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      Mechanisms of nanoparticle-mediated photomechanical cell damage

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          Abstract

          Laser-assisted killing of gold nanoparticle targeted macrophages was investigated. Using pressure transient detection, flash photography and transmission electron microscopy (TEM) imaging, we studied the mechanism of single cell damage by vapor bubble formation around gold nanospheres induced by nanosecond laser pulses. The influence of the number of irradiating laser pulses and of particle size and concentration on the threshold for acute cell damage was determined. While the single pulse damage threshold is independent of the particle size, the threshold decreases with increasing particle size when using trains of pulses. The dependence of the cell damage threshold on the nanoparticle concentration during incubation reveals that particle accumulation and distribution inside the cell plays a key role in tissue imaging or cell damaging.

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          Biocompatibility of gold nanoparticles and their endocytotic fate inside the cellular compartment: a microscopic overview.

          Macrophages are one of the principal immune effector cells that play essential roles as secretory, phagocytic, and antigen-presenting cells in the immune system. In this study, we address the issue of cytotoxicity and immunogenic effects of gold nanoparticles on RAW264.7 macrophage cells. The cytotoxicity of gold nanoparticles has been correlated with a detailed study of their endocytotic uptake using various microscopy tools such as atomic force microscopy (AFM), confocal-laser-scanning microscopy (CFLSM), and transmission electron microscopy (TEM). Our findings suggest that Au(0) nanoparticles are not cytotoxic, reduce the production of reactive oxygen and nitrite species, and do not elicit secretion of proinflammatory cytokines TNF-alpha and IL1-beta, making them suitable candidates for nanomedicine. AFM measurements suggest that gold nanoparticles are internalized inside the cell via a mechanism involving pinocytosis, while CFLSM and TEM studies indicate their internalization in lysosomal bodies arranged in perinuclear fashion. Our studies thus underline the noncytotoxic, nonimmunogenic, and biocompatible properties of gold nanoparticles with the potential for application in nanoimmunology, nanomedicine, and nanobiotechnology.
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            Simulation of the Optical Absorption Spectra of Gold Nanorods as a Function of Their Aspect Ratio and the Effect of the Medium Dielectric Constant

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              The macrophage foam cell as a target for therapeutic intervention.

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                Author and article information

                Journal
                Biomed Opt Express
                BOE
                Biomedical Optics Express
                Optical Society of America
                2156-7085
                07 February 2012
                01 March 2012
                07 February 2012
                : 3
                : 3
                : 435-446
                Affiliations
                [1 ]Institute of Applied Physics, University of Bern; Sidlerstrasse 5, 3012 Bern, Switzerland
                [2 ]Department of Clinical Research, University of Bern, 3010 Bern, Switzerland
                [3 ]Institute of Anatomy, University of Bern, Baltzerstrasse 2, 3000 Bern 9, Switzerland
                [4 ]Now at Adolphe Merkle Institute for nanoscience,University of Fribourg, 1723 Marby, Switzerland
                [5 ]Department of Urology, University of Bern, 3010 Bern, Switzerland
                [6 ]Now at Department of Pathobiology and Diagnostic Investigation, Michigan State University, East Lansing, Michigan, USA
                [7 ]Scitech Instruments, North Vancouver, BC, V7J 2S5 Canada
                Author notes
                Article
                158922
                10.1364/BOE.3.000435
                3296532
                22435092
                51c5c88a-30f5-463b-a0da-be0fc5358154
                ©2012 Optical Society of America

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially.

                History
                : 28 November 2011
                : 30 January 2012
                : 31 January 2012
                Funding
                Funded by: Swiss National Science Foundation
                Award ID: 205320-103872
                Funded by: 6th Framework Program of the European Commission
                Award ID: Specific Targeted Research Project No. LSHC-CT-2006-018858 PROMET
                Categories
                Cell Studies
                Custom metadata
                True
                0

                Vision sciences
                (170.0170) medical optics and biotechnology,(170.5120) photoacoustic imaging,(170.5180) photodynamic therapy

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