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Potential-modulated release of ceftriaxone using chitosan hydrogel-based composite involving ordered mesoporous carbon and graphene | ||
Advances in Nanochemistry | ||
مقاله 5، دوره 2، شماره 1، فروردین 2020، صفحه 21-26 اصل مقاله (1.4 M) | ||
نوع مقاله: Original Article | ||
شناسه دیجیتال (DOI): 10.22126/anc.2020.4839.1019 | ||
نویسندگان | ||
Toraj Ahmadi-Jouibari1؛ Mari Ataee1؛ Negar Noori1؛ Nazir Fattahi* 2 | ||
1Clinical Research Development Center, Imam Khomeini and Dr. Mohammad Kermanshahi and Farabi Hospitals, Kermanshah University of Medical Sciences, Kermanshah, Iran | ||
2Research Center for Environmental Determinants of Health (RCEDH), Kermanshah University of Medical Sciences, Kermanshah, Iran | ||
چکیده | ||
We report on the successful release-modulation of ceftriaxone (CEF) by an applied potential on a chitosan hydrogel-based composite. Here, the performance of chitosan (CHIT)-based composites were evaluated on glassy carbon electrode (GC), GC-ordered mesoporous carbons (OMCs) and Graphene (Gr), which offer attractive features such as good electronic conductivity and effectiveness in delivering electroactive surface area. Ceftriaxone was selected as an indicator of cephalosporins as a model drug. Besides this, based on the fact that CEF has three pKa, we carefully studied the electronic structures, hardness, and HOMO-LUMO gaps of deprotonated forms, for the first time, using DFT-B3LYP/6-31G* method. The optimized structures of the anions 1, 2, and 3 implied that the proton (H+), located in an electronic sponge, changes its position from -COO-, in anion 1 to -NH3+ in anions 2 and 3. Due to its porous morphology and high surface area, the prepared OMCs/CHIT film found to have a significantly higher capability in the time-controlled release of the CEF and prevention of its fast depletion into the aqueous medium, compared to GR/CHIT and GC/CHIT films. | ||
کلیدواژهها | ||
Ordered mesoporous carbons؛ Graphene؛ Chitosan؛ Electrically-controlled drug release؛ Cephalosporins | ||
آمار تعداد مشاهده مقاله: 258 تعداد دریافت فایل اصل مقاله: 238 |