Léa Guerassimoff, Jingming Cao, Michaella Auguste, Amaury Bossion, Chen Zhu, Dao Le, Catherine Cailleau, Safa Mohamed Ismail, Françoise Mercier-Nomé, Julien Nicolas
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引用次数: 0
Abstract
Chemotherapy is primarily administered intravenously (IV), but this route poses significant challenges (e.g., 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.
化疗主要是静脉内给药(IV),但这一途径带来了重大挑战(例如,高成本,患者不适,后勤困难,副作用,如使用导管感染)。尽管口服和皮下(SC)途径因其便利性和更好的患者舒适度和降低成本的潜力而受到青睐,但口服化疗面临生物利用度和依从性差等问题,而由于局部毒性,SC递送不适合刺激性或泡状药物。为了克服这些限制,研究人员探索了聚合物前药策略,将药物与聚合物连接,降低毒性并增强药物传递。紫杉醇(Ptx)是一种疏水性和囊泡性药物,它成功地与一种非常亲水的生物相容性聚合物聚丙烯酰胺(PAAm)偶联,从而使SC注射更安全,并增强了对肿瘤小鼠的治疗效果。然而,这种策略的潜力取决于将其应用于其他抗肿瘤药物。使聚合物可降解以方便排泄也是一个关键的改进。在这项工作中,这种方法已经成功地扩展到吉西他滨(Gem),一种广泛使用但具有刺激性的抗癌药物,以及可降解的paam基促进剂,在主链上具有可切割的酯基。由此产生的基于Gem的前药具有较高的临界溶液温度,以确保在SC组织温度下完全溶解,持续的Gem释放,在生理条件下显着降解,与游离Gem相比,改善了全身毒性并且没有局部毒性。值得注意的是,Gem- paam聚合物前药在Mia pa - ca2肿瘤小鼠中表现出显著的抗癌功效,优于Gem的商业配方Gemzar®。这些进展表明,这些亲水聚合物前药有可能改变SC化疗,使更广泛的抗癌药物的使用成为可能,同时减少副作用并改善患者的预后。
期刊介绍:
Chemical Science is a journal that encompasses various disciplines within the chemical sciences. Its scope includes publishing ground-breaking research with significant implications for its respective field, as well as appealing to a wider audience in related areas. To be considered for publication, articles must showcase innovative and original advances in their field of study and be presented in a manner that is understandable to scientists from diverse backgrounds. However, the journal generally does not publish highly specialized research.