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ultraviolet visible diffuse reflectance spectroscopy  (JASCO Inc)


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    Structured Review

    JASCO Inc ultraviolet visible diffuse reflectance spectroscopy
    Ultraviolet Visible Diffuse Reflectance Spectroscopy, supplied by JASCO Inc, used in various techniques. Bioz Stars score: 99/100, based on 18783 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/diffusion/V-750/10__3390_slash_polym18202555-115-0-15
    Average 99 stars, based on 18783 article reviews
    ultraviolet visible diffuse reflectance spectroscopy - by Bioz Stars, 2026-11
    99/100 stars

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    Related Articles

    Microbial Assay:

    Article Title: Multifunctional Halloysite-Glutathione Nanocomposite for Solar CO2 Conversion and Pollutant Sensing
    Article Snippet: The ultraviolet visible-diffusion (UV–vis DRS) spectra were acquired using a Jasco V-670 instrument equipped with an integrating sphere, using BaSO 4 as reference.

    Circular Dichroism:

    Article Title: Multifunctional Halloysite-Glutathione Nanocomposite for Solar CO2 Conversion and Pollutant Sensing
    Article Snippet: The ultraviolet visible-diffusion (UV–vis DRS) spectra were acquired using a Jasco V-670 instrument equipped with an integrating sphere, using BaSO 4 as reference.

    Spectroscopy:

    Article Title: Multifunctional Halloysite-Glutathione Nanocomposite for Solar CO2 Conversion and Pollutant Sensing
    Article Snippet: The ultraviolet visible-diffusion (UV–vis DRS) spectra were acquired using a Jasco V-670 instrument equipped with an integrating sphere, using BaSO 4 as reference.

    Diffusion-based Assay:

    Article Title: Multifunctional Halloysite-Glutathione Nanocomposite for Solar CO2 Conversion and Pollutant Sensing
    Article Snippet: The ultraviolet visible-diffusion (UV–vis DRS) spectra were acquired using a Jasco V-670 instrument equipped with an integrating sphere, using BaSO 4 as reference.

    Spectrophotometry:

    Article Title: Multifunctional Halloysite-Glutathione Nanocomposite for Solar CO2 Conversion and Pollutant Sensing
    Article Snippet: The ultraviolet visible-diffusion (UV–vis DRS) spectra were acquired using a Jasco V-670 instrument equipped with an integrating sphere, using BaSO 4 as reference.

    Transmission Assay:

    Article Title: Multifunctional Halloysite-Glutathione Nanocomposite for Solar CO2 Conversion and Pollutant Sensing
    Article Snippet: The ultraviolet visible-diffusion (UV–vis DRS) spectra were acquired using a Jasco V-670 instrument equipped with an integrating sphere, using BaSO 4 as reference.

    X-ray Diffraction:

    Article Title: Multifunctional Halloysite-Glutathione Nanocomposite for Solar CO2 Conversion and Pollutant Sensing
    Article Snippet: The ultraviolet visible-diffusion (UV–vis DRS) spectra were acquired using a Jasco V-670 instrument equipped with an integrating sphere, using BaSO 4 as reference.

    Transformation Assay:

    Article Title: Multifunctional Halloysite-Glutathione Nanocomposite for Solar CO2 Conversion and Pollutant Sensing
    Article Snippet: The ultraviolet visible-diffusion (UV–vis DRS) spectra were acquired using a Jasco V-670 instrument equipped with an integrating sphere, using BaSO 4 as reference.

    Nuclear Magnetic Resonance:

    Article Title: Multifunctional Halloysite-Glutathione Nanocomposite for Solar CO2 Conversion and Pollutant Sensing
    Article Snippet: The ultraviolet visible-diffusion (UV–vis DRS) spectra were acquired using a Jasco V-670 instrument equipped with an integrating sphere, using BaSO 4 as reference.



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    Image Search Results


    Experimental workflow of the comparative IVPT study. Two commercial diclofenac gels, Voltaren® and Olfen®, were evaluated using Franz diffusion cells and two structurally distinct barrier models: Strat-M® and the HaCaT construct. The main permeation outputs included cumulative permeated amount, Jss, t lag, and Kp. The study was designed to assess whether the selection of a barrier model influences the comparative interpretation of formulation performance. Created in BioRender.com .

    Journal: Frontiers in Pharmacology

    Article Title: Barrier model selection alters apparent diclofenac permeation parameters: a controlled in vitro comparison of Strat-M ® and a HaCaT-based epidermal construct

    doi: 10.3389/fphar.2026.1934405

    Figure Lengend Snippet: Experimental workflow of the comparative IVPT study. Two commercial diclofenac gels, Voltaren® and Olfen®, were evaluated using Franz diffusion cells and two structurally distinct barrier models: Strat-M® and the HaCaT construct. The main permeation outputs included cumulative permeated amount, Jss, t lag, and Kp. The study was designed to assess whether the selection of a barrier model influences the comparative interpretation of formulation performance. Created in BioRender.com .

    Article Snippet: Permeation experiments were performed using an automated Franz diffusion cell system (Logan System 912-6; Logan Instruments Corp., Somerset, NJ, United States) equipped with vertical glass diffusion cells with a diffusion area of 3.14 cm 2 and a receptor compartment volume of 15 mL.

    Techniques: Diffusion-based Assay, Construct, Selection, Formulation

    Schematic representation of the two barrier systems as mounted in the Franz diffusion cell. In both panels, the formulation is applied to the donor side (top), and the receptor medium lies below. Left: the Strat-M® synthetic membrane, comprising two polyethersulfone layers of high diffusional resistance over a more permeable polyolefin support, with synthetic lipids distributed throughout the porous structure; this depiction follows the manufacturer’s description of the membrane. Right: the HaCaT construct, comprising keratinocytes cultured at the air–liquid interface on a porous PET insert membrane. The right-hand panel is a generic depiction of this class of model and not a representation of the construct used here: no cross-sectional imaging was performed, multilayer architecture was not confirmed, and neither the number nor the arrangement of the cell layers shown was measured in this study. No stratum corneum is depicted, and none was demonstrated. The drawing is not to scale and is intended solely to contrast the architectural principles of the two model types. Created in BioRender.com .

    Journal: Frontiers in Pharmacology

    Article Title: Barrier model selection alters apparent diclofenac permeation parameters: a controlled in vitro comparison of Strat-M ® and a HaCaT-based epidermal construct

    doi: 10.3389/fphar.2026.1934405

    Figure Lengend Snippet: Schematic representation of the two barrier systems as mounted in the Franz diffusion cell. In both panels, the formulation is applied to the donor side (top), and the receptor medium lies below. Left: the Strat-M® synthetic membrane, comprising two polyethersulfone layers of high diffusional resistance over a more permeable polyolefin support, with synthetic lipids distributed throughout the porous structure; this depiction follows the manufacturer’s description of the membrane. Right: the HaCaT construct, comprising keratinocytes cultured at the air–liquid interface on a porous PET insert membrane. The right-hand panel is a generic depiction of this class of model and not a representation of the construct used here: no cross-sectional imaging was performed, multilayer architecture was not confirmed, and neither the number nor the arrangement of the cell layers shown was measured in this study. No stratum corneum is depicted, and none was demonstrated. The drawing is not to scale and is intended solely to contrast the architectural principles of the two model types. Created in BioRender.com .

    Article Snippet: Permeation experiments were performed using an automated Franz diffusion cell system (Logan System 912-6; Logan Instruments Corp., Somerset, NJ, United States) equipped with vertical glass diffusion cells with a diffusion area of 3.14 cm 2 and a receptor compartment volume of 15 mL.

    Techniques: Diffusion-based Assay, Formulation, Membrane, Construct, Cell Culture, Imaging