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用于定量测定溴马唑仑及其降解产物的稳定性指示分光光度法。

Stability indicating spectrophotometric methods for quantitative determination of bromazepam and its degradation product.

机构信息

Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia; Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr El-Aini St., Cairo 11562, Egypt.

Toxicology Laboratory, Forensic Medicine Authority, Justice Ministry,114 Bairam El Tounsy St., El Sayeda Zeinab, 11647 Cairo, Egypt.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2020 Sep 5;238:118433. doi: 10.1016/j.saa.2020.118433. Epub 2020 May 5.

Abstract

Four simple, sensitive and selective stability indicating spectrophotometric methods are presented for quantitative determination of the benzodiazepine drug; bromazepam (BMZ) and one of its reported potential impurities and degradation product; 2-(2-amino-5-bromobenzoyl) pyridine (ABP) in methanol. Method A, is isoabsorptive point coupled with D method, where good linearity was obtained by measuring the absorbance of BMZ at 264 nm (A) in the concentration range of 2-25 μg mL, and the absorbance of ABP at its λ 396 nm in concentration range of 0.5-24 μg mL. Method B, is ratio subtraction; the absorbance was measured at 233 nm for BMZ using 20 μg mL of ABP, while ABP was determined directly at its λ 396 nm using methanol as a solvent. Method C, was based on measuring the total peak amplitude of the first derivative of the ratio spectra (DD) of BMZ from 301 to 326 nm using 10 μg mL of ABP as a divisor and determination of ABP at peak amplitude of 293 nm using 5 μg mL of BMZ as a divisor. In method D, ratio difference method, good linearity was achieved for determination of BMZ and ABP by measuring the differences between the amplitudes of ratio spectra at 312 nm and 274 nm and differences between the amplitudes of ratio spectra at 274 nm and 312 nm, respectively. The stability of BMZ was investigated under different ICH recommended forced degradation conditions. The suggested methods were then successfully applied for determination of BMZ in its pharmaceutical formulations.

摘要

四种简单、灵敏和选择性的稳定指示分光光度法被提出,用于定量测定苯并二氮䓬类药物;溴马唑仑(BMZ)及其一种报道的潜在杂质和降解产物;2-(2-氨基-5-溴苯甲酰)吡啶(ABP)在甲醇中。方法 A 是等吸收点结合 D 法,通过测量 BMZ 在 264nm 处的吸光度(A)在 2-25μg mL 的浓度范围内,以及 ABP 在 396nm 处的吸光度在 0.5-24μg mL 的浓度范围内得到良好的线性关系。方法 B 是比率减法;在 233nm 处测量 BMZ 的吸光度,使用 20μg mL 的 ABP,而 ABP 则直接在其 396nm 处使用甲醇作为溶剂进行测定。方法 C 是基于测量比值光谱(DD)的第一导数的总峰幅度,其中 BMZ 从 301 到 326nm,使用 10μg mL 的 ABP 作为除数,以及使用 5μg mL 的 BMZ 作为除数在 293nm 处测定 ABP 的峰幅度。在方法 D 中,通过测量 312nm 和 274nm 处比值光谱的幅度差以及 274nm 和 312nm 处比值光谱的幅度差,实现了对 BMZ 和 ABP 的良好线性测定。在不同 ICH 推荐的强制降解条件下研究了 BMZ 的稳定性。然后,这些方法成功地应用于其药物制剂中 BMZ 的测定。

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