坎地沙坦西蕾蒂酯和氢氯噻嗪片剂型的同时分光光度测定

M. M. Annapurna, J. Kumar
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引用次数: 4

摘要

建立了一种简便的导数分光光度法同时测定片剂中坎地沙坦西莱西地酯和氢氯噻嗪的含量。坎地沙坦通过阻断血管平滑肌和肾上腺的血管紧张素受体而拮抗血管紧张素II(血管收缩和醛固酮分泌)的作用并降低血压,而氢氯噻嗪通过干扰钠离子在肾小管上皮上的运输而增加氯、钠和水的排泄。这里显示了利尿作用。一阶导数法是基于测量一种药物在另一种药物的零交叉点处的吸光度。分别在222.69 nm(氢氯噻嗪的零点交叉点)和254.63 nm(坎地沙坦的零点交叉点)两个不同波长处测定坎地沙坦西莱西酯和氢氯噻嗪。在磷酸盐缓冲液中,坎地沙坦西拉西地酯和氢氯噻嗪分别在0.5 ~ 50µg/ml和0.1 ~ 50µg/ml浓度范围内呈线性关系。该方法可用于坎地沙坦西莱西地酯与氢氯噻嗪复方片剂的常规分析。关键词:坎地沙坦西莱西蒂酯,导数光谱,氢氯噻嗪,同时测定
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Simultaneous Spectrophotometric Estimation of Candesartan Cilexetil and Hydrochlorothiazidein Tablet Dosage Form
A new simple derivative spectrophotometric method has been developed for the simultaneous determination of Candesartan Cilexetil and Hydrochlorothiazide in tablet dosage forms. Candesartan antagonizes the effect of angiotensin II (vasoconstriction and aldosterone secretion) by blocking the angiotensin II receptor in vascular smooth muscle and the adrenal gland and decrease the blood pressure whereas Hydrochlorothiazide increases chloride, sodium and water excretion by interfering with transport of sodium ions across renal tubular epithelium. And there by show the diuretic action. The first derivative method is based on the measurement of absorbance of one drug at the zero crossing point of another drug. Candesartan Cilexetil and Hydrochlorothiazide were determined at two different wavelengths 222.69 (zero crossing point of Hydrochlorothiazide) and 254.63 nm (zero crossing point of Candesartan Cilexetil) from the derivative spectra respectively. The methods hows linearity over the concentration range 0.5-50 and 0.1-50 µg/ml for Candesartan Cilexetil and Hydrochlorothiazide respectively in phosphate buffer. The proposed method was validated and can be used for routine analysis of combined tablet dosage forms containing Candesartan Cilexetil and Hydrochlorothiazide. Key words: Candesartan Cilexetil, Derivative spectroscopy, Hydrochlorothiazide, Simultaneous determination.
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