Fan Yueyue, Cui Yuexin, Hao Wenyan, Chen Mengyu, Liu Qianqian, Wang Yuli, Yang Meiyan, Li Zhiping, Gong Wei, Song Shiyong, Yang Yang, Gao Chunsheng
College of Pharmacy, Henan University, Kaifeng, 475000, PR China.
State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, Beijing, 100850, PR China.
Bioact Mater. 2021 May 1;6(12):4402-4414. doi: 10.1016/j.bioactmat.2021.04.027. eCollection 2021 Dec.
Nanosuspensions, as a new drug delivery system for insoluble drugs, are only composed of a drug and a small amount of stabilizer, which is dispersed in an aqueous solution with high drug-loading, small particle size, high dispersion, and large specific surface area. It can significantly improve the dissolution, bioavailability, and efficacy of insoluble drugs. In this study, paclitaxel nanosuspensions ((PTX)NS) were prepared by an ultrasonic precipitation method, with the characteristics of simple preparation and easy repetition. With the help of a homologous targeting mechanism, a kind of glioma C6 cancer cell membrane (CCM)-coated (PTX)NS was developed and modified with WSW peptide to obtain WSW-CCM-(PTX)NS with the functions of BBB penetration and tumor targeting. The results showed that the cancer cell membrane could effectively camouflage the nanosuspensions so that it was not cleared by the immune system and could cross the blood-brain-barrier (BBB) and selectively target tumor tissues. Cell uptake experiments and imaging confirmed that the uptake of WSW-CCM-(PTX)NS by tumor cells and the distribution in intracranial gliomas increased. Cytotoxicity test and anti-glioma studies showed that WSW-CCM-(PTX)NS could significantly inhibit the growth of glioma cells and significantly prolong the survival time of glioma-bearing mice. Finally, the cancer cell membrane coating endowed the nanosuspensions with the biological properties of homologous adhesion and immune escape. This study provides an integrated solution for improving the targeting of nanosuspensions and demonstrates the encouraging potential of biomimetic nanosuspensions applicable to tumor therapy.
纳米混悬液作为一种用于难溶性药物的新型给药系统,仅由药物和少量稳定剂组成,以高载药量、小粒径、高分散性和大比表面积分散于水溶液中。它能显著提高难溶性药物的溶出度、生物利用度和疗效。在本研究中,采用超声沉淀法制备了紫杉醇纳米混悬液((PTX)NS),其具有制备简单、易于重复的特点。借助同源靶向机制,开发了一种包被神经胶质瘤C6癌细胞膜(CCM)的(PTX)NS,并使用WSW肽进行修饰,以获得具有血脑屏障穿透和肿瘤靶向功能的WSW-CCM-(PTX)NS。结果表明,癌细胞膜能够有效地伪装纳米混悬液,使其不被免疫系统清除,并能穿过血脑屏障(BBB),选择性地靶向肿瘤组织。细胞摄取实验和成像证实,肿瘤细胞对WSW-CCM-(PTX)NS的摄取以及在颅内胶质瘤中的分布增加。细胞毒性试验和抗胶质瘤研究表明,WSW-CCM-(PTX)NS能够显著抑制胶质瘤细胞的生长,并显著延长荷瘤小鼠的存活时间。最后,癌细胞膜包被赋予了纳米混悬液同源黏附及免疫逃逸的生物学特性。本研究为提高纳米混悬液的靶向性提供了一个综合解决方案,并证明了仿生纳米混悬液在肿瘤治疗中的应用潜力令人鼓舞。