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电纺纤维的长效药物释放用于体内炎症预防,以防止腱周粘连。

Long-term drug release from electrospun fibers for in vivo inflammation prevention in the prevention of peritendinous adhesions.

机构信息

Department of Orthopedics, The First Affiliated Hospital of Soochow University, 188 Shizi Street, Suzhou, Jiangsu 215006, People's Republic of China.

出版信息

Acta Biomater. 2013 Jul;9(7):7381-8. doi: 10.1016/j.actbio.2013.03.040. Epub 2013 Apr 6.

DOI:10.1016/j.actbio.2013.03.040
PMID:23567943
Abstract

Physical barriers such as electrospun fibrous membranes are potentially useful in preventing peritendinous adhesions after surgery. However, inflammatory responses caused by degradation of barrier materials remain a major challenge. This study aimed to fabricate electrospun composite fibrous membranes based on drug-loaded modified mesoporous silica (MMS) and poly (l-lactic acid) (PLLA). Using a co-solvent-based electrospinning method ibuprofen (IBU)-loaded MMS was successfully and uniformly encapsulated in the PLLA fibers. The electrospun PLLA-MMS-IBU composite fibrous membranes showed significantly lower initial burst release (6% release in the first 12h) compared with that of electrospun PLLA-IBU fibrous membranes (46% release in the first 12h) in in vitro release tests. Moreover, the release from PLLA-MMS-IBU was also for significantly longer than that from PLLA-IBU (100 vs. 20days). In animal studies both PLLA-IBU and PLLA-MMS-IBU showed improved anti-adhesion properties and anti-inflammatory effects compared with PLLA fibrous membrane alone 4weeks after implantation. Further, animals implanted with PLLA-MMS-IBU for 8weeks showed the lowest inflammation and best recovery compared with those implanted with PLLA-IBU and PLLA, most likely as a result of its long-term IBU release profile. Therefore, this study provides a platform technique for fabricating fibrous membranes with long-term sustained drug release characteristics which may function as a novel carrier for long-term anti-inflammation and anti-adhesion to prevent peritendinous adhesions.

摘要

物理屏障,如电纺纤维膜,在预防手术后腱周粘连方面具有潜在的应用价值。然而,屏障材料降解引起的炎症反应仍然是一个主要挑战。本研究旨在制备基于载药改性介孔硅(MMS)和聚(L-乳酸)(PLLA)的电纺复合纤维膜。采用共溶剂静电纺丝法,成功且均匀地将布洛芬(IBU)载入 MMS 中。与电纺 PLLA-IBU 纤维膜(第 12 小时释放 46%)相比,体外释放试验表明电纺 PLLA-MMS-IBU 复合纤维膜的初始突释释放明显较低(第 12 小时释放 6%)。此外,PLLA-MMS-IBU 的释放时间也明显长于 PLLA-IBU(100 天 vs. 20 天)。动物研究表明,与 PLLA 纤维膜相比,植入后 4 周时,PLLA-IBU 和 PLLA-MMS-IBU 均表现出更好的抗粘连和抗炎效果。此外,植入 PLLA-MMS-IBU 8 周的动物与植入 PLLA-IBU 和 PLLA 的动物相比,炎症程度最低,恢复情况最好,这可能是由于其具有长期的 IBU 释放特性。因此,本研究提供了一种制造具有长期持续药物释放特性的纤维膜的平台技术,可作为一种新型载体用于长期抗炎和抗粘连,以预防腱周粘连。

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