药物分析杂志2024,Vol.44Issue(1) :126-133.DOI:10.16155/j.0254-1793.2024.01.13

HPLC法测定替米沙坦中的有关物质

Determination of related substances in telmisartan by HPLC

王春 张素珍 陶鸿珠 彭亚 赵斌锋
药物分析杂志2024,Vol.44Issue(1) :126-133.DOI:10.16155/j.0254-1793.2024.01.13

HPLC法测定替米沙坦中的有关物质

Determination of related substances in telmisartan by HPLC

王春 1张素珍 1陶鸿珠 1彭亚 1赵斌锋1
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作者信息

  • 1. 浙江金立源药业有限公司,绍兴 312369
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摘要

目的:建立高效液相色谱法测定替米沙坦原料药中的有关物质.方法:采用Waters Symmetry Shield RP8(150 mm ×4.6 mm,3.5 μm)色谱柱,以0.1%磷酸溶液(用三乙胺调pH至3.0)-乙腈为流动相,梯度洗脱,流速0.8 mL·min-1,柱温25 ℃,检测波长230 nm.结果:替米沙坦与9种已知杂质色谱峰之间的分离度均>1.5,定量限均<40 ng·mL-1,检测限均<10 ng·mL-1.替米沙坦及各杂质质量浓度在30~600 ng·mL-1范围内线性关系良好(r>0.999 5).杂质Ⅰ~杂质Ⅸ的平均回收率分别为93.8%、99.8%、97.5%、99.2%、99.8%、98.3%、98.4%、99.2%、99.7%,RSD 均<2.0%.改变流速、柱温、波长、流动相比例及pH后,对有关物质的检测结果无影响.3批替米沙坦中最大单杂含量均为0.02%,杂质总量<0.10%.结论:经方法学验证,本方法专属性强,灵敏、精密,准确度高,可用于替米沙坦原料药有关物质的测定.

Abstract

Objective:To establish an HPLC method for the determination of the related substances in telmisartan.Methods:Waters Symmetry Shield RP8(150 mm x4.6 mm,3.5 µm)column was adopted.The mobile phase A was 0.1%phosphoric acid solution(pH was adjusted to 3.0 with triethylamine),and the mobile phase B was acetonitrile.The gradient elution was performed.The flow rate,column temperature and wavelength were 0.8 mL·min-1,25 ℃ and 230 nm,respectively.Results:The resolutions between the peaks of telmisartan and nine known impurities were greater than 1.5.The limits of quantitation of all impurities were less than 40 ng·mL-1,and the limits of detection of all impurities were less than 10 ng·mL-1.The standard curves of telmisartan and its impurities were linear within the range 30-600 ng·mL-1,and the correlation coefficients were all greater than 0.999 5.The average recovery rates of impurities Ⅰ-Ⅸ were 93.8%,99.8%,97.5%,99.2%,99.8%,98.3%,98.4%,99.2%and 99.7%,respectively,and the RSDs of 9 results were all less than 2.0%.Changing the flow rate,column temperature,wavelength,mobile phase ratio and pH did not affect the detection results of the related substances.The results of maximum single impurity were 0.02%in three batches of telmisartan,and the results of total impurities were less than 0.10%.Conclusion:The method is highly specific,sensitive,precise and accurate,and can be used for the determination of related substances of telmisartan.

关键词

替米沙坦/原料药/有关物质/药典标准/质量控制/高效液相色谱法/梯度洗脱

Key words

telmisartan/active pharmaceutical ingredient/related substances/pharmacopoeia standard/quality control/HPLC/gradient elution

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出版年

2024
药物分析杂志
中国药学会

药物分析杂志

CSTPCDCSCD北大核心
影响因子:1.039
ISSN:0254-1793
被引量1
参考文献量16
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