S. Swarnalatha
Central Leather Research Institute
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Publication
Featured researches published by S. Swarnalatha.
Journal of Applied Microbiology | 2007
A. Ganesh Kumar; S. Swarnalatha; S. Gayathri; Narayana Nagesh; G. Sekaran
Aims: The aim of the study was to optimize microbial degradation of keratinous waste and to characterize the alkaline active keratinase showing its biotechnological importance.
Colloids and Surfaces B: Biointerfaces | 2008
S. Swarnalatha; P.K. Selvi; A. Ganesh Kumar; G. Sekaran
A new carrier matrix for nanoemulsion drug delivery was synthesized from glycine as the raw material, using mesoporous/microporous electron rich carbon-silica composite surface (MAC(800)). MAC(800) was prepared from rice husk in two-stage carbonization. The surface area, pore volume, and pore size distribution of MAC(800) were measured, using nitrogen adsorption isotherms at 77K. The unpaired electron density of MAC(800) was measured in electron spin resonance spectroscopy (ESR), using TEMPOL (4-hydroxy-2,2,6,6-tetramethyl piperidine-1-oxyl) as the reference spin probe. Glycine was converted into ketene at the surface of MAC(800), which further underwent radical polymerization to form a low molecular weight ketene polymer (LMKP) of ester structure. The structure and the properties of LMKP were confirmed through (13)C, (1)H and DEPT nuclear magnetic resonance (NMR) spectroscopy, attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR) and size exclusion chromatography (SEC). The two hydrophilic drugs namely ciprofloxacin hydrochloride (CPH) and gentamicin sulphate (GS) were chosen for the nanoemulsion preparation and characterization. They were characterized for morphology, interaction of drugs with the polymer and their crystallinity, using HR-TEM, DSC and XRD, respectively. The encapsulation efficiency of the LMKP towards the drugs ciprofloxacin hydrochloride and gentamicin sulphate were 26% and 12%, respectively. The dissolution studies of the nanoemulsion were carried out for the pH 6.5, 7.4 and 8.0. The cytocompatibility studies were done for LMKP as well as nanoemulsion using Hep2 epithelial cells.
Engineering in Life Sciences | 2009
Arumugam Ganesh Kumar; R. Venkatesan; Burusa Prasad Rao; S. Swarnalatha; G. Sekaran
Synergistes sp. DQ560074 produced a protease in submerged fermentation (SmF) at 400–420 U/mL and in solid‐state fermentation (SSF) at 745–755 U/g. The protease, which belongs to the aspartic protease class, was active over a wide range of pH (5–7) and at high temperatures (25–45°C). The protease is stable and active in various polar protic solvents (50% v/v) like ethanol, isopropanol, n–butanol, in polar aprotic solvents (50% v/v) like acetonitrile, and in non‐polar solvents (50% v/v) such as ethylacetate and toluene, but not in hydrophilic organic solvents (methyl alcohol and acetone). As far as we know, this is the first contribution to the production of a mesophilic protease with solvent stability in SSF using a proteinaceous solid waste.
Bioresource Technology | 2008
A. Ganesh Kumar; S. Swarnalatha; B. Sairam; G. Sekaran
Biochemical Engineering Journal | 2009
A. Ganesh Kumar; S. Swarnalatha; P. Kamatchi; G. Sekaran
Journal of Chemical Technology & Biotechnology | 2006
S. Swarnalatha; Arumugam Gnanamani; G. Sekaran
Journal of Chemical Technology & Biotechnology | 2009
S. Swarnalatha; Arumugam Ganesh Kumar; Srinivasulu Tandaiah; G. Sekaran
Journal of Porous Materials | 2009
S. Swarnalatha; A. Ganesh Kumar; G. Sekaran
Journal of Materials Science: Materials in Medicine | 2008
S. Swarnalatha; R. Gopi; A. Ganesh Kumar; P.K. Selvi; G. Sekaran
Journal of Porous Materials | 2009
A. Ganesh Kumar; S. Swarnalatha; P. Kamatchi; R. Kirubagaran; K. Perinmbam; G. Sekaran