Superhigh-magnetization nanocarrier as a doxorubicin delivery platform for magnetic targeting therapy
Superhigh-magnetization nanocarrier as a doxorubicin delivery platform for magnetic targeting therapy
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DOI:
10.1016/j.biomaterials.2011.08.014
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发表时间:
2011-12-01
期刊:
影响因子:
14
通讯作者:
Chuang, Cheng-Keng
中科院分区:
文献类型:
--
作者:
Hua, Mu-Yi;Yang, Hung-Wei;Chuang, Cheng-Keng
comprised of a magnetic Fe3O4 (SHMNPs) core and a shell of aqueous stable self-doped poly[N-(1-one-butyric acid)]aniline (SPAnH), which have a high drug loading capacity (similar to 27.1 wt%) of doxorubicin (DOX). The SHMNCs display superparamagnetic property with a magnetization of 89.7 emu/g greater than that of Resovist (a commercial contrast agent used for magnetic resonance imaging; 73.7 emu/g). Conjugating the anticancer drug DOX to these nanocarriers enhances the drug's thermal stability and maximizes the efficiency with which it is delivered by magnetic targeting (MT) therapy to MGH-U1 bladder cancer cells, in part by avoiding the effects of p-glycoprotein (P-gp) pumps to enhance the intracellular concentration of DOX The high R2 relaxivity (434.7 mM(-1)s(-1)) of SHMNCs not only be a most effective MT carrier of chemotherapeutic agent but be an excellent contrast agent of MRI, allowing the assessment of the distribution and concentration of DOX in various tissues and organs. This advanced drug delivery system promises to provide more effective MT therapy and tumor treatment using lower therapeutic doses and potentially reducing the side effects of cardiotoxicity caused by DOX. (C) 2011 Elsevier Ltd. All rights reserved.