Crystalline silicon carbide (SiC) and silicon (Si) biocompatibility was evaluated by directly culturing three mammalian cell lines on these semiconducting substrates. Cell proliferation and adhesion quality were studied using MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] assays and fluorescent microscopy. The reported results show that SiC is indeed a more biocompatible substrate than Si. The surface wettability of SiC and Si samples was evaluated through static contact angle measurements, which provided interesting information regarding the influence of different cleaning procedures on the SiC surfaces. The cell proliferation data are discussed in light of the contact angle measurements results. This joint analysis leads to interesting conclusions that may help to uncover the main factors that define a semiconductor's biocompatibility.
We have analyzed red and blue luminescence from porous silicon as a function of oxidation parameters and feature dimension determined with an atomic force microscope. We have found correlation between blue luminescence intensity and the increase in feature size caused by oxidation. We have further shown that blue luminescence, is identical, with respect to spectrum and fast decay, to that of high microelectronic quality SiO, grown on crystalline silicon using dry oxygen plus an organic chlorine compound. Thus, we conclude that blue luminescence originates from SiOZ film rather than from the silicon nanocrystals in the porous material. Intensity enhancement, as compared to SiO, on crystalline wafers, comes from the gigantic surface area of porous silicon.
The photodissociation of iron-boron pairs in p-type silicon produces lifetime killing interstitial iron and may be combined with noncontact surface photovoltage (SPV) measurement of the minority carrier diffusion length to achieve fast detection of iron. We found that, for iron concentrations ranging from 8×108 to 1×1013 atoms/cm3, the pair dissociation using a white light (10 W/cm2) was completed within 15 s. Surface recombination was a major rate limiting factor. Passivation of the surface enhanced the rate by as much as a factor of 20. The photodissociation rate increased with increasing temperature, however, the increase was smaller than that of the thermal dissociation rate. These characteristics are consistent with a previously proposed recombination enhanced dissociation mechanism. For practical iron detection, it is important that the detection limit of the approach is close to one part per quadrillion.
Non-viral delivery of cell-impermeant drugs and DNA in vivo has traditionally relied upon either chemical or physical stress applied directly to target tissues. Physical methods typically use contact between an applicator, or electrode, and the target tissue and may involve patient discomfort. To overcome contact-dependent limitations of such delivery methodologies, an atmospheric helium plasma source was developed to deposit plasma products onto localized treatment sites. Experiments performed in murine skin showed that samples injected with plasmid DNA encoding luciferase and treated with plasma demonstrated increased levels of expression relative to skin samples that received injections of DNA alone. Increased response relative to injection alone was observed when either positive or negative voltage was used to generate the helium plasma. Quantitative results over a 26-day follow-up period showed that luciferase levels as high as 19-fold greater than the levels obtained by DNA injection alone could be achieved. These findings indicate that plasmas may compete with other physical delivery methodologies when skin is the target tissue.
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