Development of itaconic acid-based molecular imprinted polymers using supercritical fluid technology for pH-triggered drug delivery

被引:53
|
作者
Marcelo, Goncalo [1 ]
Ferreira, Ines C. [1 ]
Viveiros, Raquel [1 ]
Casimiro, Teresa [1 ]
机构
[1] Univ Nova Lisboa, Fac Ciencias & Tecnol, Dept Quim, LAQV REQUIMTE, P-2829516 Caparica, Portugal
关键词
Supercritical carbon dioxide; Molecular imprinting; Crosslinked polymer; pH-responsive; Metronidazole; CARBON-DIOXIDE; API PURIFICATION; RELEASE; POLYMERIZATION; HYDROGELS; SYSTEMS; METRONIDAZOLE; RECOGNITION; COMBINATION; STRATEGY;
D O I
10.1016/j.ijpharm.2018.03.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A novel pH-responsive molecularly imprinted polymer (MIP) based on Itaconic acid: Ethylene glycol dimethacrylate was developed as a potential body-friendly oral drug delivery system for metronidazole (MZ), a pH-independent drug. MIP performance was evaluated in a simulated oral administration situation, at pHs 2.2 and 7.4. Itaconic acid-based copolymers were synthesized using two different molar ratios of template: monomer:crosslinker (T:M:C), 1:5:25 and 1:5:50, in supercritical carbon dioxide (scCO(2)) in high yields. Further, impregnation of MZ was performed in scCO(2) environment. Morphological and chemical properties of the copolymers produced were assessed by SEM, Morphologi G3 and FTIR analyses. Non-molecularly imprinted polymer (NIP) matrices presented swelling over time in opposition to the molecularly imprinted ones. In the scCO(2)-impregnation process, MIPs showed a significant molecular recognition towards MZ, presenting higher drug uptake ability with MZ loading of 18-61 wt% in MIPs, compared to 7-20 wt% in NIPs. In vitro drug release experiments presented different release profiles at the different pHs, where MZ-MIPs could release higher amounts of MZ at the lowest pH than at pH 7.4.
引用
收藏
页码:125 / 131
页数:7
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