Source:http://linkedlifedata.com/resource/pubmed/id/20138213
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2010-3-8
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pubmed:abstractText |
Standard treatment for inflammatory bowel diseases (IBD) necessitates frequent intake of anti-inflammatory and/or immunosuppressive drugs, leading to significant adverse events. To evaluate the role solid lipid nanoparticles (SLN) play as drug delivery system in enhancing anti-inflammatory activity for drugs such as dexamethasone and butyrate in a human inflammatory bowel diseases whole-blood model. ELISA assay and the peripheral blood mononuclear cell (PBMC) cytokine mRNA expression levels were evaluated by quantitative SYBR Green real-time RT-PCR to determine the IL-1beta, TNF-alpha, IFN-gamma and IL-10 secretion in inflammatory bowel diseases patients' PBMC culture supernatants. There was a significant decrease in IL-1beta (p<0.01) and TNF-alpha (p<0.001) secretion, whilst IL-10 (p<0.05) secretion significantly increased after cholesteryl butyrate administration, compared to that of butyrate alone at the highest concentration tested (100 microM), at 24h exposure. There was a significant decrease in IL-1beta (p<0.01), TNF-alpha (p<0.001) and IL-10 (p<0.001) secretion after dexamethasone loaded SLN administration, compared to dexamethasone alone at the highest concentration tested (250 nM) at 24h exposure. No IFN-gamma was detected under any conditions and no cytotoxic effects observed even at the highest concentration tested. The incorporation of butyrate and dexamethasone into SLN has a significant positive anti-inflammatory effect in the human inflammatory bowel disease whole-blood model.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1879-0720
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pubmed:author |
pubmed-author:CanaparoRobertoR,
pubmed-author:DapernoMarcoM,
pubmed-author:EandiMarioM,
pubmed-author:GascoMaria RosaMR,
pubmed-author:IppolitoLauraL,
pubmed-author:MartinassoGermanaG,
pubmed-author:MuntoniElisabettaE,
pubmed-author:PeraAngeloA,
pubmed-author:SerpeLoredanaL,
pubmed-author:SostegniRaffaelloR,
pubmed-author:VivenzaNicolettaN,
pubmed-author:ZaraGian PaoloGP
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pubmed:copyrightInfo |
Copyright 2010 Elsevier B.V. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
18
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pubmed:volume |
39
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
428-36
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pubmed:meshHeading |
pubmed-meshheading:20138213-Anti-Inflammatory Agents,
pubmed-meshheading:20138213-Chromatography, High Pressure Liquid,
pubmed-meshheading:20138213-Cytokines,
pubmed-meshheading:20138213-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:20138213-Female,
pubmed-meshheading:20138213-Humans,
pubmed-meshheading:20138213-Inflammatory Bowel Diseases,
pubmed-meshheading:20138213-Lipids,
pubmed-meshheading:20138213-Male,
pubmed-meshheading:20138213-Nanoparticles,
pubmed-meshheading:20138213-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:20138213-Spectrophotometry, Ultraviolet
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pubmed:year |
2010
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pubmed:articleTitle |
Solid lipid nanoparticles as anti-inflammatory drug delivery system in a human inflammatory bowel disease whole-blood model.
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pubmed:affiliation |
Department of Anatomy, Pharmacology and Forensic Medicine, University of Torino, Via P. Giuria 13, 10125 Torino, Italy. loredana.serpe@unito.it
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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