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聚己内酯-b-聚环氧乙烷嵌段共聚物胶束作为神经营养因子FK506和L-685,818的新型药物递送载体。

Polycaprolactone-b-poly(ethylene oxide) block copolymer micelles as a novel drug delivery vehicle for neurotrophic agents FK506 and L-685,818.

作者信息

Allen C, Yu Y, Maysinger D, Eisenberg A

机构信息

Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montreal P.Q, Canada H3A 2K6.

出版信息

Bioconjug Chem. 1998 Sep-Oct;9(5):564-72. doi: 10.1021/bc9702157.

Abstract

Micelles formed from polycaprolactone-b-poly(ethylene oxide) (PCL-b-PEO) diblock copolymers were investigated as a novel drug delivery system. The affinity of the micelles for hydrophobic solubilizates was assayed by determining the partition coefficient for the lipophilic compound, pyrene, between the micelles and water; the partition coefficient was found to be on the order of 10(2). The Trypan blue and Alamar blue survival assays were used to assess the in vitro biocompatibility of the micelles with PC 12 cells, MCF-7 breast cancer cells, and primary cultures of human microglia, astrocytes, and cortical neurons. The micelles were then studied as a delivery vehicle for the neurotrophic agents FK506 and L-685,818 in PC 12 cell cultures. In both cases, the micelle-incorporated drugs, in the presence of nerve growth factor (5 ng/mL), were able to promote the degree of differentiation of the PC 12 rat pheochromocytoma cells.

摘要

研究了由聚己内酯-b-聚环氧乙烷(PCL-b-PEO)二嵌段共聚物形成的胶束作为一种新型药物递送系统。通过测定亲脂性化合物芘在胶束和水之间的分配系数,来测定胶束对疏水性增溶物的亲和力;发现分配系数约为10(2)。使用台盼蓝和alamar蓝存活试验来评估胶束与PC 12细胞、MCF-7乳腺癌细胞以及人小胶质细胞、星形胶质细胞和皮质神经元原代培养物的体外生物相容性。然后研究了胶束作为PC 12细胞培养物中神经营养剂FK506和L-685,818的递送载体。在这两种情况下,在存在神经生长因子(5 ng/mL)的情况下,掺入胶束的药物能够促进PC 12大鼠嗜铬细胞瘤细胞的分化程度。

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