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替加环素免疫检测:用于药物监测目的的开发的具有特异性和选择性的抗体。

Tigecycline Immunodetection Using Developed Group-Specific and Selective Antibodies for Drug Monitoring Purposes.

机构信息

I. Mechnikov Research Institute for Vaccines and Sera, Moscow 105064, Russia.

Faculty of Medicine, M.V. Lomonosov Moscow State University, Moscow 119991, Russia.

出版信息

Biosensors (Basel). 2023 Mar 4;13(3):343. doi: 10.3390/bios13030343.

Abstract

Tigecycline (TGC), a third-generation tetracycline, is characterized by a more potent and broad antibacterial activity, and the ability to overcome different mechanisms of tetracycline resistance. TGC has proven to be of value in treatment of multidrug-resistant infections, but therapy can be complicated by multiple dangerous side effects, including direct drug toxicity. Given that, a TGC immunodetection method has been developed for therapeutic drug monitoring to improve the safety and efficacy of therapy. The developed indirect competitive ELISA utilized TGC selective antibodies and group-specific antibodies interacting with selected coating TGC conjugates. Both assay systems showed high sensitivity (IC50) of 0.23 and 1.59 ng/mL, and LOD of 0.02 and 0.05 ng/mL, respectively. Satisfactory TGC recovery from the spiked blood serum of healthy volunteers was obtained in both assays and laid in the range of 81-102%. TGC concentrations measured in sera from COVID-19 patients with secondary bacterial infections were mutually confirmed by ELISA based on the other antibody-antigen interaction and showed good agreement (R = 0.966). A TGC pharmacokinetic (PK) study conducted in three critically ill patients proved the suitability of the test to analyze the therapeutic concentrations of TGC. Significant inter-individual PK variability revealed in this limited group supports therapeutic monitoring of TGC in individual patients and application of the test for population pharmacokinetic modelling.

摘要

替加环素(TGC)是第三代四环素,具有更强和更广泛的抗菌活性,并且能够克服四环素耐药的不同机制。TGC 已被证明对治疗多重耐药感染有价值,但由于多种危险的副作用,包括直接药物毒性,治疗可能会变得复杂。鉴于此,已经开发了 TGC 免疫检测方法用于治疗药物监测,以提高治疗的安全性和疗效。开发的间接竞争 ELISA 利用 TGC 选择性抗体和与选定的涂层 TGC 缀合物相互作用的组特异性抗体。两种检测系统均显示出较高的灵敏度(IC50),分别为 0.23 和 1.59ng/mL,以及较低的检测限(LOD),分别为 0.02 和 0.05ng/mL。在两种检测系统中,从健康志愿者的添加血液血清中回收 TGC 的效果均令人满意,回收率均在 81-102%之间。通过 ELISA 基于另一种抗体-抗原相互作用测量的 COVID-19 继发细菌感染患者血清中的 TGC 浓度相互证实,并且显示出良好的一致性(R=0.966)。在三名重症患者中进行的 TGC 药代动力学(PK)研究证明了该测试适用于分析 TGC 的治疗浓度。在该有限组中发现的显著个体间 PK 变异性支持对个体患者的 TGC 进行治疗监测,并应用该测试进行群体药代动力学建模。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2351/10046529/a07440ddbf7b/biosensors-13-00343-g001.jpg

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