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喷雾固化富含蛋白质的脂质微球:制备与固态特性研究。

Spray congealed lipid microparticles with high protein loading: preparation and solid state characterisation.

机构信息

Dipartimento di Scienze Farmaceutiche, Università di Bologna, Via S. Donato 19/2, 40127 Bologna, Italy.

出版信息

Eur J Pharm Sci. 2012 Aug 15;46(5):346-56. doi: 10.1016/j.ejps.2012.02.021. Epub 2012 Mar 21.

Abstract

The spray-congealing technique, a solvent-free drug encapsulation process, was successfully employed to obtain lipid-based particulate systems with high (10-20% w/w) protein loading. Bovine serum albumin (BSA) was utilised as model protein and three low melting lipids (glyceryl palmitostearate, trimirystin and tristearin) were employed as carriers. BSA-loaded lipid microparticles were characterised in terms of particle size, morphology and drug loading. The results showed that the microparticles exhibited a spherical shape, mean diameter in the range 150-300 μm and an encapsulation efficiency higher than 90%. Possible changes in the protein structure as a result of the manufacturing process was then investigated for the first time using UV spectrophotometry in fourth derivative mode and FT-Raman spectroscopy. The results suggested that the structural integrity of the protein was maintained within the particles. Thermal analysis indicated that the effect of protein on the thermal properties of the carriers could be detected. Spray-congealing could thus be considered a suitable technique to produce highly BSA-loaded microparticles preserving the structure of the protein.

摘要

喷雾凝结技术是一种无溶剂的药物包封过程,成功地用于获得具有高(10-20%w/w)蛋白载量的基于脂质的颗粒系统。牛血清白蛋白(BSA)被用作模型蛋白,三种低熔点脂质(甘油棕榈硬脂酸酯、三硬脂精和三硬脂酸甘油酯)被用作载体。载有 BSA 的脂质微球在粒径、形态和药物载量方面进行了表征。结果表明,微球呈球形,平均直径在 150-300μm 范围内,包封效率高于 90%。然后首次使用紫外分光光度法在四阶导数模式和傅里叶变换拉曼光谱法中研究了制造过程中蛋白质结构可能发生的变化。结果表明,蛋白质在颗粒内的结构完整性得以保持。热分析表明,可以检测到蛋白质对载体热性能的影响。因此,喷雾凝结技术可以被认为是一种合适的技术,可以生产出高载量的 BSA 微球,同时保持蛋白质的结构。

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