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用于乳腺癌治疗的多西他赛负载甲氧基聚(乙二醇)-聚(L-乳酸)纳米粒:合成、表征、方法验证及细胞毒性

Docetaxel-Loaded Methoxy poly(ethylene glycol)-poly (L-lactic Acid) Nanoparticles for Breast Cancer: Synthesis, Characterization, Method Validation, and Cytotoxicity.

作者信息

Miraj Shumaila, Saeed Hamid, Iqtedar Mehwish, Albekairi Norah A, Ahmed Nadeem, Danish Muhammad Zeeshan, Islam Muhammad, Rasool Muhammad Fawad, Deen Kashif Mairaj, Rathore Hassaan Anwer

机构信息

Department of Pharmaceutics, College of Pharmacy, University of the Punjab, Lahore 54000, Pakistan.

Department of Biotechnology, Lahore College for Women University, Jail Road, Lahore 54000, Pakistan.

出版信息

Pharmaceuticals (Basel). 2023 Nov 13;16(11):1600. doi: 10.3390/ph16111600.

Abstract

This study aimed to synthesize and characterize DTX-mPEG-PLA-NPs along with the development and validation of a simple, accurate, and reproducible method for the determination and quantification of DTX in mPEG-PLA-NPs. The prepared NPs were characterized using AFM, DLS, zetasizer, and drug release kinetic profiling. The RP-HPLC assay was developed for DTX detection. The cytotoxicity and anti-clonogenic effects were estimated using MTT and clonogenic assays, respectively, using both MCF-7 and MDA-MB-231 cell lines in a 2D and 3D culture system. The developed method showed a linear response, high precision, accuracy, RSD values of ≤2%, and a tailing factor ≤2, per ICH guidelines. The DTX-mPEG-PLA-NPs exhibited an average particle size of 264.3 nm with an encapsulation efficiency of 62.22%. The in vitro drug kinetic profile, as per the Krosmeyers-Peppas model, demonstrated Fickian diffusion, with initial biphasic release and a multistep sustained release over 190 h. The MTT assay revealed improved in vitro cytotoxicity against MCF-7 and MDA-MB-231 in the 2D cultures and MCF-7 3D mammosphere cultures. Significant inhibitions of the clonogenic potential of MDA-MB-231 were observed for all concentrations of DTX-mPEG-PLA-NPs. Our results highlight the feasibility of detecting DTX via the robust RP-HPLC method and using DTX-mPEG-PLA-NPs as a perceptible and biocompatible delivery vehicle with greater cytotoxic and anti-clonogenic potential, supporting improved outcomes in BC.

摘要

本研究旨在合成并表征多西他赛-甲氧基聚乙二醇-聚乳酸纳米粒(DTX-mPEG-PLA-NPs),同时开发并验证一种简单、准确且可重复的方法,用于测定和定量mPEG-PLA-NPs中的多西他赛。使用原子力显微镜(AFM)、动态光散射(DLS)、zeta电位仪和药物释放动力学分析对制备的纳米粒进行表征。开发了用于多西他赛检测的反相高效液相色谱(RP-HPLC)测定法。分别使用MTT和克隆形成试验评估细胞毒性和抗克隆形成作用,在二维和三维培养系统中使用MCF-7和MDA-MB-231细胞系。根据国际协调会议(ICH)指南,所开发的方法显示出线性响应、高精度、准确性、相对标准偏差(RSD)值≤2%以及拖尾因子≤2。DTX-mPEG-PLA-NPs的平均粒径为264.3 nm,包封率为62.22%。根据Krosmeyers-Peppas模型,体外药物动力学分析表明为菲克扩散,具有初始双相释放和190小时以上的多步持续释放。MTT试验显示,在二维培养以及MCF-7三维乳腺球培养中,对MCF-7和MDA-MB-231的体外细胞毒性有所改善。对于所有浓度的DTX-mPEG-PLA-NPs,均观察到MDA-MB-231的克隆形成潜力受到显著抑制。我们的结果突出了通过稳健的RP-HPLC方法检测多西他赛以及使用DTX-mPEG-PLA-NPs作为一种可感知且生物相容的递送载体的可行性,该载体具有更大的细胞毒性和抗克隆形成潜力,有助于改善乳腺癌(BC)的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ed/10675362/a44db52d6dcd/pharmaceuticals-16-01600-g001.jpg

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