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用于皮下递送刺激性抗癌药物的可降解水溶性聚合物前药。

Degradable water-soluble polymer prodrugs for subcutaneous delivery of irritant anticancer drugs.

作者信息

Guerassimoff Léa, Cao Jingming, Auguste Michaella, Bossion Amaury, Zhu Chen, Le Dao, Cailleau Catherine, Ismail Safa Mohamed, Mercier-Nomé Françoise, Nicolas Julien

机构信息

Université Paris-Saclay, CNRS, Institut Galien Paris-Saclay 91400 Orsay France

Université Paris-Saclay, IPSIT, INSERM UMR 996 91400 Orsay France.

出版信息

Chem Sci. 2025 Jul 10. doi: 10.1039/d5sc02967h.

Abstract

Chemotherapy is primarily administered intravenously (IV), but this route poses significant challenges (, high costs, patient discomfort, logistical difficulties, side effects such as infections from catheter use). Although oral and subcutaneous (SC) routes are preferred for their convenience and have the potential for better patient comfort and cost reduction, oral chemotherapy faces issues like poor bioavailability and adherence, while SC delivery is unsuitable for irritant or vesicant drugs due to local toxicity. To overcome these limitations, the polymer prodrug strategy has been explored, where drugs are linked to a polymer, reducing toxicity and enhancing drug delivery. Recent work has focused on creating water-soluble polymer prodrugs for SC delivery of paclitaxel (Ptx), a hydrophobic and vesicant drug, which was successfully conjugated to polyacrylamide (PAAm), a very hydrophilic biocompatible polymer, resulting in safer SC injection and enhanced therapeutic efficacy in tumor-bearing mice. However, this strategy's potential depends on adapting it to other vesicant anticancer drugs. Making the polymer degradable for facilitated excretion would also be a key improvement. In this work, this approach has been successfully extended to gemcitabine (Gem), a widely used but irritant anticancer drug, and to a degradable PAAm-based promoiety, having cleavable ester groups in the main chain. The resulting Gem-based prodrugs featured upper critical solution temperature to ensure complete solubility at the temperature of the SC tissue, sustained Gem release, significant degradation under physiological conditions, improved systemic toxicity and absence of local toxicity compared to free Gem. Remarkably, Gem-PAAm polymer prodrugs exhibited significant anticancer efficacy in mice bearing Mia Pa-Ca 2 tumors, outperforming Gemzar®, the commercial formulation of Gem. These advances suggest the potential of these hydrophilic polymer prodrugs to transform SC chemotherapy, enabling the use of a broader range of anticancer drugs while reducing side effects and improving patient outcomes.

摘要

化疗主要通过静脉注射(IV)给药,但这种给药途径存在重大挑战(成本高、患者不适、后勤困难、诸如因使用导管导致感染等副作用)。尽管口服和皮下(SC)给药途径因其便利性而更受青睐,并且有可能提高患者舒适度并降低成本,但口服化疗面临生物利用度差和依从性等问题,而皮下给药由于局部毒性不适用于刺激性或发泡性药物。为了克服这些限制,人们探索了聚合物前药策略,即将药物与聚合物连接,降低毒性并增强药物递送。最近的工作集中在制备用于皮下递送紫杉醇(Ptx)的水溶性聚合物前药,紫杉醇是一种疏水性发泡性药物,已成功与聚丙烯酰胺(PAAm)偶联,聚丙烯酰胺是一种非常亲水的生物相容性聚合物,在荷瘤小鼠中实现了更安全的皮下注射并提高了治疗效果。然而,该策略的潜力取决于将其应用于其他发泡性抗癌药物。使聚合物可降解以促进排泄也将是一项关键改进。在这项工作中,该方法已成功扩展到吉西他滨(Gem),一种广泛使用但具有刺激性的抗癌药物,并扩展到基于可降解PAAm的前体部分,其主链中具有可裂解的酯基。所得的基于Gem的前药具有上临界溶液温度,以确保在皮下组织温度下完全溶解,实现Gem的持续释放,在生理条件下显著降解,与游离Gem相比全身毒性改善且无局部毒性。值得注意的是,Gem-PAAm聚合物前药在携带Mia Pa-Ca 2肿瘤的小鼠中表现出显著的抗癌疗效,优于Gem的商业制剂Gemzar®。这些进展表明这些亲水性聚合物前药在改变皮下化疗方面的潜力,能够使用更广泛的抗癌药物,同时减少副作用并改善患者预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ef/12327024/639e278535b9/d5sc02967h-f1.jpg

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