We report on high-performance, white light emission from polyfluorene co-polymers blend and study of the opto-electrical properties of polymer blend light-emitting devices (PLEDs) fabricated on ...plastic substrate. Our results show that efficient white light emission via energy transfer, producing higher device efficiencies and luminance in comparison with the conventional single PLEDs, can be realized by blending carrier donor (host) and acceptor (guest) organic polyfluorene co-polymers. A maximum luminance of /spl sim/7400 cd/m/sup 2/ was achieved at 13 V with Internationale de L'Eclairage coordinates of (0.33, 0.33). Maximum emission efficiency of /spl sim/2.0 cd/A and power efficiency of /spl sim/1.1 lm/W are obtained for white light PLEDs on plastic substrate.
이 연구의 목적은 임상 Candida albicans의 바이오필름억제을 위한 Rhadachlorin과 적색발광다이오드를 이용한 광역학치료의 체외적 효과를 평가하고자 하였다. Candida albicans 부유액을 9×10(8)CFU/mL을 5% 당이 함유된 YNB배지에 준비하였다. Candida albicans의 바이오필름은 96웰 플레이트에 100 ...uL씩 분주후 3시간 배양하고 상층액을 제거하였다. 각 웰에 50 μg/mL 부터 0.39 μg/mL 농도로 Rhadachlorin을 부착된 세포위에 처리하였다. 30분간 배양 후 빛을 30, 60, 90분을 630 nm 광원의 LED를 이용하여 조사하였고, 이때 각각의 에너지밀도는 14, 29, 43 J/cm2 이였다. 모든 상층액을 제거후에 건조시켰다. 부착된 세포를 safranin O로 염색하였다. 490 nm 파장으로 마이크로플레이트 리더로 흡광도를 측정하였다. 또한, 광감작제포화에 의해 Candida albicans의 형광시그널을 관찰하였다. 결론적으로 확연한 억제는 Rhadachlorin의 농도 50 μg/mL과 630 nm LED치료에서 Candida albicans의 바이오필름의 72.5%가 감소되었다. 또한 광감작제 Rhadachlorin은 Candida albicans의 30분에서 충분한 축적을 보였다. 전체적으로 이 결과들은 바이오필름형성의 억제는 Rhadachlorin의 농도에 의존되었다. 이 결과들은 Rhadachlorin과 630 nm LED의 광역학치료는 Candida albicans의 바이오필름 억제가 가능한 것으로 제의된다.
The purpose of this study was to evaluate the in-vitro efficacy of PDT using red light emitting diode (LED) with Radachlorin for biofilm inhibition of clinical Candida albicans isolates. The suspensions containing C. albicans at 9×10(8)CFU/mL were prepared on yeast nitrogen base containing 5% glucose. The biofilm formation was grown for 3 h after seeding suspensions each 100 ul on a 96-well plate and then supernatant was discarded. Each well was treated with 0.39 μg/mL from 50 μg/mL concentrations of Radachlorin on adherent biofilm. After a 30-minute incubation, light was irradiated for 30, 60, or 90 minutes using the following light source of wavelength 630 nm LED, at energy densities of 14, 29, and 43 J/cm2. Afterwards, all supernatant was removed and dried. Adherent cells were stained with safranin O and dried. The cell viability was measured using a microplate reader at 490 nm. Also, a fluorescent signal on C. albicans was observed by saturation of a photosensitizer. In conclusion, a significant inhibition of 72.5% was observed to C. albicans on biofilm at the Radachlorin dose of 50 μg/mL with 630 nm LED. The Photosensitizer (Radachlorin) was adequate at 30 minuttes for C. albicans. Overall, the results showed that inhibition of biofilm formation was Radachlorine dose-dependent. The results suggest that PDT, using Radachlorin with 630 nm LED, is able to decrease biofilm formation of C. albicans.
Non-aqueous capillary electrophoresis was evaluated for the separation of five hydrophobic basic blue dyes for application in forensic dye analysis. The use of a red light emitting diode as a high ...intensity, low-noise light source provided sensitive detection of the blue dyes while also allowing the evaluation of solvents that absorb strongly in the UV region. Excellent peak shapes and separation selectivity were obtained in methanol, ethanol, acetonitrile and dimethylsulfoxide, however water, tetrahydrofuran, dimethylformamide and acetone were unsuitable as solvents due to poor peak shapes and a lack of sensitivity, most likely due to adsorption onto the capillary wall. Due to the known compatibility of methanol with capillary electrophoresis–mass spectrometry, this solvent was examined further with the relative acidity/basicity of the electrolyte being optimised with an artificial neural network. The optimised method was examined for the separation of ink samples from 6 fibre tip and 2 ball point blue or black pens and showed that a unique migration time for the main dye component in seven of the eight pens could be obtained.
Genetic Algorithm is based on natural evolution. The genetic algorithm is a probabilistic search algorithm that iteratively transforms a set (called a population) of mathematical objects (typically ...fixed-length binary character strings), each with an associated fitness value, into a new population of offspring objects using the Darwinian principle of natural selection. The research in genetic algorithm mainly concentrates on the software implementation, which is lagging in term of speed. Genetic algorithm, processor consists lots of sub-modules like ALU unit, memory unit and control unit. From all the sub-module, ALU module is responsible of bringing the genetic variation. In this paper, Enhanced ALU unit consisting of Mutation Operator like Flap, Uniform, Virus mutation and Crossover operators like One point, Multi Point, Uniform crossover was designed using VHDL language and was implemented using Spartan 3E FPGA.
