Process and formulation variables in the preparation of injectable and biodegradable magnetic microspheres.

Hong Zhao, Jeffrey Gagnon, Urs O Häfeli
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Abstract

The aim of this study was to prepare biodegradable sustained release magnetite microspheres sized between 1 to 2 microm. The microspheres with or without magnetic materials were prepared by a W/O/W double emulsion solvent evaporation technique using poly(lactide-co-glycolide) (PLGA) as the biodegradable matrix forming polymer. Effects of manufacturing and formulation variables on particle size were investigated with non-magnetic microspheres. Microsphere size could be controlled by modification of homogenization speed, PLGA concentration in the oil phase, oil phase volume, solvent composition, and polyvinyl alcohol (PVA) concentration in the outer water phase. Most influential were the agitation velocity and all parameters that influence the kinematic viscosity of oil and outer water phase, specifically the type and concentration of the oil phase. The magnetic component yielding homogeneous magnetic microspheres consisted of magnetite nanoparticles of 8 nm diameter stabilized with a polyethylene glycole/polyacrylic acid (PEG/PAA) coating and a saturation magnetization of 47.8 emu/g. Non-magnetic and magnetic microspheres had very similar size, morphology, and size distribution, as shown by scanning electron microscopy. The optimized conditions yielded microspheres with 13.7 weight% of magnetite and an average diameter of 1.37 microm. Such biodegradable magnetic microspheres seem appropriate for vascular administration followed by magnetic drug targeting.

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制备可注射和可生物降解磁性微球的工艺和配方变量。
本研究的目的是制备生物可降解缓释磁铁矿微球,尺寸在 1 到 2 微米之间。使用聚乳酸-共聚乙二醇(PLGA)作为生物可降解基质形成聚合物,通过 W/O/W 双乳液溶剂蒸发技术制备了含或不含磁性材料的微球。用非磁性微球研究了制造和配方变量对粒度的影响。通过改变均质速度、油相中的 PLGA 浓度、油相体积、溶剂成分和外层水相中的聚乙烯醇 (PVA) 浓度,可以控制微球的大小。影响最大的是搅拌速度以及所有影响油相和外水相运动粘度的参数,特别是油相的类型和浓度。产生均质磁性微球的磁性成分由直径为 8 纳米的磁铁矿纳米颗粒组成,并用聚乙二醇/聚丙烯酸(PEG/PAA)涂层稳定,饱和磁化率为 47.8 emu/g。扫描电子显微镜显示,非磁性和磁性微球的大小、形态和尺寸分布非常相似。优化条件下产生的微球含有 13.7% 的磁铁矿,平均直径为 1.37 微米。这种可生物降解的磁性微球似乎很适合在血管给药后进行磁性药物靶向。
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