4.7 Article

Development of the dried blood spot preparation protocol for comprehensive evaluation of the hematocrit effect

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ANALYTICA CHIMICA ACTA
卷 1239, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.aca.2022.340650

关键词

Dried blood spots; Hematocrit effect; Distribution bias; Azole drugs

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This study proposed an effective DBS preparation protocol to comprehensively evaluate the hematocrit (Hct) effect for accurate quantification of DBS samples. An LC-MS/MS method was used to quantify the target drugs in DBS samples, and the results showed the validity of the proposed protocol. This new protocol eliminated common pitfalls in studying the Hct effect and provided a comprehensive strategy for further DBS studies.
The application of dried blood spots (DBS) has gradually increased in different fields because of its several ad-vantages. The hematocrit (Hct) effect is one major analytical challenge that may affect the quantification ac-curacy of DBS samples and should be investigated when developing a novel DBS method. However, previous studies usually overlooked the Hct-related distribution bias when evaluating the Hct effect. This study aimed to propose an effective DBS preparation protocol for the comprehensive evaluation of the Hct effect. We selected voriconazole and posaconazole as the demonstration drugs. Fifteen microliters of the blood samples were spotted on DBS cards followed by whole spot extraction. An LC-MS/MS method was first developed to quantify vor-iconazole and posaconazole in DBS samples. The quantitation accuracy for both azole drugs was within 93.5%- 111.7%, except for the accuracies of posaconazole at the LLOQ, which were less than 119%. The intra-and interday precision were below 11%. The validated LC-MS/MS method was used to develop the DBS preparation protocol for evaluating the Hct effect. Three critical parameters that may affect the observed Hct effect were investigated. The results showed that using the solid-state of the target analytes, spiking the target analytes before preparing different Hct levels, and allowing enough equilibrium time after spiking target analytes can provide a more holistic Hct effect evaluation. The validity of the proposed new protocol was verified by con-version factors obtained from 71 paired DBS and plasma samples. Conversion factors calculated by clinical samples were consistent with the Hct effect evaluated by manually prepared DBS samples. This new DBS preparation protocol eliminated the common pitfalls in studying the Hct effect and offered a comprehensive strategy to assess the Hct effect for further DBS studies.

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