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A novel cell transfection platform based on laser optoporation mediated by Au nanostar layers

机译:基于Au纳米载体层介导的激光邻晶体的新细胞转染平台

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摘要

The recently developed laser-induced cell transfection mediated by Au nanoparticles is a promising alternative to the well-established lipid-based transfection or to electroporation. Optoporation is based on the laser plasmonic heating of nanoparticles located near the cell membrane. However, the uncontrollable cell damage from intense laser pulses and from random attachment of nanoparticles may be crucial for transfection. We present a novel plasmonic optoporation technique that uses Au nanostar layers immobilized in culture microplate wells. HeLa cells were grown directly on Au nanostar layers, after which they were subjected to continuous-wave 808 nm laser irradiation. An Au monolayer density similar to 15 mu g/cm(2) and an absorbed energy of about 15 to 30 J were found to be optimal for optoporation. Propidium iodide molecules were used as model penetrating agent. The transfection efficiency evaluated using fluorescence microscopy for HeLa cells transfected with pGFP under optimized optoporation conditions (95% +/- 5%) was similar to the efficiency of TurboFect. The technique's efficiency (295 +/- 10 relative light units, RLU), demonstrated by transfecting HeLa cells with the pCMV-GLuc 2 control plasmid, was greater than that obtained by transfection of HeLa cells with the TurboFect agent (220 +/- 10 RLU). The cell viability in plasmonic optoporation (92% +/- 7%), too, was greater than that in transfection with TurboFect (75% +/- 7%).
机译:由Au纳米粒子介导的最近开发的激光诱导的细胞转染是对良好的脂质的转染或电穿孔的有希望的替代方案。邻孔透镜基于位于细胞膜附近的纳米颗粒的激光等离子体加热。然而,来自强烈的激光脉冲和随机连接的纳米颗粒的无法控制的细胞损伤对于转染至关重要。我们提出了一种新的等离子体透镜技术,使用固定在培养微孔板孔中的Au纳米菌层。 Hela细胞直接生长在Au纳米罩层上,之后将它们进行连续波808nm激光照射。发现类似于15μg/ cm(2)的Au单层密度和约15至30 j的吸收能量是最佳的逆光孔。碘化丙锭分子用作模型渗透剂。使用荧光显微镜评估的转染效率使用PGFP在优​​化的邻孔孔条件下(95%+/- 5%)转染的Hela细胞(95%+/- 5%)类似于涡轮孔的效率。该技术的效率(295 +/- 10相对光单元,RLU)通过转染PCMV-Gluc2对照质粒,大于通过用涡轮胶剂转染HeLa细胞(220 +/- 10 RLU)。等离子体致孔的细胞活力也大于涡轮孔的转染(75%+/- 7%)。

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