散装和剂型 BCS-II 的等度 RP-HPLC 方法开发、验证和优化

IF 0.7 4区 医学 Q4 PHARMACOLOGY & PHARMACY Current Pharmaceutical Analysis Pub Date : 2024-01-26 DOI:10.2174/0115734129283491240103071614
Uditi Handa, Anuj Malik, Kumar Guarve, Fatimah Jan, Kajal Nagpal
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引用次数: 0

摘要

背景以往对氢溴酸右美沙芬的研究基本上是与其他化合物同时进行的。因此,需要开发一种采用等度洗脱模式的新型方法。目标::为了检测不同基质中的氢溴酸右美沙芬(DXM),设计并验证了一种使用 Waters 2487 双 λ 检测器的简单、准确、灵敏的反相高效液相色谱技术。方法:在本实验中,采用甲醇/pH 3.0 磷酸二氢钾缓冲液(70:30,v/v)作为流动相,在 C-18 HPLC 色谱柱(长 4.6 cm,内径 4.6 mm,粒径 5 μm)上以等度洗脱模式在 7 分钟内完成分离,流速为 1.0 mL/min,紫外检测波长为 278 nm。使用 Empower 2.4 软件对色谱响应进行整合:R2 为 0.9987,当前方法在 10- 60 ppm 范围内对 DXM 的线性度较高(保留时间为 4.281 ± 0.505 min)。对于 DXM Hbr,检测限(LOD & LOQ)分别为 10.633 μg/mL 和 32.221 μg/mL。样品在基质中保持稳定,无明显影响。结论这种新方法采用直接的液/液萃取程序,两种不同分析物的回收率在 100 ± 10 % 之间,准确度高。日内和日间的精确度均小于 2.0%(RSD)。该技术被证明具有可靠性和可重复性,可用于药理学(活性成分、糖浆)和生物(血液)基质,可用于未来生物分析方法开发的研究工作,如药代动力学研究。
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Isocratic RP-HPLC Method Development, Validation, and Optimization of BCS-II in Bulk and Dosage Form
Background:: Previous studies of dextromethorphan hydrobromide basically worked on simultaneous research with other compounds. So, the development of a novel method using the isocratic elution mode is needed. Objective:: For the detection of dextromethorphan hydrobromide (DXM) in diverse matrices, a straightforward, accurate, and sensitive reversed-phase HPLC technique using a Waters 2487 Dual λ Absorbance detector has been designed and validated. Method:: In this experimental work, utilizing methanol/pH 3.0 potassium dihydrogen phosphate buffer (70:30, v/v) as the mobile phase, the separation was completed in 7 minutes on a C-18 HPLC column (4.6 cm length, 4.6 mm internal diameter; 5 μm particle size) utilizing an isocratic elution mode, flow rate of 1.0 mL/min, and UV-detection at 278 nm. Integration of the chromatography response was carried out using Empower 2.4 software Results:: With an R2 of 0.9987, the current approach showed high linearity for DXM in the 10- 60 ppm range (retention time 4.281 ± 0.505 min). For DXM Hbr, the limits of detection (LOD & LOQ) were 10.633 μg/mL and 32.221μg/mL, respectively. Samples remained stable in the presence of the matrices without any apparent influence. Conclusion:: The novel approach, which used a straightforward liquid/liquid extraction procedure with recovery ranging from 100 ± 10 % performed by two different analytes, was accurate. The precision within and between days was ≤ 2.0% (RSD). The technique was proven to be reliable and repeatable, and it can be utilized with pharmacological (active ingredients, syrups) and also for biological (blood) matrices which can be used in future research work for bioanalytical method development such as pharmacokinetics studies.
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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
85
审稿时长
3 months
期刊介绍: Aims & Scope Current Pharmaceutical Analysis publishes expert reviews and original research articles on all the most recent advances in pharmaceutical and biomedical analysis. All aspects of the field are represented including drug analysis, analytical methodology and instrumentation. The journal is essential to all involved in pharmaceutical, biochemical and clinical analysis.
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