On the possibility of low cost, adherent therapeutic drug monitoring in oncology

Silvia Dalla Marta, Stefano Fornasaro, A. Jaworska, G. Toffoli, A. Bonifacio, V. Sergo
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引用次数: 1

Abstract

A frequent quantification of drugs concentrations in plasma of patients subject to chemotherapy is seldom performed, mostly because the standard methods (Gas or Liquid Chromatography coupled with Mass Spectroscopy) are expensive and time consuming. In this paper we report the approach pursued in one of the research units of the EU project RAMAN4CLINICS to tackle the problem of a low cost, time adherent quantification of drugs used for oncological patients using a Surface Enhanced Raman Scattering (SERS) spectroscopy. More specifically, the issues concerning the repeatability of the nanostructured substrates will be presented and some promising results to increase the selectivity of the measures toward specific drugs will be discussed, with examples concerning one cytotoxic agent, Irinotecan and one kinase inhibitor, Sunitinib.
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肿瘤低成本、持续治疗药物监测的可能性
很少对化疗患者的血浆中药物浓度进行频繁的定量分析,主要是因为标准方法(气相或液相色谱与质谱相结合)昂贵且耗时。在本文中,我们报告了欧盟项目RAMAN4CLINICS的一个研究单位所采用的方法,以解决使用表面增强拉曼散射(SERS)光谱对肿瘤患者使用的药物进行低成本,时间粘附定量的问题。更具体地说,有关纳米结构底物的可重复性的问题将被提出,并将讨论一些有希望的结果,以增加对特定药物的选择性,例如一种细胞毒性药物伊立替康和一种激酶抑制剂舒尼替尼。
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