Capryloyl glycine and soy isoflavonoids in hypertrichosis: An experimental and placebo‐controlled clinical study
Autor: | Luisa Angileri, Mauro Barbareschi, Stefano Veraldi, Elisa Gaio, Federico Benetti |
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Rok vydání: | 2021 |
Předmět: |
Adult
Hypertrichosis Eflornithine soy isoflavonoids capryloyl glycine Glycine Dermatology Pharmacology Hair Removal Placebo Ornithine decarboxylase Clinical study 030207 dermatology & venereal diseases 03 medical and health sciences 0302 clinical medicine medicine Humans Skin CAPRYLOYL GLYCINE business.industry ornithine decarboxylase 1 Original Articles medicine.disease Tolerability Eflornithine Hydrochloride 030220 oncology & carcinogenesis Original Article Female business glycine soy‐fermented extract |
Zdroj: | Journal of Cosmetic Dermatology |
ISSN: | 1473-2165 1473-2130 |
DOI: | 10.1111/jocd.14096 |
Popis: | Background The management of acquired hypertrichosis (HT) is based on the search of the causes and subsequent specific treatment. However, simultaneous hair removal is important. No single method for hair removal is appropriate for all patients and skin areas. Treatment options are actually limited and clinical results are often unsatisfactory. Ornithine decarboxylase 1 (ODC1), an enzyme present in hair follicles, is considered as a potential target to inhibit hair growth. Only eflornithine hydrochloride, an inhibitor of ODC1, showed to be partially effective in the management of acquired HT. Aims The aim of our study was to evaluate the potential inhibition of ODC1 activity by a cream containing 4% capryloyl glycine, an ODC1 inhibitor, and 1% glycine soy‐fermented extract (soy isoflavonoids). Furthermore, we present the results of a placebo‐controlled clinical study that evaluated the efficacy and tolerability of this cream. Methods The ODC1 activity was detected by measuring absorbance at 340 nm. In the presence of ODC1 inhibitors, absorbance decreases as a function of inhibition. Difluoromethylornithine (DFMO) was provided as an inhibitor control. ODC1 activity inhibition was expressed as percentage of control (untreated sample). All data were presented as mean ± standard deviation of three independent experiments. To determine if statistically significant differences between treatments were present, a t test analysis was performed. The differences between groups were considered significant at p |
Databáze: | OpenAIRE |
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