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Mesoporous Silica Nanostructure Modified With Azo Gatekeepers for Colon Targeted Delivery of 5-Fluorouracil Publisher



Farjadian F1 ; Moghadam M1, 2 ; Monfared M3 ; Mohammadisamani S1, 2
Authors
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Authors Affiliations
  1. 1. Pharmaceutical Sciences Research Center, School of Pharmacy, Shiraz University of Medical Science, Shiraz, Iran
  2. 2. Department of Pharmaceutics, School of Pharmacy, Shiraz University of Medical Science, Shiraz, Iran
  3. 3. Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran

Source: AIChE Journal Published:2022


Abstract

In this study, amino-functionalized mesoporous silica (MS) particles were synthesized and loaded with the anticancer drug, 5-Fu. In a post-modification reaction, the pores were gated by an azobenzene derivative to act as an enzyme-responsive drug delivery system. The synthesis and characterization of the MS structure were validated using various instrumental techniques such as XRD, N2 adsorption/desorption, and FE-SEM and TEM. The loading efficiency and capacity of 5-Fu adsorption onto MS were evaluated; the adsorption isotherm graphs were plotted. The enzyme responsiveness feature of this nanocarrier was tested in the 5-Fu release study. The 5-Fu release from MS and the azo-capped compound was measured, and when sodium dithionite was used as a reducing agent and an azoreductase enzyme mimicker, the controlled release was observed. Finally, the cytotoxicity of 5-Fu loaded and azo-capped MS in normal medium and sodium dithionate-containing medium was evaluated and compared with the cytotoxicity of the free drug. © 2022 American Institute of Chemical Engineers.