Joseph Jan F, Gronbach Leonie, García-Miller Jill, Cruz Leticia M, Wuest Bernhard, Keilholz Ulrich, Zoschke Christian, Parr Maria K
Freie Universität Berlin, Core Facility BioSupraMol, 14195 Berlin, Germany.
Freie Universität Berlin, Institute of Pharmacy (Pharmacology & Toxicology), 14195 Berlin, Germany.
Pharmaceutics. 2020 Apr 30;12(5):413. doi: 10.3390/pharmaceutics12050413.
Cancer treatment often lacks individual dose adaptation, contributing to insufficient efficacy and severe side effects. Thus, personalized approaches are highly desired. Although various analytical techniques are established to determine drug levels in preclinical models, they are limited in the automated real-time acquisition of pharmacokinetic profiles. Therefore, an online UHPLC-MS/MS system for quantitation of drug concentrations within 3D tumor oral mucosa models was generated. The integration of sampling ports into the 3D tumor models and their culture inside the autosampler allowed for real-time pharmacokinetic profiling without additional sample preparation. Docetaxel quantitation was validated according to EMA guidelines. The tumor models recapitulated the morphology of head-and-neck cancer and the dose-dependent tumor reduction following docetaxel treatment. The administration of four different docetaxel concentrations resulted in comparable courses of concentration versus time curves for 96 h. In conclusion, this proof-of-concept study demonstrated the feasibility of real-time monitoring of drug levels in 3D tumor models without any sample preparation. The inclusion of patient-derived tumor cells into our models may further optimize the pharmacotherapy of cancer patients by efficiently delivering personalized data of the target tissue.
癌症治疗常常缺乏个体化剂量调整,导致疗效不佳和严重的副作用。因此,非常需要个性化的治疗方法。尽管已经建立了各种分析技术来测定临床前模型中的药物水平,但它们在自动实时获取药代动力学曲线方面存在局限性。因此,我们构建了一个用于定量三维肿瘤口腔黏膜模型内药物浓度的在线超高效液相色谱-串联质谱(UHPLC-MS/MS)系统。将采样端口集成到三维肿瘤模型中,并在自动进样器中对其进行培养,从而无需额外的样品制备即可实现实时药代动力学分析。多西他赛的定量分析按照欧洲药品管理局(EMA)的指南进行了验证。肿瘤模型重现了头颈癌的形态以及多西他赛治疗后剂量依赖性的肿瘤缩小情况。给予四种不同浓度的多西他赛后,96小时内浓度-时间曲线的变化过程具有可比性。总之,这项概念验证研究证明了在无需任何样品制备的情况下实时监测三维肿瘤模型中药物水平的可行性。将患者来源的肿瘤细胞纳入我们的模型中,可能通过有效地提供靶组织的个性化数据,进一步优化癌症患者的药物治疗。