4.8 Article

In vivo quantitative molecular absorption of glycerol in human skin using coherent anti-Stokes Raman scattering (CARS) and two-photon auto-fluorescence

Journal

JOURNAL OF CONTROLLED RELEASE
Volume 308, Issue -, Pages 190-196

Publisher

ELSEVIER
DOI: 10.1016/j.jconrel.2019.07.018

Keywords

In vivo molecular cutaneous absorption; Coherent anti-Stokes Raman Scattering (CARS); Quantitative molecular imaging; Molecular penetration pathways; Human skin

Funding

  1. Centre National de la Recherche Scientifique (CNRS), France Aix-Marseille University, France [ANR-11-IDEX-0001-02]
  2. ANR, France grant France Bio Imaging [ANR-10-INSB-04-01]
  3. ANR, France grant France Life Imaging [ANR-11-INSB-0006]

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The penetration of small molecules through the human skin is a major issue for both safety and efficacy issues in cosmetics and pharmaceutic domains. To date, the quantification of active molecular compounds in human skin following a topical application uses ex vivo skin samples mounted on Franz cell diffusion set-up together with appropriate analytical methods. Coherent anti-Stokes Raman scattering (CARS) has also been used to perform active molecule quantification on ex vivo skin samples, but no quantification has been described in human skin in vivo. Here we introduce and validate a framework for imaging and quantifying the active molecule penetration into human skin in vivo. Our approach combines nonlinear imaging microscopy modalities, such as two-photon excited auto-fluorescence (TPEF) and coherent anti-Stokes Raman scattering (CARS), together with the use of deuterated active molecules. The imaging framework was exemplified on topically applied glycerol diluted in various vehicles such as water and xanthan gel. In vivo glycerol quantitative percutaneous penetration over time was demonstrated, showing that, contrary to water, the xanthan gel vehicle acts as a film reservoir that releases glycerol continuously over time. More generally, the proposed imaging framework provides an enabling platform for establishing functional activity of topically applied products in vivo.

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