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通过乳液静电纺丝将药物储库封装于纤维中:形态表征与初步释放评估

Encapsulation of drug reservoirs in fibers by emulsion electrospinning: morphology characterization and preliminary release assessment.

作者信息

Qi Hongxu, Hu Ping, Xu Jun, Wang Aijun

机构信息

The Laboratory of Advanced Materials and Department of Chemical Engineering, Tsinghua University, Beijing, China.

出版信息

Biomacromolecules. 2006 Aug;7(8):2327-30. doi: 10.1021/bm060264z.

Abstract

In this paper, we prepared composite fibers via electrospinning from either W/O or O/W emulsion. SEM images demonstrate the beads-in-string structures in these fibers and proved this technique to be an effective method for microencapsulation. As a practical application, Ca-alginate microspheres, which serve as reservoirs for hydrophilic drugs, were prepared in a reverse emulsion and then incorporated into poly (l-lactic acid) (PLLA) fibers by electrospinning. With the bovine serum albumin (BSA) loaded into the microspheres, the beads-in-string structure thus entrapped hydrophilic proteins in hydrophobic polymeric matrix. In the in vitro release test, BSA, which was released from composite fibers, achieved prolonged release profiles and lower burst release rates than those from naked Ca-alginate microspheres. In comparison with other well-established techniques to prepare microcapsules, such as solvent evaporation and spray-drying techniques, emulsion electrospinning features partly competing, partly complementary characteristics. Extension to other emulsion systems will be able to fabricate new types of functional structures.

摘要

在本文中,我们通过静电纺丝从水包油(W/O)或油包水(O/W)乳液制备了复合纤维。扫描电子显微镜(SEM)图像展示了这些纤维中的串珠结构,并证明该技术是一种有效的微囊化方法。作为实际应用,作为亲水性药物储存库的海藻酸钙微球在反相乳液中制备,然后通过静电纺丝掺入聚左旋乳酸(PLLA)纤维中。将牛血清白蛋白(BSA)载入微球后,这种串珠结构从而将亲水性蛋白质包裹在疏水性聚合物基质中。在体外释放试验中,从复合纤维中释放的BSA呈现出比未包裹的海藻酸钙微球更长的释放曲线和更低的突释率。与其他成熟的微囊制备技术(如溶剂蒸发和喷雾干燥技术)相比,乳液静电纺丝具有部分竞争、部分互补的特性。扩展到其他乳液体系将能够制造新型功能结构。

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