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Surface Engineered Mesoporous Silica Carriers for the Controlled Delivery of Anticancer Drug 5-Fluorouracil: Computational Approach for the Drug-Carrier Interactions Using Density Functional Theory

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dc.contributor.author Rehman, Fozia
dc.contributor.author Khan, Asif Jamal
dc.contributor.author Sama, Zaib Us
dc.contributor.author Alobaid, Hussah M.
dc.contributor.author Gilani, Mazhar Amjad
dc.contributor.author Safi, Sher Zaman
dc.contributor.author Muhammad, Nawshad
dc.contributor.author Rahim, Abdur
dc.contributor.author Ali, Abid
dc.contributor.author Guo, Jiahua
dc.contributor.author Arshad, Muhammad
dc.contributor.author Emran, Talha Bin
dc.date.accessioned 2024-08-29T06:40:33Z
dc.date.available 2024-08-29T06:40:33Z
dc.date.issued 2023-04-13
dc.identifier.uri http://dspace.daffodilvarsity.edu.bd:8080/handle/123456789/13289
dc.description.abstract "Introduction: Drug delivery systems are the topmost priority to increase drug safety and efficacy. In this study, hybrid porous silicates SBA-15 and its derivatives SBA@N and SBA@3N were synthesized and loaded with an anticancer drug, 5-fluorouracil. The drug release was studied in a simulated physiological environment. Method: These materials were characterized for their textural and physio-chemical properties by scanning electron microscopy (SEM), nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FTIR), small-angle X-ray diffraction (SAX), and nitrogen adsorption/desorption techniques. The surface electrostatics of the materials was measured by zeta potential. Results: The drug loading efficiency of the prepared hybrid materials was about 10%. In vitro drug release profiles were obtained in simulated fluids. Slow drug release kinetics was observed for SBA@3N, which released 7.5% of the entrapped drug in simulated intestinal fluid (SIF, pH 7.2) and 33% in simulated body fluid (SBF, pH 7.2) for 72 h. The material SBA@N presented an initial burst release of 13% in simulated intestinal fluid and 32.6% in simulated gastric fluid (SGF, pH 1.2), while about 70% of the drug was released within the next 72 h. Density functional theory (DFT) calculations have also supported the slow drug release from the SBA@3N material. The release mechanism of the drug from the prepared carriers was studied by first-order, second-order, Korsmeyer–Peppas, Hixson–Crowell, and Higuchi kinetic models. The drug release from these carriers follows Fickian diffusion and zero-order kinetics in SGF and SBF, whereas first-order, non-Fickian diffusion, and case-II transport were observed in SIF. Discussion: Based on these findings, the proposed synthesized hybrid materials may be suggested as a potential drug delivery system for anti-cancer drugs such as 5-fluorouracil." en_US
dc.language.iso en_US en_US
dc.publisher Frontier Scientific Publishing en_US
dc.subject Drug en_US
dc.subject Anticancer drug en_US
dc.subject Drug carriers en_US
dc.title Surface Engineered Mesoporous Silica Carriers for the Controlled Delivery of Anticancer Drug 5-Fluorouracil: Computational Approach for the Drug-Carrier Interactions Using Density Functional Theory en_US
dc.type Article en_US


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