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Controlled release behaviour of protein-loaded microparticles prepared via coaxial or emulsion electrospray

机译:通过同轴或乳液电喷雾制备的负载蛋白质的微粒的控制释放行为

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摘要

Biodegradable poly (lactic-co-glycolic acid) (PLGA) microparticles are an effective way to achieve sustained drug release. In this study, we investigated a sustained release model of PLGA microparticles with incorporated protein via either emulsion or coaxial electrospray techniques. PLGA (75:25) was used as the carrier, and bovine serum albumin as a model protein. Coaxial electrospray resulted in a type of core–shell structure with mean diameters of 2.41 ± 0.60 µm and a centralised protein distribution within the core. Emulsion electrospray formed bigger microparticles with mean diameters of 22.75 ± 8.05 µm and a heterogeneous protein distribution throughout the microparticles. The coaxial electrospray microparticles presented a much slighter burst release than the emulsion electrospray microparticles. Loading efficiency was significantly higher (p < 0.05) in the coaxial group than emulsion group. This indicated that both emulsion and coaxial electrospray could produce protein-loaded microparticles with sustained release behaviour, but the former revealed a superior approach for drug delivery.
机译:可生物降解的聚乳酸-乙醇酸共聚物(PLGA)微粒是实现药物持续释放的有效方法。在这项研究中,我们通过乳液或同轴电喷雾技术研究了掺入蛋白质的PLGA微粒的缓释模型。 PLGA(75:25)被用作载体,牛血清白蛋白被用作模型蛋白。同轴电喷雾导致一种核壳结构,平均直径为2.41±0.60μm,蛋白质在核内集中分布。乳液电喷雾形成较大的微粒,平均直径为22.75±8.05μm,蛋白质分布在整个微粒中。同轴电喷雾微粒呈现出比乳液电喷雾微粒更小的突发释放。同轴组的负载效率显着高于乳液组(p <0.05)。这表明乳液和同轴电喷雾均可以产生具有持续释放行为的负载蛋白质的微粒,但前者揭示了一种更好的药物递送方法。

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