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Advances in Fingerprint Technology.pdf

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nanocrystals. Photolum<strong>in</strong>escent semiconductor nanoparticles have recently<br />

become the subject of <strong>in</strong>tense <strong>in</strong>vestigation <strong>in</strong> the biotechnology arena,<br />

mostly for label<strong>in</strong>g purposes. 19,20 DNA sequenc<strong>in</strong>g is an example. The salient<br />

virtues that dist<strong>in</strong>guish the nanoparticles (referred to also as quantum dots,<br />

nanocrystals, and nanocomposites, depend<strong>in</strong>g on morphology) from ord<strong>in</strong>ary<br />

fluorescent labels are that their absorption and lum<strong>in</strong>escence wavelengths<br />

(colors) can be tuned by vary<strong>in</strong>g the particle size and that the lum<strong>in</strong>escence<br />

lifetimes are long, rang<strong>in</strong>g from roughly 10 –8 to 10 –6 s, thus mak<strong>in</strong>g<br />

the nanoparticles suitable for time-resolved spectroscopy and time-resolved<br />

imag<strong>in</strong>g, with flexibility <strong>in</strong> terms of useful laser light sources. These features<br />

are valuable from a biotechnology perspective and are, <strong>in</strong> pr<strong>in</strong>ciple, equally<br />

pert<strong>in</strong>ent to the f<strong>in</strong>gerpr<strong>in</strong>t context, thus prompt<strong>in</strong>g a study of their potential<br />

utility <strong>in</strong> f<strong>in</strong>gerpr<strong>in</strong>t detection that commenced <strong>in</strong> 1999. 9 Because of f<strong>in</strong>ancial<br />

and manpower constra<strong>in</strong>ts, this <strong>in</strong>vestigation has to date only aimed at reduction<br />

to practice 21 (i.e., demonstration of feasibility rather than work-up of<br />

rout<strong>in</strong>e recipes). Nonetheless, a variety of nanoparticle systems and f<strong>in</strong>gerpr<strong>in</strong>t<br />

chemistries have been exam<strong>in</strong>ed. Practical recipes will presumably follow<br />

once the best general approaches have been del<strong>in</strong>eated.<br />

CdS Nanocrystals 22<br />

Photolum<strong>in</strong>escent semiconductor nanocrystals may be expected to be used<br />

for f<strong>in</strong>gerpr<strong>in</strong>t detection <strong>in</strong> various ways, namely by <strong>in</strong>corporation <strong>in</strong>to dust<strong>in</strong>g<br />

powder <strong>in</strong> a manner ak<strong>in</strong> to fluorescent dye blend<strong>in</strong>g with magnetic<br />

powder 9 by sta<strong>in</strong><strong>in</strong>g, especially once f<strong>in</strong>gerpr<strong>in</strong>ts have been exposed to<br />

cyanoacrylate ester; or by chemical bond<strong>in</strong>g to constituents of f<strong>in</strong>gerpr<strong>in</strong>t<br />

residue. In photolum<strong>in</strong>escence detection of f<strong>in</strong>gerpr<strong>in</strong>ts, the sta<strong>in</strong><strong>in</strong>g<br />

approach generally tends to be more effective when applicable to the article<br />

under exam<strong>in</strong>ation, than dust<strong>in</strong>g. Thus, the focus <strong>in</strong> this chapter section is<br />

on sta<strong>in</strong><strong>in</strong>g with CdS nanocrystals. As a preface to this mode of f<strong>in</strong>gerpr<strong>in</strong>t<br />

detection, the photophysical properties of CdS quantum dots are exam<strong>in</strong>ed,<br />

primarily to assess suitability for phase-resolved imag<strong>in</strong>g to suppress background<br />

fluorescence, but also to determ<strong>in</strong>e suitable excitation wavelengths.<br />

The employed CdS nanocrystal samples, prepared <strong>in</strong> <strong>in</strong>verse micelles 23,24<br />

and capped with dioctyl sulfosucc<strong>in</strong>ate (sodium salt), were obta<strong>in</strong>ed from<br />

Professor John T. McDevitt (Chemistry Department, University of Texas,<br />

Aust<strong>in</strong>). Solubilization of the nanocrystals utilized heptane or a mixture of<br />

hexanes (CH 3C 4H 8CH 3). Solutions had quantum dot concentrations of milligram/milliliter<br />

order. Absorption spectra <strong>in</strong> these solvents exhibited band<br />

edges at about 440 nm and very broad absorbance (with some structure, but<br />

not absorption peaks as <strong>in</strong> typical atomic or molecular spectra) that <strong>in</strong>creased<br />

with decreas<strong>in</strong>g wavelength to 300 nm, the lowest wavelength <strong>in</strong> our absorption<br />

measurements. The spectra, fairly typical of semiconductor absorption

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