Degradation of vancomycin in external quality assessment samples is a factor to underestimate its concentration

Author:

Fan Yaxin123ORCID,Wang Yu123ORCID,Chen Mengting123,Chen Yuancheng23ORCID,Guo Beining123,Liu Xiaofen123,Wu Hailan123,Li Yi123,Hu Jiali123,Zhang Jing123ORCID

Affiliation:

1. Institute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, 200040, China

2. Key Laboratory of Clinical Pharmacology of Antibiotics, National Population & Family Planning Commission, Shanghai, 200040, China

3. National Clinical Research Center for Aging & Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, China

Abstract

Aim: To compare the difference between the measured and target values in vancomycin external quality assessment (EQA) samples and to investigate the factors for underestimating its concentration. Materials & methods: A retrospective analysis of 195 international vancomycin EQA results was performed. Deviations of the concentrations determined by TDx fluorescence polarization immunoassay (FPIA), Axsym FPIA and Architect chemiluminescence microparticle immunoassay (CMIA) method were -2.43, -16.28 and -10.53%, respectively. Chromatographic peaks of the crystalling degradation products appeared in samples with large deviations. Vancomycin were degraded after long-term transporting and high temperature. Conclusion: Vancomycin concentrations measured by Axsym FPIA and Architect CMIA methods were likely to be underestimated. Long-term transporting resulted in low EQA results, suggesting that establishing a local EQA system for vancomycin is essential.

Funder

Municipal Hospital Emerging Frontier Technology Joint Research Project of Shanghai Shenkang Development Center

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

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