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Building immune microsphere against tumor necrosis factor-alpha (TNF-alpha) / 生物医学工程学杂志
J. biomed. eng ; Sheng wu yi xue gong cheng xue za zhi;(6): 1219-1222, 2005.
Article de Zh | WPRIM | ID: wpr-309917
Bibliothèque responsable: WPRO
ABSTRACT
We have constructed the immune microsphere against tumor necrosis factor-alpha (TNF-alpha) prospectively, hoping to establish the experiment groundwork in more researches which could be used in specific elimination of the TNF-alpha by blood purification method for the future. The recombinant human tumor necrosis factor-alpha monoclonal antibody (rHTNF-alpha McAb) was wrapped on the polystyrene microsphere (PSM) carrier connecting poly-L-lysine (PLL) beforehand. They were earmarked by the fluorescein isothiocyanate (FITC) respectively. The packing conditions were examined using the inversted and fluorescence microscopes and the spectrophotometer. The results showed that the best conditions for wrapping were 20 degrees C, pH9.5 and 60 minutes. The PLL content was not changed in the washing fluid after coating, which indicated the wrapping was quite firm. At the same temperature and same coating time, the rHTNF-alpha McAb coated on the PLL was obviously substantial when the concentration of glutaraldehyde solution was 0.2%. The findings demonstrated that the built immune microsphers can be used as a novel adsorption material. This method is simple and economic, and it offers a new approach to the related studies.
Sujet(s)
Texte intégral: 1 Indice: WPRIM Sujet Principal: Polylysine / Polystyrènes / Protéines recombinantes / Chimie / Facteur de nécrose tumorale alpha / Fluorescéine / Allergie et immunologie / Microsphères / Anticorps monoclonaux Limites du sujet: Humans langue: Zh Texte intégral: J. biomed. eng / Sheng wu yi xue gong cheng xue za zhi Année: 2005 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Polylysine / Polystyrènes / Protéines recombinantes / Chimie / Facteur de nécrose tumorale alpha / Fluorescéine / Allergie et immunologie / Microsphères / Anticorps monoclonaux Limites du sujet: Humans langue: Zh Texte intégral: J. biomed. eng / Sheng wu yi xue gong cheng xue za zhi Année: 2005 Type: Article