首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Development of a Triplet-Triplet Absorption Ruler: DNA- and Chromatin-Mediated Drug Molecule Release from a Nanosurface
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Development of a Triplet-Triplet Absorption Ruler: DNA- and Chromatin-Mediated Drug Molecule Release from a Nanosurface

机译:三重-三重吸收标尺的开发:DNA和染色质介导的药物分子从纳米表面的释放。

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Triplet-triplet (T-T) absorption spectroscopy has been used successfully as a molecular ruler to understand the actual release process of sanguinarine as a drug molecule from a gold nanoparticle surface in the presence of cell components, that is, DNA and chromatin. The obtained results have been verified by fluorescence and surface-enhanced Raman spectroscopy (SERS), and a plausible explanation has been put forward to describe the underestimation and overestimation of the percentage (%) of the release of drug molecules measured by fluorescence- and SERS-based techniques, respectively, over the highlighted T-T absorption spectroscopy. Because of the intrinsic nature of absorption, the reported T-T absorption spectroscopic assay overpowers fluorescence- and SERS-based assays, which are limited by the long-range interaction and nonlinear dependence of the concentration of analytes, respectively.
机译:三重态三重态(T-T)吸收光谱已成功地用作分子标尺,以了解在细胞成分(即DNA和染色质)存在的情况下,血红素作为药物分子从金纳米颗粒表面的实际释放过程。通过荧光和表面增强拉曼光谱(SERS)验证了所获得的结果,并提出了合理的解释来描述通过荧光和SERS测得的药物分子释放百分比(%)的低估和高估突出的TT吸收光谱法中分别使用了基于C的技术。由于吸收的内在性质,所报道的T-T吸收光谱分析法优于基于荧光和基于SERS的分析法,后者分别受分析物浓度的长期相互作用和非线性依赖性的限制。

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