文獻名： Bioinspired red blood cell membrane-encapsulated biomimetic nanoconstructs for synergistic and efficacious chemo-photothermal therapy

作者：Pei Wanga; Fuquan Jiangb; Biaoqi Chenc; Hanxiao Tangc; Xiaojiao Zenga; Duanhua Caic; Mingzhi Zhuc; Ruimin Longc; Dayun Yange; Ranjith Kumar Kankalacd; Shibin Wangad; Yuangang Liucdf 

aCollege of Materials Science and Engineering, Huaqiao University, Xiamen, Fujian 361021, PR China

bSchool of Pharmaceutical Sciences, Fujian Provincial Key Laboratory of Innovative Drug Target Research, Xiamen University, Xiamen, Fujian, 361021, PR China

cCollege of Chemical Engineering, Huaqiao University, Xiamen, Fujian, 361021, PR China

dFujian Provincial Key Laboratory of Biochemical Technology, Xiamen, Fujian, 361021, PR China

eSchool of Basic Medical Science, Fujian Medical University, Fuzhou, Fujian, 350122, PR China

fInstitute of Pharmaceutical Engineering, Huaqiao University, Xiamen, Fujian, 361021, PR China

摘要：Recently, the fabrication of nanotechnology-based co-delivery systems has garnered enormous interest for efficacious cancer therapy. However, these systems still face certain challenges such as codelivery of drugs with different chemistries, inadequate loading efficiency, immune rejection resulting in rapid clearance and substantially poor bioavailability in vivo. To address the challenges, we have developed a biomimetic and stable design based on bovine serum albumin (BSA) nanoparticles that are encapsulated with a hydrophilic photothermal agent, indocyanine green (ICG), as well as a hydrophobic agent, gambogic acid (GA), via the desolvation method. Furthermore, these nanoconstructs have been coated with the red blood cell membranes (RBCm), which exhibit pronounced long-term circulation in addition to avoiding premature leakage of drugs. RBCm-coated BSA nanoparticles show a higher affinity towards both GA and ICG (RmGIB NPs), resulting in high loading efficiencies of 24.3 ± 1.2 % and 25.0 ± 1.2 %, respectively. Moreover, the bio-efficacy investigations of these biomimetic constructs (RmGIB NPs) in cells in vitro as well as in tumor-bearing mice in vivo confirm augmented inhibition, demonstrating potential synergistic chemo-photothermal therapeutic efficacy. Altogether, we provide an efficient delivery platform for designing and constructing BSA nanovehicles toward synergistic and effective co-delivery of therapeutics.