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基于载有 PHBHHx 纳米粒的磷脂复合物的速效-长效胰岛素制剂。

A rapid-acting, long-acting insulin formulation based on a phospholipid complex loaded PHBHHx nanoparticles.

机构信息

Key Laboratory of Drug Targeting and Drug Delivery Systems, Ministry of Education, West China School of Pharmacy, Sichuan University, Chengdu, PR China.

出版信息

Biomaterials. 2012 Feb;33(5):1583-8. doi: 10.1016/j.biomaterials.2011.10.072. Epub 2011 Nov 21.

Abstract

The application of poly(hydroxybutyrate-co-hydroxyhexanoate) (PHBHHx) for sustained and controlled delivery of hydrophilic insulin was made possible by preparing insulin phospholipid complex loaded biodegradable PHBHHx nanoparticles (INS-PLC-NPs). The INS-PLC-NPs produced by a solvent evaporation method showed a spherical shape with a mean particle size, zeta potential and entrapment efficiency of 186.2 nm, -38.4 mv and 89.73%, respectively. In vitro studies demonstrated that only 20% of insulin was released within 31 days with a burst release of 5.42% in the first 8 h. The hypoglycaemic effect in STZ induced diabetic rats lasted for more than 3 days after the subcutaneous injection of INS-PLC-NPs, which significantly prolonged the therapeutic effect compared with the administration of insulin solution. The pharmacological bioavailability (PA) of INS-PLC-NPs relative to insulin solution was over 350%, indicating that the bioavailability of insulin was significantly enhanced by INS-PLC-NPs. Therefore, the INS-PLC-NPs system is promising to serve as a long lasting insulin release formulation, by which the patient compliance can be enhanced significantly. This study also showed that phospholipid complex loaded biodegradable nanoparticles (PLC-NPs) have a great potential to be used as a sustained delivery system for hydrophilic proteins to be encapsulated in hydrophobic polymers.

摘要

聚(羟基丁酸酯-共-羟基己酸酯)(PHBHHx)在亲水性胰岛素的持续和控制释放中的应用成为可能,通过制备载有胰岛素磷脂复合物的可生物降解的 PHBHHx 纳米颗粒(INS-PLC-NPs)。通过溶剂蒸发法制备的 INS-PLC-NPs 呈球形,平均粒径、Zeta 电位和包封效率分别为 186.2nm、-38.4mv 和 89.73%。体外研究表明,在 31 天内只有 20%的胰岛素释放,在最初的 8 小时内有 5.42%的突释。在 STZ 诱导的糖尿病大鼠中,皮下注射 INS-PLC-NPs 后的降血糖作用持续超过 3 天,与胰岛素溶液给药相比,显著延长了治疗效果。与胰岛素溶液相比,INS-PLC-NPs 的药效生物利用度(PA)超过 350%,表明 INS-PLC-NPs 显著增强了胰岛素的生物利用度。因此,INS-PLC-NPs 系统有望成为一种长效胰岛素释放制剂,可显著提高患者的顺应性。本研究还表明,载有胰岛素磷脂复合物的可生物降解纳米颗粒(PLC-NPs)具有作为亲水性蛋白质的持续释放系统的巨大潜力,可将其包裹在疏水性聚合物中。

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