Intense Blue Light Research Articles

Retinas of the Diurnal RodentArvicanthis ansorgeiAre Highly Resistant to Experimentally Induced Stress and Degeneration

Environmentally induced stress plays a significant role in retinal degeneration and blindness both in animals and in humans. Among such sources of stress, phototoxicity is well studied and has been shown to lead to photoreceptor-specific loss in a number of species. However, the vast majority of studies have been conducted in nocturnal, albino rod-dominant rat and mouse strains, and the pertinence of such findings to human pathology and cone loss is debatable. The authors examined retinal vulnerability to damage in the diurnal murid rodent Arvicanthis ansorgei, a pigmented species with a large number of cones. The authors used established protocols for exposing animals to a wide range of lighting conditions (variable intensity, duration, spectrum, previous light history, and time of exposure) and injecting N-methyl-N-nitrosourea (MNU); each procedure is reported to produce rapid and complete photoreceptor-specific damage. Animals then underwent electroretinography to record rod and cone function and were subsequently euthanized and used for immunohistochemical analysis of retinal structure and quantification of free fatty acids. These standard regimens produced no detectable detrimental effects on A. ansorgei retinal phenotype, function, or structure. Partial retinal damage in A. ansorgei was induced by very intense blue light or elevated doses of MNU. This resistance was not attributable to differences in lipid composition (specifically, docosahexaenoic acid) between A. ansorgei and susceptible strains of mice and rats. The retina of this species exhibits exceptionally high resistance to damage from light and toxins such as MNU.

Tissue-Autonomous Promotion of Palisade Cell Development by Phototropin 2 inArabidopsis

Light is an important environmental information source that plants use to modify their growth and development. Palisade parenchyma cells in leaves develop cylindrical shapes in response to blue light; however, the photosensory mechanism for this response has not been elucidated. In this study, we analyzed the palisade cell response in phototropin-deficient mutants. First, we found that two different light-sensing mechanisms contributed to the response in different proportions depending on the light intensity. One response observed under lower intensities of blue light was mediated exclusively by a blue light photoreceptor, phototropin 2 (PHOT2). Another response was elicited under higher intensities of light in a phototropin-independent manner. To determine the tissue in which PHOT2 perceives the light stimulus to regulate the response, green fluorescent protein (GFP)-tagged PHOT2 (P2G) was expressed under the control of tissue-specific promoters in the phot1 phot2 mutant background. The results revealed that the expression of P2G in the mesophyll, but not in the epidermis, promoted palisade cell development. Furthermore, a constitutively active C-terminal kinase fragment of PHOT2 fused to GFP (P2CG) promoted the development of cylindrical palisade cells in the proper direction without the directional cue provided by light. Hence, in response to blue light, PHOT2 promotes the development of cylindrical palisade cells along a predetermined axis in a tissue-autonomous manner.

Effects of light quality on leaf morphogenesis of a heterophyllous amphibious plant, Rotala hippuris

For heterophyllous amphibious plants that experience fluctuating water levels, it is critical to control leaf development precisely in response to environmental cues that can serve as a quantitative index of water depth. Light quality can serve as such a cue because the ratio of red light relative to far-red light (R/FR) increases and blue-light intensity decreases with increasing water depth. Growth experiments were conducted to examine how R/FR and blue-light intensity alter leaf morphology of a heterophyllous amphibious plant, Rotala hippuris. Using combinations of far red (730 nm), red (660 nm) and blue (470 nm) light-emitting diodes (LEDs), growth experiments were used to quantitatively evaluate the effects of the R/FR ratio and blue-light intensity on leaf morphology. Under the natural light regime in an outside growth garden, R. hippuris produced distinct leaves under submerged and aerial conditions. R/FR and blue-light intensity were found to markedly affect heterophyllous leaf formation. Higher and lower R/FR caused leaf characters more typical of submerged and aerial leaves, respectively, in both aerial and submerged conditions, in accordance with natural distribution of leaf types and light under water. High blue light caused a shift of trait values toward those of typical aerial leaves, and the response was most prominent under conditions of R/FR that were expected near the water surface. R/FR and blue-light intensity provides quantitative cues for R. hippuris to detect water depth and determine the developmental fates of leaves, especially near the water surface. The utilization of these quantitative cues is expected to be important in habitats where plants experience water-level fluctuation.

Copoly(1,3,4-oxadiazole-naphthylimide)s containing siloxane units in the main chain: synthesis and properties

This study was concerned with the synthesis and properties of new soluble copolyimides containing naphthalene, oxadiazole and tetramethyldisiloxane units. These copolyimides were prepared by two-step polycondensation reaction in solution of aromatic diamines containing preformed oxadiazole ring with a mixture 1 : 1 of naphthalene tetracarboxylic dianhydride and tetramethyldisiloxane- [1,3-bis(4′-phthalic anhydride)]. The structure of these polymers was confirmed by Fourier transform infrared and 1 H-NMR spectroscopy. The solubility, thermal stability and glass transition temperature of these copolyimides were measured and compared with those of related polyimides which do not contain siloxane groups. All these polymers emitted an intense blue color light upon irradiation with UV light. These copoly(oxadiazole-naphthylimide)s could be considered promising candidates for organo-soluble high-performance polymers for use in novel technological applications.

Momentary adjusting methods for simulating the color temperature, hues and brightness of daylight illumination with RGB LEDs for indoor lighting

Methods for simulating the color temperature, hue and brightness of daylight illumination for indoor lighting simply by adjusting the intensity of red, green, and blue light emitting diodes are proposed. We obtain uniform color mixing with a light box by adjusting the ratios between the intensities of red, green and blue LEDs. The intensity can be found by measuring the CIE chromaticity coordinates (x, y) and the luminance Y of the daylight with a chroma meter. After the chromaticity coordinates (x, y) and the luminance Y are found, the tristimulus values can be calculated and then transferred to red, green, and blue primaries by linear transformation. With the correct ratio of red, green, and blue intensities, the color temperature, hues and brightness of daylight can be rebuilt by red, green, and blue light emitting diodes.

Macular Pigment Changes in Pseudophakic Eyes Quantified with Resonance Raman Spectroscopy

We examined changes in macular pigment optical density (MPOD) levels after cataract surgery and compared the MPOD between eyes with clear intraocular lenses (IOLs) and yellow-tinted IOLs. Prospective, comparative case series. The MPOD levels were measured in 480 eyes of 337 patients after cataract surgery. Among them, the data from 259 eyes (clear IOL group, 121 eyes; yellow-tinted IOL group, 138 eyes) of 259 Japanese patients were selected for statistical analyses on the basis of the inclusion criteria: a postoperative visual acuity (VA) of ≥0.8 and no fundus diseases. Only 1 eye of each patient was enrolled. Patients provided informed consent to participate in this study on the basis of the approval of the institutional review board before surgery. The patients selected the type of IOL to be implanted. The MPOD levels were measured using resonance Raman spectroscopy on day 1 (baseline value); months 1, 3, and 6; and years 1 and 2 postoperatively. The difference in MPOD levels between the IOL groups was analyzed by unpaired t tests. The following parameters were analyzed by multiple regression analysis: age, gender, body mass index (BMI), smoking history, glaucoma, diabetes, preoperative VA, preoperative refractive error, and IOL power and type. We found no significant differences in the baseline characteristics between the 2 groups. Until 6 months postoperatively, the MPOD levels did not differ significantly between the groups. However, from 1 year onward, the levels were significantly higher in the yellow-tinted IOL group compared with the clear IOL group. By multiple regression analysis, 1 day postoperatively, older age and diabetes were correlated with lower MPOD levels; 1 year postoperatively and thereafter, however, lower MPOD levels were correlated with clear IOLs. Cataract surgery with clear IOLs induced a greater decrease in macular pigment levels compared with yellow-tinted IOLs during a longer follow-up period. These findings agreed with observations that excessive light exposure is associated inversely with MPOD, because clear IOLs transmit higher intensities of blue light than yellow-tinted IOLs.

Improving color rendering of Y3Al5O12:Ce3+ white light‐emitting diodes based on dual‐blue‐emitting active layers

AbstractAn InGaN/GaN blue‐violet light‐emitting diode (LED) structure and an InGaN/GaN blue LED structure were grown sequentially on the same sapphire substrate by metal‐organic chemical vapor deposition (MOCVD). At the low injection current, the intensity ratio of blue‐violet light to blue light was almost constant, while the blue light intensity increased gradually with increasing injection current when the latter was more than 40 mA. High color rendering has been realized for a Y3Al5O12:Ce3+ phosphor‐converted white LED based on dual‐blue‐emitting active layers relative to a single blue‐emitting active layer at the same injection current.

Blue emitting amino-DPQ with PS and PMMA phosphors for organic light emitting diode

New conjugated polymer, 2(4′-aminophenyl)-4-phenylquinoline i.e., amino-DPQ have been synthesized by Friedlander condensation method at 140 °C. The Optical, structural and thermal properties of the amino-DPQ has been studied. The blended thin films of amino-DPQ with PMMA and PS at different wt% concentrations have been prepared. The UV–vis absorption spectra could provide a good deal of information on the electronic structures of the polymeric compound. When powder form of amino-DPQ is excited at 385 nm, it emits intense blue light of wavelength 486 nm. The blended thin films of amino-DPQ with PMMA and PS at different wt% concentrations show the emission peak in the range of 415–450 nm. Hence, the blue emitting 2(4′-aminophenyl)-4-phenylquinoline (amino-DPQ) has generated considerable interest owing to their good photoluminescence efficiencies.

Quantitative analysis of pupillary light reflex by real-time autofluorescent imaging in a diabetic mouse model

Here we (i) introduce a novel laser-based quantitative method of measuring pupillary light reflex (PLR) and applied it for the in vivo PLR monitoring of early diabetic retinopathy (DR) in a mouse model, (ii) investigate if melanopsin-expressing retinal ganglion cells (mRGCs) are implicated in the early progression of DR and, if so, is there an impact on PLR and (iii) determine if changes in PLR precede the onset of retinal hypoperfusion. A base-line PLR measurement is captured from C57BL/6J wild type mice followed by a single intraperitoneal administration of 200 mg/kg streptozotocin (STZ) and citrate buffer (vehicle) for the “diabetic” ( n = 5) and “control” ( n = 5) mice respectively, the very next day. PLR measurements are repeated once a week for four weeks. The PLR data comprises retinal autofluorescence intensity (AFI) values sampled over a 5-min period under confocal excitation with 488 nm high intensity blue laser light. AFI is used here as an indirect measure of pupil size since the amount of excitation light entering and emission light leaving the eye is proportional to the pupil area. Immunohistochemistry (IHC) staining of mRGCs and RT-PCR of melanopsin mRNA are performed at the end-point. The vascular calibre of both control and STZ-treated diabetic mice is assessed via in vivo fluorescein angiography (FA) on day 0 (base-line), 1/2, 1 and 4 months post-STZ treatment. The PLR profile shows a more rapid pupil constriction and slower dilation in diabetic mice compared to the control. Changes in PLR coincide or even precede the onset of retinal hypoperfusion. Extensive dendritic network of the mRGCs in retinal whole-mounts and increased melanopsin mRNA from the whole eye are also observed in diabetic mice. These pathological changes to mRGCs during early DR may in turn contribute towards changes in PLR. We present here a quantitative method of measuring PLR which enables an early detection of DR with potential application in the clinical setting. In contrast to conventional measurements of PLR, we are able to calibrate the amount of light reaching the retina which is a crucial parameter in longitudinal studies.

A POSSIBLE MECHANISM FOR THE BACTERICIDAL EFFECT OF VISIBLE LIGHT

Visible light at high intensity was found to kill bacteria while low-power light in the visible and near infrared region enhances bacterial proliferation. The present review summarizes evidence demonstrating that the mechanism of visible light- bacteria interaction involves reactive oxygen species (ROS) generation. The ROS are photo induced by bacterial endogenous photosensitizers. Phototoxic effects were found to involve induction of high amounts of reactive oxygen species (ROS) by the bacteria while low amounts of ROS may promote their proliferation. Intense blue light, preferably at 415nm, is better than red light for bacteria killing.

Effects of Light Wavelength and Intensity on the Expression of Photoresponse Genes in Oyster Mushroom Mycelia

When oyster mushroom mycelia photoresponse genes responded to blue light, there was an inherent induction period, which lasted until the light stimulation caused up- and downregulation of the genes. The expression levels of the genes were highly dependent on the intensity of blue (470 nm) and green light (525 nm), while far-red (735 nm) and red light (660 nm) did not affect the expression level regardless of the intensity. In addition, when the mycelia were stimulated for 36 h using blue light at 105 μmol m-2 s-1 of photon flux density and then kept in the dark for 4 d, the expression levels of a few downregulated genes became ca. 2.2 to 3 times greater than before irradiation. These findings have the potential to lead to the development of new phototechnology and techniques in which light-emitting diodes are used in the cultivation of edible mushrooms.

Synthesis and optical property of large-scale centimetres-long silicon carbide nanowires by catalyst-free CVD route under superatmospheric pressure conditions

Large-scale centimetres-long single-crystal β-SiC nanowires have been prepared using CH(4) as the carbon source and SiO or the mixture of Si and SiO(2) as the silicon source by a simple catalyst-free CVD route under superatmospheric pressure conditions. The nanowries grown on ceramic boat or corundum substrates, with lengths of several centimetres and the average diameters of around 40 nm, were composed of single-crystal β-SiC core along the [111] direction and amorphous SiO(2) shell of about 1-30 nm thick depending on the growth position along the flowing direction of the carrier gas. The total gas pressure is an important factor for the synthesis of the large-scale centimetres-long β-SiC nanowires, which can easily adjust the pressure of the vapors to supersaturation condition. The growth of the nanowires was governed by the Vapor-Solid mechanism. The β-SiC nanowires showed an intense blue light emission at room temperature.

Construction of efficient solid emitters with conventional and AIE luminogens for blue organic light-emitting diodes

9,9-Bis(9-heptyl-3-carbazolyl)fluorenes (BPyBCF, BAnBCF, BTPABCF, and BTPEBCF, where B = Bis, Py = pyrene, C = carbazole, F = fluorene, An = anthracene, TPA = triphenylamine, and TPE = tetraphenylethene) with different chromophoric units at the 2,7-positions are synthesized in moderate to high yields (52–89%) by Suzuki coupling reactions of 9,9-bis(9-heptyl-3-carbazolyl)-2,7-dibromofluorene with the corresponding arylboronic acid and utilized as active layers for the construction of blue organic light-emitting diodes (OLEDs). BPyBCF, BAnBCF and BTPABCF emit intense blue light with high fluorescence quantum yields (ΦF = 75–94%) in solution. However, they exhibit much lower ΦF values (30–61%) in the film state, revealing that aggregate formation has quenched their light emission. On the contrary, BTPEBCF is weakly emissive in solution (ΦF = 0.3%) but becomes a strong emitter (ΦF = 100%) when fabricated into solid film, demonstrating a phenomenon of aggregation-induced emission (AIE). Restriction of intramolecular rotation and suppression of intermolecular interactions due to the propeller-like tetraphenylethene unit are responsible for the AIE phenomenon. All the luminogens are thermally and morphologically stable, showing high glass-transition (Tg = 109–147 °C) and thermal-degradation temperatures (Td = 396–478 °C). Non-doped OLEDs using BPyBCF, BAnBCF, and BTPABCF as light-emitting layers are constructed, which give blue electroluminescence with maximum current (ηC,max) and external quantum (ηext,max) efficiencies of 4.8 cd A−1 and 2.3%. With the same device configuration, BTPEBCF shows higher ηC,max and ηext,max values of 7.9 cd A−1 and 2.9%, respectively, thanks to its AIE feature.

Human Lens Transmission of Blue Light: A Comparison of Autofluorescence-Based and Direct Spectral Transmission Determination

Purpose: Direct measurement of the transmission of light through the human lens is not possible in vivo unless invasive techniques are used. In the current study, a reliable in vivo estimate of the transmission of blue light through the lens was assessed by comparing an indirect and noninvasive method based on autofluorescence measurements with a direct method. Methods: Total transmission of blue light was measured in human donor lenses using a direct method applicable only in vitro and compared with transmittance estimates made by an in vivo applicable autofluorescence technique. Results: Human lens transmission of blue light decreases with age by 0.7–0.8% per year at 480 nm. The comparison of methods showed that the autofluorescence-based method correlated significantly with the direct measurements (R = 0.83, p < 0.001) and acceptable agreement between the two methods was found. Discussion: In conclusion, the human lens transmittance of blue light can be measured reliably in vivo. This enables the possibility to correct for retinal light intensities when studying the mechanisms of the circadian rhythm in clinical studies and related disorders and in addition when working with clinical and experimental methods affected by retinal blue light intensities.

Photoluminescence study of the surface modified and MEH-PPV coated cotton fibers

In this paper, we report a study on the photoluminescence properties of pure cotton fibers from chemically surface and morphology modified and coated with MEH-PPV polymer samples by dip-coating method. The treated and coated fibers surfaces were characterized using scanning electron microscopy (SEM), luminescence and FT-IR spectroscopy. The SEM photos showed that cotton fiber surface was covered by a layer of MEH-PPV with the thickness around 1 μm. The effects on the crystalline structure and photoluminescence (PL) were studied as a function of the alkali modification conditions. It was found that the blue light intensity of the mercerized and bleached specimen is approximately two orders higher than the scoured one. The performance of fibers with MEH-PPV polymer as a coating component was investigated and an excellent white-light emission which consists of blue-, green-, and red-light-emitting bands was demonstrated.

Intense and Tunable Electrochemiluminescence of Corannulene

Electrochemiluminescence of corannulene in acetonitrile by the use of coreactants is reported here for the first time. The investigation has been carried out utilizing both benzoyl peroxide as a sacrificial coreactant and arylamine derivatives as nonsacrificial species to perform mixed-annihilation processes. The electrochemiluminescence produces an intense blue light. The use of different tris(arylamines) as mixed-annihilation coreactants gives rise to exciplexes with corannulene that emit at different wavelengths, thus allowing the emission color to be tuned by changing the coreactant molecule. This opens a potential pathway to exploitation of such an intriguing carbon structure for building efficient blue-light emitting devices.

Integration of phot1, phot2, and PhyB signalling in light-induced chloroplast movements

In Arabidopsis thaliana, chloroplasts move towards the periclinal cell walls upon exposure to low blue light intensities and to anticlinal walls under high light. The regulation of these chloroplast movements involves members of both the phototropin and phytochrome families of photoreceptors. Examination of fluence-rate response dependencies in phot1 and phot2 mutants revealed that although both photoreceptors are capable of inducing chloroplast accumulation under low-light conditions, the signals from these photoreceptors appear to be antagonistic. Chloroplast movements in wild-type plants were intermediate between those of the single phot mutants, consistent with each operating through separate signalling cascades. Mutants in phot2 showed transient chloroplast avoidance responses upon exposure to intense blue light, and slow but sustained chloroplast avoidance under intense white light, indicating that in the absence of phot2, phot1 is capable of generating both a low and a high-light response signal. Mutations in phytochrome B (phyB) caused an enhanced avoidance response at intermediate and high light intensities. Examination of phyB, phot1phyB, and phot2phyB mutants indicated that this enhancement is caused by PhyB inhibition of the high-light avoidance response in wild-type plants. In addition, our results suggest that the inhibition by PhyB is not exclusive to either of the phot1 or phot2 signalling pathways.

Near white light emission from GaN based light emitting diode with GaN/AlGaN distributed Bragg reflector

A near white GaN-based multiple quantum well (MQW) light emitting diode (LED) was grown by metal–organic chemical vapor deposition on top of a 20-period GaN/Al z Ga 1− z N distributed Bragg reflector (DBR). Photoluminescence, electroluminescence and high resolution X-ray diffraction were performed to analyze the sample characteristics. The results show that the introduction of the DBR increases the ratio of the green to blue light intensities. Near white light emission with commission international de l’Eclairage color coordinates x=0.18, y=0.28 was achieved at injection current 20 mA for the sample with DBR.

Visible light‐induced killing of bacteria as a function of wavelength: Implication for wound healing

Visible light (400-800 nm) at high intensity was previously found to kill bacteria that are frequently found in infected wounds, while low-power white light enhances bacterial proliferation. The phototoxic effect was found to involve induction of reactive oxygen species (ROS) production by the bacteria. The aim of the present study was to identify the most effective wavelengths in the visible range for inducing a bactericidal effect. ROS production in Staphylococcus aureus and Escherichia coli as a function of wavelengths in the visible range (400-500, 500-800, 415, and 455 nm) was studied using the electron paramagnetic resonance (EPR) spin trapping technique. The phototoxicity of 415 and 455 nm light at different fluencies on the survival of S. aureus and E. coli was assessed by colony count of the bacteria following irradiation. ROS production following blue (400-500 nm) light illumination was found to be higher than that of red (500-800 nm). Within the blue range, light of 415 nm induced more ROS than 455 nm, which correlated with results obtained for the reduction in colony count of S. aureus and E. coli following illumination using equal intensities of these two wavelengths. At low fluencies, both 415 and 455 nm enhanced proliferation of S. aureus but reduced viability of E. coli. Intense blue light, preferably at 415 nm, could be used for bacterial eradication. However, it should be noted that low intensity of visible light can be dangerous since it may promote proliferation of the microorganisms.

Light controls phospholipase A2α and β gene expression in Citrus sinensis

The low-molecular weight secretory phospholipase A2α (CssPLA2α) and β (CsPLA2β) cloned in this study exhibited diurnal rhythmicity in leaf tissue of Citrus sinensis. Only CssPLA2α displayed distinct diurnal patterns in fruit tissues. CssPLA2α and CsPLA2β diurnal expression exhibited periods of approximately 24 h; CssPLA2α amplitude averaged 990-fold in the leaf blades from field-grown trees, whereas CsPLA2β amplitude averaged 6.4-fold. Diurnal oscillation of CssPLA2α and CsPLA2β gene expression in the growth chamber experiments was markedly dampened 24 h after transfer to continuous light or dark conditions. CssPLA2α and CsPLA2β expressions were redundantly mediated by blue, green, red and red/far-red light, but blue light was a major factor affecting CssPLA2α and CsPLA2β expression. Total and low molecular weight CsPLA2 enzyme activity closely followed diurnal changes in CssPLA2α transcript expression in leaf blades of seedlings treated with low intensity blue light (24 μmol m−2 s−1). Compared with CssPLA2α basal expression, CsPLA2β expression was at least 10-fold higher. Diurnal fluctuation and light regulation of PLA2 gene expression and enzyme activity in citrus leaf and fruit tissues suggests that accompanying diurnal changes in lipophilic second messengers participate in the regulation of physiological processes associated with phospholipase A2 action.