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载顺铂和齐墩果酸的硅纳米粒子增强肺癌细胞凋亡和逆转多药耐药。

Co-delivery of cisplatin and oleanolic acid by silica nanoparticles-enhanced apoptosis and reverse multidrug resistance in lung cancer.

机构信息

Department of Thoracic Oncosurgery-2, Jilin Province Tumor Hospital, Changchun, China.

Oral and Maxillofacial Surgery, Jilin Province Tumor Hospital, Changchun, China.

出版信息

Kaohsiung J Med Sci. 2021 Jun;37(6):505-512. doi: 10.1002/kjm2.12365. Epub 2021 Feb 8.

Abstract

Multidrug resistance (MDR) of chemotherapy is one of the significant concerns in cancer therapy. Here in our study, cisplatin (DDP) and oleanolic acid (OA) were co-loaded in mesoporous silica nanoparticles (Nsi) to construct DDP/OA-Nsi and solve the DDP-resistance in lung cancer therapy. The cytotoxicity and apoptosis assays demonstrated that in DDP-resistant A549/DDP cells, the cytotoxicity of DDP/OA-Nsi was significantly higher than that of free DDP or DDP single delivery system (DDP-Nsi). The intracellular drug accumulation study revealed that the intracellular DDP concentration in the DDP/OA-Nsi group was also higher than that in free DDP and DDP-Nsi groups. In the A549/DDP xenograft tumor model, DDP/OA-Nsi showed the best anticancer effect. In summary, DDP/OA-Nsi was a promising drug delivery system to solve MDR in lung cancer therapy.

摘要

多药耐药(MDR)是癌症治疗中的一个重大问题。在本研究中,顺铂(DDP)和齐墩果酸(OA)被共载于介孔硅纳米粒子(Nsi)中,构建了 DDP/OA-Nsi,以解决肺癌治疗中的 DDP 耐药问题。细胞毒性和细胞凋亡实验表明,在 DDP 耐药的 A549/DDP 细胞中,DDP/OA-Nsi 的细胞毒性明显高于游离 DDP 或 DDP 单一给药系统(DDP-Nsi)。细胞内药物积累研究表明,DDP/OA-Nsi 组的细胞内 DDP 浓度也高于游离 DDP 和 DDP-Nsi 组。在 A549/DDP 异种移植肿瘤模型中,DDP/OA-Nsi 显示出最佳的抗癌效果。综上所述,DDP/OA-Nsi 是一种有前途的药物传递系统,可解决肺癌治疗中的 MDR 问题。

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