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仿生红细胞膜包裹的仿生纳米构建体用于协同增效的化学-光热治疗。

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

机构信息

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

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

出版信息

Colloids Surf B Biointerfaces. 2020 May;189:110842. doi: 10.1016/j.colsurfb.2020.110842. Epub 2020 Feb 3.

Abstract

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.

摘要

最近,基于纳米技术的共递药系统的制备在有效的癌症治疗方面引起了极大的兴趣。然而,这些系统仍然面临一些挑战,如不同化学性质的药物共递、载药效率不足、免疫排斥导致快速清除和体内生物利用度极低等。为了解决这些挑战,我们开发了一种基于牛血清白蛋白(BSA)纳米粒子的仿生稳定设计,该纳米粒子通过去溶剂化法包裹亲水性光热剂吲哚菁绿(ICG)和疏水性药物藤黄酸(GA)。此外,这些纳米结构被红细胞膜(RBCm)包裹,具有显著的长循环特性,同时避免了药物的过早泄漏。RBCm 包裹的 BSA 纳米粒子对 GA 和 ICG 具有更高的亲和力(RmGIB NPs),分别达到 24.3±1.2%和 25.0±1.2%的高载药效率。此外,这些仿生构建体(RmGIB NPs)在体外细胞和荷瘤小鼠体内的生物功效研究证实了增强的抑制作用,显示出潜在的协同化疗-光热治疗效果。总之,我们为设计和构建 BSA 纳米载体提供了一种有效的递药平台,以实现治疗药物的协同有效共递。

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