4.6 Article

A novel LC-MS/MS method for quantification of unstable endogenous 3,4-dihydroxyphenylacetaldehyde in rat brain after chemical derivatization

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Publisher

ELSEVIER
DOI: 10.1016/j.jpba.2020.113822

Keywords

LC-MS/MS; Mass spectrometry; 3,4-dihydroxyphenylacetaldehyde; Aldehyde; Derivatization; Instablitiy

Funding

  1. National Natural Science Foundation of China [81603077, 81960682]
  2. First -Class Disciplines Fund of Education Department of Guizhou Province [GNYL [2017]006]
  3. Science and Technology Fund of Science and Technology Department of Guizhou Province [QKH-y1201811186, [2017]1221]
  4. Youth Talent Project of Zunyi Medical University [18zy-007]

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DOPAL, a toxic metabolite of dopamine, causes neurodegeneration by covalent binding with proteins; a sensitive UPLC-MS/MS method was developed for quantification of DOPAL in rat brain tissue samples; significant increase of DOPAL level was found in the striatum of rats in a 6-OHDA-induced Parkinson's disease model.
3,4-dihydroxyphenylacetaldehyde (DOPAL), a toxic intermediary metabolite of dopamine (DA), causes catecholaminergic neurodegeneration via covalent binding with functional proteins or other biomolecules. Accurate quantification of DOPAL is essential to investigate the etiological factors associated with DOPAL and the pathogenetic role of DOPAL in Parkinson's disease (PD). However, no validated quantitative methods are available. Quantification of DOPAL in biosample is challenging since it is a reactive endogenous aldehyde with poor ionization efficiency and chromatographic behavior in the LC-MS system. Here, a sensitive, simple, and robust UPLC-MS/MS method has been established and validated for the determination of DOPAL in rat brain tissue specimens. DOPAL was found to be unstable in biosample due to reactive aldehyde whereas it was stable in acidic condition. The analyte was stabilized by pH and temperature control during the sample preparation and derivatization. Then, a chemical derivatization method that can be readily performed in acidic conditions and at low temperature was employed using 2-hydrazino-4-(trifluoromethyl)-pyrimidine (HTP) to block the reactive aldehyde and improve the detection sensitivity (about 100-fold increase) and chromatographic retention. Bovine serum albumin was used as a surrogate matrix, which was validated by the parallelism assay and post-column infusion experiment. This method was fully validated and the lower limit of quantification (LLOQ) was 0.5 ng/mL. With the method, a significant increase of DOPAL level was found in striatum region of rats received 6-hydroxydopamine (6-OHDA) injection for 12 h, indicating DOPAL may play a pathogenic role in 6-OHDA-induced PD model. (C) 2020 Elsevier B.V. All rights reserved.

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