scholarly journals Environmental influence on blood serum detection using ultraviolet 365

2021 ◽  
Vol 5 (1) ◽  
pp. 030-036
Author(s):  
Kearse Kelly P
Keyword(s):  
Visible Light ◽  
Blood Serum ◽  
Environmental Conditions ◽  
Whole Blood ◽  
Uv Light ◽  
Environmental Influence ◽  
Crime Scene ◽  
Light Sources ◽  
Color Changes ◽  
Serum Detection

The major use of alternative light sources (ALS) in the evaluation of bloodstains has been primarily focused on detection of whole blood, with relatively little attention to visualization of blood serum. Serum may become separated from blood pools during clotting, and because it is relatively invisible on certain backgrounds, go undetected by a perpetrator attempting to clean up a crime scene. Recently, Ultraviolet 365 (UV 365) was shown to be an effective tool in blood evaluation, useful for detection of even minute quantities of blood serum. Here the effects of environmental conditions on blood serum stain appearance were evaluated, including temperature, pH, protease sensitivity, solubility, and aging. Interestingly, it was found that the UV fluorescence of serum increases upon exposure to heat, which was accompanied by color changes under visible light and decreased solubility in multiple solvents. The efficiency of visualization of serum stains was somewhat variable, depending on the type of material on which it was dried. Finally, the current study documents the effect of heating on formation of fluorescent serum halo rings in dried bloodstains. Taken together, these data demonstrate that blood serum detection may be affected by certain conditions that influence its visualization under both visible and UV light.

scholarly journals Visible-Light Photoswitching of G-Quadruplex Ligand Binding Mode Allows Reversible Control of G-Tetrad Structure

2020 ◽  
Author(s):  
Michael O'Hagan ◽  
Javier Ramos Soriano ◽  
Susanta Haldar ◽  
Juan Carlos Morales ◽  
Adrian Mulholland ◽  
...  
Keyword(s):  
Ligand Binding ◽  
Visible Light ◽  
Uv Light ◽  
Binding Mode ◽  
High Energy ◽  
Light Sources ◽  
Biologically Relevant ◽  
G Quadruplex ◽  
Potential Applications ◽  
Robust Regulation

<div><p>Photoresponsive ligands for G-quadruplex oligonucleotides (G4) offer exciting opportunities for the reversible regulation of these assemblies with potential applications in biological chemistry and responsive nanotechnology. However, achieving the robust regulation of G4 ligand activity with low-energy visible light sources that are easily accessible and compatible with biological systems remains a significant challenge to realizing these applications. Herein, we report the G4-binding properties of a photoresponsive dithienylethene (DTE). We demonstrate the first example of G4-specific acceleration of the photoswitching kinetics of a small molecule and the visible-light mediated switching of the G4 ligand binding mode in physiologically-relevant conditions, which in turn allows control over the G4 tetrad structure of telomeric G4 in potassium buffer. The process is fully reversible and avoids the need for high-energy UV light. This affords an efficient, practical and biologically-relevant means of control that may be applied in the generation of new responsive G4/ligand supramolecular systems.</p></div><br>

scholarly journals Visible-Light Photoswitching of G-Quadruplex Ligand Binding Mode Allows Reversible Control of G-Tetrad Structure

2020 ◽  
Author(s):  
Michael O'Hagan ◽  
Javier Ramos Soriano ◽  
Susanta Haldar ◽  
Juan Carlos Morales ◽  
Adrian Mulholland ◽  
...  
Keyword(s):  
Ligand Binding ◽  
Visible Light ◽  
Uv Light ◽  
Binding Mode ◽  
High Energy ◽  
Light Sources ◽  
Biologically Relevant ◽  
G Quadruplex ◽  
Potential Applications ◽  
Robust Regulation

<div><p>Photoresponsive ligands for G-quadruplex oligonucleotides (G4) offer exciting opportunities for the reversible regulation of these assemblies with potential applications in biological chemistry and responsive nanotechnology. However, achieving the robust regulation of G4 ligand activity with low-energy visible light sources that are easily accessible and compatible with biological systems remains a significant challenge to realizing these applications. Herein, we report the G4-binding properties of a photoresponsive dithienylethene (DTE). We demonstrate the first example of G4-specific acceleration of the photoswitching kinetics of a small molecule and the visible-light mediated switching of the G4 ligand binding mode in physiologically-relevant conditions, which in turn allows control over the G4 tetrad structure of telomeric G4 in potassium buffer. The process is fully reversible and avoids the need for high-energy UV light. This affords an efficient, practical and biologically-relevant means of control that may be applied in the generation of new responsive G4/ligand supramolecular systems.</p></div><br>

scholarly journals Visible-Light Photoswitching of G-Quadruplex Ligand Binding Mode Allows Reversible Control of G-Tetrad Structure

2020 ◽  
Author(s):  
Michael O'Hagan ◽  
Javier Ramos Soriano ◽  
Susanta Haldar ◽  
Juan Carlos Morales ◽  
Adrian Mulholland ◽  
...  
Keyword(s):  
Ligand Binding ◽  
Visible Light ◽  
Uv Light ◽  
Binding Mode ◽  
High Energy ◽  
Light Sources ◽  
Biologically Relevant ◽  
G Quadruplex ◽  
Potential Applications ◽  
Robust Regulation

<div><p>Photoresponsive ligands for G-quadruplex oligonucleotides (G4) offer exciting opportunities for the reversible regulation of these assemblies with potential applications in biological chemistry and responsive nanotechnology. However, achieving the robust regulation of G4 ligand activity with low-energy visible light sources that are easily accessible and compatible with biological systems remains a significant challenge to realizing these applications. Herein, we report the G4-binding properties of a photoresponsive dithienylethene (DTE). We demonstrate the first example of G4-specific acceleration of the photoswitching kinetics of a small molecule and the visible-light mediated switching of the G4 ligand binding mode in physiologically-relevant conditions, which in turn allows control over the G4 tetrad structure of telomeric G4 in potassium buffer. The process is fully reversible and avoids the need for high-energy UV light. This affords an efficient, practical and biologically-relevant means of control that may be applied in the generation of new responsive G4/ligand supramolecular systems.</p></div><br>

scholarly journals Degradation of Phenol By Photolysis Using N-doped TiO2 Catalyst

Molekul ◽  
2019 ◽  
Vol 14 (1) ◽  
pp. 6
Author(s):  
Safni Safni ◽  
Mechy Rezita Wahyuni ◽  
Khoiriah Khoiriah ◽  
Yulizar Yusuf
Keyword(s):  
Blood Pressure ◽  
Visible Light ◽  
Uv Light ◽  
Phenol Degradation ◽  
Light Sources ◽  
Lower Blood Pressure ◽  
Dose Irradiation ◽  
Lower Blood ◽  
Liver And Kidney ◽  
Liver And Kidney Damage

Phenol (C6H5OH) is a common contaminant in wastewater. In certain concentrations, phenol can inhibit the activity of microorganisms and give adverse effects tohumanhealth, such as liver and kidney damage, perfect heart rate, and lower blood pressure. In this study, phenol was degraded with andwithoutN-doped TiO2under photolysis UV-light (10 Watts, λ = 365 nm) and visible-light (13 watt Philips, lux= 1400, λ = 465-640 nm)irradiation. The reductionof phenol concentrationwas measured by a UV-Vis spectrophotometer at a wavelength 200-400 nm. Some parameters such as catalyst dose, irradiation timesand type of light sources were studied. The XRD and DRS UV-Vis characterization confirmthat the nitrogen modified of titania catalyst potentially actives in visible-light. The N-doped TiO2is able to catalyze and improve the efficiency of phenol degradation in photocatalysissystem. Phenol with initialconcentration 8 mg/L was degraded by 33.89% and 30.51% without catalyst and increased to be 90.8% and 67.80%by additionof 15 mg N-doped TiO2catalyst under UV-light and visible-lightfor 210 minutes photolysis, respectively. From the results,irradiation using UV-light achieveshigherefficiency than visible-lightonphenol degradation.

scholarly journals Photo-Degradation of Orange G as an Environmental Pollutant with TiO2-ZnO Composite Material

2021 ◽  
pp. 29-38
Author(s):  
Md Abdullah Bin Samad ◽  
Md. Amjad Hossain ◽  
Tajmeri S. A. Islam ◽  
Waziha Farha
Keyword(s):  
Visible Light ◽  
Uv Light ◽  
Pure Water ◽  
Environmental Pollutant ◽  
Contaminated Water ◽  
Light Sources ◽  
Light Penetration ◽  
Surrounding Water ◽  
Photo Degradation ◽  
Orange G

The increasing water pollution is a great concern as millions of people don't have access to pure water in Bangladesh. A considerable number of people are dying of contaminated water each year not only in Bangladesh but all over the world. Many industries, tanneries, companies, etc. are emitting lots of environmentally hazardous materials into the surrounding water. Many of these pollutants are industrial dyes. The dyes loss from the industrial water during dyeing operation damage the esthetic merit of surface water. They minimize light penetration, hamper aquatic lives and hinder photosynthesis. Some dyes may also have toxic, mutagenic, and carcinogenic characteristics. The purpose of this research is to get rid of the pollutant dye Orange G before the water is contaminated. A method named photo-degradation using different light sources is used to mineralize Orange G dye with composite materials including TiO2-ZnO. This composite was prepared by the hydrothermal method. The photocatalytic behavior of the prepared composite TiO2-ZnO helps in minimizing the effect of this dye to save the water from contamination. The composite compoundwas studied by experimenting on photo-degradation with Orange G under different light sources such as visible light, UV light, and sunlight. The photo-degradation percentage was found to maximum of 79.60 in the presence of sunlight. The percentages of photo-degradation under UV light and visible light were 48.0 and 18.40 respectively.

Antiheparin Activity of Human Serum and Platelet Factor 4

1973 ◽  
Vol 30 (01) ◽  
pp. 093-105 ◽  
Author(s):  
C.H.J Sear ◽  
L Poller ◽  
F.R.C Path
Keyword(s):  
Molecular Weight ◽  
Ionic Strength ◽  
Blood Serum ◽  
Whole Blood ◽  
Platelet Rich Plasma ◽  
Gel Filtration ◽  
Normal Serum ◽  
Platelet Factor ◽  
Mean Values ◽  
Antiheparin Activity

SummaryThe antiheparin activity of normal serum has been studied by comparing the antiheparin activities of sera obtained from normal whole blood, platelet-rich plasma and platelet-’free’ plasma with a purified platelet extract during differential isoelectric precipitation and by gel filtration chromatography.The mean values for the activity of PRP-serum and PFP-serum were 106% (S.D. 11) and 10% (S.D. 3) of untreated whole blood respectively. The activity of whole blood serum, PRP serum and whole blood serum plus platelet extract precipitated under identical physical conditions, i.e. pH 7.0, I =0.008, indicating that the activities of the three samples are probably associated with PF4. PF4 precipitated from human platelet extract at pH 4.0, but this is probably due to the difference in the two biochemical environments investigated, i.e. serum and platelet extract.The gel filtration experiments revealed striking similarities between the major antiheparin activities of serum and platelet extract. At physiological pH and ionic strength both activities were associated with high molecular weight material, but at physiological pH and elevated ionic strength both activities behaved as much smaller entities of molecular weight between 25,000 and 30,000 daltons and it seems very likely that both activities are associated with the same molecule, i.e. PF4.

Immobilization of ZnO Suspension on Glass Substrate to Remove Filtration During the Removal of Remazol Red R from Aqueous Solution

2016 ◽  
Vol 12 (6) ◽  
pp. 4127-4133
Author(s):  
Nazmul Kayes ◽  
Jalil Miah ◽  
Md. Obaidullah ◽  
Akter Hossain ◽  
Mufazzal Hossain
Keyword(s):  
Aqueous Solution ◽  
Glass Substrate ◽  
Uv Light ◽  
Aqueous Suspension ◽  
Light Irradiation ◽  
Zno Films ◽  
Light Sources ◽  
Zno Film ◽  
Semiconductor Oxides ◽  
Remazol Red

Photodegradation of textile dyes in the presence of an aqueous suspension of semiconductor oxides has been of growing interest. Although this method of destruction of dyes is efficient, the main obstacle of applying this technique in the industry is the time and cost involving separation of oxides from an aqueous suspension. In this research, an attempted was made to develop ZnO films on a glass substrate by simple immobilization method for the adsorption and photodegradation of a typical dye, Remazol Red R (RRR) from aqueous solution. Adsorption and photodegradation of  RRR were performed in the presence of glass supported ZnO film. Photodegradation of the dye was carried out by varying different parameters such as the catalyst dosage, initial concentrations of RRR, and light sources. The percentage of adsorption as well as photodegradation increased with the amount of ZnO, reaches a maximum and then decreased. Maximum degradation has been found under solar light irradiation as compared to UV-light irradiation. Removal efficiency was also found to be influenced by the pre-sonication of ZnO suspension.

Visible-Light Activated [2+2] Photocycloaddition Reaction Enabled Identification of Carbon-Carbon Double Bonds Position Isomerism in Structural Lipidomics

2020 ◽  
Author(s):  
Guifang Feng ◽  
Yanhong Hao ◽  
Liang Wu ◽  
Suming Chen
Keyword(s):  
Visible Light ◽  
Uv Light ◽  
Practical Importance ◽  
Side Reactions ◽  
Potential Health ◽  
Fundamental Interest ◽  
Unsaturated Lipids ◽  
Health Damage ◽  
Global Identification ◽  
Polyunsaturated Lipids

The photocycloaddition of olefins with carbonyls is of fundamental interest and practical importance in C=C bond location in unsaturated lipids. However, the traditional UV light activated [2+2] photocycloaddition reaction suffers side reactions and potential health damage. Here, we reported the first example of visible-light activated [2+2] photocycloaddition of anthraquinone with unsaturated lipids. This reaction showed great capability for locating the C=C bonds in various kinds of monounsaturated and polyunsaturated lipids by combining with tandem mass spectrometry (MS), such as fatty acids, phospholipids and glycerides. Based on this developed reaction, a workflow with liquid chromatography tandem MS method was developed for the global identification of unsaturated lipids in human serum, and 86 of monounsaturated and complicated polyunsaturated lipids were identified with definitive positions of C=C bonds. This approach provides new insights both on the photocycloaddition reactions and the structural lipidomics.

Green Synthesis of ZnO/Dy/NiO Heterostructures for Enhanced Photocatalytic Applications

2020 ◽  
Vol 1 (1) ◽  
pp. 30-36
Author(s):  
Shubha Jayachamarajapura Pranesh ◽  
Diwya Lanka
Keyword(s):  
Visible Light ◽  
Uv Light ◽  
Combustion Method ◽  
Hybrid Nanocomposites ◽  
Synthetic Dyes ◽  
Hybrid Nanostructure ◽  
Wide Range ◽  
Visible Light Active ◽  
Textile Industries ◽  
Photocatalytic Applications

Background: Textile industries discharge harmful synthetic dyes to nearby water sources. These colour effluents should be treated before discharge to reduce the toxicity caused by synthetic colours. Objective: To synthesize visible light active superstructures to reduce water pollution caused by textile industries. Methods: We have successfully synthesized ZnO/Dy/NiO hybrid nanocomposites using waste curd as fuel by a simple combustion method. The obtained material was able to reduce recombination and enhanced the photocatalytic degradation of organic pollutants. The as-synthesized material was characterized by XRD, absorption spectroscopy, FESEM, EDAX, etc. The obtained hybrid nanostructure was used as a photocatalyst for the degradation of methylene blue under sunlight, UV light as well as in dark. Comparative experiments were carried out with a variation of catalytic load, pH, dye concentrations, etc. for a better understanding of the performance of the catalyst at various conditions. Results and Conclusion: The ternary compound shows wide range of absorption by expanding absorption band both in UV and visible regions. ZnO/Dy/NiO hybrid nanocomposites performed well and showed uniqueness in the activity uder visible light.

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