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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Producing monodisperse drug-loaded polymer microspheres via cross-flow membrane emulsification: The effects of polymers and surfactants
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Producing monodisperse drug-loaded polymer microspheres via cross-flow membrane emulsification: The effects of polymers and surfactants

机译:通过错流膜乳化生产单分散载药聚合物微球:聚合物和表面活性剂的作用

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Cross-flow membrane emulsification (XME) is a method for producing highly uniform droplets by forcing a fluid through a small orifice into a transverse flow of a second, immiscible fluid. We investigate the feasibility of using XME to produce monodisperse solid microspheres made of a hydrolyzable polymer and a hydrophobic drug, a model system for depot drug delivery applications. This entails the emulsification of a drug and polymer-loaded volatile solvent into water followed by evaporation of the solvent. We use a unique side-view visualization technique to observe the details of emulsion droplet production, providing direct information regarding droplet size, dripping frequency, wetting of the membrane surface by the two phases, neck thinning during droplet break off, and droplet deformation before and after break off. To probe the effects that dissolved polymers, surfactants, and dynamic interfacial tension may have on droplet production, we compare our results to a polymer and surfactant-free fluid system with closely matched physical properties. Comparing the two systems, we find little difference in the variation of particle size as a function of continuous phase flow rate. In contrast, at low dripping frequencies, dynamic interfacial tension causes the particle size to vary significantly with drip frequency, which is not seen in simple fluids. No effects due to shear thinning or fluid elasticity are detected. Overall, we find no significant impediments to the application of XME to forming highly uniform drug-loaded microspheres.
机译:错流膜乳化(XME)是一种通过迫使流体通过一个小孔进入第二种不混溶流体的横向流动来产生高度均匀的液滴的方法。我们研究了使用XME生产由可水解聚合物和疏水性药物制成的单分散固体微球的可行性,该模型系统是用于储库药物递送应用的模型系统。这需要将药物和负载聚合物的挥发性溶剂乳化到水中,然后蒸发溶剂。我们使用独特的侧视图可视化技术观察乳液液滴的产生细节,提供有关液滴尺寸,滴落频率,两相膜表面润湿,液滴破裂过程中颈部变细以及液滴在变形之前和之后的变形的直接信息。分手后。为了探究溶解的聚合物,表面活性剂和动态界面张力对液滴产生的影响,我们将我们的结果与物理性能紧密匹配的不含聚合物和表面活性剂的流体系统进行了比较。比较这两个系统,我们发现随着连续相流速的变化,粒径变化几乎没有差异。相反,在低滴落频率下,动态界面张力会导致粒径随滴落频率而显着变化,这在简单的流体中是看不到的。没有检测到由于剪切稀化或流体弹性引起的影响。总体而言,我们发现将XME应用于形成高度均一的载药微球没有重大障碍。

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