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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Preparation, co-assembling and interfacial crosslinking of photocurable and folate-conjugated amphiphilic block copolymers for controlled and targeted drug delivery: Smart armored nanocarriers
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Preparation, co-assembling and interfacial crosslinking of photocurable and folate-conjugated amphiphilic block copolymers for controlled and targeted drug delivery: Smart armored nanocarriers

机译:光固化和叶酸共轭的两亲嵌段共聚物的制备,共组装和界面交联,用于可控和靶向药物递送:智能铠装纳米载体

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Novel pH-sensitive, biodegradable and biocompatible copolymers based on polycaprolactone-poly(ethylene glycol) (PCL/PEG) were synthesized and further modified with folic acid and/or acryloyl chloride. The mixed polymeric micelles were formed by self-assembling of folated-copolymer and non-folated-copolymer with different compositions via nanoprecipitation method. The solubilization of quercetin as anti-cancer drug by the mixed micelle with the optimized composition (folatedon-folated 20/80) was more efficient than those made of each one alone. Nanogels with different crosslinking density were produced in the presence of ethylene glycol dimethacrylate (EGDMA) as the crosslinker via a photochemical method. Interfacial crosslinking of acrylated groups were utilized to produce a core-shell spherical nanoparticle to evaluate their in-vitro drug release and degradation rate.
机译:合成了基于聚己内酯-聚(乙二醇)(PCL / PEG)的新型pH敏感,可生物降解和生物相容性共聚物,并进一步用叶酸和/或丙烯酰氯进行了改性。通过纳米沉淀法将具有不同组成的叶酸共聚物和非叶酸共聚物进行自组装,形成了混合的聚合物胶束。槲皮素作为抗癌药物,其混合胶束具有优化的组成(叶酸/非叶酸20/80),比单独使用槲皮素更有效。在乙二醇二甲基丙烯酸酯(EGDMA)作为交联剂的存在下,通过光化学方法制备了具有不同交联密度的纳米凝胶。丙烯酸酯基团的界面交联被用于生产核-壳球形纳米颗粒,以评估它们的体外药物释放和降解速率。

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