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Catechin is found in several natural sources, as Eugenia dysenterica and Syzygium cumini extracts. Its antioxidant and UV-protective properties suggest a potential use in cosmetic and dermatological formulations. A simple analytical method capable of giving support to experiments performed along the development of topical formulations containing this natural substance (i.e., drug assay, skin permeation and stability studies), however, is still demanded. Thus, this work aimed to develop and validate a selective HPLC method for catechin determination during the development of topical formulations. Separation was achieved using a RP-C18 column (300 x 3.9 mm; 10 μm), with a mobile phase of methanol/phosphoric acid 0.01 M (15: 85, v/v), flow rate of 0.8 mL/min, temperature set at 40°C, and UV detection at 230 nm. Method was linear in a range from 0.5 to 10.0 μg/mL (r = 0.9998); precise with an overall variation coefficient of 5.5% and accurate with catechin recovery from the skin layers higher than 85%. Additionally, the method was sensitive (limit of detection = 0.109 μg/mL, limit of quantification = 0.342 μg/mL) and selective against plant extracts, skin matrices and formulation interferents, as well as catechin degradation products. It was also robust regarding both methodology parameters and analytical stability.

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This page is a summary of: Versatile chromatographic method for catechin determination in development of topical formulations containing natural extracts, Biomedical Chromatography, September 2017, Wiley,
DOI: 10.1002/bmc.4062.
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