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1.
ACS Appl Mater Interfaces ; 4(1): 338-50, 2012 Jan.
Article in English | MEDLINE | ID: mdl-22128903

ABSTRACT

A novel method to exfoliate the montmorillonite clay was developed previously to generate random nanosilicate platelets (NSP), one kind of delaminated clay. To improve their dispersion in a polymer, we modified NSPs by three types of surfactants (cationic Qa, nonionic Qb, and anionic Qc) in this study and used them to prepare nanocomposites with polyurethane (PU). The zeta potential, antimicrobial ability, and biocompatibility of these surfactant-modified NSPs (abbreviated "NSQ") were characterized. It was found that the zeta potential of Qa-modified NSP (NSQa) was positive, whereas those of NSP and the other two NSQs (NSQb and NSQc) were negative. All NSQ presented less cytotoxicity than NSP. NSQa and NSQc showed excellent antimicrobial activities against S. aureus (Gram-positive strain) and E. coli (Gram-negative strain). The nanocomposites of NSQ with PU were then characterized for surface and mechanical properties, cell attachment and proliferation, antimicrobial activity in vitro, and biocompatibility in vivo. A higher surfactant to NSP ratio was found to improve the dispersion of NSQ in PU matrix. The mechanical properties of all PU/NSQ nanocomposites were significantly enhanced. Among various NSQ, only NSQa were observed to migrate to the composite surface. The attachment and proliferation of endothelial cells and fibroblasts in vitro as well as biocompatibility in vivo were significantly better for PU/NSQa containing 1% of NSQa than other materials. The microbiostasis ratios of PU/NSQ nanocomposites containing 1% NSQa or NSQc were >90%. These results proposed the safety and potential antimicrobial applications of surfactant-modified delaminated clays and their nanocomposites with PU polymer.


Subject(s)
Aluminum Silicates/chemistry , Anti-Bacterial Agents/chemistry , Nanocomposites/chemistry , Polyurethanes/chemistry , Aluminum Silicates/toxicity , Anti-Bacterial Agents/pharmacology , Bacterial Adhesion/drug effects , Biocompatible Materials/chemistry , Biocompatible Materials/pharmacology , Cell Adhesion/drug effects , Clay , Endothelial Cells/cytology , Escherichia coli/drug effects , Fibroblasts/cytology , Nanocomposites/toxicity , Polyurethanes/pharmacology , Staphylococcus aureus/drug effects
2.
ACS Appl Mater Interfaces ; 1(11): 2556-64, 2009 Nov.
Article in English | MEDLINE | ID: mdl-20356127

ABSTRACT

Nanometer-scale silicate platelet (NSP) materials were previously developed by increasing the interlayer space and exfoliation of layered silicate clays such as montmorillonite and synthetic fluorinated mica by the process of polyamine exfoliation. In this study, the antibacterial activity and cytotoxicity of these nanometer-scale silicate clays were evaluated. The derivatives of NSP (NSP-S) which were modified by C18-fatty amine salts via ionic exchange association exhibited the highest antibacterial activity in the aqueous state among all clays. The high antibacterial activity, however, was accompanied by elevated cytotoxicity. The variations of cell surface markers (CD29 and CD44) and type I collagen expression of fibroblasts treated with the clays were measured to clarify the mechanism of the silicate-induced cytotoxicity. The signal transduction pathway involved the downregulation of extracellular-signal-regulated kinase (ERK), which appeared to participate in silicate-induced cytotoxicity. This study helped to understand the antibacterial potential of NSP and the interaction of natural and modified clays with cellular activities.


Subject(s)
Aluminum Silicates/pharmacology , Amines/chemistry , Anti-Infective Agents/pharmacology , Endothelial Cells/cytology , Fibroblasts/cytology , Salts/chemistry , Silicates/pharmacology , Animals , Bentonite/pharmacology , Cations , Cattle , Cell Death/drug effects , Clay , Collagen Type I/genetics , Collagen Type I/metabolism , Colony Count, Microbial , Endothelial Cells/drug effects , Endothelial Cells/enzymology , Escherichia coli/drug effects , Escherichia coli/growth & development , Escherichia coli/ultrastructure , Extracellular Signal-Regulated MAP Kinases/metabolism , Fibroblasts/drug effects , Fibroblasts/enzymology , Gene Expression Regulation/drug effects , Humans , Hyaluronan Receptors/metabolism , Integrin beta1/metabolism , Microbial Sensitivity Tests , Phosphorylation/drug effects , Staphylococcus aureus/drug effects , Staphylococcus aureus/growth & development , Staphylococcus aureus/ultrastructure
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