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Advances in Fingerprint Technology.pdf

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ZnS<br />

encapsulant<br />

CdSe<br />

conjugat<strong>in</strong>g<br />

ligand<br />

Figure 6.21 Structure of encapsulated and functionalized CdSe nanocrystal.<br />

biotechnology arena, and the functionalization has tended to <strong>in</strong>volve carboxylate<br />

and am<strong>in</strong>o groups. Given the above-described dendrimer <strong>in</strong>vestigation,<br />

we have <strong>in</strong> place a chemistry that should lend itself to the f<strong>in</strong>gerpr<strong>in</strong>t context.<br />

Because of the high cost and low availability of CdSe nanocrystals, we have to<br />

date only addressed f<strong>in</strong>gerpr<strong>in</strong>t development with carboxylate-functionalized<br />

ones (obta<strong>in</strong>ed from Quantum Dot Corp., Palo Alto, CA). Diimide mediation<br />

of the chemical f<strong>in</strong>gerpr<strong>in</strong>t label<strong>in</strong>g was essential (f<strong>in</strong>gerpr<strong>in</strong>ts 1-month-old on<br />

alum<strong>in</strong>um foil). Heat<strong>in</strong>g was not useful, destroy<strong>in</strong>g the nanocrystals. Nanocrystals<br />

are generally stored at low temperature (about 4°C) to prevent flocculation.<br />

No f<strong>in</strong>gerpr<strong>in</strong>t development was obta<strong>in</strong>ed at that temperature, even with<br />

sample immersion for up to 5 days. At room temperature, 24-hr f<strong>in</strong>gerpr<strong>in</strong>t<br />

immersion <strong>in</strong> a water solution conta<strong>in</strong><strong>in</strong>g <strong>in</strong> 1 µM concentration the watersoluble<br />

CdSe/ZnS/carboxylate functionalized nanocrystals and <strong>in</strong> 8 µM concentration<br />

the water-soluble 1-(3-dimethylam<strong>in</strong>opropyl)-3-ethylcarbodiimide<br />

hydrochloride produced development of lum<strong>in</strong>escent f<strong>in</strong>gerpr<strong>in</strong>ts. An example<br />

is shown <strong>in</strong> Figure 6.22. The carbodiimide relative concentration was kept low<br />

(one would normally use higher concentration) to prevent flocculation of<br />

nanocrystals. The low nanocrystal concentration itself was dictated by the<br />

limited nanocrystal supply.<br />

In keep<strong>in</strong>g with semiconductor characteristics (i.e., broad band-structure<br />

characteristics <strong>in</strong> absorption), the utilized nanocrystals lum<strong>in</strong>esced under<br />

excitation that could range from the ultraviolet to the red. This makes for<br />

greater flexibility <strong>in</strong> terms of the excitation light source. The comparatively<br />

rather sharp red lum<strong>in</strong>escence peaked at 635 nm and had full-width at halfmaximum<br />

of 35 nm (comparable to molecular fluorescence); the absorption/lum<strong>in</strong>escence<br />

spectra are shown <strong>in</strong> Figure 6.23. Lum<strong>in</strong>escence lifetime<br />

measurements were best <strong>in</strong>terpreted by two-component fits. These yielded

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