Wan Shengli, Fan Qingze, Wu Yuesong, Zhang Jingqing, Qiao Gan, Jiang Nan, Yang Jie, Liu Yuanzhi, Li Jingyan, Chiampanichayakul Sawitree, Tima Singkome, Tong Fei, Anuchapreeda Songyot, Wu Jianming
Division of Clinical Microscopy, Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, Thailand.
Department of Pharmacy, The Affiliated Hospital of Southwest Medical University, Luzhou 646000, China.
Pharmaceutics. 2023 Feb 13;15(2):631. doi: 10.3390/pharmaceutics15020631.
Cancer is a serious threat to human health, and chemotherapy for cancer is limited by severe side effects. Curcumin (CUR) is a commonly used natural product for antitumor treatment without safety concerns. However, low bioavailability and poor tumor accumulation are great obstacles for its clinical application. Our previous research has demonstrated that platelet membrane-camouflaged nanoparticles can efficiently ameliorate the in vivo kinetic characteristics and enhance the tumor affinity of payloads. Nevertheless, the antitumor efficiency of this formulation still needs to be thoroughly investigated, and its drug release behavior is limited. Herein, CUR-loaded platelet membrane bioinspired chitosan-modified liposome (PCLP-CUR) was constructed to improve CUR release. PCLP-CUR was shown to have long retention time, improved bioavailability, strong tumor targeting capacity and effective cellular uptake. The incorporation of chitosan enabled PCLP-CUR to release cargoes quickly under mild acidic tumor conditions, leading to more complete drug release and favoring subsequent treatment. Both in vitro and in vivo investigations showed that PCLP-CUR could significantly enhance the anticancer efficacy of CUR with minimal side effects through biomimetic membrane and chitosan modification. In summary, this developed delivery system can provide a promising strategy for tumor-targeting therapy and phytochemical delivery.
癌症是对人类健康的严重威胁,癌症化疗受到严重副作用的限制。姜黄素(CUR)是一种常用的用于抗肿瘤治疗的天然产物,不存在安全性问题。然而,低生物利用度和较差的肿瘤蓄积性是其临床应用的巨大障碍。我们之前的研究表明,血小板膜伪装的纳米颗粒可以有效改善体内动力学特征并增强所载药物的肿瘤亲和力。尽管如此,这种制剂的抗肿瘤效率仍需深入研究,并且其药物释放行为也受到限制。在此,构建了负载姜黄素的血小板膜仿生壳聚糖修饰脂质体(PCLP-CUR)以改善姜黄素的释放。PCLP-CUR显示出具有较长的保留时间、提高的生物利用度、强大的肿瘤靶向能力和有效的细胞摄取。壳聚糖的加入使PCLP-CUR能够在温和的酸性肿瘤条件下快速释放所载物,从而实现更完全的药物释放并有利于后续治疗。体外和体内研究均表明,PCLP-CUR通过仿生膜和壳聚糖修饰能够显著增强姜黄素的抗癌疗效,且副作用最小。总之,这种开发的递送系统可为肿瘤靶向治疗和植物化学物质递送提供一种有前景的策略。