On the assessment of hydroxyapatite fluoridation by means of Raman scattering.

Hydroxyapatite is the main mineral component of bones and teeth. Fluorapatite, a bioceramic that can be obtained from hydroxyapatite by chemical substitution of the hydroxide ions with fluoride, exhibits lower mineral solubility and larger mechanical strength. Despite the widespread use of fluoride against caries, a reliable technique for unambiguous assessment of fluoridation in in vitro tests is still lacking. Here we present a method to probe fluorapatite formation in fluoridated hydroxyapatite by combining Raman scattering with thermal annealing. In synthetic minerals, we found that effectively fluoride substituted hydroxyapatite transforms into fluorapatite only after heat treatment, due to the high activation energy for this first order phase transition.

Influence of photostability on single-molecule surface enhanced Raman scattering enhancement factors.

Experimental determinations of enhancement factors in Surface Enhanced Raman Scattering (SERS) are intimately intertwined with the photostability of the probes. We study the effect of the limited photostability in single-molecule SERS (SM-SERS) events and show explicitly how this may result in a large under-estimation of the SERS enhancement factors (EFs) obtained experimentally. To this end, we use the bianalyte technique with isotopically edited probes to provide the best-case scenario for the isolation of single molecule events, and study the statistics of EFs at different incident laser powers. When photobleaching stops playing an important role within the integration time used to capture the spectra, SM-SERS EFs approach an upper bound, which is in agreement with estimations of the EFs within the electromagnetic theory of SERS enhancements. Our results reinforce, in addition, the fact that the highest SM-SERS EFs observed experimentally are typically of the order of approximately 10(10).

Guiding molecules with electrostatic forces in surface enhanced Raman spectroscopy.

In surface enhanced raman scattering (SERS) the problem of drawing molecules to the places where surface plasmon resonance enhancements will produce signals is one of the most basic ones, and the initial obstacle to every application of the effect. We explore the possibility of using electrostatic forces as a means to "guide" charged molecules in solution toward SERS active substrates. We also show explicitly the possibility of selectively enhancing different types of dyes according to their charge, and we discuss briefly possible extensions for other applications where "electrostatic guiding" could be an option.