Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Mar 15;30(1):26-37.
doi: 10.38212/2224-6614.3399.

Direct immersion solid-phase microextraction combined with ambient ionization tandem mass spectrometry to rapidly distinguish pesticides in serum for emergency diagnostics

Affiliations

Direct immersion solid-phase microextraction combined with ambient ionization tandem mass spectrometry to rapidly distinguish pesticides in serum for emergency diagnostics

Hung Su et al. J Food Drug Anal. .

Abstract

Despite the fact that carbamates and organophosphates cause acute poisoning via different mechanisms and require disparate management, they are indistinguishable by current clinical assays. Herein, direct immersion solid-phase microextraction (DI-SPME) plus thermal desorption-electrospray ionization tandem mass spectrometry (TD-ESI/MS/MS) was developed to discern them. Both pesticides spiked in human serum were extracted by SPME and analyzed by TD-ESI/MS/MS. This is a promising emergency care platform as rapid analyses could be done in tiny sample volumes with satisfactory recovery (89.46%-116.32%), precision (covariance <20%), sensitivity (LOD <0.1 μg/mL), turnaround time (<5 minutes), and linearity (R2 = 0.9827-0.9992) within 0.1-100 μg/mL.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Schematic diagram of the analytical processes in this study: (a) pesticides were spiked in human serum, (b) an SPME fiber was used to extract pesticides from diluted human serum, (c) the SPME fiber was attached to the sampling probe and rinsed with pure water, (d) TD-ESI/MS/MS analysis was performed, (e) acquired MS data were compared with data in pesticide databases to identify analytes.
Fig. 2
Fig. 2
DI-SPME-TD-ESI/MS mass spectra of (a) diluted human serum, (b) diluted human serum from (a) spiked with six carbamate (■) and organophosphate (●) insecticides (5 μg/mL each), and (c) diluted human serum spiked with six insecticides (0.5 μg/mL each).
Fig. 3
Fig. 3
Carbaryl ion intensity vs. SPME adsorption time for 5 μg/mL of carbaryl spiked in diluted human serum. Six replicates were performed for each adsorption duration.
Fig. 4
Fig. 4
Triplicate DI-SPME-TD-ESI/MS/MS analyses of diluted human serum spiked with a mixture of 6 pesticide standards (0.5 μg/mL each), where two ion pairs were monitored for each pesticide in MRM mode (a–f). Pesticide ion signals detected in the sample: a) carbaryl, b) methiocarb, c) methomyl, d) chlorpyrifos, e) ethion, and f) fenthion. (g–l) Six randomly selected pesticide ion signals which were absent in the sample: g) acephate, h) carbofuran, i) isoprocarb, j) methidatihion, k) terbufos, and l) thiobencarb.

Similar articles

Cited by

References

    1. Ellenhorn MJ, Barceloux DG. Diagnosis and treatment of human poisoning. Amsterdam: Elsevier/ North Holland; 1988. Medical toxicology; pp. 1077–8.
    1. Rumack BH, Spoerke DG, editors. POISINDEX(R) information system. 1986. Consensus: pesticide specialty board.
    1. Aquilonius SM, Eckernas SA, Hartvig P, Hultman J, Lindstrom B, Osterman PO. A pharmacokinetic study of neostigmine in man using gas chromatography-mass spectroscopy. Eur J Clin Pharmacoi. 1979;15:367–71. - PubMed
    1. Unni LK, Hannant ME, Bccker RE, Giacobini E. Determination of physostigmine in plasma and cerebrospinal fluid by liquid chromatography with electrochemical detection. Clin Chem. 1989;35:292–5. - PubMed
    1. Ellin RJ, Zvirblis P, Wilson MR. Method for isolation and determination of pyridostigmine and metabolites in urine and blood. J Chromatogr. 1982;22g:235–44. - PubMed

Publication types

LinkOut - more resources