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Uv visible spectroscopy

Manufactured by Shimadzu
Sourced in Japan

UV/visible spectroscopy is a technique used to measure the absorption or transmission of light by a sample in the ultraviolet and visible regions of the electromagnetic spectrum. It provides information about the chemical composition and structure of a sample.

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6 protocols using uv visible spectroscopy

1

Evaluating Crosslinked Vancomycin-Loaded Gelatin Beads

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To evaluate the crosslinking level of the gelatin, the beads were validated by Ninhydrin assay (Sigma-Alderich, St. Louis, MO, USA) by a 100 °C water bath for 20 min. The free amine amount was evaluated by 570 nm absorption using UV/visible spectroscopy (Shimadzu, Kyoto, Japan). The drug loading capacity was evaluated by grinding weighted vancomycin-loaded gelatin bead samples. Drug releasing was achieved by the continuous shaking of bead debris in 400 mL of PBS using an orbital shaker (Benchmark Scientific, Sayreville, NJ, USA) for 2 h. The supernatant was collected and evaluated by 280 nm absorption using UV/visible spectroscopy (Shimadzu, Kyoto, Japan). The evaluation of drug releasing kinetics follows a similar process without grinding. Similar weight vancomycin-loaded gelatin bead samples were incubated in the 96-well culture plates with 200 μL of PBS added in a 37 °C incubator for monitoring the in vivo environment and evaluated by spectroscopy by fixed time points.
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2

Evaluating Vancomycin-Loaded Gelatin Beads

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Staphylococcus aureus was cultured in a Lysogeny broth (LB) culture medium at 37 °C. Bacteria were collected and diluted to McFland 0.5, referring to a standard concentration of 1.5 × 108 CFU/mL. Vancomycin-loaded gelatin beads containing a total of 2.15 mg of vancomycin were suspended in 17.2 mL of LB culture medium and diluted to a final concentration of 128, 64, 32, 16, 8, 4, 2, 1, 0.5, and 0.25 μg/mL of suspension medium. The bacteria solution was diluted in this bead suspension medium to form a concentration of 1.5 × 106 CFU/mL. The control groups were prepared by free vancomycin LB solutions with similar concentrations. Both the experimental and control groups were incubated at 37 °C for 24 h. OD600 was evaluated by UV/visible spectroscopy (Shimadzu, Kyoto, Japan) before and after incubation.
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3

Amikacin Release from LADNP

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100 mg of LADNP was placed in a dialysis bag and immersed in 50 mL of phosphate buffer saline (pH 7.4/37 °C) with a magnetic bead swirling at 1000 rpm for 7 h. The burst release phase was assessed after 30 min. After that, 3 mL of medium was removed from the tube every hour. The samples were analyzed using UV/visible spectroscopy in Shimadzu, Japan. The release pattern was determined by extrapolating the optical density against amikacin concentration.
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4

Structural Characterization of Nano-MgO

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The initial characterization for prepared nano-MgO was monitored by measuring the UV–vis absorbance spectrum by using a UV-Visible Spectroscopy (Shimadzu, Tokyo, Japan) to detect the surface plasmon resonance band6 ,8 (link)–10 (link). The structural properties (real estate properties) of the nano-MgO were analyzed by transmission electron microscope (JEOL JEM2100F- Japan), scanning electronmicroscopy (SEM) (JEOL JSM 6360LA, Japan), scientific particle size analyzer (PSA) and its chemical composition was demonstrated by an energy dispersive X-Ray (EDX) analyzer. The FTIR spectrums were measured using Shimadzu FTIR-8400 S, Japan, over the wavelength range 400–4000 cm−1. X-ray diffraction patterns were obtained using Schimadzu 7000 diffractometer operating with Cu Kα1 radiation(λ = 0.15406 nm) generated at 30 kV and 30 mA with the scan rate of 2°/min for 2θ values between 20° and 80°. The average particle size was estimated using the Scherrer formula Eq. (1). D=kλ/βcosθ where D is particle diameter, k is a constant equals 0.9, λ is wavelength of X-ray source (0.1541 nm), β is the full width at half maximum (FWHM) and θ is the half diffraction angle.
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5

Determination of Nicotine Entrapment Efficiency in SLNs

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The percentage entrapment efficiency (%EE) of nicotine loading into SLNs was determined by the ultrafiltration method using centrifugal filter tubes (molecular weight cut-off: 10 kDa) (Amicon Ultra®-0.5 mL) [30 (link),31 (link)] by placing 0.5 mL of SLN suspension into a centrifugal filter tube and centrifuging the samples at 10,000 rpm for 20 min at 20 °C. The amount of unentrapped nicotine in the aqueous phase (filtrate) was measured by UV–visible spectroscopy (Shimadzu, Kyoto, Japan) at λmax of 261 nm. The following equations were used for calculating the entrapment efficiency and loading capacity: Entrapment efficiency (%EE)=100×[WiWfWi]
Wi is the amount of nicotine initially added and Wf is the mount of free nicotine.
Loading capacity (%LC)=100×WiWfWlipid+Wi
Wi is the amount of nicotine initially added, Wf is the amount of free nicotine, and Wlipid is the amount of lipid added.
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6

Carotenoid Extraction and Characterization

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Dried carotenoids isolated from C. sakazakii BAA894, DH5α/pWSK29-EiZYIB and DH5α/pWSK29-EiZYIBX were dissolved in methanol, and that from DH5α/pWSK29-EiIB and DH5α/pWSK29-EiYIB were dissolved in hexane. Their absorption spectra were determined by a Shimadzu UV-visible spectroscopy.
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