高效液相色谱法同时测定苯磺酸氨氯地平、氢氯噻嗪和替米沙坦复方剂型的方法建立与验证

Bhavin P. Marolia, K. Bodiwala, Shailesh A Shah, P. Prajapati, Bhavik Himmatbhai Satani, S. A. Desai
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引用次数: 10

摘要

背景:复方氨氯地平、氢氯噻嗪和替米沙坦合用治疗高血压。用超高效液相色谱法(UPLC)同时测定了该组合物的含量。目的:建立并验证高效液相色谱法同时测定苯磺酸氨氯地平、氢氯噻嗪和替米沙坦三片剂型的含量。材料与方法:以硅胶60F254预包覆的铝板为固定相,氯仿:丁-1-醇:氨(6:4:0.1,v/v/v)为流动相进行色谱分离。在254 nm处进行光谱-密度扫描。方法按照ICH Q2R1标准进行验证。结果与讨论:苯磺酸氨氯地平、氢氯噻嗪和替米沙坦在200 ~ 1000 ng/波段、500 ~ 2500 ng/波段和1600 ~ 8000 ng/波段均呈线性关系,相关系数r 2 = 0.9952、0.9992和0.9979。苯磺酸氨氯地平、氢氯噻嗪和替米沙坦的R f值分别为0.27±0.02、0.43±0.02和0.14±0.02。该方法对苯磺酸氨氯地平、氢氯噻嗪和替米沙坦的回收率分别为99.43 ~ 101.57%、100.22 ~ 101.54%和100.12 ~ 100.44%。苯磺酸氨氯地平、氢氯噻嗪和替米沙坦的检出限和定量限分别为8.6、58.0和186.9 ng/带,26.1、175.8和566.4 ng/带。应用:建立的高效液相色谱法同时测定了三种药物的复方片剂剂型,结果与标签上的说法吻合较好。结论:建立的方法准确、精密度高、特异性好、灵敏度高。可用于苯磺酸氨氯地平、氢氯噻嗪、替米沙坦联用片的常规分析(测定)。关键词:苯磺酸氨氯地平(AML),氢氯噻嗪(HCTZ),替米沙坦(TLM),高效薄层色谱(HPTLC),同时估计
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development and Validation of HPTLC Method for Simultaneous Estimation of Amlodipine Besylate, Hydrochlorothiazide and Telmisartan In Their Combined Tablet Dosage Form
Background: The combination of Amlodipine Besylaye, Hydrochlorthiazide and Telmisartan is prescribed for the treatment of hypertension. An Ultra Performance Liquid Chromatography (UPLC) method has been reported for simultaneous estimation of this combination. Objective: To develop and validate HPTLC Method for simultaneous estimation of Amlodipine Besylate, Hydrochlorothiazide and Telmisartan in their combined tablet dosage form. Materials and Method: The chromatographic separation was performed using aluminum plates pre-coated with silica gel 60F254 as stationary phase and chloroform: butan-1-ol: ammonia (6: 4: 0.1, v/v/v) as mobile phase. Spectro-densitometric scanning was performed at 254 nm. The developed method was validated according to ICH Q2R1 guideline. Results and Discussion: The linearity was established over a concentration range of 200-1000 ng/band, 500-2500 ng/band and 1600-8000 ng/band with correlation coefficient r 2 = 0.9952, 0.9992 and 0.9979 for Amlodipine besylate, Hydrochlorothiazide and Telmisartan, respectively. The R f values of Amlodipine besylate, Hydrochlorothiazide and Telmisartan were found to be 0.27 ± 0.02, 0.43 ± 0.02 and 0.14 ± 0.02 respectively. Recovery of drug was achieved in the range of 99.43–101.57%, 100.22–101.54% and 100.12–100.44% for Amlodipine besylate, Hydrochlorothiazide and Telmisartan, respectively by developed method. Limit of detection and limit of quantitation was found to be 8.6, 58.0 and 186.9 ng/band and 26.1, 175.8 and 566.4 ng/band for Amlodipine besylate, Hydrochlorothiazide and Telmisartan, respectively. Application: The developed HPTLC method was applied for simultaneous estimation of three drugs in their combined tablet dosage forms and results were found to be in good agreement with the labeled claim. Conclusion: The developed HPTLC method was found to be accurate, precise, specific and sensitive. It can be applied for routine analysis (assay) of tablets containing combination of Amlodipine besylate, Hydrochlorothiazide and Telmisartan. Key words: Amlodipine besylate (AML), Hydrochlorothiazide (HCTZ), Telmisartan (TLM), High Performance Thin Layer Chromatography (HPTLC), Simultaneous estimation.
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