Development of a biocompatible green drug release system using salidroside-TiO2-doped chitosan oligosaccharide molecularly imprinted polymers
文献类型: 外文期刊
作者: Liu, Zijie 1 ; Ma, Xingbin 1 ; Li, Shuyu 1 ; Qiu, Jiajie 1 ; Liu, Siyu 1 ; Huang, Zhifeng 1 ; Lin, Hongling 2 ; Abd El-Aty, A. M. 3 ;
作者机构: 1.Guangdong Ocean Univ, Coll Coastal Agr Sci, Zhanjiang 524088, Guangdong, Peoples R China
2.Chinese Acad Trop Agr Sci, Southern Subtrop Crop Res Inst, Zhanjiang Expt Stn, Zhanjiang 524013, Peoples R China
3.Cairo Univ, Fac Vet Med, Dept Pharmacol, Giza 12211, Egypt
4.Qilu Univ Technol, Shandong Acad Sci, State Key Lab Biobased Mat & Green Papermaking, Jinan 250353, Peoples R China
5.Ataturk Univ, Med Fac, Dept Med Pharmacol, TR-25240 Erzurum, Turkiye
关键词: Surface molecularly; imprinted polymer; Novel functional monomer; Diethylene glycol; Sustained release; Salidroside; dimethacrylate
期刊名称:ARABIAN JOURNAL OF CHEMISTRY ( 影响因子:6.0; 五年影响因子:5.9 )
ISSN: 1878-5352
年卷期: 2023 年 16 卷 10 期
页码:
收录情况: SCI
摘要: This study focuses on creating a green drug release system using a food-grade titanium dioxide (TiO2) material through surface molecular imprinting. Salidroside (SD) was chosen as the template molecule to synthesize molecularly imprinted polymers (SDT-MIP) utilizing TiO2-doped chitosan oligosaccharides as the functional monomer. The SDT-MIPs were characterized using multiple techniques, and their effectiveness was evaluated through an in vitro release study. Additionally, the affinity of SDT-MIPs toward the template molecule was examined using Langmuir and Freundlich adsorption models. The Langmuir model revealed a maximum capacity of 170.41 mg/g and an imprinted factor of 3.4. The study demonstrated that drug release from the SDT-MIPs in simulated gastrointestinal fluid primarily occurred through pure Fick diffusion. The release kinetics exhibited diffusion coefficients ranging from 3.38 x 10-3 cm2/s to 2.78 x 10-2 cm2/s, indicating their biocompatibility and potential application in drug delivery. Furthermore, the SDT-MIP demonstrated no adverse impact on cell viability even at concentrations as high as 1000 lg/mL. The survival rate of cells cultivated in the presence of SDT-MIP solution exceeded 120 & PLUSMN; 12.46%,
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