根据ICHQ2(R2)指南:应用反相高效液相色谱法定量脂质体中紫杉醇和小檗碱的含量。

IF 1.7 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Debanjan Mukherjee, Raj Kamal, Akshay Kumar Lunawat, Tarun Sharma, Nitish Kumar, Ankit Awasthi, Shubham Thakur
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引用次数: 0

摘要

小檗碱(Berberine, BER)是一种抗氧化、抗炎和抗肿瘤的药物,而紫杉醇(paclitaxel, PTX)是一种广泛应用于乳腺癌的合成化疗药物。一些报告建议使用PTX和BER联合治疗乳腺癌,许多制药科学家正在努力开发一种结合这种组合的新型药物输送系统。然而,文献中缺乏一种可靠的同时估计方法。因此,在本研究中,我们旨在建立一种可靠的反相高效液相色谱法,用于同时估计脂质体制剂中游离药物形式的PTX和BER。方法采用C18色谱柱(250 × 4.6 mm, 5µm),乙腈和水(70:30,v/v)为流动相,流速为0.8 mL/min,检测波长为250 nm。PTX和BER的滞留时间分别为2.84 min和5.62 min。对理论极板>2000进行了验证,得到了0.9979 (PTX)和0.9975 (BER) 2个值的峰值尾迹。体外释放度为98.83±2.94% (PTX),体外释放度为96.56±1.92% (BER), 24 h内释放度均在可接受范围内。验证的方法精密度高、准确度高、可靠性好,适用于药物制剂分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reversed-Phase High-Performance Liquid Chromatography Assisted Simultaneous Estimation and Validation as per ICHQ2(R2) Guidelines: Application of Method in Quantification of Paclitaxel and Berberine in Liposomes-Based Delivery System.

Berberine (BER) is an antioxidant, anti-inflammatory, and antitumor agent, while paclitaxel (PTX) is a widely used synthetic chemotherapeutic agent for breast cancer. Several reports have suggested the use of a PTX and BER combination for the effective treatment of breast cancer, and many pharmaceutical scientists are working to develop a novel drug delivery system incorporating this combination. However, the literature lacks a reliable simultaneous estimation method for this combination. Therefore, in the present study, we aimed to develop a robust reversed-phase high-performance liquid chromatography method for the simultaneous estimation of PTX and BER in free drug form in liposomal formulation. The method employed a C18 column (250 × 4.6 mm, 5 µm) with acetonitrile and water (70:30, v/v) as the mobile phase at a flow rate of 0.8 mL/min and detection at 250 nm. Retention times were 2.84 and 5.62 min for PTX and BER, respectively. Theoretical plates >2000 were demonstrated, and peak tailing of <2 in validation as per ICH Q2(R2) was observed. In the 10-50 ppm range, linearity was found with R2 values of 0.9979 (PTX) and 0.9975 (BER). Furthermore, the method achieved within acceptable limits precision (<2% relative standard deviation) and accuracy (90%-110%). Robustness assessments checked method reliability in small variations. In addition, using the method effectively, entrapment efficiencies of 85.27 ± 1.74% and 78.62 ± 2.38% were obtained for PTX and BER in liposomal formulations. Moreover, in vitro release studies revealed 98.83 ± 2.94% (PTX) and 96.56 ± 1.92% (BER) release over 24 h. The validated method was precise, accurate, and reliable, making it suitable for application in drug formulation analysis.

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来源期刊
Assay and drug development technologies
Assay and drug development technologies 医学-生化研究方法
CiteScore
3.60
自引率
0.00%
发文量
33
审稿时长
>12 weeks
期刊介绍: ASSAY and Drug Development Technologies provides access to novel techniques and robust tools that enable critical advances in early-stage screening. This research published in the Journal leads to important therapeutics and platforms for drug discovery and development. This reputable peer-reviewed journal features original papers application-oriented technology reviews, topical issues on novel and burgeoning areas of research, and reports in methodology and technology application. ASSAY and Drug Development Technologies coverage includes: -Assay design, target development, and high-throughput technologies- Hit to Lead optimization and medicinal chemistry through preclinical candidate selection- Lab automation, sample management, bioinformatics, data mining, virtual screening, and data analysis- Approaches to assays configured for gene families, inherited, and infectious diseases- Assays and strategies for adapting model organisms to drug discovery- The use of stem cells as models of disease- Translation of phenotypic outputs to target identification- Exploration and mechanistic studies of the technical basis for assay and screening artifacts
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