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Multi-target-responsive AIE material for in situ visualization of level 3 features in latent fingerprints
Guoxin Zhuang1, Jinxin Wei2, Yonglin Wen2
1Scientific Research and Experiment Center, Fujian Police College, Fujian, 350007, China.
Analytica Chimica Acta
|August 1, 2025
Summary
A novel aggregation-induced emission (AIE) material visualizes latent fingerprints (LFPs) by targeting multiple secretions, including amino acids and lipids. This breakthrough enhances the identification of damaged or fragmentary fingerprints using aqueous solutions.
Area of Science:
- Forensic Science
- Materials Science
- Chemistry
Background:
- Latent fingerprint (LFP) Level 3 features (ridge shape, pore size) are crucial for matching damaged prints.
- Current LFP developers primarily target lipids, often requiring mixed solvents and neglecting amino acids.
- LFP component degradation limits visualization of Level 3 features in diverse fingerprint states.
Purpose of the Study:
- Develop hydrophilic, multi-target-responsive aggregation-induced emission (AIE) materials.
- Advance forensic individual identification by improving LFP visualization.
- Enable reliable LFP analysis despite variations in secretion composition and degradation.
Main Methods:
- Designed a cationic amphipathic AIE material with -COOMe groups (AIE-COOMe).
- Utilized fluorescence assays and DFT calculations to assess AIE-COOMe's targeting capabilities.
- Investigated intermolecular forces (hydrogen bonding, hydrophobic, electrostatic) for AIE material anchoring.
Main Results:
- AIE-COOMe visualized multiple secretions (amino acids, proteins, lipids) in LFPs using aqueous solutions.
- Achieved accurate visualization of Level 3 features despite dynamic secretion composition.
- DFT revealed -COOMe groups enhance hydrogen bonding for amino acid targeting; hydrophobic/electrostatic forces drive lipid targeting.
Conclusions:
- Multiple intermolecular forces enable rapid AIE material anchoring to diverse LFP secretions.
- Overcame limitations of single-secretion-reliant methods for LFP recognition and imaging.
- Established a foundation for precise identification of fragmentary LFPs.

