(2021) Switch off inflammation in spleen cells with CD40-targeted PLGA nanoparticles containing dimethyl fumarate. Colloids and Surfaces B: Biointerfaces.
![]() |
Text
1-s2.0-S092777652100535X-main.pdf Download (1MB) |
Abstract
The purpose of this study was designing and synthesizing a PLGA formulation targeted with anti-CD40 monoclonal antibody, which has suitable physicochemical properties as a dimethyl fumarate (DMF) drug delivery system having minimal cytotoxicity. Therefore, this research was performed to determine the effect of anti-CD40mAb-DMF-NPs on the expression of IL-1β, IL-6 and TNF-α cytokine genes in mouse splenocytes. The toxicity of different groups, namely free PLGA, free DMF, DMF-containing PLGA, anti-CD40mAb-DMF-NPs, was evaluated by MTT assay. PLGA formulations conjugated with mAbCD40 were loaded with DMF drug that showed little cytotoxic effect against mouse splenocytes. QRT-PCR method was subsequently used to assess the effect of the mentioned groups on the expression of IL-1β, TNF-α and IL-6 genes. After treatment of the cells with DMF alone or with polymer carriers, the expression of IL-1β, IL-6 and TNF-α cytokine genes was significantly reduced. The decrease in expression was markedly higher in the antibody-targeted nanoparticles group relative to other treatment groups. Our results in this area are promising and provide a good basis for further future studies in this regard. © 2021
Item Type: | Article |
---|---|
Keywords: | Cytotoxicity; Monoclonal antibodies; Organic solvents; Physicochemical properties; Polymerase chain reaction; Synthesis (chemical), Cytokine genes; Dimethyl fumarate; Drug-delivery systems; Mabcd40; Multiple sclerosis; Physicochemical property; PLGA; PLGA nanoparticles; Spleen cells; Splenocytes, Nanoparticles |
Journal or Publication Title: | Colloids and Surfaces B: Biointerfaces |
Volume: | 208 |
Depositing User: | ms soheila Bazm |
URI: | http://eprints.ssu.ac.ir/id/eprint/12266 |
Actions (login required)
![]() |
View Item |