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
| 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.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." | |
| dc.identifier.other | http://dspace.daffodilvarsity.edu.bd:8080/handle/123456789/13289 | |
| dc.identifier.uri | http://dspace.daffodilvarsity.edu.bd:8080/handle/123456789/13289 | |
| dc.language.iso | en_US | |
| dc.publisher | Frontier Scientific Publishing | |
| dc.source | DIU Institutional Repository | |
| dc.subject | Drug | |
| dc.subject | Anticancer drug | |
| dc.subject | Drug carriers | |
| 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 | |
| dc.type | Article |
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