4.8 Article

Glutathione-Triggered Off-On Release of Anticancer Drugs from Dendrimer-Encapsulated Gold Nanoparticles

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 135, 期 26, 页码 9805-9810

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ja402903h

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资金

  1. Science and Technology of Shanghai Municipality [11DZ2260300]
  2. National Natural Science Foundation of China [21274044]
  3. Program for New Century Excellent Talents in University of Ministry of Education of China [NCET-11-0138]
  4. Innovation Program of Shanghai Municipal Education Commission [12ZZ044]

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Polymeric nanoparticles that can stably load anticancer drugs and release them in response to a specific trigger such as glutathione are of great interest in cancer therapy. In the present study, dendrimer-encapsulated gold nanoparticles (DEGNPs) were synthesized and Used as carriers of thiolated anticancer drugs. Thiol-containing drugs such as captopril and 6-mercaptopurine loaded within DEGNPs showed an Off-On release behavior in the presence of thiol-reducing agents such as glutathione and dithiothreitol. Thiolated doxorubicin and cisplatin, loaded within the nanoparticle, showed much reduced cytotoxicity as compared to the free anticancer compounds. The toxicity of drug-loaded DEGNPs can be enhanced by improving the intracellular glutathione. Glutathione-triggered release of thiolated doxorubicin within cancer cells is further confirmed by flow cytometry and confocal laser scan microscopy studies. In addition, DEGNPs showed excellent biocompatibility on several cell lines. This study provides a new insight into biomedical applications of dendrimers and dendrimer-encapsulated nanoparticles.

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