分子印迹对水凝胶晶状体中难水溶性药物的装载和释放的影响

A. Al-Shohani, Zahraa Yahya Sabri
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引用次数: 0

摘要

治疗性隐形眼镜tcl是一种用于延长角膜停留时间和减少频繁滴入的方法,这是眼药水的一个问题。CLs的问题是装载了疏水药物。本研究采用分子印迹技术制备了抗真菌药物伊曲康唑(itraconazole),以提高其在真菌性角膜炎中的负载。以PEGDA (25 μL)和AIBN (37 mg)分别为交联剂和引发剂,制备了不同浓度的甲基丙烯酸羟乙酯HEMA和甲基丙烯酸MAA的氯离子聚合体(cl)。所制备的CLs透明,具有良好的折叠性能。micl的载药量明显高于常规CLs。与常规CLs相比,micl的伊曲康唑释放持续。优选的最佳配方为8%的MAA,最大载药量为1077 μg,而非MI (288 μg),缓释时间超过24 h。MI成功地作为一种工具,提高了水凝胶CL中难溶性药物的载药量。
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The Effect of Molecular Imprinting on the Loading and Release of Poorly Water Soluble Drug in Hydrogel Gontact Lenses
Therapeutic contact lenses TCLs is an approach used to enhance corneal residence time and reduce frequent instillation, which is a problem with eye drops.  The problem with CLs is loading of hydrophobic drugs. In this research the CLs were prepared with molecular imprinting MI to enhance the loading of itraconazole, which is used as antifungal drug for fungal keratitis. CLs using different  concentration of hydroxyethyl methacrylate HEMA and methacrylic acid MAA were prepared with and without MI using PEGDA (25 μL) and AIBN (37 mg) as crosslinker and initiator respectively. All the prepared CLs were clear and have good folding endurance. MICLs had significantly higher drug loading compared to conventional CLs. The release of itraconazole from MICLs was sustained compared to conventional CLs. The optimum formula chosen had 8% MAA due to maximum drug loading (1077 μg) compared to non-MI (288 μg) and sustained release for more than 24 h. MI was successfully utilized as a tool to enhance the loading of poorly water soluble drug into a hydrogel CL.
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