Poly (hydroxyethyl methacrylate-co-hydroxyethyl acrylate) soft contact lenses for acetazolamide release

被引:0
作者
Amel Oucif
Nabila Haddadine
Dria Zakia
Naima Bouslah
Ahmed Benaboura
Khaled Beyaz
Bendiba Guedouar
M. Samy El-Shall
机构
[1] USTHB,Laboratoire de Synthèse Macromoléculaire et Thio
[2] Centre de Développement Des Technologie Avancées,Organique Macromoléculaire (LSMTM)
[3] CDTA,Division Des Milieux ionisés et Laser
[4] Virginia Commonwealth University,Department of Chemistry
来源
Polymer Bulletin | 2022年 / 79卷
关键词
Hydroxyethyl methacrylate; Hydroxyethyl acrylate; Hydrogel; Acetazolamide; Soft contact lenses; Optimization;
D O I
暂无
中图分类号
学科分类号
摘要
In this study, different ratios of poly (hydroxyethyl methacrylate-co-hydroxyethyl acrylate) hydrogels (HEMA-co-HEA), corresponding to (100/0, 70/30, 60/40, 50/50, 40/60, 30/70, and 0/100) were successfully prepared by free radical polymerization leading to tunable drug release materials for therapeutic soft contact lenses (SCLs) applications. The microstructures of the materials were investigated using Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM), and their thermal properties were examined with differential scanning calorimetry (DSC) and thermogravimetric (TGA) analyses. The results showed that the presence of HEA in the hydrogels matrix improved the materials’ microstructure and enhanced the swelling capacity in a 0.9% NaCl solution (pH = 5.5) at 37 °C. Furthermore, in vitro study of the loading and release of acetazolamide, as a model drug, showed a non-Fickian drug release behavior for all the studied hydrogels, whereas the highest drug release/loading capacity was observed for the hydrogel ratio HEMA/HEA of 40/60. Therefore, it can be concluded that the corresponding hydrogel is a promising curative SCLs material for a sustainable drug release application.
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页码:1535 / 1554
页数:19
相关论文
共 73 条
[21]  
Khutoryanskaya OV(2000)Hydrogels in pharmaceutical formulations Eur J Pharm Biopharm 50 27-46
[22]  
Dursch TJ(1980)Sorption and transport in glassy polymers–a review Polym Eng Sci 20 2-13
[23]  
Pradas MM(1985)Analysis of fickian and non-fickian drug release from polymers Pharm Acta Helv 60 110-111
[24]  
Bevington JC(1983)The swelling interface number as a criterion for prediction of diffusional solute release mechanisms in swellable polymers J Polym Sci Polym Phys Edit 21 983-997
[25]  
Melville HW(1985)Kinetics of drug release from hydrogel matrices J Control Release 2 277-288
[26]  
Taylor RP(2017)Generalized model for the diffusion of solvents in glassy polymers: from fickian to super case II J Chem Phys 147 044904-1464
[27]  
Al-Musa S(1965)Investigation of factors influencing release of solid drug dispersed in inert matrices J Pharm Sci 54 1459-1234
[28]  
Fara DA(1966)Investigation of factors influencing release of solid drug dispersed in inert matrices III. Quantitative studies involving the polyethylene plastic matrix J Pharm Sci 55 1230-1199
[29]  
Badwan A(2004)Investigation into the diffusion of water into HEMA-co-MOEP Hydrogels Biomacromol 5 1194-810
[30]  
Nobuhiko Y(2007)Swelling and drug release behavior of poly (2-hydroxyethyl methacrylate/itaconic acid) copolymeric hydrogels obtained by gamma irradiation Radiat Phys Chem 76 801-566