Eco-conscious chromatographic determination of an anti-depressant free-dose combination in the presence of related impurities.

IF 2.7 3区 化学 Q2 CHEMISTRY, ANALYTICAL
Naglaa A Kabil, Hawaa M Khalil, Hind E El Ghwas, Shymaa Bibars, Sara Abdulwahab
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Abstract

According to the World Health Organization (WHO), an estimated 10% of pharmaceutical products distributed in developing countries are counterfeit or of substandard quality. A crucial strategy to help overcome this problem is to develop simple and easily applicable analytical methods for quality control testing of drugs, especially those administered in combinations due to their complex nature. Here, we worked towards this goal through the development of a simple, and rapid method based on High Performance Liquid Chromatography coupled with Ultraviolet detection (HPLC-UV) for the simultaneous determination of an anti-depressant free-drug combination consisting of brexpiprazole (BREX) and fluoxetine (FLX) in the presence of fluoxetine related impurities (FLX-A). Chromatographic separation was carried out employing a mixture of 45% ethanol and 55% aqueous solvent consisting of 0.1% triethylamine, 0.15 M sodium dodecyl sulfate and 0.057 M sodium dihydrogen phosphate adjusted to pH 6 using orthophosphoric acid. Separation was performed using a hypersil BDS C18 column at 50 °C, employing isocratic elution; the flow rate was set at 1.5 mL min-1, and UV detection was performed at 220 nm. The results of the developed method reflect excellent analytical performance. Linearity was observed over a concentration range of 5-80 μg mL-1 for both drugs with correlation coefficients of 0.9996 and 0.9998 for BREX and FLX, respectively. The respective LOQ and LOD values were found to be 2.70 and 4.41 μg mL-1 and 0.83 and 1.46 μg mL-1 for BREX and FLX; in addition, the developed method was utilized to test the purity of both drugs in pharmaceutical formulations by monitoring fluoxetine-related impurities. The developed method was also determined to be eco-friendly, as testing with four available assessment tools demonstrated its superior greenness, especially represented by an AGREE score of 0.83.

存在相关杂质的抗抑郁自由剂量组合的生态意识色谱测定。
据世界卫生组织(世卫组织)估计,在发展中国家销售的药品中有10%是假冒或质量不合格的。帮助克服这一问题的一个关键战略是开发简单和易于应用的分析方法,用于药物的质量控制测试,特别是那些由于其复杂性而以联合方式给药的药物。在此,我们通过建立一种基于高效液相色谱-紫外检测(HPLC-UV)的简单、快速的方法来同时测定含有氟西汀相关杂质(FLX- a)的由brexpiprazole (BREX)和fluoxetine (FLX)组成的抗抑郁药物组合。色谱分离采用45%乙醇和55%水溶液的混合物,该溶剂由0.1%三乙胺、0.15 M十二烷基硫酸钠和0.057 M磷酸二氢钠组成,用正磷酸调节pH为6。采用高sil BDS C18色谱柱在50℃下进行分离,采用等密度洗脱;流速为1.5 mL min-1,紫外检测波长为220 nm。该方法具有良好的分析性能。BREX和FLX在5 ~ 80 μ mL-1浓度范围内呈线性关系,相关系数分别为0.9996和0.9998。BREX和FLX的定量限分别为2.70和4.41 μg mL-1, 0.83和1.46 μg mL-1;此外,所开发的方法还用于通过监测氟西汀相关杂质来检测药物制剂中两种药物的纯度。开发的方法也被确定为生态友好型,因为使用四种可用的评估工具进行测试表明其具有优越的绿色,特别是以0.83的AGREE得分为代表。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Analytical Methods
Analytical Methods CHEMISTRY, ANALYTICAL-FOOD SCIENCE & TECHNOLOGY
CiteScore
5.10
自引率
3.20%
发文量
569
审稿时长
1.8 months
期刊介绍: Early applied demonstrations of new analytical methods with clear societal impact
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