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Toward Point-of-Care Diagnostics to Monitor MMP-9 and TNF-α Levels in Inflammatory Bowel Disease

[Image: see text] We have investigated the association of matrix metallopeptidase 9 (MMP-9) and tumor necrosis factor α (TNF-α) levels with colitis severity using an established IL10–/– mouse model, which reflects the severity of inflammation in humans with inflammatory bowel disease (IBD). We found...

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Detalles Bibliográficos
Autores principales: Liu, Dandan, Viennois, Emilie, Fang, Jieqiong, Merlin, Didier, Iyer, Suri S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7970462/
https://www.ncbi.nlm.nih.gov/pubmed/33748570
http://dx.doi.org/10.1021/acsomega.0c05115
Descripción
Sumario:[Image: see text] We have investigated the association of matrix metallopeptidase 9 (MMP-9) and tumor necrosis factor α (TNF-α) levels with colitis severity using an established IL10–/– mouse model, which reflects the severity of inflammation in humans with inflammatory bowel disease (IBD). We found that MMP-9 and TNF-α correlated with colitis severity. In parallel, we developed assays to detect fecal MMP-9 and serum TNF-α using “cap and release” mesoporous silica nanoparticles (MSNs). MMP-9 peptide substrates as “caps” were attached to dye-loaded MSNs. The introduction of MMP-9 resulted in substrate cleavage and subsequent dye release, which was rapidly detected using a fluorometer. For TNF-α, an anti-TNF antibody was used as the “cap”. The introduction of TNF-α antigen leads to the release of the dyes because the antigen binds more strongly to the antibody cap. The MSN-based assays can detect MMP-9 and TNF-α effectively, although signal amplification is required to meet clinical sensitivity.