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In this study the in vitro activities of seven antibiotics (ciprofloxacin, ceftazidime, tetracycline, trimethoprim, sulfamethoxazole, polymyxin B and piperacillin) and six phytochemicals (protocatechuic acid, gallic acid, ellagic acid, rutin, berberine and myricetin) against five P. aeruginosa isolates, alone and in combination are evaluated. All the phytochemicals under investigation demonstrate potential inhibitory activity against P. aeruginosa. The combinations of sulfamethoxazole plus protocatechuic acid, sulfamethoxazole plus ellagic acid, sulfamethoxazole plus gallic acid and tetracycline plus gallic acid show synergistic mode of interaction. However, the combinations of sulfamethoxazole plus myricetin shows synergism for three strains (PA01, DB5218 and DR3062). The synergistic combinations are further evaluated for their bactericidal activity against P. aeruginosa ATCC strain using time-kill method. Sub-inhibitory dose responses of antibiotics and phytochemicals individually and in combination are presented along with their interaction network to suggest on the mechanism of action and potential targets for the phytochemicals under investigation. The identified synergistic combinations can be of potent therapeutic value against P. aeruginosa infections. These findings have potential implications in delaying the development of resistance as the antibacterial effect is achieved with lower concentrations of both drugs (antibiotics and phytochemicals).

Low density polythene (LDPE) is the most widely used packaging material primarily because of its excellent mechanical properties, barrier properties against water, light weight, low cost and high energy effectiveness. However, due to its ubiquitous nature, and resistance to biodegradability, the disposal strategies are crucial and need attention. Recently, microorganisms have become the focus of interest for environmental friendly disposal of plastic and polymer-based waste. This manuscript aims to investigate the extent of biodegradability of LDPE by four different strains of Pseudomonas bacteria-Pseudomonas aeruginosa PAO1 (ATCC 15729), Pseudomonas aeruginosa (ATCC 15692), Pseudomonas putida (KT2440 ATCC 47054) and Pseudomonas syringae (DC3000 ATCC 10862). Degradation of LDPE was determined by weight loss of the sample, morphological changes, mechanical and spectroscopic variations. The eluted compounds after degradation were analysed by gas chromatography coupled with mass spectroscopy. Our results show that Pseudomonas spp. can degrade LDPE films.

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The wide bandgap and large exciton binding energy of ZnO may generate new applications in bio-imaging after careful surface modifications. Formation of chemically pure ZnO colloidal nanocrystals with controlled size without unwanted by-products or agglomeration has been the major challenge to fully utilize ZnO's unique properties. In this research, colloidal ZnO nanocrystals were synthesized by a soft chemical method. Particle size and colloidal stability were controlled by capping agents. Influences of the surface modifications on particle size, size distribution and photoluminescence properties were investigated. Pure ZnO showed high intensity UV emission and very low intensity in the visible range, indicating good surface morphology of the ZnO nanoparticles with little surface defects. Transmission electron microscopy (TEM) analysis revealed that the capped crystals were close to spherical shape with single-crystal size about 6 nm. X-ray diffraction (XRD) analyses revealed single-phase ZnO nanoparticles. For bio-imaging, emission in visible wavelength range is preferred. Both TiO 2 and SiO 2 were effective in shifting the emission peak to the visible range with high intensity. Optimum capping thickness is 0.5 nm. ZnO-TiO 2 quantum dots (QDs) showed good bio-imaging capability on plant cells. Quantum yields of the pure ZnO and TiO 2 capped ZnO were measured and compared to commercial fluorescence materials.

This letter reports the measurement of single living cells' refractive index ͑RI͒ using an on-chip fiber-based Fabry-Pérot cavity by a differential method. In experiment a single cell is captured into the cavity, then the spectral shift in response to the buffer change and the cell presence/absence can be used to determine the cell's RI and size. Experiment on kidney cancer cells measures an effective RI of 1.399 at 0.1% accuracy. Compared with other approaches, the differential method eliminates uncertain factors and thus ensures high accuracy. The microchip facilitates automatic detection and makes it promising for label-free drug screening.

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