4.6 Article

One pot synthesis of doxorubicin loaded gold nanoparticles for sustained drug release

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RSC ADVANCES
卷 5, 期 118, 页码 97330-97334

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ra12892g

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  1. Indian Institute of Technology Mandi (IIT Mandi)
  2. Department of Science & Technology India [SR/FT/CS-152/2011]
  3. Department of Biotechnology India [BT/PR4067/BRB/10/1128/2012]

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Here, we report a facile, versatile and simple one-pot synthesis of doxorubicin (Dox) loaded gold nanoparticles (Dox-GNP conjugate), where Dox can act both as a reducing as well as a capping agent. Interestingly, when the conjugate was placed into the transporter protein environment, it avoided the undesirable multilayer protein corona formation, which is very common for nanomaterials. The in vitro drug release kinetic studies and the cytotoxicity assay and cellular update efficiency advocates that the system is capable of sustained release of the drug even in the presence of a complex biological environment.

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