Department of Analytical Chemistry, Physical Chemistry and Chemical Engineering, University of Alcala, Alcala de Henares, 28805, Madrid, Spain; Department of Analytical Chemistry, Faculty of Chemistry, Universidad Complutense de Madrid, Plaza de las Ciencias, Ciudad Universitaria, 28040, Madrid, Spain.
Department of Analytical Chemistry, Physical Chemistry and Chemical Engineering, University of Alcala, Alcala de Henares, 28805, Madrid, Spain; Chemical Research Institute "Andres M. del Rio", University of Alcala, Alcala de Henares, Madrid, E28805, Spain.
Biosens Bioelectron. 2024 Jan 15;244:115796. doi: 10.1016/j.bios.2023.115796. Epub 2023 Oct 28.
Tacrolimus (FK506) is a macrolide lactone immunosuppressive drug that is commonly used in transplanted patients to avoid organ rejection. FK506 exhibits high inter- and intra-patient pharmacokinetic variability, making monitoring necessary for organ graft survival. This work describes the development of a novel bioassay for monitoring FK506. The bioassay is based on using polycaprolactone-based (PCL) magnetic Janus micromotors and a recombinant chimera receptor that incorporates the immunophilin tacrolimus binding protein 1A (FKBP1A) tagged with Emerald Green Fluorescent Protein (EmGFP). The approach relies on a fluorescence competitive bioassay between the drug and the micromotors decorated with a carboxylated FK506 toward the specific site of the fluorescent immunophilin. The proposed homogeneous assay could be performed in a single step without washing steps to separate the unbound receptor. The proposed approach fits the therapeutic requirements, showing a limit of detection of 0.8 ng/mL and a wide dynamic range of up to 90 ng/mL. Assay selectivity was evaluated by measuring the competitive inhibition curves with other immunosuppressive drugs usually co-administered with FK506. The magnetic propulsion mechanism allows for efficient operation in raw samples without damaging the biological binding receptor (FKBP1A-EmGFP). The enhanced target recognition and micromixing strategies hold considerable potential for FK506 monitoring in practical clinical use.
他克莫司(FK506)是一种大环内酯类免疫抑制剂药物,常用于移植患者以避免器官排斥。FK506 表现出高度的个体内和个体间药代动力学变异性,因此需要监测以确保器官移植物的存活。本工作描述了一种用于监测 FK506 的新型生物测定法的开发。该生物测定法基于使用聚己内酯基(PCL)磁 Janus 微马达和一种重组嵌合受体,该受体将免疫抑制剂结合蛋白 1A(FKBP1A)与 Emerald Green 荧光蛋白(EmGFP)标记物融合。该方法依赖于药物与用羧基化 FK506 修饰的微马达之间的荧光免疫抑制剂的荧光竞争生物测定,该微马达的修饰物针对荧光免疫抑制剂的特定结合位点。该拟议的均相测定法可以在不进行洗涤步骤以分离未结合的受体的情况下一步完成。所提出的方法符合治疗要求,检测限为 0.8ng/mL,动态范围宽达 90ng/mL。通过测量与通常与 FK506 联合使用的其他免疫抑制剂的竞争性抑制曲线来评估测定法的选择性。磁推进机制允许在不损坏生物结合受体(FKBP1A-EmGFP)的情况下在原始样本中进行高效操作。增强的目标识别和微混合策略在实际临床应用中具有很大的 FK506 监测潜力。