Microneedle-mediated vascular endothelial growth factor delivery promotes angiogenesis and functional recovery after stroke

Ischemic stroke is still the major cause of disability worldwide. Although vascular endothelial growth factor (VEGF) is able to promote both angiogenesis and functional recovery, its use is limited by needle-induced injury, nonhomogenous VEGF distribution, and limited VEGF retention in the brain aft...

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Veröffentlicht in:Journal of controlled release 2021-10, Vol.338, p.610-622
Hauptverfasser: Liu, Yang, Long, Linyu, Zhang, Fanjun, Hu, Xuefeng, Zhang, Jieyu, Hu, Cheng, Wang, Yunbing, Xu, Jianguo
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Sprache:eng
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Zusammenfassung:Ischemic stroke is still the major cause of disability worldwide. Although vascular endothelial growth factor (VEGF) is able to promote both angiogenesis and functional recovery, its use is limited by needle-induced injury, nonhomogenous VEGF distribution, and limited VEGF retention in the brain after intracranial or intravenous injection. Here, we first present a gelatin methacryloyl (GelMA) microneedle (MN)-based platform for the sustained and controlled local delivery of an adeno-associated virus (AAV) expressing human VEGF (AAV-VEGF) that achieves homogenous distribution and high transfection efficiency in ischemic brains. An ischemic stroke model was established in adult rats, and MNs loaded with AAV-VEGF were epicortically inserted into both the ischemic core and penumbra of these rats one day after the onset of ischemia. One week later, the inflammatory response and microneedle biocompatibility were assessed by enzyme-linked immunosorbent assay (ELISA) and immunofluorescence. Eight weeks later, angiogenesis and neural stem cell proliferation and migration were assessed. GelMA MN implantation did not elicit an obvious inflammatory response and had good biocompatibility in the brain. AAV–green fluorescent protein (GFP)-loaded MNs could achieve successful transfection and homogeneous distribution in the brain cortex three weeks postoperatively. MNs loaded with AAV-VEGF increased VEGF expression and enhanced functional angiogenesis and neurogenesis. In summary, MNs might emerge as a promising platform for delivering various therapeutics to treat ischemic stroke and repair other neurologically diseased tissues. [Display omitted] •Microneedle-based platform can achieve sustained and controlled drug release with homogenous distribution.•GelMA Microneedles loaded with AAV-VEGF significantly stimulate angiogenesis and maturation in infarct area.•GelMA Microneedles loaded with AAV-VEGF promote the proliferation, migration and differentiation of NSCs after stroke.•GelMA Microneedles loaded with AAV-VEGF enhance long-term neurological recovery after stroke.
ISSN:0168-3659
1873-4995
DOI:10.1016/j.jconrel.2021.08.057