Liu Yanhong, Wang Meiyan, Liu Wanru, Jing Jili, Ma Hongshuang
Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital, Jilin University, Changchun, China.
Department of Rheumatology and Immunology, First Hospital, Jilin University, Changchun, China.
Front Bioeng Biotechnol. 2022 May 2;10:904344. doi: 10.3389/fbioe.2022.904344. eCollection 2022.
Although great progress has been made in improving the efficacy of cancer treatment through combination treatment using drug agents, there are still challenges in improving the efficiency of drug delivery. In this study, olaparib and doxorubicin were co-loaded on disulfide bond cross-linked polypeptide nanogels for the treatment of breast cancer in mouse models. Under stimulation of a high glutathione environment in cancer cells, the drug is quickly released from the nanogel to target cancer cells. In addition, compared with free drugs and single-drug-loaded nanogels, dual-drug- co-loaded nanogels exhibit the best anti-cancer effect and demonstrated excellent biological safety. Therefore, the co-delivery of olaparib and doxorubicin through polypeptide nanogels presents good prospects for application as anti-cancer treatment.
尽管通过使用药物进行联合治疗在提高癌症治疗疗效方面取得了巨大进展,但在提高药物递送效率方面仍存在挑战。在本研究中,奥拉帕利和阿霉素共负载于二硫键交联的多肽纳米凝胶上,用于治疗小鼠模型中的乳腺癌。在癌细胞的高谷胱甘肽环境刺激下,药物迅速从纳米凝胶中释放出来以靶向癌细胞。此外,与游离药物和单药负载的纳米凝胶相比,双药共负载的纳米凝胶表现出最佳的抗癌效果,并显示出优异的生物安全性。因此,通过多肽纳米凝胶共递送奥拉帕利和阿霉素作为抗癌治疗具有良好的应用前景。