期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 130, 期 32, 页码 10643-10647出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja801631c
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资金
- NCI NIH HHS [R21 CA120536, R21 CA120536-02, R21 CA120536-01, CA120536] Funding Source: Medline
A highly efficient drug vector for photodynamic therapy (PDT) drug delivery was developed by synthesizing PEGylated gold nanoparticle conjugates, which act as a water-soluble and biocompatible cage that allows delivery of a hydrophobic drug to its site of PDT action. The dynamics of drug release in vitro in a two-phase solution system and in vivo in cancer-bearing mice indicates that the process of drug delivery is highly efficient, and passive targeting prefers the tumor site. With the Au NP-Pc 4 conjugates, the drug delivery time required for PDT has been greatly reduced to less than 2 h, compared to 2 days for the free drug.
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