4.8 Article

Nucleosome-inspired nanocarrier obtains encapsulation efficiency enhancement and side effects reduction in chemotherapy by using fullerenol assembled with doxorubicin

期刊

BIOMATERIALS
卷 167, 期 -, 页码 205-215

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2018.03.015

关键词

Fullerenol; Doxorubicin; PEG-PLGA; Encapsulation efficiency; Reduced side effects

资金

  1. Ministry of Science and Technology of China (National Basic Research Program) [2016YFA0201600]
  2. National Science Foundation of China [21320102003, U1532122, 31571027, 21705151]
  3. Science Fund for Creative Research Groups of the National Natural Science Foundation of China [11621505]
  4. CAS Key Research Program for Frontier Sciences [QYZDJ-SS-SLH022]
  5. CAS Interdisciplinary Innovation Team
  6. Project of Beijing National Science Foundation [2174085]
  7. National Science Fund for Distinguished Young Scholars [11425520]

向作者/读者索取更多资源

Chemodrugs have been widely used to treat cancer; however, the chemotherapy usually leads to serious side effects and failure. Various nanomaterials and strategies have been explored for drug delivery to improve the efficacy of chemodrugs. One key to loading chemodrugs onto a nano-delivery system is enhancement of the encapsulation efficiency, especially for polymeric nanoparticles being loaded with hydrophilic drugs. Inspired by the ability of eukaryote to package millions of genes in the nucleus wrapping and condensing DNA around histones to form chromosomes, here we developed a karyon-like hybrid nanoparticle to achieve ultra-high encapsulation of doxorubicin (Dox) with reduced side effects. We utilized fullerenol as a histone, packaged a great number of Dox, and used PEG-PLGA as the karyotheca coating the nucleosome (fullerenol and Dox complex) to stabilize the complex. It is noteworthy that the encapsulation efficiency of Dox in the polymeric micelles was increased from similar to 5% to similar to 79%. What's more, the biomimetic-inspired delivery system significantly reduced the chemodrug side effects by utilizing the radical scavenging ability of fullerenol. This novel drug-delivery design approach provides useful insights for improving the applicability of fullerenol in drug delivery systems for cancer therapy. (C) 2018 Elsevier Ltd. All rights reserved.

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