceutical formulations using bromocresol green, bromocresol purple and bromophenol blue.采用溴甲酚绿、溴甲酚紫和溴酚蓝,用萃取分光光度法测定原料药及药物制剂中的盐酸奥索马嗪。
Arch Pharm (Weinheim). 2005 Apr;338(4):190-7. doi: 10.1002/ardp.200400947.
3
Development and validation of spectrophotometric methods for estimation of antimigraine drug eletriptan hydrobromide in pure form and pharmaceutical formulations.建立并验证分光光度法测定纯态及药物制剂中抗偏头痛药物氢溴酸依来曲普坦的含量。
Ann Pharm Fr. 2021 Jul;79(4):395-408. doi: 10.1016/j.pharma.2020.11.002. Epub 2020 Nov 19.
4
Spectrophotometric determination of gatifloxacin in pure form and in pharmaceutical formulation.分光光度法测定纯加替沙星及药物制剂中的加替沙星。
Spectrochim Acta A Mol Biomol Spectrosc. 2007 Aug;67(5):1306-12. doi: 10.1016/j.saa.2006.09.041. Epub 2006 Oct 14.
5
Sensitive and selective spectrophotometric assay of piroxicam in pure form, capsule and human blood serum samples via ion-pair complex formation.通过离子对络合物形成对纯吡罗昔康、胶囊和人血清样品进行灵敏且选择性的分光光度测定。
Spectrochim Acta A Mol Biomol Spectrosc. 2014 Sep 15;130:238-44. doi: 10.1016/j.saa.2014.03.074. Epub 2014 Apr 2.
6
Spectrophotometric determination of diphenhydramine. HC1 in pharmaceutical preparations.分光光度法测定药物制剂中的盐酸苯海拉明。
J Assoc Off Anal Chem. 1977 Jul;60(4):926-8.
7
Extractive spectrophotometric method for the determination of tropicamide.用于测定托吡卡胺的萃取分光光度法。
J Young Pharm. 2012 Jan;4(1):42-8. doi: 10.4103/0975-1483.93572.
8
Spectrophotometric Methods for Determination of Sunitinib in Pharmaceutical Dosage Forms Based on Ion-pair Complex Formation.基于离子对络合物形成的分光光度法测定药物剂型中的舒尼替尼
Iran J Pharm Res. 2020 Summer;19(3):103-109. doi: 10.22037/ijpr.2020.1101119.
9
Ion-pair spectrophotometric estimation of gemifloxacin.吉米沙星的离子对分光光度法测定
Pharm Methods. 2012 Jan;3(1):26-30. doi: 10.4103/2229-4708.97713.
10
Spectrophotometric determination of tranexamic acid in pharmaceutical bulk and dosage forms.分光光度法测定原料药及剂型中的氨甲环酸
Anal Sci. 2005 Sep;21(9):1133-5. doi: 10.2116/analsci.21.1133.

引用本文的文献

1
Green HPLC-Fluorescence detection method for concurrent analysis of Tamsulosin hydrochloride and Tolterodine tartrate in dosage forms and biological fluids.用于同时分析剂型和生物流体中盐酸坦索罗辛和酒石酸托特罗定的绿色高效液相色谱-荧光检测法
Sci Rep. 2025 Mar 27;15(1):10615. doi: 10.1038/s41598-025-92183-6.
2
Development of Green HPTLC method for simultaneous determination of a promising combination Tamsulosin and Mirabegron: stability-indicating assay was examined.开发用于同时测定坦索罗辛和米拉贝隆这一有前景组合的绿色高效薄层色谱法:进行了稳定性指示分析。
BMC Chem. 2023 Sep 30;17(1):130. doi: 10.1186/s13065-023-01043-9.
3

本文引用的文献

1
Spectrophotometric estimation of tamsulosin hydrochloride by acid-dye method.酸性染料法分光光度法测定盐酸坦索罗辛
Pharm Methods. 2011 Jan;2(1):53-60. doi: 10.4103/2229-4708.81089.
2
A sensitive HPLC method for simultaneous estimation of tamsulosin hydrochloride and its impurity.一种同时测定盐酸坦索罗辛及其杂质的灵敏高效液相色谱法。
Pak J Pharm Sci. 2008 Jul;21(3):307-10.
3
Development of a validated RP-LC/ESI-MS-MS method for separation, identification and determination of related substances of tamsulosin in bulk drugs and formulations.
Validated Spectrophtometric Method for Simultaneous Determination of Buprenorphine and Naloxone in Pharmaceutical Dosage Forms.
验证的分光光度法同时测定药物制剂中丁丙诺啡和纳洛酮的含量
Iran J Pharm Res. 2017 Winter;16(1):112-119.
4
UV Spectrophotometric Determination and Validation of Hydroquinone in Liposome.脂质体中对苯二酚的紫外分光光度法测定及验证
Iran J Pharm Res. 2015 Spring;14(2):473-8.
5
Development of a rapid derivative spectrophotometric method for simultaneous determination of acetaminophen, diphenhydramine and pseudoephedrine in tablets.一种同时测定片剂中对乙酰氨基酚、苯海拉明和伪麻黄碱的快速导数分光光度法的开发。
Iran J Pharm Res. 2015 Spring;14(2):435-42.
开发一种经过验证的反相液相色谱/电喷雾串联质谱法,用于原料药和制剂中坦索罗辛相关物质的分离、鉴定和测定。
J Pharm Biomed Anal. 2008 Jan 7;46(1):94-103. doi: 10.1016/j.jpba.2007.09.009. Epub 2007 Sep 14.
4
Determination of tamsulosin in human aqueous humor and serum by liquid chromatography-electrospray ionization tandem mass spectrometry.液相色谱-电喷雾电离串联质谱法测定人房水和血清中的坦索罗辛。
J Pharm Biomed Anal. 2007 Jan 17;43(2):606-12. doi: 10.1016/j.jpba.2006.07.016. Epub 2006 Aug 22.
5
Chiral separation of tamsulosin by capillary electrophoresis.
J Pharm Biomed Anal. 2005 Sep 15;39(3-4):691-6. doi: 10.1016/j.jpba.2005.04.023.
6
Rapid, simple and highly sensitive LC-ESI-MS/MS method for the quantification of tamsulosin in human plasma.一种用于定量测定人血浆中坦索罗辛的快速、简便且高灵敏度的液相色谱-电喷雾串联质谱法。
Biomed Chromatogr. 2005 Dec;19(10):709-19. doi: 10.1002/bmc.498.
7
Rapid determination of tamsulosin in human plasma by high-performance liquid chromatography using extraction with butyl acetate.采用乙酸丁酯萃取的高效液相色谱法快速测定人血浆中的坦索罗辛。
J Chromatogr B Analyt Technol Biomed Life Sci. 2004 Oct 5;809(2):307-11. doi: 10.1016/j.jchromb.2004.06.043.
8
Chiral separation of tamsulosin isomers by HPLC using cellulose tris (3,5-dimethhylphenylcarbamate) as a chiral stationary phase.
J Pharm Biomed Anal. 2004 Feb 18;34(3):689-93. doi: 10.1016/s0731-7085(03)00555-7.
9
Validation of high-performance liquid chromatography methods for pharmaceutical analysis. Understanding the differences and similarities between validation requirements of the US Food and Drug Administration, the US Pharmacopeia and the International Conference on Harmonization.用于药物分析的高效液相色谱法的验证。了解美国食品药品监督管理局、美国药典和国际协调会议验证要求之间的异同。
J Chromatogr A. 2003 Feb 14;987(1-2):57-66. doi: 10.1016/s0021-9673(02)01536-4.
10
Quantitation of tamsulosin in human plasma by liquid chromatography-electrospray ionization mass spectrometry.采用液相色谱-电喷雾电离质谱法对人血浆中的坦索罗辛进行定量分析。
J Chromatogr B Analyt Technol Biomed Life Sci. 2002 Feb 5;767(1):75-81. doi: 10.1016/s0378-4347(01)00546-1.