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基于亲水作用色谱-二极管阵列检测-质谱联用分析非法肽类药物。

Analysis of illegal peptide drugs via HILIC-DAD-MS.

机构信息

Division of Food, Medicines and Consumer Safety, Section Medicines and Healthcare Products, Scientific Institute of Public Health (WIV-ISP), J. Wytsmansstraat 14, B-1050 Brussels, Belgium; Laboratory for Drug Quality & Registration (DruQuaR), Department of Pharmaceutical analysis, University of Ghent, Ottergemsesteenweg 460, B-9000 Ghent, Belgium.

Laboratory for Drug Quality & Registration (DruQuaR), Department of Pharmaceutical analysis, University of Ghent, Ottergemsesteenweg 460, B-9000 Ghent, Belgium.

出版信息

Talanta. 2017 Nov 1;174:562-571. doi: 10.1016/j.talanta.2017.06.034. Epub 2017 Jun 13.

Abstract

Biopharmaceuticals have established themselves as highly efficient medicines, and are still one of the fastest growing parts of the health-product industry. Unfortunately, the introduction of these promising new drugs went hand in hand with the creation of a black market for illegal and counterfeit biotechnology drugs. Particularly popular are the lyophilised peptides with a molecular weight of less than 5kDa. Most of them are meant for subcutaneous injection and are easily accessible via the internet. In recent years, different methods based on reversed phase liquid chromatography have been developed to detect and quantify these peptides. The emerging of more polar peptides however requires the introduction of other separation techniques. Therefore, we set out to develop and validate an analytical method based on hydrophilic interaction liquid chromatography (HILIC) to identify and quantify the most frequently encountered illegal peptides on the European market. For this objective, five different HILIC columns were selected and screened for their chromatographic performance. Among those columns, the ZIC HILIC column showed the best performance under the tested screening conditions in terms of resolution and symmetry factor for the targeted peptide set. Hence, the operational conditions were further optimised for the identification of illegal preparations via mass spectrometry (MS) and quantification via UV. Validation was performed via accuracy profiles based on the ISO 17025 guideline. The obtained validated HILIC-method allows for the detection and quantification of the most frequently encountered illegal peptides on the internet in a total run time of 35min including post gradient equilibration and online cleaning step. Combined with a previously developed RPLC-method, the ZIC HILIC system allows for the detection and quantification of a wide spectrum of illicit peptide drugs available on the internet. Furthermore, the developed method could also be envisaged for the detection of new emerging polar peptide drugs.

摘要

生物制药已被证明是高效的药物,并且仍然是保健品行业增长最快的领域之一。不幸的是,这些有前途的新药的推出伴随着非法和假冒生物技术药物黑市的出现。特别受欢迎的是分子量小于 5kDa 的冻干肽。它们大多用于皮下注射,通过互联网很容易获得。近年来,已经开发出基于反相液相色谱的不同方法来检测和定量这些肽。然而,由于出现更多极性的肽,因此需要引入其他分离技术。因此,我们着手开发和验证一种基于亲水相互作用液相色谱(HILIC)的分析方法,以鉴定和定量欧洲市场上最常见的非法肽。为此,选择了五种不同的 HILIC 柱,并对其色谱性能进行了筛选。在这些柱中,ZIC HILIC 柱在测试的筛选条件下针对目标肽集显示出最佳的分辨率和对称因子性能。因此,进一步优化了操作条件,以便通过质谱(MS)进行非法制剂的鉴定和通过 UV 进行定量。验证是通过基于 ISO 17025 指南的准确度概况进行的。所获得的经验证的 HILIC 方法允许在 35 分钟的总运行时间内检测和定量互联网上最常见的非法肽,包括梯度后平衡和在线清洗步骤。与之前开发的 RPLC 方法结合使用,ZIC HILIC 系统允许检测和定量互联网上广泛存在的非法肽药物。此外,该方法还可以用于检测新出现的极性肽药物。

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