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Remotely Triggered Liposome Release by Near-Infrared Light Absorption via Hollow Gold Nanoshells

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Department of Chemical Engineering and Department of Chemistry, University of California, Santa Barbara, California 93106, and Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, Texas 77030
†Department of Chemical Engineering, University of California, Santa Barbara.
‡Department of Chemistry, University of California, Santa Barbara.
§Baylor College of Medicine.
Cite this: J. Am. Chem. Soc. 2008, 130, 26, 8175–8177
Publication Date (Web):June 11, 2008
https://doi.org/10.1021/ja802656d
Copyright © 2008 American Chemical Society

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    Abstract

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    An elusive goal for systemic drug delivery is to provide both spatial and temporal control of drug release. Liposomes have been evaluated as drug delivery vehicles for decades, but their clinical significance has been limited by slow release or poor availability of the encapsulated drug. Here we show that near-complete liposome release can be initiated within seconds by irradiating hollow gold nanoshells (HGNs) with a near-infrared (NIR) pulsed laser. Our findings reveal that different coupling methods such as having the HGNs tethered to, encapsulated within, or suspended freely outside the liposomes, all triggered liposome release but with different levels of efficiency. For the underlying content release mechanism, our experiments suggest that the microbubble formation and collapse due to the rapid temperature increase of the HGN is responsible for liposome disruption, as evidenced by the formation of solid gold particles after the NIR irradiation and the coincidence of a laser power threshold for both triggered release and pressure fluctuations in the solution associated with cavitation. These effects are similar to those induced by ultrasound and our approach is conceptually analogous to the use of optically triggered nano-“sonicators” deep inside the body for drug delivery. We expect HGNs can be coupled with any nanocarriers to promote spatially and temporally controlled drug release. In addition, the capability of external HGNs to permeabilize lipid membranes can facilitate the cellular uptake of macromolecules including proteins and DNA and allow for promising applications in gene therapy.

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    TEM image of HGNs, data showing pulsed NIR laser has no effect on the control solutions, absorption spectra of liposome/HGNs/CF complex exposed to pulsed laser, cryo-EM micrographs of tomographic imaging to demonstrate encapsulation and tethering, comparison of different methods of coupling HGNs to liposomes, as well as Materials and Methods. This material is available free of charge via the Internet at http://pubs.acs.org.

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