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adapalene  (Biosynth Carbosynth)


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    Structured Review

    Biosynth Carbosynth adapalene
    <t>Adapalene</t> chemical structure.
    Adapalene, supplied by Biosynth Carbosynth, used in various techniques. Bioz Stars score: 93/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/adapalene/product/Biosynth Carbosynth
    Average 93 stars, based on 2 article reviews
    adapalene - by Bioz Stars, 2026-02
    93/100 stars

    Images

    1) Product Images from "Environmentally sensitive fluorescence of the topical retinoid adapalene"

    Article Title: Environmentally sensitive fluorescence of the topical retinoid adapalene

    Journal: Frontiers in Chemistry

    doi: 10.3389/fchem.2024.1438751

    Adapalene chemical structure.
    Figure Legend Snippet: Adapalene chemical structure.

    Techniques Used:

    Normalized UVA absorption band in the different solvents. ( acetonitrile, ethyl acetate, 1,4-dioxane, ethanol, hexane, methanol, dichloromethane, DMF, THF). Inset: Normalized UV-vis absorption spectra of adapalene in acetonitrile, ethanol and hexane.
    Figure Legend Snippet: Normalized UVA absorption band in the different solvents. ( acetonitrile, ethyl acetate, 1,4-dioxane, ethanol, hexane, methanol, dichloromethane, DMF, THF). Inset: Normalized UV-vis absorption spectra of adapalene in acetonitrile, ethanol and hexane.

    Techniques Used:

    Absorption (λ A , nm) and fluorescence (λ F , nm) maxima, Stokes shift (Δν, cm −1 ) of  adapalene  in solvents of different polarity (dielectric constant, є, refractive index, n, and E T (30) parameter).
    Figure Legend Snippet: Absorption (λ A , nm) and fluorescence (λ F , nm) maxima, Stokes shift (Δν, cm −1 ) of adapalene in solvents of different polarity (dielectric constant, є, refractive index, n, and E T (30) parameter).

    Techniques Used: Fluorescence, Refractive Index

    Absorption of adapalene alone (10 μM, gray), DNA (50 μM in bp, dotted green line) or adapalene in the presence of DNA (full green line) in PBS at pH 7.4. Inset: adapalene alone (10 μM, gray), HSA alone (2 μM, dotted blue line), of adapalene in the presence of HSA (full blue line).
    Figure Legend Snippet: Absorption of adapalene alone (10 μM, gray), DNA (50 μM in bp, dotted green line) or adapalene in the presence of DNA (full green line) in PBS at pH 7.4. Inset: adapalene alone (10 μM, gray), HSA alone (2 μM, dotted blue line), of adapalene in the presence of HSA (full blue line).

    Techniques Used:

    Normalized fluorescence spectra of adapalene in different solvents.
    Figure Legend Snippet: Normalized fluorescence spectra of adapalene in different solvents.

    Techniques Used: Fluorescence

    (A) Position of the emission maxima in wavenumber of adapalene versus the polarity E T (30) in different solvents or in dioxane:ethanol mixtures (inset). (B) Lippert-Mataga plot for adapalene in different solvents or in dioxane:ethanol mixtures (inset).
    Figure Legend Snippet: (A) Position of the emission maxima in wavenumber of adapalene versus the polarity E T (30) in different solvents or in dioxane:ethanol mixtures (inset). (B) Lippert-Mataga plot for adapalene in different solvents or in dioxane:ethanol mixtures (inset).

    Techniques Used:

    Fluorescence emission (λ exc = 315 nm) of a solution containing adapalene (10 μM) and HSA (12 μM) in PBS at pH 7.4, adapalene alone in PBS (gray dotted line). Inset emission changes as a function of the protein concentration.
    Figure Legend Snippet: Fluorescence emission (λ exc = 315 nm) of a solution containing adapalene (10 μM) and HSA (12 μM) in PBS at pH 7.4, adapalene alone in PBS (gray dotted line). Inset emission changes as a function of the protein concentration.

    Techniques Used: Fluorescence, Protein Concentration

    Fluorescence emission (λ exc = 315 nm) of adapalene (10 μM) alone in PBS at pH 7.4 (black) and in the presence of duplex salmon sperm DNA (from 25 to 400 μM in bp). Inset: Stern-Volmer plot for the quenching of adapalene fluorescence in PBS (blue), with 10 μM bp (orange) or 100 μM bp (grey) of DNA.
    Figure Legend Snippet: Fluorescence emission (λ exc = 315 nm) of adapalene (10 μM) alone in PBS at pH 7.4 (black) and in the presence of duplex salmon sperm DNA (from 25 to 400 μM in bp). Inset: Stern-Volmer plot for the quenching of adapalene fluorescence in PBS (blue), with 10 μM bp (orange) or 100 μM bp (grey) of DNA.

    Techniques Used: Fluorescence

    Emission spectra of adapalene (10 μM) varying CTAB concentration (from 0.05 to 4 mM) in PBS and adapalene alone in PBS (gray dotted line), λ exc = 315 nm. Inset: Representation of the changes of 390 nm emission vs. the logarithm of CTAB concentration.
    Figure Legend Snippet: Emission spectra of adapalene (10 μM) varying CTAB concentration (from 0.05 to 4 mM) in PBS and adapalene alone in PBS (gray dotted line), λ exc = 315 nm. Inset: Representation of the changes of 390 nm emission vs. the logarithm of CTAB concentration.

    Techniques Used: Concentration Assay



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    Image Search Results


    Mechanisms of flavonoid and polyphenol compounds in the antibacterial and anti-inflammatory treatment of acne.

    Journal: Pharmaceuticals

    Article Title: Nanoparticle-Encapsulated Plant Polyphenols and Flavonoids as an Enhanced Delivery System for Anti-Acne Therapy

    doi: 10.3390/ph18020209

    Figure Lengend Snippet: Mechanisms of flavonoid and polyphenol compounds in the antibacterial and anti-inflammatory treatment of acne.

    Article Snippet: Resveratrol , Nanoemulsion gel containing adapalene and 5 mg of resveratrol (F1), applied once daily. Nanoemulsion gel containing adapalene and 10 mg of resveratrol (F2), applied once daily. , Surfactant-based nanocarrier , The prepared nanoemulsion gel formulation containing adapalene and resveratrol showed better efficacy in treating acne pustules compared to the marketed formulation. The treatment time was significantly shorter for the prepared formulations. , [ ] .

    Techniques: Activity Assay, Bacteria, Activation Assay, Phospho-proteomics, Expressing

    Efficacy of flavonoid and polyphenol nanoparticle formulations in acne treatment.

    Journal: Pharmaceuticals

    Article Title: Nanoparticle-Encapsulated Plant Polyphenols and Flavonoids as an Enhanced Delivery System for Anti-Acne Therapy

    doi: 10.3390/ph18020209

    Figure Lengend Snippet: Efficacy of flavonoid and polyphenol nanoparticle formulations in acne treatment.

    Article Snippet: Resveratrol , Nanoemulsion gel containing adapalene and 5 mg of resveratrol (F1), applied once daily. Nanoemulsion gel containing adapalene and 10 mg of resveratrol (F2), applied once daily. , Surfactant-based nanocarrier , The prepared nanoemulsion gel formulation containing adapalene and resveratrol showed better efficacy in treating acne pustules compared to the marketed formulation. The treatment time was significantly shorter for the prepared formulations. , [ ] .

    Techniques: Polymer, Activity Assay, Formulation, Liposomes, Antioxidant Activity Assay, Concentration Assay

    Adapalene chemical structure.

    Journal: Frontiers in Chemistry

    Article Title: Environmentally sensitive fluorescence of the topical retinoid adapalene

    doi: 10.3389/fchem.2024.1438751

    Figure Lengend Snippet: Adapalene chemical structure.

    Article Snippet: Adapalene was purchased from BIOSYNTH Carbosynth and was used without further purification.

    Techniques:

    Normalized UVA absorption band in the different solvents. ( acetonitrile, ethyl acetate, 1,4-dioxane, ethanol, hexane, methanol, dichloromethane, DMF, THF). Inset: Normalized UV-vis absorption spectra of adapalene in acetonitrile, ethanol and hexane.

    Journal: Frontiers in Chemistry

    Article Title: Environmentally sensitive fluorescence of the topical retinoid adapalene

    doi: 10.3389/fchem.2024.1438751

    Figure Lengend Snippet: Normalized UVA absorption band in the different solvents. ( acetonitrile, ethyl acetate, 1,4-dioxane, ethanol, hexane, methanol, dichloromethane, DMF, THF). Inset: Normalized UV-vis absorption spectra of adapalene in acetonitrile, ethanol and hexane.

    Article Snippet: Adapalene was purchased from BIOSYNTH Carbosynth and was used without further purification.

    Techniques:

    Absorption (λ A , nm) and fluorescence (λ F , nm) maxima, Stokes shift (Δν, cm −1 ) of  adapalene  in solvents of different polarity (dielectric constant, є, refractive index, n, and E T (30) parameter).

    Journal: Frontiers in Chemistry

    Article Title: Environmentally sensitive fluorescence of the topical retinoid adapalene

    doi: 10.3389/fchem.2024.1438751

    Figure Lengend Snippet: Absorption (λ A , nm) and fluorescence (λ F , nm) maxima, Stokes shift (Δν, cm −1 ) of adapalene in solvents of different polarity (dielectric constant, є, refractive index, n, and E T (30) parameter).

    Article Snippet: Adapalene was purchased from BIOSYNTH Carbosynth and was used without further purification.

    Techniques: Fluorescence, Refractive Index

    Absorption of adapalene alone (10 μM, gray), DNA (50 μM in bp, dotted green line) or adapalene in the presence of DNA (full green line) in PBS at pH 7.4. Inset: adapalene alone (10 μM, gray), HSA alone (2 μM, dotted blue line), of adapalene in the presence of HSA (full blue line).

    Journal: Frontiers in Chemistry

    Article Title: Environmentally sensitive fluorescence of the topical retinoid adapalene

    doi: 10.3389/fchem.2024.1438751

    Figure Lengend Snippet: Absorption of adapalene alone (10 μM, gray), DNA (50 μM in bp, dotted green line) or adapalene in the presence of DNA (full green line) in PBS at pH 7.4. Inset: adapalene alone (10 μM, gray), HSA alone (2 μM, dotted blue line), of adapalene in the presence of HSA (full blue line).

    Article Snippet: Adapalene was purchased from BIOSYNTH Carbosynth and was used without further purification.

    Techniques:

    Normalized fluorescence spectra of adapalene in different solvents.

    Journal: Frontiers in Chemistry

    Article Title: Environmentally sensitive fluorescence of the topical retinoid adapalene

    doi: 10.3389/fchem.2024.1438751

    Figure Lengend Snippet: Normalized fluorescence spectra of adapalene in different solvents.

    Article Snippet: Adapalene was purchased from BIOSYNTH Carbosynth and was used without further purification.

    Techniques: Fluorescence

    (A) Position of the emission maxima in wavenumber of adapalene versus the polarity E T (30) in different solvents or in dioxane:ethanol mixtures (inset). (B) Lippert-Mataga plot for adapalene in different solvents or in dioxane:ethanol mixtures (inset).

    Journal: Frontiers in Chemistry

    Article Title: Environmentally sensitive fluorescence of the topical retinoid adapalene

    doi: 10.3389/fchem.2024.1438751

    Figure Lengend Snippet: (A) Position of the emission maxima in wavenumber of adapalene versus the polarity E T (30) in different solvents or in dioxane:ethanol mixtures (inset). (B) Lippert-Mataga plot for adapalene in different solvents or in dioxane:ethanol mixtures (inset).

    Article Snippet: Adapalene was purchased from BIOSYNTH Carbosynth and was used without further purification.

    Techniques:

    Fluorescence emission (λ exc = 315 nm) of a solution containing adapalene (10 μM) and HSA (12 μM) in PBS at pH 7.4, adapalene alone in PBS (gray dotted line). Inset emission changes as a function of the protein concentration.

    Journal: Frontiers in Chemistry

    Article Title: Environmentally sensitive fluorescence of the topical retinoid adapalene

    doi: 10.3389/fchem.2024.1438751

    Figure Lengend Snippet: Fluorescence emission (λ exc = 315 nm) of a solution containing adapalene (10 μM) and HSA (12 μM) in PBS at pH 7.4, adapalene alone in PBS (gray dotted line). Inset emission changes as a function of the protein concentration.

    Article Snippet: Adapalene was purchased from BIOSYNTH Carbosynth and was used without further purification.

    Techniques: Fluorescence, Protein Concentration

    Fluorescence emission (λ exc = 315 nm) of adapalene (10 μM) alone in PBS at pH 7.4 (black) and in the presence of duplex salmon sperm DNA (from 25 to 400 μM in bp). Inset: Stern-Volmer plot for the quenching of adapalene fluorescence in PBS (blue), with 10 μM bp (orange) or 100 μM bp (grey) of DNA.

    Journal: Frontiers in Chemistry

    Article Title: Environmentally sensitive fluorescence of the topical retinoid adapalene

    doi: 10.3389/fchem.2024.1438751

    Figure Lengend Snippet: Fluorescence emission (λ exc = 315 nm) of adapalene (10 μM) alone in PBS at pH 7.4 (black) and in the presence of duplex salmon sperm DNA (from 25 to 400 μM in bp). Inset: Stern-Volmer plot for the quenching of adapalene fluorescence in PBS (blue), with 10 μM bp (orange) or 100 μM bp (grey) of DNA.

    Article Snippet: Adapalene was purchased from BIOSYNTH Carbosynth and was used without further purification.

    Techniques: Fluorescence

    Emission spectra of adapalene (10 μM) varying CTAB concentration (from 0.05 to 4 mM) in PBS and adapalene alone in PBS (gray dotted line), λ exc = 315 nm. Inset: Representation of the changes of 390 nm emission vs. the logarithm of CTAB concentration.

    Journal: Frontiers in Chemistry

    Article Title: Environmentally sensitive fluorescence of the topical retinoid adapalene

    doi: 10.3389/fchem.2024.1438751

    Figure Lengend Snippet: Emission spectra of adapalene (10 μM) varying CTAB concentration (from 0.05 to 4 mM) in PBS and adapalene alone in PBS (gray dotted line), λ exc = 315 nm. Inset: Representation of the changes of 390 nm emission vs. the logarithm of CTAB concentration.

    Article Snippet: Adapalene was purchased from BIOSYNTH Carbosynth and was used without further purification.

    Techniques: Concentration Assay