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Advances in Fingerprint Technology.pdf

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of DNA us<strong>in</strong>g RFLP. 130 No adverse effects were reported. Newall et al. <strong>in</strong>vestigated<br />

the effect of CA fum<strong>in</strong>g on blood pr<strong>in</strong>ts and also found no <strong>in</strong>hibition.<br />

131 Another light source study was conducted by Andersen and<br />

Bramble. 132 They found that exposure of DNA to 255-nm shortwave UV<br />

radiation (1 mW/cm 2 at a distance of 25 to 35 cm) for as little as 30 sec could<br />

drastically reduce the chances of recover<strong>in</strong>g and identify<strong>in</strong>g DNA us<strong>in</strong>g PCR-<br />

STR analysis.<br />

A study of the effect of seven different blood reagents (amido black, DFO,<br />

n<strong>in</strong>hydr<strong>in</strong>, Hungarian Red, Crowle’s Double Sta<strong>in</strong>, lum<strong>in</strong>ol, and Leucomalachite<br />

Green) on DNA recovered from diluted blood pr<strong>in</strong>ts on several porous<br />

and nonporous substrates and analyzed us<strong>in</strong>g the PCR-STR/Profiler Plus<br />

multiplex system found no adverse results. 133 Miller reported success with<br />

these reagents with a blood dilution factor of up to 1:10,000. 134 The report<br />

also mentioned that as the length of exposure to the reagents and the extent<br />

of dilution of the blood sample <strong>in</strong>creased (beyond 1:10,000), the possibility<br />

of recover<strong>in</strong>g DNA dim<strong>in</strong>ished significantly. A similar result for lum<strong>in</strong>ol was<br />

reported by Gross et al. 135 Champod reported on PCR-STR analysis work<br />

done by Brignoli and Coquoz that found difficulties with LMG and o-tolid<strong>in</strong>e,<br />

but not with MMD. 136 Hochmeister et al. reported a similar result for<br />

LMG and o-tolid<strong>in</strong>e us<strong>in</strong>g RFLP analysis. 137 Roux et al. also looked at the<br />

effect of visualization reagents on blood pr<strong>in</strong>ts. 138 MMD, magnetic f<strong>in</strong>gerpr<strong>in</strong>t<br />

powder, and UV radiation were found to <strong>in</strong>terfere with PCR DNA<br />

analysis. The study also found that DFO, Sticky-side powder, n<strong>in</strong>hydr<strong>in</strong> with<br />

secondary metal salt treatment, amido black, diam<strong>in</strong>obenzid<strong>in</strong>e, lum<strong>in</strong>ol,<br />

CA with rhodam<strong>in</strong>e 6G, and black powder could adversely affect recovery<br />

and analysis of DNA us<strong>in</strong>g the D1S80 system primers. Most of these problems<br />

were resolved by us<strong>in</strong>g CTT system primers. Their study also <strong>in</strong>dicated problems<br />

with the blood reagent benzid<strong>in</strong>e dissolved <strong>in</strong> glacial acetic acid.<br />

DNA From Developed Latent Pr<strong>in</strong>ts<br />

Very few studies have been published that exam<strong>in</strong>e the possibility of recover<strong>in</strong>g<br />

DNA from treated latent pr<strong>in</strong>ts (rather than treated bloodsta<strong>in</strong>s or<br />

blood pr<strong>in</strong>ts). Recently, Zamir et al. <strong>in</strong>vestigated the effect of DFO treatment<br />

of latent pr<strong>in</strong>ts on DNA analysis and found that it had no adverse effect. 139<br />

Another related issue <strong>in</strong>volves the possibility of recover<strong>in</strong>g DNA from undeveloped<br />

f<strong>in</strong>gerpr<strong>in</strong>ts left on commonly handled objects. This issue was highlighted<br />

by van Oorschot and Jones <strong>in</strong> the journal Nature <strong>in</strong> 1997. 140 The<br />

quantity of DNA recovered from objects like a car key, briefcase handle, and<br />

a telephone handset was found to be sufficient to identify the person who<br />

had handled the item. In some cases DNA transferred from another source<br />

(a secondary transfer) was detected and identified. However, a similar study

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