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Biodegradable silicon nanoneedles delivering nucleic acids intracellularly induce localized in vivo neovascularization

机译:可生物降解的硅纳米针可在细胞内递送核酸诱导局部体内新血管形成

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摘要

The controlled delivery of nucleic acids to selected tissues remains an inefficient process mired by low transfection efficacy, poor scalability because of varying efficiency with cell type and location, and questionable safety as a result of toxicity issues arising from the typical materials and procedures employed. High efficiency and minimal toxicity in vitro has been shown for intracellular delivery of nuclei acids by using nanoneedles, yet extending these characteristics to in vivo delivery has been difficult, as current interfacing strategies rely on complex equipment or active cell internalization through prolonged interfacing. Here, we show that a tunable array of biodegradable nanoneedles fabricated by metal-assisted chemical etching of silicon can access the cytosol to co-deliver DNA and siRNA with an efficiency greater than 90%, and that in vivo the nanoneedles transfect the VEGF-165 gene, inducing sustained neovascularization and a localized sixfold increase in blood perfusion in a target region of the muscle.
机译:核酸向选定组织的受控递送仍然是效率低下的过程,其被低转染效率,由于细胞类型和位置的效率变化而导致的可扩展性差,以及由于使用的典型材料和程序引起的毒性问题而导致的安全性受到质疑。已经显示出通过使用纳米针在细胞内递送核酸的体外高效和最小毒性,但是将这些特征扩展到体内递送是困难的,因为当前的接口策略依赖于复杂的设备或通过延长接口的活性细胞内在化。在这里,我们证明了通过金属硅化学刻蚀制造的可生物降解纳米针的可调阵列可以访问细胞溶质,以高于90%的效率共同递送DNA和siRNA,并且在体内纳米针可以转染VEGF-165。基因,导致持续的新血管形成,并在肌肉目标区域局部灌注了六倍的血液。

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