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一种基于超滤的无抗体检测方法,用于使用纳升液相色谱-高分辨率质谱/质谱法在低皮克/毫升浓度下检测尿液中的生长激素释放激素。

An antibody-free, ultrafiltration-based assay for the detection of growth hormone-releasing hormones in urine at low pg/mL concentrations using nanoLC-HRMS/MS.

作者信息

Coppieters Gilles, Deventer Koen, Polet Michaël, Van Eenoo Peter, Judák Péter

机构信息

Doping Control Laboratory (DoCoLab), Ghent University, Department of Diagnostic Sciences (GE32), Ottergemsesteenweg 460, B-9000 Ghent, Belgium.

Doping Control Laboratory (DoCoLab), Ghent University, Department of Diagnostic Sciences (GE32), Ottergemsesteenweg 460, B-9000 Ghent, Belgium.

出版信息

J Pharm Biomed Anal. 2022 May 30;214:114726. doi: 10.1016/j.jpba.2022.114726. Epub 2022 Mar 12.

DOI:10.1016/j.jpba.2022.114726
PMID:35298973
Abstract

This work presents an ultrafiltration-based, validated method for the screening and confirmation of prohibited growth hormone-releasing hormone (GHRH) analogues (sermorelin/CJC-1293, sermorelin metabolite, CJC-1295 and tesamorelin) in urine by nanoLC-HRMS/MS. Sample preparation avoids the use of laborious antibody-based extraction approaches and consists solely of preconcentration by ultrafiltration. Even in the absence of immuno-affinity purification steps, high sensitivity was still ensured as limits of detection between 5 and 25 pg/mL and limits of identification between 25 and 50 pg/mL were established. The robustness of the miniaturized chromatographic setup was evaluated through the injection of 200 + preconcentrated urinary extracts. In a comparison with immuno-affinity purification, enhanced recoveries (59 - 115%) and similar sensitivity were achieved, yet at lower operational costs. Stability experiments showed the importance of the proper handling of urine samples to avoid degradation of these peptide hormones, especially for sermorelin and its metabolite which were found to rapidly degrade at temperatures > 4 °C and pH values < 7 in accordance with earlier studies. Without the need for specific antibodies, this method may be expanded to cover emerging peptide drugs (≥ ~3 kDa), as well as their metabolites in the future to facilitate coverage for this class of prohibited substances.

摘要

这项工作提出了一种基于超滤的、经过验证的方法,用于通过纳升液相色谱-高分辨质谱/质谱法筛选和确证尿液中违禁的生长激素释放激素(GHRH)类似物(舍莫瑞林/CJC-1293、舍莫瑞林代谢物、CJC-1295和替沙莫瑞林)。样品制备避免了使用费力的基于抗体的提取方法,仅通过超滤进行预浓缩。即使没有免疫亲和纯化步骤,仍确保了高灵敏度,因为检测限在5至25 pg/mL之间,鉴定限在25至50 pg/mL之间。通过注入200多个预浓缩尿液提取物评估了小型化色谱装置的稳健性。与免疫亲和纯化相比,回收率提高(59 - 115%)且灵敏度相似,但运营成本更低。稳定性实验表明正确处理尿液样品对于避免这些肽类激素降解的重要性,特别是对于舍莫瑞林及其代谢物,根据早期研究发现,它们在温度> 4°C和pH值< 7时会迅速降解。由于无需特定抗体,该方法未来可能会扩展以涵盖新兴的肽类药物(≥ ~3 kDa)及其代谢物,以便于对这类违禁物质进行检测。

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