No abstract

Bacterial fouling on surfaces significantly increases the resistance of bacteria toward antibiotics, which leads to medical complications and a corresponding financial burden. Here, we report on a general and robust technique for facile modification of various surfaces with different antibacterial agents. Our approach in this study was inspired by the strong adhesion of mussel adhesion proteins (MAPs) to many types of surfaces, including metals, polymers, and inorganic materials. Thus, glass and polymeric slides were dip-coated with dopamine, as a MAP mimic, and the resulting surfaces were characterized. The reactivity of dopamine-coated surfaces toward nucleophilic addition was then confirmed by reacting them with fluorescent probes containing either a free amino or a free thiol group. Laser scanning confocal microscopy (LSCM), X-ray photoelectron spectroscopy (XPS), confocal Raman microscopy, matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) mass spectroscopy, and cyclic voltammetry studies collectively suggested that the probes had covalently attached to the surfaces. Fabrication of dopamine-coated surfaces with an antibacterial quaternary amine or an ultrashort lipopeptide analog generated surfaces that effectively kill Escherichia coli and Staphylococcus aureus cells on contact. Moreover, minimal leaching of the fabricated agent was detected after prolonged incubation. This technique could be further developed to a ''paint-like'' or selfassembling monolayer-like procedure for the preparation of antibacterial surfaces on various materials.

Collagen is the main connective tissue protein of vertebrates and shows exceptional mechanical and optical properties. The alignment of collagen fibrils correlates to the function of a specific tissue and leads to optical anisotropy. The effect of the molecular alignment on Raman scattering, however, has barely been investigated. We found that the peak intensities of the C-C, C=O, and N-H vibrational modes, which are typical for the Raman bands of the protein backbone, change with the orientation of the collagen fibrils. These observations demonstrate that Raman spectra contain specific information regarding molecular and fiber alignment.

Silicon carbide (SiC) is often used for electronic devices operating at elevated temperatures. Spectroscopic temperature measurements are of high interest for device monitoring because confocal Raman microscopy provides a very high spatial resolution. To this end, calibration data are needed that relate Raman line-shift and temperature. The shift of the phonon wavenumbers of single crystal SiC was investigated by Raman spectroscopy in the temperature range from 3 to 112 • C. Spectra were obtained in undoped 6H-SiC as well as in undoped and nitrogen-doped 4H-SiC. All spectra were acquired with the incident laser beam oriented parallel as well as perpendicular to the c-axis to account for the anisotropy of the phonon dispersion. Nearly all individual peak centers were shifting linearly towards smaller wavenumbers with increasing temperature. Only the peak of the longitudinal optical phonon A 1 (LO) in nitrogen-doped 4H-SiC was shifting to larger wavenumbers. For all phonons, a linear dependence of the Raman peaks on both parameters, temperature and phonon frequency, was found in the given temperature range. The linearity of the temperature shift allows for precise spectroscopic temperature measurements. Temperature correction of Raman line-shifts also provides the ability to separate thermal shifts from mechanically induced ones.