Substructure-Specific Antibodies Against Fentanyl Derivatives

Structural variants of the synthetic opioid fentanyl are a major threat to public health. Following an investigation showing that many derivatives are poorly detected by commercial lateral flow and related assays, we created hapten conjugate vaccines using an immunogenic virus-like particle carrier and eight synthetic fentanyl derivatives designed to mimic the structural features of several of the more dangerous analogues. Immunization of mice elicited strong antihapten humoral responses, allowing the screening of hundreds of hapten-specific hybridomas for binding strength and specificity. A panel of 13 monoclonal IgG antibodies were selected, each showing a different pattern of recognition of fentanyl structural variations, and all proving to be highly efficient at capturing parent fentanyl compounds in competition ELISA experiments. These results provide antibody reagents for assay development as well as a demonstration of the power of the immune system to create binding agents capable of both broad and specific recognition of small-molecule targets.

Authors

Institutions

Publication Details

Journal
ACS Nano
Published
2025-01-10
DOI
https://doi.org/10.1021/acsnano.4c14369
Citations
4
Primary Topic
Neuropeptides and Animal Physiology
Type
article
Field-Weighted Citation Impact
3.64

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Substructure-Specific Antibodies Against Fentanyl Derivatives

Michelle Schroeder, Rebekah E. Wharton, M. G. Finn, Jason Goldstein et al.
4 citations
ACS Nano
Neuropeptides and Animal Physiology
3.64
article

Substructure-Specific Antibodies Against Fentanyl Derivatives

Michelle Schroeder, Rebekah E. Wharton, M. G. Finn, Jason Goldstein, Asiya Seema Chida, Minghao Xu, Joo R. Lee, Xiaoling Tang, Asheley P. Chapman
article en
4 citations

Abstract

Structural variants of the synthetic opioid fentanyl are a major threat to public health. Following an investigation showing that many derivatives are poorly detected by commercial lateral flow and related assays, we created hapten conjugate vaccines using an immunogenic virus-like particle carrier and eight synthetic fentanyl derivatives designed to mimic the structural features of several of the more dangerous analogues. Immunization of mice elicited strong antihapten humoral responses, allowing the screening of hundreds of hapten-specific hybridomas for binding strength and specificity. A panel of 13 monoclonal IgG antibodies were selected, each showing a different pattern of recognition of fentanyl structural variations, and all proving to be highly efficient at capturing parent fentanyl compounds in competition ELISA experiments. These results provide antibody reagents for assay development as well as a demonstration of the power of the immune system to create binding agents capable of both broad and specific recognition of small-molecule targets.

ACS NanoVol. 19(3)
Centers for Disease Control and Prevention (US), Georgia Institute of Technology (US), Center for Environmental Health (US), National Center for Environmental Health (US)
Brigham Young University, National Institutes of Health, Centers for Disease Control and Prevention, National Institute of Allergy and Infectious Diseases
Zero hunger
Openalex Percentile: Top 9%
Neuropeptides and Animal Physiology
3.64
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.