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Examination of Firearms Review: 2007 to 2010 - Interpol

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Reinholz chose <strong>to</strong> target albumin, a protein constituting ca. 60% <strong>of</strong> the serum-protein<br />

volume and secreted by the eccrine sweat glands (277). More precisely, given that<br />

an “anti-human whole serum” was used, the whole serum constituents were actually<br />

targeted, and not specifically the albumin. Fingermarks were left on five porous<br />

substrates (i.e., white and manila envelopes, recycled paper, post-it, and<br />

nitrocellulose), and aged from 15 <strong>to</strong> 130 days under artificial and natural light. Once<br />

processed, purple fingermark ridges could be observed on a more or less clearer<br />

background (depending on the substrate), with visible third-level details. It should be<br />

noted that the detected marks progressively fade with time. Finally, the integration <strong>of</strong><br />

this technique in the existing detection sequences was assessed. A DFO-processed<br />

fingermark (fresh mark on white paper) gave more details once subsequently<br />

processed with the albumin recognition technique. However, when applied after<br />

ninhydrin, the visible mark vanished and no detail could be further observed. Finally,<br />

this procedure gave equivalent results when applied after physical developer. The<br />

described procedure seems promising. Nevertheless, it is extremely time-consuming<br />

and labour-intensive, with several blocking/staining and rinsing baths.<br />

Drapel et al. identified and targeted three proteins present in the secretion residue<br />

and implicated in the skin regeneration process (i.e., keratin, cathepsin, and<br />

dermcidin) (276). Using a chromophoric enhancement process, positive results were<br />

obtained on fingermarks left on PVDF (a substrate commonly used in biology <strong>to</strong> fix<br />

proteins), but also on paper. Further research is currently performed, especially <strong>to</strong><br />

decrease the time required by the procedure (several hours) and <strong>to</strong> introduce<br />

luminescent markers.<br />

2.2.8 Detection <strong>of</strong> fingermarks on thermal paper<br />

Some techniques specifically developed for thermal papers were<br />

described or renewed: incorporation <strong>of</strong> polyvinylpyrrolidones in a ninhydrin<br />

solution <strong>to</strong> avoid the darkening <strong>of</strong> the substrate (279), dry-application <strong>of</strong><br />

1,2-indanedione (280), use <strong>of</strong> heat and steam (281, 282), iodine fuming<br />

(283), or vacuum metal deposition (282). The use <strong>of</strong> pDMAC <strong>to</strong> detect<br />

marks on thermal papers was also assessed (227), with the conclusion<br />

that classical amino acid reagents are better choices.<br />

In the previous report (284), we mentioned the “solution G3” as a powerful posttreatment<br />

for ninhydrin- and DFO-processed thermal papers whose reactive layer<br />

could have darkened due <strong>to</strong> the polar solvents contained in the reagent solutions<br />

(285). Recently, Schwarz & Klenke proposed a modified ninhydrin formulation<br />

containing polyvinylpyrrolidones (PVP) (279). The introduction <strong>of</strong> PVP in the working<br />

solution prevents the darkening <strong>of</strong> the thermal layer, and allows a one-step detection<br />

<strong>of</strong> fingermarks which readily appear in clear contrast with the background. PVP being<br />

non<strong>to</strong>xic and reasonably priced, it could constitute a promising alternative <strong>to</strong> the<br />

existing two-steps discolouration procedure. One drawback <strong>of</strong> the currently proposed<br />

formulation is the ratio <strong>of</strong> polar solvent (compared <strong>to</strong> non-polar ones) that could<br />

cause ink running in particular cases. Further research is still undergoing, especially<br />

about the possibility <strong>to</strong> include PVP in DFO or 1,2-indanedione working solutions.<br />

260

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