Rahman Nafisur, Khan Sumaiya
Department of Chemistry, Aligarh Muslim University, Aligarh 202002, Uttar Pradesh, India.
ACS Omega. 2019 Feb 26;4(2):4252-4258. doi: 10.1021/acsomega.8b03384. eCollection 2019 Feb 28.
Simple and selective zero- and second-order derivative circular dichroism (CD) spectroscopic methods have been designed for the assay of captopril in commercially available dosage forms. A normal CD spectroscopic scan (zero order) exhibits a negative band at 208 nm (method A) in distilled water. The calibration curve shows a linear response over the concentration range of 10-80 μg mL. The second-order derivative (D2) CD spectrum shows one positive band at 208 nm (method B) and one negative band at 225 nm (method C). Linear calibration curves were obtained in the concentration range of 10-70 μg mL for both the methods (B and C). The detection limits were found to be 1.26, 1.48, and 2.38 μg mL for methods A, B, and C, respectively. The study under stressed acidic, basic, and oxidative conditions showed the degradation of captopril. The proposed methods were validated as per ICH guidelines. All the proposed methods were compared with the reference method to demonstrate its suitability for quality control of captopril in its dosage forms.
已设计出简单且具有选择性的零阶和二阶导数圆二色光谱法(CD),用于测定市售剂型中的卡托普利。普通的CD光谱扫描(零阶)在蒸馏水中于208 nm处呈现一个负峰(方法A)。校准曲线在10 - 80 μg/mL的浓度范围内呈线性响应。二阶导数(D2)CD光谱在208 nm处显示一个正峰(方法B),在225 nm处显示一个负峰(方法C)。方法B和C在10 - 70 μg/mL的浓度范围内均获得了线性校准曲线。方法A、B和C的检测限分别为1.26、1.48和2.38 μg/mL。在酸性、碱性和氧化应激条件下的研究表明卡托普利会降解。所提出的方法按照国际人用药品注册技术协调会(ICH)指南进行了验证。将所有所提出的方法与参考方法进行比较,以证明其适用于卡托普利剂型的质量控制。