Goñi-de-Cerio Felipe, Thevenot Julie, Oliveira Hugo, Pérez-Andrés Encarnación, Berra Edurne, Masa Marc, Suárez-Merino Blanca, Lecommandoux Sébastien, Heredia Pedro
J Biomed Nanotechnol. 2015 Nov;11(11):2034-49. doi: 10.1166/jbn.2015.2148.
Encapsulating chemotherapy drugs in targeted nanodelivery systems is one of the most promising approaches to tackle cancer disease, avoiding side effects of common treatment. In the last decade, several nanocarriers with different nature have been tested, but polypeptide-based copolymers have attracted considerable attention for their biocompatibility, controlled and slow biodegradability as well as their low toxicity. In this work, we synthesized, characterized and evaluated poly(trimethylene carbonate)-bock-poly(L-glutamic acid) derived polymersomes, targeted to epidermal growth factor receptor (EGFR), loaded with plitidepsin and ultimately tested in HT29 and LS174T colorectal cancer cell lines for specificity and efficacy. Furthermore, morphology, physico-chemical properties and plitidepsin loading were carefully investigated. A thorough in vitro cytotoxicity analysis of the unloaded polymersomes was carried out for biocompatibility check, studying viability, cell membrane asymmetry and reactive oxygen species levels. Those cytotoxicity assays showed good biocompatibility for plitidepsin-unloaded polymersomes. Cellular uptake and cytotoxic effect of EGFR targeted and plitidepsin loaded polymersome indicated that colorectal cancer cell lines were.more sensitive to anti-EGFR-drug-loaded than untargeted drug-loaded polymersomes. Also, in both cell lines, the use of untargeted polymersomes greatly reduced plitidepsin cytotoxicity as well as the cellular uptake, indicating that the use of this targeted nanocarrier is a promising approach to tackle colorectal cancer disease and avoid the undesired effects of the usual treatment. Furthermore, in vivo assays support the in vitro conclusions that EGFR targeted polymersomes could be a good drug delivery system. This work provides a proof of concept for the use of encapsulated targeted drugs as future therapeutic treatments for cancer.
将化疗药物封装在靶向纳米递送系统中是攻克癌症疾病、避免常规治疗副作用的最具前景的方法之一。在过去十年中,已经测试了几种不同性质的纳米载体,但基于多肽的共聚物因其生物相容性、可控且缓慢的生物降解性以及低毒性而备受关注。在这项工作中,我们合成、表征并评估了靶向表皮生长因子受体(EGFR)的聚(三亚甲基碳酸酯)-嵌段-聚(L-谷氨酸)衍生的聚合物囊泡,其负载了普利替辛,并最终在HT29和LS174T结肠癌细胞系中测试了特异性和疗效。此外,还仔细研究了其形态、物理化学性质和普利替辛负载情况。对未负载的聚合物囊泡进行了全面的体外细胞毒性分析以检查生物相容性,研究细胞活力、细胞膜不对称性和活性氧水平。这些细胞毒性试验表明未负载普利替辛的聚合物囊泡具有良好的生物相容性。EGFR靶向且负载普利替辛的聚合物囊泡的细胞摄取和细胞毒性作用表明,结肠癌细胞系对负载抗EGFR药物的聚合物囊泡比未靶向负载药物的聚合物囊泡更敏感。此外,在这两种细胞系中,使用未靶向的聚合物囊泡大大降低了普利替辛的细胞毒性以及细胞摄取,这表明使用这种靶向纳米载体是攻克结肠直肠癌疾病并避免常规治疗不良影响的一种有前景的方法。此外,体内试验支持了体外结论,即EGFR靶向的聚合物囊泡可能是一种良好的药物递送系统。这项工作为使用封装的靶向药物作为未来癌症治疗方法提供了概念验证。