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基于表面增强拉曼散射的胶体纳米传感器用于开发治疗药物监测。

A surface enhanced Raman scattering based colloid nanosensor for developing therapeutic drug monitoring.

机构信息

Department of Chemical Sciences, University of Padova, v. Marzolo 1, 35313 Padova, Italy.

SOC Farmacologia Sperimentale e Clinica, Centro di Riferimento Oncologico, Via Franco Gallini 2, 33081 Aviano, Italy.

出版信息

J Colloid Interface Sci. 2019 Jan 1;533:621-626. doi: 10.1016/j.jcis.2018.08.107. Epub 2018 Aug 29.

Abstract

Competitive reactions, on the surface of plasmonic nanostructures, allow exploiting SERS signals for quantitative Therapeutic Drug Monitoring. As an example, the concentration of Erlotinib, an anti-EGFR small molecule, used for the treatment of non-small cell lung and pancreatic cancer, is determined. The numerous side effects and the variability of patient responses make Erlotinib a good candidate for monitoring. The new SERS based sensor can estimate Erlotinib down to nanomolar concentration and is based on the chemical reaction of the drug and of a competitor SERS reporter on the surface of gold nanostructures. Colloid solutions of naked gold nanoparticles obtained by laser ablation in solution were used for obtaining nanostructures with very efficient hot spots for SERS and with a clean surface for chemistry. Detection of the drug in the nanomolar concentration range is shown to be possible also in spiked plasma samples.

摘要

在等离子体纳米结构的表面上进行竞争反应,可以利用 SERS 信号进行定量治疗药物监测。例如,确定了表皮生长因子受体 (EGFR) 小分子埃罗替尼的浓度,埃罗替尼用于治疗非小细胞肺癌和胰腺癌。由于其众多的副作用和患者反应的可变性,埃罗替尼是监测的一个很好的候选药物。新的基于 SERS 的传感器可以估计埃罗替尼低至纳摩尔浓度,并且基于药物和金纳米结构表面上的竞争 SERS 报告分子的化学反应。通过溶液中激光烧蚀获得的裸露金纳米粒子的胶体溶液用于获得具有非常有效的 SERS 热点和清洁表面化学的纳米结构。在掺杂的血浆样品中也显示出可以在纳摩尔浓度范围内检测到药物。

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