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Evaluation of physicochemical properties, and antimicrobial efficacy of monoclinic sulfur-nanocolloid
Stable nanocolloids of monoclinic sulfur (β-SNPs) were prepared through ‘water-in-oil microemulsion technique’ at room temperature after suitable modifications of the surface. The morphology (rod shaped; ~50 nm in diameter) and allotropic nature (monoclinic) of the SNPs were investigated with Transm...
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Published in: | Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology 2013-04, Vol.15 (4), p.1, Article 1491 |
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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: | Stable nanocolloids of monoclinic sulfur (β-SNPs) were prepared through ‘water-in-oil microemulsion technique’ at room temperature after suitable modifications of the surface. The morphology (rod shaped; ~50 nm in diameter) and allotropic nature (monoclinic) of the SNPs were investigated with Transmission Electron Microscopy and X-ray Diffraction technique. The surface modification, colloidal stability, and surface topology of β-SNPs were evaluated with Fourier Transform Infrared Spectroscopy, zeta potential analysis, and Atomic Force Microscopy. Thermal decomposition pattern of these nanosized particles was determined by Thermo Gravimetric Analysis (TGA). β-SNPs-colloids expressed excellent antimicrobial activities against a series of fungal and bacterial isolates with prominent deformities at their surface. In contrast, insignificant cytotoxicity was achieved against the human derived hepatoma (HepG2) cell line upon treatment with β-SNPs. A simultaneous study was performed to determine the stock concentration of β-SNP-colloids using a novel high phase liquid chromatographic method. Cumulative results of this study hence, elucidate the stabilization of nanosized monoclinic sulfur at room temperature and their potential antimicrobial efficacy over micron-sized sulfur. |
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ISSN: | 1388-0764 1572-896X |
DOI: | 10.1007/s11051-013-1491-y |