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首页> 外文期刊>Colloid and polymer science >Self-assembled liposomes from electrosprayed polymer-based microparticles
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Self-assembled liposomes from electrosprayed polymer-based microparticles

机译:由电喷涂聚合物基微粒自组装的脂质体

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Composite poly(iV-isopropylacrylamide) (PNIPAAm)/phosphatidylcholine (PC) microparticles were prepared by electrospraying. PC-based liposomes were subsequently generated upon the addition of water. The microparticles have an average diameter of ca. 1 urn, while the liposomes produced were found to have much smaller diameters of ca. 225-280 nm. The liposomes had zeta potentials of -44 to -50 mV, consistent with the formation of a stable suspension. Upon heat treatment, the liposomes exhibit phase transitions due to the influence of PNIPAAm. The liposomes containing 33 % PC have a phase transition temperature of approximately 36 °C, close to physiological conditions. The model drug ketoprofen could be loaded into electrosprayed microparticles and subsequently incorporated into self-assembled liposomes, with an entrapment efficiency for the latter process of ca. 75 %. Sustained drug release regulated by temperature was observed from these drag-loaded materials. At 25 °C, only 45 % of the total drug loading was released after 110 hours, while at 37 °C drug release approached 90 % over the same time period. The self-assembled liposomes reported here, therefore, have great potential as drug delivery devices.
机译:通过电喷雾制备复合聚(N-异丙基丙烯酰胺)(PNIPAAm)/磷脂酰胆碱(PC)微粒。随后在加水后生成基于PC的脂质体。微粒的平均直径为约3μm。 1微米,而发现产生的脂质体的直径小得多。 225-280 nm。脂质体的ζ电势为-44至-50 mV,与形成稳定的悬浮液一致。在热处理时,由于PNIPAAm的影响,脂质体显示出相变。含有33%PC的脂质体的相变温度约为36°C,接近生理条件。可以将模型药物酮洛芬装填到电喷雾的微粒中,然后掺入自组装脂质体中,从而对后一过程的包封效率较高。 75%。从这些药物负载的材料中观察到受温度调节的持续药物释放。在25°C下,110小时后仅释放了总载药量的45%,而在37°C下,同一时期的药物释放量接近90%。因此,这里报道的自组装脂质体作为药物输送装置具有巨大的潜力。

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