化学
肿胀 的
自愈水凝胶
体内
核化学
MTT法
控制释放
生物利用度
药物输送
赫拉
体外
最大值
色谱法
高分子化学
药理学
生物化学
材料科学
有机化学
纳米技术
复合材料
生物
医学
生物技术
作者
Samiullah Khan,Muhammad Usman Minhas,Muhammad Tahir Aqeel,Ihsan Shah,Shahzeb Khan,Mohsin Kazi,Zachary N. Warnken
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2022-05-13
卷期号:14 (5): 1050-1050
被引量:15
标识
DOI:10.3390/pharmaceutics14051050
摘要
This study was aimed to develop novel in situ forming gels based on N-vinylcaprolactam, sodium alginate, and N,N-methylenebisacrylamide. The in situ Poly (NVRCL-g-NaAlg) gels were developed using the cold and free radical polymerization method. The structure formation, thermal stability, and porous nature of gels was confirmed by FTIR, NMR, DSC, TGA, and SEM. The tunable gelation temperature was evaluated by tube titling and rheological analysis. Optical transmittance showed that all formulations demonstrated phase transition around 33 °C. The swelling and release profile showed that gels offered maximum swelling and controlled 5-FU release at 25 °C and pH (7.4), owing to a relaxed state. Porosity and mesh size showed an effect on swelling and drug release. The in vitro degradation profile demonstrated a controlled degradation rate. An MTT assay confirmed that formulations are safe tested against Vero cells. In vitro cytotoxicity showed that 5-FU loaded gels have controlled cytotoxic potential against HeLa and MCF-7 cells (IC50 = 39.91 µg/mL and 46.82 µg/mL) compared to free 5-FU (IC50 = 50.52 µg/mL and 53.58 µg/mL). Histopathological study demonstrated no harmful effects of gels on major organs. The in vivo bioavailability in rabbits showed a controlled release in gel form (Cmax, 1433.59 ± 45.09 ng/mL) compared to a free drug (Cmax, 2263.31 ± 13.36 ng/mL) after the subcutaneous injection.
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