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1.
Langmuir ; 28(24): 8915-9, 2012 Jun 19.
Article in English | MEDLINE | ID: mdl-22444199

ABSTRACT

Ultrasmall water-soluble silver nanoclusters are synthesized, and their properties are investigated. The silver nanoclusters have high colloidal stability and show fluorescence in the red. This demonstrates that like gold nanoclusters also silver nanoclusters can be fluorescent.


Subject(s)
Fluorescence , Metal Nanoparticles/chemistry , Silver/chemistry , Colloids/chemical synthesis , Colloids/chemistry , Particle Size , Surface Properties
2.
Int J Nanomedicine ; 6: 1365-71, 2011.
Article in English | MEDLINE | ID: mdl-21760731

ABSTRACT

BACKGROUND: San-Huang-Xie-Xin-Tang (SHXXT) decoction, a traditional Chinese medicine containing Rhei rhizome, Coptidis rhizome, and Scutellariae radix, is widely used in hepatoprotective therapy. However, preparation of the decoction requires addition of boiling water that causes loss of numerous effective components. METHODS: To improve the bioavailability of the decoction, nanoscale SHXXT was developed. Chloroform-induced liver injury and hepatic stellate cell activity in mice were used to demonstrate the hepatoprotective characteristics of nanoscale SHXXT decoction. RESULTS: Liver/body weight ratio and serum aspartate and alanine aminotranferase levels were recovered by the nanoscale SHXXT. TIMP-1 gene expression was inhibited and MMP-2 gene expression was accelerated in activated hepatic stellate cells. CONCLUSION: Nanoscale SHXXT decoction prepared in room temperature water could have preserved hepatoprotective ability. The results of this study indicate that nanoscale SHXXT could be extracted easily. The simple preparation of this herbal decoction is more convenient and energy-efficient.


Subject(s)
Chemical and Drug Induced Liver Injury/drug therapy , Drugs, Chinese Herbal/pharmacology , Hepatic Stellate Cells/drug effects , Nanoparticles/chemistry , Protective Agents/pharmacology , Animals , Body Weight/drug effects , Chloroform/adverse effects , Drug Delivery Systems , Drugs, Chinese Herbal/chemistry , Female , Histocytochemistry , Liver/drug effects , Liver/pathology , Liver Cirrhosis/drug therapy , Matrix Metalloproteinase 2/metabolism , Mice , Mice, Inbred ICR , Nanoparticles/ultrastructure , Nanotechnology , Organ Size/drug effects , Particle Size , Protective Agents/chemistry , Tissue Inhibitor of Metalloproteinase-1/metabolism
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