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1.
Nanotechnology ; 34(50)2023 Oct 04.
Article in English | MEDLINE | ID: mdl-37714140

ABSTRACT

Zinc oxide quantum dots (ZnO QDs) have gained wide attention due to their wide excitation spectrum, large Stokes shift, adjustable photoluminescence (PL) spectrum, and excellent biocompatibility. However, low fluorescence intensity and poor stability restrict their further applications. In this work, zinc sulfide (ZnS) as a surface modifier, ZnO/ZnS core-shell QDs with type-I core-shell structure and particle size of 5 nm were prepared via sol-gel method. Transmission electron microscope characterization demonstrates the core-shell structure and spherical morphology of the as-synthesized ZnO/ZnS QDs. The PL spectra show that ultraviolet fluorescence has been greatly enhanced. The maximum fluorescence intensity of ZnO/ZnS core-shell QDs increases by 5288.6% compared with that of bare ZnO QDs. The PL quantum yield increases from 9.53% to 30.95%. After being stored for three weeks, the fluorescence performance can be well retained. Furthermore, the cytotoxicity tests confirm the excellent biocompatibility of ZnO/ZnS core-shell QDs, demonstrating they are good candidates for cell imaging.

2.
Bioengineering (Basel) ; 10(5)2023 Apr 26.
Article in English | MEDLINE | ID: mdl-37237600

ABSTRACT

The use of ultraviolet fluorescence markers in medical simulations has become popular in recent years, especially during the COVID-19 pandemic. Healthcare workers use ultraviolet fluorescence markers to replace pathogens or secretions, and then calculate the regions of contamination. Health providers can use bioimage processing software to calculate the area and quantity of fluorescent dyes. However, traditional image processing software has its limitations and lacks real-time capabilities, making it more suitable for laboratory use than for clinical settings. In this study, mobile phones were used to measure areas contaminated during medical treatment. During the research process, a mobile phone camera was used to photograph the contaminated regions at an orthogonal angle. The fluorescence marker-contaminated area and photographed image area were proportionally related. The areas of contaminated regions can be calculated using this relationship. We used Android Studio software to write a mobile application to convert photos and recreate the true contaminated area. In this application, color photographs are converted into grayscale, and then into black and white binary photographs using binarization. After this process, the fluorescence-contaminated area is calculated easily. The results of our study showed that within a limited distance (50-100 cm) and with controlled ambient light, the error in the calculated contamination area was 6%. This study provides a low-cost, easy, and ready-to-use tool for healthcare workers to estimate the area of fluorescent dye regions during medical simulations. This tool can promote medical education and training on infectious disease preparation.

3.
J Microbiol Methods ; 203: 106628, 2022 12.
Article in English | MEDLINE | ID: mdl-36442696

ABSTRACT

Thamnolia vermicularis (Tv) and Thamnolia subuliformis (Ts) are two species from the same habitat with such similar external morphological characteristics that researchers often confuse the two in their scientific work and do not distinguish between them. This study applies three different methods to distinguish them. The diversity of endophytic fungi was also compared and their antibacterial activity in vitro was evaluated. The results show that all three methods can distinguish Tv and Ts, and can be used to cross-validate each other. The ultraviolet fluorescence method and the chemical colour change method are simpler strategies, while thin-layer chromatography is relatively complicated but can more clearly distinguish the chemical composition of the two species. In the analysis of the endophytic fungi community structure of Tv and Ts, it was found that the diversity of endophytic fungi in Tv was more abundant and had wider antibacterial activity and better inhibitory activity against gram-positive bacteria in vitro.


Subject(s)
Ascomycota , Mycobiome , Anti-Bacterial Agents/pharmacology , Chromatography, Thin Layer
4.
Wiad Lek ; 75(2): 483-489, 2022.
Article in English | MEDLINE | ID: mdl-35307681

ABSTRACT

OBJECTIVE: The aim: To evaluate the quality of cleaning and disinfection of surfaces scheduled for daily cleaning and degree of bacterial contamination of hospital rooms and the patients' inanimate environment in Kyiv acute care hospitals, Ukraine. PATIENTS AND METHODS: Materials and methods: We performed a multicenter prospectively study of the quality of cleaning and disinfection of surfaces scheduled for daily cleaning in 9 acute care hospitals by use of an ultraviolet fluorescence targeting method and microbial methods. RESULTS: Results: A total 9,104 environmental samples from were collected and tested. The cleaning and disinfection of surfaces were not being performed properly in most cases. Complete removal of the mark was 49.1%, partial removal was 37,5%, and mark was still visible, i.e. this area had not been processed was 13,4% when the ultraviolet fluorescence targeting method procedures were used, respectively. The predominant bacterial agents in hospital environment surfaces were: Escherichia coli, Enterobacter spp., Pseudomonas aeruginosa, Klebsiella pneumoniae, Proteus spp., Citrobacter spp., Acinetobacter spp., and Enterococcus spp. The overall proportion of extended spectrum beta-lactamase (ESBL) production among Enterobacteriaceae was 31.5% and of methicillin-resistance in Staphylococcus aureus (MRSA) 14.9%. Vancomycin resistance was observed in 5.2% of isolated enterococci (VRE). Resistance to third-generation cephalosporins was observed in 12.7% E.coli isolates and was in 11.2% K. pneumoniae isolates. Carbapenem resistance was identified in 24.7% of P.aeruginosa isolates and 59.3% of Acinetibacter spp. isolates. CONCLUSION: Conclusions: In a hospital rooms, patient environmental surfaces can be a vehicle for the transmission of multidrug-resistant (MDR) bacterial agents that cause healthcare-associated infections.


Subject(s)
Anti-Bacterial Agents , Cross Infection , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/therapeutic use , Bacteria , Cross Infection/microbiology , Cross Infection/prevention & control , Hospitals , Humans , Ukraine
5.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-932600

ABSTRACT

Objective:To achieve rapid and accurate detection of trace uranium in drinking water by analyzing the factors influencing the accuracy of uranium measurement in drinking water using ultraviolet fluorescence method and by evaluating the uncertainty in measurement.Methods:The influence of acidity, Fe 3+ and Mn 2+ contents on the analitical result were studied to optimize the measurement conditions. The accuracy of the measurement method was verified in 7 laboratories. By studying the errors introduced in the process of standard preparation, sample pretreatment and measurement, the sources of uncertainty were analyzed and the uncertainty was synthesized. Results:At pH 1-11 in aqueous solution, the linear regression coefficient of the standard curve was greater than 0.995, which was in line with the linear measurement range of the instrument. At pH 12 or so, the linear regression coefficient was 0.761, which could not meet the measurement requirements. At pH<3 or pH>10, the increase in fluorescence count was lower, which might increase the measurement error. At Fe 3+ concentration ≥15 mg/L, a large deviation occurred in measurement value that could affect seriously measurement result. At Mn 2+ concentration ≥ 1.6 mg/L, the sample produced white precipitation, which could affect the measurement accuracy. Three spiked water samples with different concentrations were determined in 8 laboratories. Each water sample was measured six times in parallel. The relative standard uncertainty of the result were 6.42×10 -2, 4.48×10 -2 and 5.26×10 -2 μg/L, and the expanded uncertainties were 0.03, 0.06 and 0.12 μg/L( k=2), respectively. Conclusions:The optimum conditions for the determination of uranium in water using this method pH were in samples 3-10, the concentration of Fe 3+ less than 15 mg/L, and the concentration of Mn 2+ less than or equal to 1.6 mg/L. The main sources of uncertainty in the measurement of uranium in water using ultraviolet fluorescence method arise from the repeated measurement error and the volume of added standard solution.

6.
Proc Natl Acad Sci U S A ; 118(21)2021 05 25.
Article in English | MEDLINE | ID: mdl-34001606

ABSTRACT

Fluorescence in biological systems is usually associated with the presence of aromatic groups. Here, by employing a combined experimental and computational approach, we show that specific hydrogen bond networks can significantly affect fluorescence. In particular, we reveal that the single amino acid L-glutamine, by undergoing a chemical transformation leading to the formation of a short hydrogen bond, displays optical properties that are significantly enhanced compared with L-glutamine itself. Ab initio molecular dynamics simulations highlight that these short hydrogen bonds prevent the appearance of a conical intersection between the excited and the ground states and thereby significantly decrease nonradiative transition probabilities. Our findings open the door to the design of new photoactive materials with biophotonic applications.


Subject(s)
Ammonia/chemistry , Glutamine/chemistry , Peptides/chemistry , Density Functional Theory , Fluorescence , Humans , Hydrogen Bonding , Molecular Dynamics Simulation , Optics and Photonics/methods
7.
Ecotoxicology ; 29(9): 1399-1408, 2020 Nov.
Article in English | MEDLINE | ID: mdl-32785887

ABSTRACT

While large-scale oil spills can cause acute mortality events in birds, there is increasing evidence that sublethal oil exposure can trigger physiological changes that have implications for individual performance and survival. Therefore, improved methods for identifying small amounts of oil on birds are needed. Because ultraviolet (UV) light can be used to identify thin crude oil films in water and on substrate that are not visually apparent under normal lighting conditions, we hypothesized that UV light could be useful for detecting small amounts of oil present on the plumage of birds. We evaluated black skimmers (Rynchops niger), brown pelicans (Pelecanus occidentalis), clapper rails (Rallus crepitans), great egrets (Ardea alba), and seaside sparrows (Ammodramus maritimus) exposed to areas affected by the Deepwater Horizon oil spill in the Gulf of Mexico as well as from reference areas from 20 June, 2010 to 23 February, 2011. When visually assessed without UV light, 19.6% of birds evaluated from areas affected by the spill were determined to be oiled (previously published data), whereas when examined under UV light, 56.3% of the same birds were determined to have oil exposure. Of 705 individuals examined in areas potentially impacted by the spill, we found that fluorescence under UV light assessment identified 259 oiled birds that appeared to be oil-free on visual exam, supporting its utility as a simple tool for improving detection of modestly oiled birds in the field. Further, UV assessment revealed an increase in qualitative severity of oiling (approximate % of body surface oiled) in 40% of birds compared to what was determined on visual exam. Additionally, black skimmers, brown pelicans, and great egrets exposed to oil as determined using UV light experienced oxidative injury to erythrocytes, had decreased numbers of circulating erythrocytes, and showed evidence of a regenerative hematological response in the form of increased reticulocytes. This evidence of adverse effects was similar to changes identified in birds with oil exposure as determined by visual examination without UV light, and is consistent with hemolytic anemia likely caused by oil exposure. Thus, UV assessment proved useful for enhancing detection of birds exposed to oil, but did not increase detection of birds experiencing clinical signs of anemia compared to standard visual oiling assessment. We conclude that UV light evaluation can help identify oil exposure in many birds that would otherwise be identified visually as unexposed during oil spill events.


Subject(s)
Environmental Monitoring/methods , Petroleum Pollution , Petroleum , Water Pollutants, Chemical , Animals , Birds , Gulf of Mexico , Ultraviolet Rays
8.
Arthropod Struct Dev ; 54: 100913, 2020 Jan.
Article in English | MEDLINE | ID: mdl-32000010

ABSTRACT

Mate choice, copulation, genital morphology, and sperm storage are not very well understood in millipedes. The use of three-dimensional x-ray computed tomography (µCT) provides new morphological data regarding millipede reproductive systems in both the female and male, including chitinous sclerites and membranes, muscles, glands, oviducts, and sperm conduits. Here we present a complete integrated account of the morphology and function of the female genital organs in the family Polydesmidae (Diplopoda: Polydesmida) using µCT, UV fluorescence imaging, and scanning electron microscopy. These data allow us to consider competing hypotheses regarding millipede vulva formation. We additionally present the morphology of copulatory interface in Pseudopolydesmus Attems, 1898 using images of a mating pair in copula and by simulating the interface of the organs using 3D models from µCT, allowing us to tentatively identify a lock-and-key-like mechanism. Finally, we use µCT to reveal the topology of the seminal canal in the gonopod of male Pseudopolydesmus, a topic that has remained unresolved for nearly 80 years.


Subject(s)
Arthropods/anatomy & histology , Arthropods/physiology , Copulation/physiology , Animals , Arthropods/ultrastructure , Female , Genitalia, Female/anatomy & histology , Genitalia, Female/ultrastructure , Genitalia, Male/anatomy & histology , Genitalia, Male/ultrastructure , Male , Microscopy, Electron, Scanning , Optical Imaging , X-Ray Microtomography
9.
Anal Bioanal Chem ; 410(3): 853-862, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29085988

ABSTRACT

Microreactors have gained increasing attention in their application toward continuous micro flow synthesis. An unsolved problem of continuous flow synthesis is the lack of techniques for continuous product purification. Herein, we present a micro free-flow electrophoresis device and accompanying setup that enables the continuous separation and purification of unlabeled organic synthesis products. The system is applied to the separation and purification of triarylmethanes. For imaging of the unlabeled analytes on-chip a novel setup for large area (3.6 cm2) deep ultra violet excitation fluorescence detection was developed. Suitable separation conditions based on low conductivity electrophoresis buffers were devised to purify the product. With the optimized conditions, starting materials and product of the synthesis were well separated (R > 1.2). The separation was found to be very stable with relative standard deviations of the peak positions smaller than 3.5% over 15 min. The stable conditions enabled collection of the separated compounds, and purity of the product fraction was confirmed using capillary electrophoresis and mass spectrometry. This result demonstrates the great potential of free-flow electrophoresis as a technique for product purification or continuous clean-up in flow synthesis. Graphical Abstract Micro free-flow electrophoresis (µFFE) allows continuous separation and purification of small organic synthesis products. Enabled by a novel deep-UV imaging setup starting materials and product of a recently developed synthesis for triarylmethanes could be purified. Thereby demonstrating the potential of µFFE as continuous purification technique for micro flow synthesis.

10.
Sensors (Basel) ; 18(1)2017 Dec 28.
Article in English | MEDLINE | ID: mdl-29283412

ABSTRACT

The routine surveillance of oil spills in major ports is important. However, existing techniques and sensors are unable to trace oil and micron-thin oil films on the surface of seawater. Therefore, we designed and studied a coastal-mounted sensor, using ultraviolet-induced fluorescence and fluorescence-filter systems (FFSs), to monitor oil spills and overcome the disadvantages of traditional surveillance systems. Using seawater from the port of Lingshui (Yellow Sea, China) and six oil samples of different types, we found that diesel oil's relative fluorescence intensity (RFI) was significantly higher than those of heavy fuel and crude oils in the 180-300 nm range-in the 300-400 nm range, the RFI value of diesel is far lower. The heavy fuel and crude oils exhibited an opposite trend in their fluorescence spectra. A photomultiplier tube, employed as the fluorescence detection unit, efficiently monitored different oils on seawater in field experiments. On-site tests indicated that this sensor system could be used as a coastal-mounted early-warning detection system for oil spills.

11.
J Forensic Sci ; 62(1): 209-212, 2017 01.
Article in English | MEDLINE | ID: mdl-27907226

ABSTRACT

Detection of latent fingermarks on various substrates is critical in crime investigations. Conventional chemical methods using reagents could contaminate or even destruct biological information of samples. Here, an optical method and successful case application of detecting latent fingermarks through long-wave ultraviolet (UV) fluorescence (300-400 nm) by shortwave UV laser excitation is reported. Experimental results indicate that the recovery rate of the latent fingermarks on various paper items is in the range of 70-80% without chemical treatments. Moreover, the optical method allows for the preservation of samples for further examination, such as polymerase chain reaction (PCR) testing. The technique has also been successfully applied to a criminal case in identifying the suspect, which, to the best of our knowledge, has never been reported in real crime investigations. Therefore, such a method as UV-excited UV fluorescence in detecting latent fingermarks may be better for examination in cases where biological information of samples is needed for consequent testing.


Subject(s)
Dermatoglyphics , Lasers, Solid-State , Ultraviolet Rays , Fluorescence , Humans
12.
Ecohealth ; 13(1): 60-71, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26957435

ABSTRACT

White-nose syndrome is caused by the fungus Pseudogymnoascus destructans and has killed millions of hibernating bats in North America but the pathophysiology of the disease remains poorly understood. Our objectives were to (1) assess non-destructive diagnostic methods for P. destructans infection compared to histopathology, the current gold-standard, and (2) to evaluate potential metrics of disease severity. We used data from three captive inoculation experiments involving 181 little brown bats (Myotis lucifugus) to compare histopathology, quantitative PCR (qPCR), and ultraviolet fluorescence as diagnostic methods of P. destructans infection. To assess disease severity, we considered two histology metrics (wing area with fungal hyphae, area of dermal necrosis), P. destructans fungal load (qPCR), ultraviolet fluorescence, and blood chemistry (hematocrit, sodium, glucose, pCO2, and bicarbonate). Quantitative PCR was most effective for early detection of P. destructans, while all three methods were comparable in severe infections. Correlations among hyphae and necrosis scores, qPCR, ultraviolet fluorescence, blood chemistry, and hibernation duration indicate a multi-stage pattern of disease. Disruptions of homeostasis occurred rapidly in late hibernation. Our results provide valuable information about the use of non-destructive techniques for monitoring, and provide novel insight into the pathophysiology of white-nose syndrome, with implications for developing and implementing potential mitigation strategies.


Subject(s)
Ascomycota/isolation & purification , Chiroptera/microbiology , Dermatomycoses/diagnosis , Dermatomycoses/veterinary , Animals , Blood Chemical Analysis , Canada , Geography , Hibernation , Polymerase Chain Reaction , Severity of Illness Index
13.
J Chromatogr A ; 1414: 41-50, 2015 Oct 02.
Article in English | MEDLINE | ID: mdl-26341595

ABSTRACT

Surface functionalization enabled by bioinspired polydopamine (PDA) is recognized as a convenient route for fabrication of multifunctional nanoparticles. In the present work, magnetic nanoparticles with polymer (Fe3O4@PDA) and carbon shell (Fe3O4@C) were prepared by self-oxidation of dopamine, and carbonization of the PDA coating. The performance of the two magnetic sorbents in the extraction and determination of four estrogens, estrone (E1), estradiol (E2), estriol (E3) and diethylstilbestrol (DES) from water samples in the form of magnetic solid-phase extraction was investigated. Orthogonal array design was utilized to facilitate the optimization of the proposed sample preparation approach. The highest extraction capabilities of the two sorbents were achieved under different experimental conditions. Fe3O4@PDA was shown to be superior to Fe3O4@C in the enrichment of estrogens, suggesting stronger interactions were established between the PDA coating and the target compounds. The extraction and desorption operations were enabled more conveniently by magnetic separation and the extracts were analyzed by high-performance liquid chromatography coupled with ultraviolet and fluorescence detection. The limits of detection achieved in the proposed method were in the range of 0.072-0.15ng/mL for E1 and DES, and 0.0017-0.0062ng/mL for E2 and E3. Good precision (>0.9995) was obtained with the linearity ranging from 0.2 to 100ng/mL, and from 0.01 to 5ng/mL. The method developed was assessed by analysis of the estrogens in tap water, drain water and bottled mineral water samples.


Subject(s)
Carbon/chemistry , Estrogens/isolation & purification , Indoles/chemistry , Magnetite Nanoparticles/chemistry , Polymers/chemistry , Water Pollutants, Chemical/isolation & purification , Chromatography, High Pressure Liquid , Diethylstilbestrol/isolation & purification , Estradiol/isolation & purification , Estriol/isolation & purification , Estrone/isolation & purification , Solid Phase Extraction/methods
14.
Microsc Res Tech ; 74(3): 219-24, 2011 Mar.
Article in English | MEDLINE | ID: mdl-20597072

ABSTRACT

Deep ultraviolet (DUV) microscopy is a fluorescence microscopy technique to image unlabeled proteins via the native fluorescence of some of their amino acids. We constructed a DUV fluorescence microscope, capable of 280 nm wavelength excitation by modifying an inverted optical microscope. Moreover, we integrated a nanomanipulator-controlled micropipette into this instrument for precise delivery of picoliter amounts of fluid to selected regions of the sample. In proof-of-principle experiments, we used this instrument to study, in situ, the effect of a denaturing agent on the autofluorescence intensity of single, unlabeled, electrospun fibrinogen nanofibers. Autofluorescence emission from the nanofibers was excited at 280 nm and detected at ∼350 nm. A denaturant solution was discretely applied to small, select sections of the nanofibers and a clear local reduction in autofluorescence intensity was observed. This reduction is attributed to the dissolution of the fibers and the unfolding of proteins in the fibers.


Subject(s)
Fibrinogen/metabolism , Microscopy, Ultraviolet/instrumentation , Microscopy, Ultraviolet/methods , Protein Denaturation , Amino Acids/metabolism , Microscopy, Fluorescence/instrumentation , Microscopy, Fluorescence/methods , Spectrometry, Fluorescence/instrumentation , Spectrometry, Fluorescence/methods
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