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开发一种用于布洛芬和去氧肾上腺素二元混合物稳定性指示测定的环保型高效液相色谱法。

Development of an eco-friendly HPLC method for the stability indicating assay of binary mixture of ibuprofen and phenylephrine.

作者信息

Kelani Khadiga M, Fayez Yasmin M, Abdel-Raoof Ahmed M, Fekry Reham A, Hassan Said A

机构信息

Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr El-Aini Street, Cairo, 11562, Egypt.

Analytical Chemistry Department, Faculty of Pharmacy (Boys), AL-Azhar University, Nasr City, Cairo, 11751, Egypt.

出版信息

BMC Chem. 2023 Oct 24;17(1):141. doi: 10.1186/s13065-023-01056-4.

Abstract

The development and validation of the stability indicating HPLC technique has contributed to the understanding of the stability profile of ibuprofen (IBU) and phenylephrine (PHE). Stability profile was achieved for PHE; the drug was found to be liable to be influenced by stress oxidative conditions; two oxidative degradants (Deg1 & Deg2) were formed and their structures were confirmed using IR and mass spectrometry. The drugs and degradation products were successfully separated using a gradient elution method on YMC-C8 column with 0.1% hexanesulfonic acid and acetonitrile as a mobile phase at pH 6.6. The flow rate was 1.0 mL/min, and a diode array detector operating at 220 nm was used for UV detection. The retention times of degradants Deg1, Deg2, ibuprofen (IBU), and phenylephrine hydrochloride (PHE) were 2.0, 2.2, 3.2 and 7.0 min, respectively. The proposed method was validated with respect to linearity, accuracy, precision, specificity, and robustness using ICH guidelines. The linearities of ibuprofen and phenylephrine hydrochloride were in the range of 10-100 μg/mL and 0.3-10 μg/mL, respectively. The % recoveries of the two drugs were found to be 100.75 ± 1.44%, 99.67% ± 1.67, and the LOD was found to be 2.75/mL and 0.09/mL for IBU, and PHE, respectively. The method was successfully applied to the estimation of ibuprofen and phenylephrine hydrochloride combination in pharmaceutical dosage form. The proposed technique was validated using ICH guidelines and its greenness was assessed according to Analytical Eco Scale metric (AES). Molecular docking was used to assess the two drugs and PHE oxidative degradants interaction with the stationary phase and to confirm the outcomes of the proposed method with regard to the order of elution of the two drugs and PHE degradation products. Eco-friendly and environmental safety were assessed through the application of one of the most applicable greenness assessment tool; Analytical Eco Scale metric (AES).

摘要

稳定性指示高效液相色谱技术的开发与验证有助于了解布洛芬(IBU)和去氧肾上腺素(PHE)的稳定性概况。实现了去氧肾上腺素的稳定性概况;发现该药物易受氧化应激条件的影响;形成了两种氧化降解产物(Deg1和Deg2),并使用红外光谱和质谱确认了它们的结构。使用梯度洗脱法在YMC-C8柱上,以0.1%己烷磺酸钠和乙腈为流动相,pH为6.6,成功分离了药物及其降解产物。流速为1.0 mL/min,使用在220 nm处运行的二极管阵列检测器进行紫外检测。降解产物Deg1、Deg2、布洛芬(IBU)和盐酸去氧肾上腺素(PHE)的保留时间分别为2.0、2.2、3.2和7.0分钟。按照国际协调会议(ICH)指南对所提出的方法进行了线性、准确性、精密度、特异性和稳健性方面的验证。布洛芬和盐酸去氧肾上腺素的线性范围分别为10 - 100 μg/mL和0.3 - 10 μg/mL。发现两种药物的回收率分别为100.75 ± 1.44%、99.67% ± 1.67%,布洛芬和去氧肾上腺素的检测限分别为2.75/mL和0.09/mL。该方法成功应用于药物剂型中布洛芬和盐酸去氧肾上腺素组合的测定。所提出的技术按照ICH指南进行了验证,并根据分析生态尺度指标(AES)评估了其绿色度。使用分子对接来评估两种药物和去氧肾上腺素氧化降解产物与固定相的相互作用,并确认所提出方法关于两种药物和去氧肾上腺素降解产物洗脱顺序的结果。通过应用最适用的绿色度评估工具之一——分析生态尺度指标(AES),评估了生态友好性和环境安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a236/10598928/1aa903253f67/13065_2023_1056_Fig1_HTML.jpg

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