4.6 Article

Tumour-Targeted Drug Delivery with Mannose-Functionalized Nanoparticles Self-Assembled from Amphiphilic β-Cyclodextrins

期刊

CHEMISTRY-A EUROPEAN JOURNAL
卷 22, 期 43, 页码 15216-15221

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201603294

关键词

cancer chemotherapy; mannose-mediated targeting; multivalency; nanoparticles; targeted drug delivery

资金

  1. National Natural Science Foundation of China [51403081]
  2. Natural Science Foundation of Jiangsu Province [BK20140137]
  3. Fundamental Research Funds for the Central Universities [JUSRP51629B]
  4. Max Planck Society International Partner Group Program
  5. High-end Foreign Experts Recruitment Program
  6. Thousand Talents Plan (Young Professionals)
  7. China Scholarship Council
  8. Max-Planck Society

向作者/读者索取更多资源

Multivalent mannose-functionalized nanoparticles self-assembled from amphiphilic beta-cyclodextrins (beta-CDs) facilitate the targeted delivery of anticancer drugs to specific cancer cells. Doxorubicin ( DOX)-loaded nanoparticles equipped with multivalent mannose target units were efficiently taken up via receptor-mediated endocytosis by MDA-MB-231 breast cancer cells that overexpress the mannose receptor. Upon entering the cell, the intracellular pH causes the release of DOX, which triggers apoptosis. Targeting by multivalent mannose significantly improved the capability of DOX-loaded nanoparticles to inhibit the growth of MDA-MB-231 cancer cells with minimal side effects in vivo. This targeted and controlled drug delivery system holds promise as a nanotherapeutic for cancer treatment.

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