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Efficient loading of ophthalmic drugs with poor loadability into contact lenses using functional comonomers

机译:使用功能性共聚单体有效地载入较差的可容易的可载入膜质的药物

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摘要

Ophthalmic formulations have classically been administered to eyes through eye drops, which have poor delivery efficiency and require frequent instillation. As a means of overcoming these drawbacks, ocular-drug delivery via therapeutic contact lenses has caused great interest. A simple way to prepare therapeutic contact lenses is to immerse lenses in concentrated drug solution. However, not all ocular drugs can be efficiently loaded into contact lenses by a simple soaking. In particular, our previous study showed that two antibacterial ocular drugs, ofloxacin (OFX) and neomycin (NEO), were poorly loaded to poly(2-hydroxyethyl methacrylate) (pHEMA)-based contact lenses. Herein, we investigated whether alteration of lens composition using several negatively charged comonomers can enhance loading of ocular drugs with poor loadability (OFX and NEO). As comonomers, methacrylic acid (MAA), acrylic acid (AA), and 4-methyl-4-pentenoic acid (MPA) were used, generating p(HEMA-co-MAA), p(HEMA-co-AA), and p(HEMA-co-MPA) hydrogel-based contact lenses, respectively. Contact lenses containing comonomers exhibited an increase in loading of OFX and NEO. In particular, compared with pHEMA contact lenses, contact lenses containing 2.5 mol% AA exhibited enhanced loading of OFX and NEO, 18 and 53 times, respectively. Charge interactions between comonomers and the drug were considered primary factors in the substantial increase in drug loading.
机译:眼科制剂通过滴眼剂透镜施用于眼睛,其递送效率差,需要频繁滴注。作为克服这些缺点的手段,通过治疗性隐形眼镜的眼药递送引起了极大的兴趣。制备治疗隐形眼镜的简单方法是浸入浓缩药物溶液中的透镜。然而,并非所有眼部药物都可以通过简单的浸泡将所有眼药药有效地装载到隐形眼镜中。特别是,我们之前的研究表明,两种抗菌眼药物,氧氟沙星(OFX)和新霉素(Neo)均较差地加载到聚(2-羟乙基甲基丙烯酸酯)(PHEMA)的接触眼。在此,我们研究了使用几种带负电荷共聚单体的晶状体组合物的改变是否可以增强具有差的载荷性(OFX和Neo)的眼药物的负载。作为共聚单体,使用甲基丙烯酸(MAA),丙烯酸(AA)和4-甲基-4-戊烯酸(MPa),产生P(HEMA-CO-MAA),P(HEMA-CO-AA)和P(HEMA-CO-MPA)水凝胶基隐形眼镜。含有共聚单体的隐形眼镜表现出欧姆和新载荷的增加。特别地,与PhEMA隐形眼镜相比,含有2.5mol%AA的隐形眼镜分别具有增强的OFX和Neo,18和53次。共聚单体和药物之间的电荷相互作用被认为是药物载量大幅增加的主要因素。

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  • 来源
    《Biomaterials Science》 |2018年第10期|共8页
  • 作者单位

    Gwangju Inst Sci &

    Technol Sch Mat Sci &

    Engn 123 Cheomdan Gwagi Ro Gwangju 61005 South Korea;

    Gwangju Inst Sci &

    Technol Sch Mat Sci &

    Engn 123 Cheomdan Gwagi Ro Gwangju 61005 South Korea;

    Gwangju Inst Sci &

    Technol Sch Mat Sci &

    Engn 123 Cheomdan Gwagi Ro Gwangju 61005 South Korea;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子生物学;
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