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叶酸修饰壳聚糖纳米粒:新一代抗癌纳米载体。

Folate-engineered chitosan nanoparticles: next-generation anticancer nanocarriers.

机构信息

Department of Pharmaceutics, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi, 110062, India.

Department of Biological Sciences and Bioengineering (BSBE), Indian Institute of Technology, Uttar Pradesh, Kanpur, 208016, India.

出版信息

Mol Cancer. 2024 Oct 31;23(1):244. doi: 10.1186/s12943-024-02163-z.

Abstract

Chitosan nanoparticles (NPs) are well-recognized as promising vehicles for delivering anticancer drugs due to their distinctive characteristics. They have the potential to enclose hydrophobic anticancer molecules, thereby enhancing their solubilities, permeabilities, and bioavailabilities; without the use of surfactant, i.e., through surfactant-free solubilization. This allows for higher drug concentrations at the tumor sites, prevents excessive toxicity imparted by surfactants, and could circumvent drug resistance. Moreover, biomedical engineers and formulation scientists can also fabricate chitosan NPs to slowly release anticancer agents. This keeps the drugs at the tumor site longer, makes therapy more effective, and lowers the frequency of dosing. Notably, some types of cancer cells (fallopian tube, epithelial tumors of the ovary, and primary peritoneum; lung, kidney, ependymal brain, uterus, breast, colon, and malignant pleural mesothelioma) have overexpression of folate receptors (FRs) on their outer surface, which lets folate-drug conjugate-incorporated NPs to target and kill them more effectively. Strikingly, there is evidence suggesting that the excessively produced FR&αgr (isoforms of the FR) stays consistent throughout treatment in ovarian and endometrial cancer, indicating resistance to conventional treatment; and in this regard, folate-anchored chitosan NPs can overcome it and improve the therapeutic outcomes. Interestingly, overly expressed FRs are present only in certain tumor types, which makes them a promising biomarker for predicting the effectiveness of FR-targeted therapy. On the other hand, the folate-modified chitosan NPs can also enhance the oral absorption of medicines, especially anticancer drugs, and pave the way for effective and long-term low-dose oral metronomic scheduling of poorly soluble and permeable drugs. In this review, we talked briefly about the techniques used to create, characterize, and tailor chitosan-based NPs; and delved deeper into the potential applications of folate-engineered chitosan NPs in treating various cancer types.

摘要

壳聚糖纳米粒子(NPs)由于其独特的特性,被公认为是递送抗癌药物的有前途的载体。它们具有包裹疏水性抗癌分子的潜力,从而提高其溶解度、渗透性和生物利用度;而无需使用表面活性剂,即通过无表面活性剂的增溶作用。这使得肿瘤部位的药物浓度更高,防止了表面活性剂带来的过度毒性,并可能规避药物耐药性。此外,生物医学工程师和制剂科学家还可以制备壳聚糖 NPs 以缓慢释放抗癌剂。这使得药物在肿瘤部位停留更长时间,使治疗更有效,并降低给药频率。值得注意的是,某些类型的癌细胞(输卵管、卵巢上皮肿瘤和原发性腹膜;肺、肾、脑室管膜、子宫、乳腺、结肠和恶性胸膜间皮瘤)在其外表面过度表达叶酸受体(FRs),这使得叶酸-药物缀合物结合的 NPs 能够更有效地靶向和杀死它们。引人注目的是,有证据表明,在卵巢癌和子宫内膜癌的治疗过程中,过度产生的 FRαgr(FR 的同工型)始终保持一致,表明对常规治疗产生耐药性;在这方面,叶酸锚定的壳聚糖 NPs 可以克服它并改善治疗效果。有趣的是,过度表达的 FR 仅存在于某些肿瘤类型中,这使其成为预测 FR 靶向治疗效果的有前途的生物标志物。另一方面,叶酸修饰的壳聚糖 NPs 还可以增强药物的口服吸收,特别是抗癌药物,并为有效和长期低剂量口服节拍化疗铺平道路,这种化疗方案适用于溶解度和渗透性差的药物。在这篇综述中,我们简要讨论了用于制备、表征和定制壳聚糖基 NPs 的技术;并深入探讨了叶酸工程化壳聚糖 NPs 在治疗各种癌症类型中的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1008/11526716/5b92b86e1863/12943_2024_2163_Fig1_HTML.jpg

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