Curcumin-Loaded Platelet Membrane Bioinspired Chitosan-Modified Liposome for Effective Cancer Therapy

Author:

Wan Shengli1234,Fan Qingze24,Wu Yuesong45,Zhang Jingqing6,Qiao Gan45,Jiang Nan14,Yang Jie14,Liu Yuanzhi124,Li Jingyan14,Chiampanichayakul Sawitree1ORCID,Tima Singkome17ORCID,Tong Fei45,Anuchapreeda Songyot17ORCID,Wu Jianming35ORCID

Affiliation:

1. Division of Clinical Microscopy, Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, Thailand

2. Department of Pharmacy, The Affiliated Hospital of Southwest Medical University, Luzhou 646000, China

3. School of Basic Medical Sciences, Southwest Medical University, Luzhou 646000, China

4. School of Pharmacy, Southwest Medical University, Luzhou 646000, China

5. Key Laboratory of Medical Electrophysiology of Ministry of Education of China, School of Pharmacy, Southwest Medical University, Luzhou 646000, China

6. Chongqing Research Center for Pharmaceutical Engineering, Chongqing Medical University, Chongqing 400016, China

7. Center for Research and Development of Natural Products for Health, Chiang Mai University, Chiang Mai 50200, Thailand

Abstract

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.

Funder

National Natural Science Foundation of China

Science and Technology Planning Project of Sichuan Province, China

Joint Project of Luzhou Municipal People’s Government and Southwest Medical University, China

Luzhou Science and Technology Project, China

Foundation of Southwest Medical University

Publisher

MDPI AG

Subject

Pharmaceutical Science

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