Poly (ortho esters) (POEs) as cutting-edge biodegradable polymers for targeted cancer treatment and overcoming multidrug resistance.

Devansh Shah, Sankha Bhattacharya
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Abstract

Poly (ortho esters) (POEs), biodegradable polymers featuring acid-labile ortho ester bonds formed through diol-diketene acetal reactions, are transforming cancer treatment with pH-sensitive surface erosion. This analysis explores the development of POE I, II, III, and IV (POE I-IV), suggesting that their adjustable degradation and controlled drug release may address multidrug resistance (MDR) and transform targeted cancer treatment. We seek to highlight the structural adaptability of POEs, their therapeutic functions, and their potential as advanced drug delivery systems. POE I, developed in the 1970s, faced challenges with autocatalytic degradation. POE II brought in neutral byproducts for enhanced stability, POE III facilitated injectable semi-solid formulations, and POE IV, the ultimate advancement, incorporates latent acid segments for self-catalysed hydrolysis in acidic tumour micro environments (pH 6.5-6.8), removing the need for external excipients. POE nanoparticles (50-300 nm) flexibly modify their size to improve tumour infiltration through the enhanced permeability and retention effect. Surface alterations, such as PEGylation or ligand attachment (e.g. folic acid), enable accurate targeting while minimising systemic toxicity. POEs are proficient in jointly delivering chemotherapeutics and immunomodulators, addressing MDR by inducing apoptosis, necrosis, autophagy, and pyroptosis, enhancing anti-tumour immunity. The degradation products that are biocompatible, such as acids and alcohols, promote immune interaction within the tumour microenvironment (TME). The review examines the synthesis, characterisation, and applications of POEs in post-surgical chemotherapy, ocular oncology, and protein delivery, as well as their interactions with cancer cell membranes and modulation of the TME. Issues such as scalability in manufacturing, enduring biocompatibility, and regulatory challenges are tackled, along with POEs' promise in immunotherapy and gene editing for tailored medicine. Through the integration of these insights, we emphasise POEs as a symbol of optimism for targeted, less harmful cancer therapies, leading to groundbreaking oncology advancements.

聚邻苯二甲酸酯(poe)作为一种尖端的生物可降解聚合物用于靶向癌症治疗和克服多药耐药。
聚邻位酯(poe)是一种可生物降解的聚合物,具有酸不稳定的邻位酯键,通过二醇-二烯醛缩醛反应形成,正在改变ph敏感表面侵蚀的癌症治疗。本文分析了聚(邻位酯)I、II、III和IV (POE I-IV)的发展,表明它们的可调节降解和控制药物释放可能解决多药耐药(MDR)问题,并改变靶向癌症治疗。我们试图强调POEs的结构适应性,它们的治疗功能,以及它们作为先进药物输送系统的潜力。20世纪70年代开发的POE I面临着自催化降解的挑战。POE II带来了中性副产物,增强了稳定性,POE III促进了可注射的半固体配方,POE IV是最终的进步,包含了潜在的酸段,可在酸性肿瘤微环境(pH 6.5-6.8)中自催化水解,无需外部赋形剂。POE纳米颗粒(50-300 nm)灵活调整其大小,通过增强渗透性和滞留效应来改善肿瘤浸润。表面改变,如聚乙二醇化或配体附着(如叶酸),能够准确靶向,同时最大限度地减少全身毒性。POEs擅长联合输送化疗药物和免疫调节剂,通过诱导细胞凋亡、坏死、自噬和焦亡来解决MDR问题,增强抗肿瘤免疫。具有生物相容性的降解产物,如酸和醇,促进肿瘤微环境(TME)内的免疫相互作用。本文综述了POEs的合成、表征及其在术后化疗、眼肿瘤和蛋白质传递中的应用,以及它们与癌细胞膜的相互作用和TME的调节。它们解决了制造的可扩展性、持久的生物相容性和监管挑战等问题,以及POEs在免疫治疗和定制药物基因编辑方面的前景。通过整合这些见解,我们强调POEs是有针对性的、危害较小的癌症治疗的乐观象征,将导致肿瘤学的突破性进展。& # xD。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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