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首页> 外文期刊>Analyst >Tethering of spherical DOTAP liposome gold nanoparticles on cysteamine monolayer for sensitive label free electrochemical detection of DNA and transfection
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Tethering of spherical DOTAP liposome gold nanoparticles on cysteamine monolayer for sensitive label free electrochemical detection of DNA and transfection

机译:球形DOTAP脂质体金纳米颗粒在半胱胺单层上的束缚,用于DNA的无敏感标记的电化学检测和转染

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Construction of spherical liposomes is critical for developing tools for targeted gene and drug delivery applications in biotechnology and medicine, however, it has been demonstrated only in solution phase until now. Spherical liposome tethering on pristine thiol monolayer on gold transducer and its application to label free DNA sensing and transfection has rarely been reported. Here, we report tethering of spherical 1,2-dioleoyltrimethylammoniumpropane liposome–gold nanoparticle (DOTAP–AuNP) on amine terminated monolayer by simple electrostatic interaction on gold transducer for the first time. Cuddling of cationic liposome by AuNP prevents spherical vesicle fusion in both liquid and solid phases, an essential criterion required for gene and drug delivery applications. The spherical nature of DOTAP–AuNPs on a gold surface is confirmed electrochemically using both [Fe(CN)] and [Ru(NH)] redox probes. Atomic force microscopy (AFM), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), dynamic light scattering (DLS) and ultraviolet-visible (UV) spectroscopic techniques confirm the robust nature of spherical liposome–AuNPs on solid and in liquid phases. The surface is applied for label free DNA hybridization and single nucleotide polymorphism detections sensitively and selectively without signal amplification. The lowest target DNA concentration detected is 100 attomole. DNA transfection is made simply by dropping E. coli cells on DOTAP–AuNP–DNA immobilized transducer surface. The difference between the fluorescent image of transfected E. coli and the differential interference contrast image of E. coli cells by confocal laser scanning microscopy (CLSM) confirms the efficiency and simplicity of the transfection method developed in terms of reduced cost and reagents.
机译:球形脂质体的构建对于生物技术和医学中靶向基因和药物递送应用开发工具的开发至关重要,然而,迄今为止,仅在溶液阶段就得到了证明。金换能器上原始硫醇单层上的球形脂质体束缚及其在标记自由DNA感应和转染中的应用很少见报道。在这里,我们首次报道了通过金传感器上的简单静电相互作用,将球形的1,2-二油酰基三甲基铵丙烷丙烷脂质体-金纳米颗粒(DOTAP-AuNP)束缚在胺端基单层上。 AuNP包裹阳离子脂质体可防止液相和固相中的球形囊泡融合,这是基因和药物递送应用所需的基本标准。使用[Fe(CN)]和[Ru(NH)]氧化还原探针电化学证实了金表面上DOTAP–AuNPs的球形性质。原子力显微镜(AFM),傅里叶变换红外光谱(FTIR),透射电子显微镜(TEM),动态光散射(DLS)和紫外可见(UV)光谱技术证实了球形脂质体-AuNPs在固体和固体中的稳健性液相。该表面适用于无标记的DNA杂交和敏感且选择性的单核苷酸多态性检测,无需信号放大。检测到的最低目标DNA浓度为100 attomole。只需滴加E,即可完成DNA转染。 DOTAP–AuNP–DNA固定化换能器表面的大肠杆菌细胞。转染的 E的荧光图像之间的差异。大肠 E的微分干涉对比图像。通过共聚焦激光扫描显微镜(CLSM)筛选大肠杆菌细胞,证实了在降低成本和减少试剂方面开发的转染方法的效率和简便性。

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