| Literature DB >> 21389566 |
Guoting Qin1, Zheng Li, Rongmin Xia, Feng Li, Brian E O'Neill, Jessica T Goodwin, Htet A Khant, Wah Chiu, King C Li.
Abstract
A critical issue for current liposomal carriers in clinical applications is their leakage of the encapsulated drugs that are cytotoxic to non-target tissues. We have developed partially polymerized liposomes composed of polydiacetylene lipids and saturated lipids. Cross-linking of the diacetylene lipids prevents the drug leakage even at 40 °C for days. These inactivated drug carriers are non-cytotoxic. Significantly, more than 70% of the encapsulated drug can be instantaneously released by a laser that matches the plasmon resonance of the tethered gold nanoparticles on the liposomes, and the therapeutic effect was observed in cancer cells. The remote activation feature of this novel drug delivery system allows for precise temporal and spatial control of drug release.Entities:
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Year: 2011 PMID: 21389566 PMCID: PMC3157042 DOI: 10.1088/0957-4484/22/15/155605
Source DB: PubMed Journal: Nanotechnology ISSN: 0957-4484 Impact factor: 3.874