4.8 Article

Highly Stable, Nondestructive, and Simple Visualization of Latent Blood Fingerprints Based on Covalent Bonding Between the Fluorescent Conjugated Polymer and Proteins in Blood

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 13, Pages 15621-15632

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c00710

Keywords

conjugated polymer; fluorescence; latent; blood fingerprint; development; visualization; covalent bonding

Funding

  1. China Academy of Engineering [2020-YZ-01]
  2. Major Basic Research Project the Natural Science Foundation of the Jiangsu Higher Education Institutions of China [18KJA430014]
  3. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  4. National Key Research and Development Program of China [2018YFC0807205]

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The study demonstrates a simple and effective strategy for visualizing LBFPs, showing clear fingerprint patterns and details even on challenging substrates. The method exhibits superior stability over long-term storage and against solvent washing, while maintaining the integrity of DNA.
Latent blood fingerprints (LBFPs) can provide critical information of foul play and help identify the suspects at violent crime scenes. The current methods for LBFP visualization are still not satisfactory because of the low sensitivity or complicated protocol. This study demonstrates a simple and effective LBFP visualization strategy by integrating a new amphiphilic fluorescent amino-functionalized conjugated polymer with the cotton-pad developing protocol. LBFPs on various substrates are visualized by simply covering them with the polymer solution-soaked cotton pads. The images display clear fingerprint patterns, ridge details, and sweat pores, even on very challenging substrates such as painted wood and multicolored can. The gray value analysis confirms semiquantitatively the enhancement of the contrast between ridges and furrows. Even LBFPs with various contaminations or aged for more than 600 days are effectively developed and visualized. The developed fingerprint images show superior stability over long storage time and against solvent washing. Moreover, the polymer causes no degradation of DNAs in the blood, suggesting the possibility of further DNA profiling and identification after development. The mechanistic investigation suggests that the formation of positive or inverted images can be attributed to the synergistic effects from the affinity between polymer and blood, and the affinity betwen polymer and substrate, as well as the slight quenching of polymer fluorescence by blood. Furthermore, the covalent bonding between the protonated primary amino group and proteins in blood endows the stability of the developed fingerprints. The result rationalizes the molecular design of the fluorescent polymer and sheds new light on the future strategies to effective LBFP visualization in practical applications.

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