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Hp 8453 uv vis spectrophotometer

Manufactured by Agilent Technologies
Sourced in Germany, United States

The HP 8453 UV-vis spectrophotometer is a laboratory instrument designed to measure the absorption or transmission of light in the ultraviolet and visible regions of the electromagnetic spectrum. It can be used to quantify and analyze various types of samples, including solutions, suspensions, and solid materials.

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15 protocols using hp 8453 uv vis spectrophotometer

1

In Vitro Drug Release Kinetics

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Determination of the in vitro drug release was performed using USP type II dissolution apparatus Sotax AT7 from Sotax AG, Basel, Switzerland, in 900 mL of 0.1 M hydrochloric acid at 37 °C with a paddle speed of 100 rpm. Sampling was executed every 5 min for the first 20 min, every 15 min of the following 2 h, and continuing with every hour up to 4 h. Dissolution studies were performed in triplicate and the average proportional cumulative drug release was plotted as a function of time. The MSN concentration in the dissolution medium was measured using a HP 8453 UV-Vis Spectrophotometer from Agilent Technologies Inc., Santa Clara, CA, USA, at a wavelength of 223 nm in a 1 cm cell versus a blank solution consisting of 0.1 M hydrochloric acid. The applied calibration range was between 1 and 280 mg/L. The LOD and LOQ were found to be 0.17 mg/mL and 0.50 mg/L, respectively (R2 = 0.99997).
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2

Synthesis and Characterization of Charged Au NPs

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Positively and negatively charged Au NPs in aqueous dispersions were synthesized according to previously published protocols with 2-aminoethanethiol and citrate as ligands, respectively.47 (link),48 (link) Their UV-Vis absorption spectra (Figure S1) were obtained using an Agilent/HP 8453 UV-Vis spectrophotometer, and their size and molar concentration were determined according to methods described by Khlebstov49 (link) and Liu50 (link) (positively charged Au NPs: 33 nm, 6.75 × 10−10 M; negatively charged Au NPs: 11 nm, 1.22 × 10−8 M).
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3

Optical Characterization of Gold Nanorods

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The UV-vis spectrum of nanorod aqueous solution (Figure 1) was acquired with an Agilent/HP 8453 UV-vis spectrophotometer (200 nm < λ < 1100 nm, Dublin, Ireland). Extinction spectrum of gold nanorods deposited on glass coverslips (Figure 1) was acquired with an inverted IX-71 Olympus microscope under halogen lamp (100 W) illumination. The spectrum was acquired by directing the light collected by the objective into the entrance of slit of a monochromator (SP-300i, Acton Research, UK) equipped with a thermoelectrically cooled, back illuminated CCD (Spec10:100B, Princeton Instruments, UK).
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4

Spectroscopic Characterization of Compounds

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All chemicals used in synthesis are analytically pure. UV-vis absorption spectra were recorded on a HP8453 UV-vis spectrophotometer (Agilent Ltd., USA). Fluorescence spectra were recorded on a RF-5301PC spectrofluorometer (Shimadzu Ltd., Japan). Luminescence lifetimes were measured on an OB920 fluorescence lifetime instrument (Edinburgh Instruments, U.K.), and an EPL picosecond pulsed laser was used for excitation.
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5

Microparticle Extraction and Flavonoid Quantification

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Microparticles (10 mg) were extracted in 1 ml methanol, followed by agitation in a horizontal shaker (IKA HS 501 digital horizontal Shaker, Janke & Kunkel GmbH & Co. KG IKA Labortechnik, Staufen, Germany) for 2 h (n = 3). 0.1 ml of methanol extract was diluted in 10 ml of pH 7.4 phosphate buffer. The polymer was separated from aqueous solution by filtration using filter paper (Whatman ® , GE Healthcare UK Limited, Buckinghamshire, UK). Flavonoid concentration in the obtained aqueous solution was determined by UV-spectrophotometry at wavelengths of 435 nm (HP 8453 UV-Vis spectrophotometer, Agilent Technologies Deutschland GmbH, Waldbronn, Germany). The actual drug loading and encapsulation efficiency were calculated as follows:
Encapsulation efficiency (%) = (actual drug loading/theoretical drug loading) x 100 %
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6

UV-Vis Spectroscopy Protocol

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All reagents were
purchased from Sigma-Aldrich (St. Louis, MO) unless otherwise specified.
UV–visible spectra and kinetic data were recorded on an HP8453
UV–vis spectrophotometer (Agilent Technologies, Palo Alto,
CA) or a Cary 50 spectrophotometer (Agilent Technologies).
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7

UV-Vis Spectroscopy Protocol

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All reagents were purchased from Sigma-Aldrich (St. Louis, MO) unless otherwise specified. UV-visible spectra and kinetic data were recorded on an HP8453 UV-Vis spectrophotometer (Agilent Technologies, Palo Alto, CA) or a Cary 50 spectrophotometer (Agilent Technologies, Palo Alto, CA).
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8

ABTS Cation Radical Scavenging Assay

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ABTS cation radical scavenging activity was analyzed according to the protocol of Arnao et al. [30 (link)], with some modifications. ABTS test solution was made by dissolving 7.0 mmol/L ABTS and 2.45 mmol/L potassium persulfate in Milli-Q water. The test solution was kept overnight in the dark at room temperature. ABTS working solution was made by diluting with methanol to obtain the absorbance between 0.7 and 0.8 at 734 nm. ABTS working solution (1920 µL) was mixed with 20 µL of samples dilutions (four water-soluble extracts and BSF-APH in Milli-Q water) to obtain final concentrations of 0.0125, 0.025, 0.05, 0.1 and 0.2 mg/mL. The decrease in absorbance after 30 min of incubation in dark was recorded at 734 nm using an HP 8453 UV-vis spectrophotometer (Agilent Technologies, Waldbronn, Germany). Instead of sample dilutions, only Milli-Q water was used in case of the control.
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9

DPPH Radical Scavenging Activity Assay

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DPPH radical scavenging activity was analyzed according to the protocol of Brand-Willams et al. [29 (link)], with some modifications. DPPH test solution was made by dissolving 10.5 mg of DPPH in 40 mL of ethanol. Test solution was made fresh and stored in the dark until further use. DPPH working solution was made by diluting the test solution with 10 times ethanol (to obtain absorbance of 0.6 to 0.8 at 517 nm). DPPH working solution (1920 µL) was mixed with 20 µL of the sample dilutions (four water-soluble extracts and BSF-APH in Milli-Q water) to obtain a final concentration of 0.0125, 0.025, 0.05, 0.1, and 0.2 mg/mL. The decrease in absorbance after 30 min of incubation in the dark was recorded at 510 nm using an HP 8453 UV-vis spectrophotometer (Agilent Technologies, Waldbronn, Germany). Instead of sample dilutions, only Milli-Q water was used in case of control.
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10

Spectroscopic Characterization of Plasmonic Nanopastes

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UV-Vis spectra were acquired with an Agilent/HP 8453 UV-Vis Spectrophotometer (200 nm < λ < 1,100 nm). Raman spectra at 514 nm were obtained from a Renishaw inVia Raman system. An argon ion laser (1,800 l/mm grating) was employed as an excitation source. The laser beam was focused onto the sample through a Leica 20X objective with 0.4 N.A. Measured power at the sampling level was controlled at about 3 mW. Acquisition time was usually 10 s. Raman spectra at 785 nm were obtained from a Pelkin Elmer Raman station. The laser beam was focused onto the sample through a 50X objective (M Plan Achromat) with 0.75 N.A. The laser power was around 3.5 mW and typical acquisition time was 10 s. To obtain SERS spectra, 5 μL of plasmonic nanopastes were deposited on pen written lines on paper and left to evaporate for 30 min prior analysis.
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