4.6 Article

Hyaluronic acid functionalized biodegradable mesoporous silica nanocomposites for efficient photothermal and chemotherapy in breast cancer

期刊

NANOTECHNOLOGY
卷 32, 期 16, 页码 -

出版社

IOP Publishing Ltd
DOI: 10.1088/1361-6528/abda74

关键词

chemotherapy; photothermal therapy; doxorubicin; IR780; biodegradable mesoporous silica nanoparticles; breast cancer

资金

  1. National Natural Science Foundation of China [81660505]
  2. Natural Science Basic Research Plan in Ningxia Province of China [NZ17270]

向作者/读者索取更多资源

Chemotherapy is limited by drug toxicity and side effects in treating breast cancer, but the combination of photothermal therapy with chemotherapy shows promise. A biodegradable mesoporous silica nanoparticle (bMSN NPs) system for loading doxorubicin (DOX) and IR780 has shown excellent therapeutic effects on breast cancer cells in vitro and in vivo.
Chemotherapy is one of conventional treatment methods for breast cancer, but drug toxicity and side effects have severely limited its clinical applications. Photothermal therapy has emerged as a promising method that, upon combination with chemotherapy, can better treat breast cancer. In this context, a biodegradable mesoporous silica nanoparticle (bMSN NPs) system was developed for loading doxorubicin (DOX) and IR780, to be potentially applied in the treatment of breast cancer. IR780 is encapsulated in the pores of bMSN NPs by hydrophobic adsorption, while DOX is adsorbed on the surface of the bMSN NPs by hyaluronic acid electrostatically, to form the bMID NPs. Transmission electron microscopy, fluorescence spectrum and UV absorption spectrum are used to prove the successful encapsulation of IR780 and the loading of DOX. In vitro experiments have shown bMID NPs present an excellent therapeutic effect on breast cancer cells. In vivo fluorescence imaging results have indicated that bMID NPs can accumulate in tumor sites gradually and achieve in vivo long-term circulation and continuous drug release. Furthermore, bMID NPs have provided obvious antitumor effects in breast cancer mouse models, thus evolving as an efficient platform for breast cancer therapy.

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