Toward Comprehensive Sediment Nontarget Screening: A Multilayer Solid-Phase Extraction Workflow for Broader Chemical
Shuping Yang1,2,3, Zhen Yang1,2,3, Wenxiao Pan1
1State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing100085, China.
A new multilayer solid-phase extraction (SPE) method broadens the scope of emerging contaminant analysis in sediments. This advanced technique improves detection of diverse chemicals, offering a more complete picture of environmental contamination.
Area of Science:
- Environmental Chemistry
- Analytical Chemistry
- Mass Spectrometry
Background:
- Conventional sample preparation methods for nontarget screening (NTS) in environmental analysis often exhibit physicochemical selectivity.
- This selectivity limits the detectable chemical space, particularly in complex matrices like sediments, prior to high-resolution mass spectrometry (HRMS).
- Single-layer solid-phase extraction (SPE) cartridges show distinct, property-dependent applicability windows, highlighting the need for improved extraction strategies.
Purpose of the Study:
- To develop and validate a multilayer solid-phase extraction (MLSPE) workflow for broad-spectrum extraction of emerging contaminants (ECs) in sediments.
- To reduce extraction-induced selectivity inherent in conventional methods.
- To enable a more comprehensive mapping of the sedimentary exposome for ecological risk assessment.
Main Methods:
- Systematic evaluation of single-layer SPE cartridges (HLB, PWAX/PWCX, C18, PS).
- Development of an optimized MLSPE workflow integrating complementary retention mechanisms.
- Coupling MLSPE with complementary ionization (ESI/APCI) and hybrid acquisition (DDA/DIA) techniques for HRMS analysis.
- Validation using standard reference material (NIST SRM 1936) and application to field sediments.
Main Results:
- The optimized MLSPE workflow achieved balanced extraction across an expansive physicochemical range (log Kow: -2.67 to 17.17; pKa: -1.81 to 12.27).
- Significantly increased recovery (>65%) for structurally diverse validation standards within the 60%-120% range.
- High sensitivity (method detection limits <1 ng/g d.w. for 80% of compounds) and robust precision (RSDs < 20% for 83% of analytes).
- Accurate quantification confirmed by PFOS concentration agreement with certified values.
- Over 500 confident annotations obtained from SRM 1936 and field sediments.
- Revealed elevated concentrations of frequently overlooked QACs and plasticizers in urban-impacted sediments.
Conclusions:
- The developed MLSPE workflow effectively reduces preanalytical selection bias in sediment analysis.
- This coverage-oriented approach provides a comprehensive data foundation for holistic, mixture-based ecological risk assessments.
- The method enables a more authentic mapping of the sedimentary exposome, including previously under-detected contaminants.
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