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复合藻酸盐水凝胶:一种控制释放疏水性药物的创新方法。

Composite alginate hydrogels: An innovative approach for the controlled release of hydrophobic drugs.

机构信息

Inter-Departmental Program for Biotechnology, Technion-Israel Institute of Technology, Technion City, Haifa 32000, Israel.

出版信息

Acta Biomater. 2010 Dec;6(12):4642-9. doi: 10.1016/j.actbio.2010.06.032. Epub 2010 Jun 30.

DOI:10.1016/j.actbio.2010.06.032
PMID:20601237
Abstract

We present an innovative methodology for the sustained delivery of hydrophobic drugs using composite hydrogels, prepared by embedding oil-in-water microemulsions in hydrophilic hydrogels. The hydrophobic nature of the microemulsion core enhances the solubilization of hydrophobic drugs, while the crosslinked matrix could be readily used as a solid controlled delivery vehicle. A microemulsion was formulated from pharmaceutical accepted components; the droplets diameter was shown to be about 10nm by dynamic light scattering, cryo-transmission electron microscopy and small-angle X-ray scattering (SAXS). Combining the microemulsion with alginate solution and crosslinking with calcium ions resulted in a clear hydrogel. A model hydrophobic drug, Ketoprofen, precipitated from the alginate hydrogel, but the drug-containing composite hydrogel was clear and macroscopically homogeneous. The nanostructure was investigated by SAXS; scattering plots indicate that oil droplets exist in the composite hydrogel. Release profiles of the drug from the composite hydrogel with various concentrations of polymer and crosslinker demonstrate the applicability of this system as a controlled delivery vehicle, and suggest that the release rate is governed not by the microemulsion structure but, rather, by the network properties. Furthermore, it was demonstrated that the release rate could be tailored for a specific application utilizing different alginate and calcium concentrations. The generalization of the methodology of including hydrophobic drugs in composite gels is discussed.

摘要

我们提出了一种使用复合水凝胶持续递送疏水性药物的创新方法,该方法通过将油包水乳状液嵌入亲水性水凝胶中来制备。油状液滴核心的疏水性增强了疏水性药物的溶解度,而交联基质可以很容易地用作固体控制释放载体。微乳液由医药上可接受的成分组成;动态光散射、低温透射电子显微镜和小角 X 射线散射(SAXS)表明液滴直径约为 10nm。将微乳液与藻酸盐溶液混合,并用钙离子交联,得到一种透明的水凝胶。一种模型疏水性药物酮洛芬从藻酸盐水凝胶中沉淀出来,但含有药物的复合水凝胶是透明的,宏观上是均匀的。通过 SAXS 研究了纳米结构;散射图表明油滴存在于复合水凝胶中。具有不同聚合物和交联剂浓度的药物从复合水凝胶中的释放曲线表明,该系统适用于作为控制释放载体,并且表明释放速率不受微乳液结构的控制,而是受网络性质的控制。此外,还证明可以利用不同的藻酸盐和钙浓度来定制特定应用的释放速率。讨论了将疏水性药物纳入复合凝胶的方法的推广。

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