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纳米晶体技术在以转化研究范式靶向癌症化疗药物方面的新见解。

New insights in nanocrystal technology chemotherapeutic drugs targeting cancer with a translational research paradigm.

作者信息

Iqbal Furqan Muhammad, Delie Florence, Iqbal Muhammad Omer, Gul Safia, Kanwal Sumaira, Muzammal Muhammad, Ahmad Aftab, Munawar Nayla

机构信息

Institute of Pharmaceutical Sciences of Western Switzerland, University of Geneva Rue Michel-Servet 1, Geneva 1211, Switzerland.

School of Pharmaceutical Sciences, University of Geneva Rue Michel-Servet 1, Geneva 1211, Switzerland.

出版信息

Am J Transl Res. 2025 Aug 15;17(8):5829-5847. doi: 10.62347/ETMK5291. eCollection 2025.

Abstract

Nanocrystal formulation has been increasingly investigated for overcoming the limitations of Biopharmaceutical Classification System (BCS) Class II and IV chemotherapeutic agents. Nanocrystal (NC) formation is widely accepted for increasing the solubility, biological barrier permeability, and cell internalization of poorly-soluble chemotherapeutic drugs. Nanocrystalization improves the bioavailability of anticancer agents, increasing their cytotoxicity and effectiveness for cancer treatment. NCs are nanodrug particles that are coated with a thin polymer or surfactant layer, that enhance their stability, solubility, and internalization in tumor cells. For active targeting, NCs can be decorated with ligands, e.g., proteins and amino acids. NCs also undergo passive targeting by high cellular uptake and retention in the mononuclear phagocyte system (MPS). They are prepared by either top-down, or bottom-up methods or a combination and can be scaled up for industrial manufacturing. NCs are safely administered by oral, parenteral, or transdermal routes. This review highlights the role of morphology and stabilizer, with brief discussions on nanocrystal production, ligand conjugation on drug nanocrystal targeting, and uptake in cancer cells. The benefits of NC formulations over conventional drug delivery are presented by discussing aspects of cytotoxicity studies of anticancer drugs.

摘要

为克服生物药剂学分类系统(BCS)II类和IV类化疗药物的局限性,人们对纳米晶制剂展开了越来越多的研究。纳米晶(NC)的形成被广泛认可,它可提高难溶性化疗药物的溶解度、生物屏障通透性和细胞内化能力。纳米晶化提高了抗癌药物的生物利用度,增强了它们的细胞毒性以及癌症治疗效果。纳米晶是纳米药物颗粒,表面包裹着一层薄薄的聚合物或表面活性剂层,这增强了它们在肿瘤细胞中的稳定性、溶解度和内化能力。为实现主动靶向,纳米晶可缀合配体,如蛋白质和氨基酸。纳米晶还会通过在单核吞噬细胞系统(MPS)中的高细胞摄取和滞留而发生被动靶向。它们可通过自上而下、自下而上的方法或两者结合来制备,并且可以扩大规模用于工业生产。纳米晶可通过口服、肠胃外或透皮途径安全给药。本综述重点介绍了形态学和稳定剂的作用,并简要讨论了纳米晶的制备、药物纳米晶靶向中的配体缀合以及在癌细胞中的摄取。通过讨论抗癌药物细胞毒性研究的各个方面,介绍了纳米晶制剂相对于传统药物递送的优势。

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