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首页> 外文期刊>Journal of Applied Polymer Science >Biodegradable amphiphiles of grafted poly(lactide) onto 2-hydroxyethyl methacrylate-co-N-vinylpyrrolidone copolymers as drug carriers
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Biodegradable amphiphiles of grafted poly(lactide) onto 2-hydroxyethyl methacrylate-co-N-vinylpyrrolidone copolymers as drug carriers

机译:接枝的聚丙交酯可生物降解的两亲物作为药物载体的甲基丙烯酸2-羟乙酯-co-N-乙烯基吡咯烷酮共聚物

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This article describes the synthesis and characterization of 2-hydroxylethyl methacrylate-co-N-vinylpyrrolidone copolymers, (HEMA-co-NVP), via free radical polymerization followed by grafting of poly(lactide) onto (HEMA-co-NVP) copolymers, via ring opening polymerization using tin octoate as a catalyst. The copolymers and the grafted copolymers (i.e., amphiphiles) were subjected to sustained release studies using salicylic acid, as a model drug. Characterization of the formed copolymers was performed using ~1H-NMR, ~(13)C-NMR, FTIR, TGA, DSC, and SEM techniques. Derivative of TGA thermogram was used to determine %hydrophilicity and %hydrophobicity in the grafted and ungrafted copolymers. The SEM morphology revealed porous layers with crispy structure that were most likely due to the presence of poly(lactide) chains. At lower content of poly(lactide) moiety, grafted copolymers showed non-Fickian diffusion release rate, whereas Fickian diffusion release rate at higher content of poly(lactide) was observed. The increase of poly(lactide) content (i.e., larger %hydrophobicity) in the copolymer increased the drug-sustainability, due to the consistent but porous amphiphilic degradable structures that allow controllable release of drug in time interval.
机译:本文介绍了通过自由基聚合,然后将聚丙交酯接枝到(HEMA-co-NVP)共聚物上的方法,对甲基丙烯酸2-羟乙酯-co-N-乙烯基吡咯烷酮共聚物(HEMA-co-NVP)进行合成和表征通过使用辛酸锡作为催化剂的开环聚合。使用水杨酸作为模型药物对共聚物和接枝共聚物(即两亲物)进行持续释放研究。使用〜1H-NMR,〜(13)C-NMR,FTIR,TGA,DSC和SEM技术对形成的共聚物进行表征。用TGA热分析图的衍生物测定接枝和未接枝共聚物中的亲水性和疏水性%。 SEM形态揭示了具有脆性结构的多孔层,最可能的原因是存在聚(丙交酯)链。在聚丙交酯部分含量较低的情况下,接枝共聚物显示出非菲克扩散扩散速率,而在聚丙交酯含量较高的情况下观察到菲克扩散释放速率。共聚物中聚丙交酯含量的增加(即较大的%疏水性)增加了药物的可持续性,这是由于一致但多孔的两亲可降解结构允许在时间间隔内可控地释放药物。

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