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dc.contributor.authorFernandez, M R-
dc.contributor.authorCasabona, M G-
dc.contributor.authorAnupama, V N-
dc.contributor.authorKrishnakumar, B-
dc.contributor.authorCurutchet, G A-
dc.contributor.authorBernik, D L-
dc.date.accessioned2014-06-25T10:41:44Z-
dc.date.available2014-06-25T10:41:44Z-
dc.date.issued2010-
dc.identifier.citationColloids and Surfaces B-Biointerfaces 81(1):289-296;01 Nov 2010en_US
dc.identifier.issn0927-7765-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1547-
dc.description.abstractThe objective of this work is to test the performance of new synthetic polydimethylsiloxane (PDMS)-based bed particles acting as carriers for bacteria biofilms. The particles obtained have a highly interconnected porous structure which offers a large surface adsorption area to the bacteria. In addition, PDMS materials can be cross-linked by copolymerization with other polymers. In the present work we have chosen two hydrophilic polymers: xanthan gum polysaccharide and tetraethoxysilane (TEOS). This versatile composition helps to modulate the interfacial hydrophobic/hydrophilic balance at the particle surface level and the roughness topology and pore size distribution, as revealed by scanning electron microscopy. Biofilm formation of a consortium isolated from a tannery effluent enriched in Sulphate Reducing Bacteria (SRB), and pure Acidithiobacillus ferrooxidans (AF) strains were assayed in three different bed particles synthesized with pure PDMS, PDMS-xanthan gum and PDMS-TEOS hybrids. Bacterial viability assays using confocal laser scanning fluorescence microscopy indicate that inclusion of hydrophilic groups on particle's surface significantly improves both cell adhesion and viability.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectSEMen_US
dc.subjectCSLMen_US
dc.subjectPDMSen_US
dc.subjectBiofilmen_US
dc.subjectBed materialen_US
dc.subjectAcrylamideen_US
dc.subjectPoly(dimethylsiloxane) microfluidic devicesen_US
dc.titlePDMS-based porous particles as support beds for cell immobilization: Bacterial biofilm formation as a function of porosity and polymer compositionen_US
dc.typeArticleen_US
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