Evidence map›Paper›PMID 42192142›Full record

ArticleScientific reports2026

Comprehensive method validation for detecting multiple pesticide residues in blood using ultra high performance liquid chromatography-high resolution mass spectrometry.

Ketan B Patil, Ruchir V Soni, Tushar R Ahire

Abstract readValidation Study
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Ketan B PatilGreens Zoological Rescue & Rehabilitation Centre, Department of Toxicology), Jamnagar, 0000-0002, 3815-8685, 0009-0005, 2543-1928, 0009-0004, 7296-0382, Gujarat, India.ORCID http://orcid.org/0000-0002-3815-8685
Ruchir V SoniGreens Zoological Rescue & Rehabilitation Centre, Department of Toxicology), Jamnagar, 0000-0002, 3815-8685, 0009-0005, 2543-1928, 0009-0004, 7296-0382, Gujarat, India.ORCID http://orcid.org/0009-0005-2543-1928
Tushar R AhireGreens Zoological Rescue & Rehabilitation Centre, Department of Toxicology), Jamnagar, 0000-0002, 3815-8685, 0009-0005, 2543-1928, 0009-0004, 7296-0382, Gujarat, India. metushar.ahire@yahoo.com.ORCID http://orcid.org/0009-0004-7296-0382

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A comprehensive ultra-high-performance liquid chromatography-high-resolution mass spectrometry (UHPLC-HRMS) method was developed and validated for the simultaneous detection and quantification of 171 pesticide residues in wildlife blood samples. The method employed a modified QuEChERS (Quick, Easy, Cheap, Effective, Rugged, and Safe) extraction procedure, optimized for efficient recovery of analytes while minimizing matrix interferences. Chromatographic separation was achieved by optimizing the mobile phase, flow rate, and gradient programme, which significantly enhanced peak separation and stability. The mass spectrometric analysis was performed using a full scan-ddMS² mode in an Orbitrap mass spectrometer, with three intense precursor-to-fragment ion transitions for each pesticide. The method was validated according to SANTE guidelines, assessing linearity, recovery, precision, accuracy, matrix effect and limit of quantification (LOQ). The calibration curves exhibited strong linearity (R² = 0.990-0.999) over the concentration range of 1-250 µg L⁻¹. Mean recoveries for 109 pesticides ranged from 70% to 119% at 25 µg L⁻¹ spiking level, with relative standard deviations (RSD) below 20% for most compounds. LOQs ranged from 5.0 to 59.64 µg L⁻¹. The matrix effect was evaluated and addressed through matrix-matched calibration. The developed UHPLC-HRMS method enables sensitive, selective, and reliable quantification of a wide range of pesticides in blood, supporting long-term monitoring of pesticide exposure in wildlife and aiding conservation efforts.

Indexed as

Liquid Chromatography-Mass SpectrometryPesticide ResiduesAnimalsChromatography, High Pressure LiquidLimit of DetectionMass SpectrometryReproducibility of ResultsPesticide ResiduesBlood matrixMethod validationPesticide residuesQuEChERS extractionUHPLC-HRMS

Identifiers

PMID42192142
PMCPMC13377101

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.