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Advancing towards practice: A novel LC-MS/MS method for detecting retinol in dried blood spots.
Wang, Hai-Bo; Xiao, Xuan; He, Xiao-Yun; Wang, Shao-Ting.
Afiliación
  • Wang HB; Department of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
  • Xiao X; Department of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
  • He XY; Department of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
  • Wang ST; Department of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan, 430060, China. Electronic address: shaotingw@whu.edu.cn.
Talanta ; 278: 126491, 2024 Jun 29.
Article en En | MEDLINE | ID: mdl-38955103
ABSTRACT

BACKGROUND:

To date, clinical laboratories face challenges in quantifying retinol from DBS samples. Disputes arise throughout the whole detection process, encompassing the storage condition, the release strategy as well as the selection of internal standards.

METHODS:

We incubated DBS with ascorbic acid solution. Then, retinol-d4 in acetonitrile was introduced to incorporate isotopic internal standard and promote protein precipitation. Afterward, sodium carbonate solution was added to ionize cytochromes (such as bilirubin), which amplified the difference of their hydrophobicity to retinol. Subsequently, cold-induced phase separation could be facilitated to separate retinol from the impurities. In the end, the upper layer was injected for LC-MS/MS analysis.

RESULTS:

By comparing the detected retinol content in whole blood and DBS samples prepared from the same volume, we confirmed the established pretreatment was capable to extract most of retinol from DBS (recovery >90 %). Thereafter, we verified that within DBS, retinol possessed satisfying stability without antioxidation. Indoor-light exposure and storage duration would not cause obvious degradation (<10 %). Following systematic validation, the established method well met the criteria outlined in the relevant guidelines. After comparing with detected DBS results to the paired plasma samples, 54 out of 60 met the acceptance limit for cross-validation of ±20 %.

CONCLUSIONS:

We realized precise quantification of retinol from one 3.2 mm DBS disc. By circumventing conventional antioxidation, liquid-liquid/solid-phase extraction and organic solvent evaporation, the pretreatment could be completed within 15 min consuming only minimal amounts of low-toxicity chemicals (ascorbic acid, acetonitrile, and sodium carbonate). We expect this contribution holds the potential to significantly facilitate the evaluation of patients' vitamin A status by using DBS samples in the future.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Talanta Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Talanta Año: 2024 Tipo del documento: Article País de afiliación: China