纤维蛋白
PLGA公司
药物输送
化学
药理学
背根神经节
神经再支配
他克莫司
周围神经损伤
生物医学工程
周围神经
移植
体外
医学
外科
解剖
生物化学
背
免疫学
有机化学
作者
Kasra Tajdaran,Molly S. Shoichet,Tessa Gordon,Gregory H. Borschel
摘要
ABSTRACT Despite substantial improvement in microsurgical techniques for nerve repair, recovery after peripheral nerve injury is usually incomplete. FK506, an FDA approved immunosuppressant, improves functional recovery and reinnervation following peripheral nerve injury in animal models. However, systemically delivered FK506 causes undesirable global immunosuppression. We have, therefore, engineered a biodegradable local delivery system for FK506 using fibrin gel as a drug reservoir that could be placed at a site of nerve injury. FK506 was incorporated into fibrin gel in solubilized, particulated, and poly(lactic‐co‐glycolic) acid (PLGA) microspheres‐encapsulated forms. A tunable release of FK506 in the fibrin gel from days to weeks was observed with the rate of release being most rapid for the solubilized form and then the particulate form. The most prolonged period of release was seen with the PLGA microsphere‐encapsulated form. As analyzed by in vitro dorsal root ganglion (DRG) neurite extension assay, PLGA microsphere encapsulation of FK506 did not alter the drug's properties and the released FK506 maintained its bioactivity over the entire period of release. This study suggests that local delivery of FK506 with fibrin hydrogel could be used to enhance peripheral nerve regeneration. Biotechnol. Bioeng. 2015;112: 1948–1953. © 2015 Wiley Periodicals, Inc.
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