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Uv lamp

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Sourced in United States

The UV lamp is a device that emits ultraviolet (UV) radiation. UV radiation is a type of electromagnetic radiation with wavelengths shorter than visible light, but longer than X-rays. The core function of the UV lamp is to generate UV light for various applications, such as disinfection, curing, and analytical purposes. The specific details and intended use of the UV lamp may vary depending on the model and manufacturer.

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Lab products found in correlation

4 protocols using uv lamp

1

Antimicrobial and Cytotoxic Evaluation of Self-Disinfecting Paints

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The samples used in the tests were the unmodified acrylic water-based paint (Un_Paint) and the self-disinfecting paints containing CLX in the concentration 0.15 g/L, TRP in the concentration of 6.0 g/L, and the mixture CLX+TRP in the concentration of 3.0 g/L. For antibacterial assessment, the paints were applied in 50 × 50 mm polymeric film square, according to ISO 22196 [18 ]. For cytotoxicity assessment, the paints were applied in a 10 × 10 mm polymeric film square. Before each test, every sample and parafilm were sterilized with UV-C light (294 nm) using a UV lamp from VWR (Radnor, PA, USA) for 15 min on each side.
For the tests by direct contact, samples of transparent polymeric film (W) and Copper (Cu2+) were used as negative and positive control of the surface, respectively.
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2

Antimicrobial Evaluation of Self-Disinfecting Paints

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The paints were prepared and characterized in the previous work by Querido et al. [6 (link)]. The samples used in the tests by direct contact and on extracts were the unmodified commercial water-based paint (Un_Paint) and the self-disinfecting paints containing TCS in the concentration 0.0012 g/L and ISB in the concentration of 1.2 g/L applied in a 10 × 10 mm polymeric film square. For the tests by direct contact, samples of transparent polymeric film (W) were used as the negative control of the surface and copper (Cu2+) was used as the positive control.
Before each test, every sample was sterilized with UV-C light (294 nm) using a UV lamp from VWR (Radnor, PA, USA) for 15 min on each side.
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3

Thin-Layer Chromatography for Compound Identification

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The identification of the main compounds was performed with thin-layer chromatography (TLC) using an UV lamp VWR (Austria). For chromatographic determination, 2.5 µL of sample solutions were spotted on 20 x 20 cm Merck (Germany) pre-coated TLC plates (60 F 254 , 250 µm).The first mobile phase (1) was consisted of toluene: ethyl acetate (9.3:0.7 v/v), the second mobile phase (2) was consisted of ethyl acetate:glacial acetic acid (9.5:0.5 v/v), the third mobile phase (3) was a mixture of dichloromethane:acetone:glacial acetic acid (7.6:1.5:0.5 v/v/v), while the fourth one (4) was only toluene as an organic solvent used as a mobile phase.
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4

Optimized Photocrosslinking Peptide Assay

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Photocrosslinking experiments were performed on samples containing 10 nmol peptide and 100 nmol lipid (MLVs) in PBS, 200 μL total volume, as previously described. 13 The published protocol was significantly optimised on the following points. (1) Fully oxidised peptides using Biot(O2) and Met(O2) were synthesised. (2) A narrow spectrum UV-lamp (6 W, VWR) was used. (3) Sample irradiation was performed under controlled agitation and temperature (45°C) over 1h. (4) Saponification was performed over a short time (10 min) in 2 M NaOH. Photoadducts were captured on streptavidin-coated magnetic beads. For MALDI-TOF analysis, samples were eluted with 2,5-DHB matrix (1% H3PO4, pH 1). For ESI analysis, samples were eluted with 20 % HCO2H, the recovery was less efficient than with 2,5-DHB.
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