PubMed · 11355091
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G Hillmann, W Geurtsen. 2001. Tissue engineering--an exciting future.. https://doi.org/10.1007/pl00010678
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Modifying the surfaces of polymers has received a great deal of attention, because it could bring about specific surface characteristics such as antithrombogenic property. Therefore, N-vinyl pyrrolidone/sodium acrylate (NVP/Na-AAc) binary monomers were introduced onto polypropylene (PP) films by a radiation grafting method. The effect of solvent and comonomer composition on the degree of grafting was determined. Studies of the mechanical properties and water content of such graft copolymers showed that as the grafting yield increases the elongation percent decreases. However, the water content increases with increasing grafting yield. The blood compatibility of the original PP and PP-g-NVP/Na-AAc films was evaluated by determination of the extent of platelet adsorption and thrombus formation. The blood compatibility of PP-g-NVP/Na-AAc seems to be better than that of original PP.
Surface-enhanced Raman scattering (SERS) spectra of four amphiphilic nucleolipids in single-layer Langmuir-Blodgett (LB) films deposited on silver island film substrates from pure water and complementary nucleotide-containing subphase and corresponding powder normal Raman spectra were obtained. The analysis of these spectra indicates that the SERS effect is mainly caused by a charge-transfer mechanism, and only the nucleobase headgroup moieties and complementary bases combined with them through hydrogen bonds, which are directly in contact with the silver island film substrates, could be enhanced. For the amphiphilic nucleolipids with the identical nucleobase headgroups, the SERS spectra of the LB films are similar, implying that the orientations of these nucleobase moieties on the silver substrates are analogous. However, the nucleobase takes different orientations on the silver substrates before and after complementary binding. The nucleobases in the LB films deposited from pure water are nearly lying flat on the silver surface, while the complementary binding pairs transferred from the air/water interface tend to take an end-on orientation on the metal surface.
Colloidal semiconductor quantum dots are attractive fluorophores for multicolor imaging because of broad absorption and narrow emission spectra, and they are brighter and far more photostable than organic dyes. However, severe intermittence in emission (also known as blinking) has been universally observed from single dots and has been considered an intrinsic limitation difficult to overcome. This is unfortunate because growing applications in spectroscopy of single biological molecules and quantum information processing using single photon sources could greatly benefit from long-lasting and nonblinking single-molecule emitters. For instance, in a recent application of single-dot imaging, the tracking of membrane receptors was interrupted frequently due to the stroboscopic nature of recording. Blinking can also reduce the brightness in ensemble imaging via signal saturation. Here we show that the quantum dot blinking can be suppressed with the emission duty cycle approaching 100% while maintaining biocompatibility.