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Uptake and Toxicity Studies of Poly-Acrylic Acid Functionalized Silicon Nanoparticles in Cultured Mammalian Cells
Poly‐acrylic acid (PAAc) terminated silicon nanoparticles (SiNPs) have been synthesized and employed as a synchronous fluorescent signal indicator in a series of cultured mammalian cells: HHL5, HepG2 and 3T3‐L1. Their biological effects on cell growth and proliferation in both human and mouse cell l...
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Published in: | Advanced healthcare materials 2012-03, Vol.1 (2), p.189-198 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Poly‐acrylic acid (PAAc) terminated silicon nanoparticles (SiNPs) have been synthesized and employed as a synchronous fluorescent signal indicator in a series of cultured mammalian cells: HHL5, HepG2 and 3T3‐L1. Their biological effects on cell growth and proliferation in both human and mouse cell lines have been studied. There was no evidence of in vitro cytotoxity in the cells exposed to PAAc terminated SiNPS when assessed by cell morphology, cell proliferation and viability, and DNA damage assays. The uptake of the nanocrystals by both HepG2 and 3T3‐L1 cells was investigated by confocal microscopy and flow cytometry, which showed a clear time‐dependence at higher concentrations. Reconstructed 3‐D confocal microscope images exhibited that the PAAc‐SiNPs were evenly distributed throughout the cytosol rather than attached to outer membrane. This study provides fundamental evidence for the safe application and further modification of silicon nanoparticles, which could broaden their application as cell markers in living systems and in micelle encapsulated drug delivery systems.
Poly‐acrylic acid grafted silicon nanoparticles are bio‐compatible and can be suspended in water. No evidence of in vitro cytotoxicity is demonstrated upon exposure of cells to the nanoparticles. When incubated into mammalian cells, the nanoparticles display intense luminescence, and the cellular uptake of the nanoparticles shows a clear time dependence at higher concentrations. This study provides fundamental evidence for safe application of silicon nanoparticles, which could broaden their potential uses as cell markers in living systems and in micelle encapsulated drug‐delivery systems. |
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ISSN: | 2192-2640 2192-2659 |
DOI: | 10.1002/adhm.201100010 |