| Literature DB >> 26218339 |
Judith Taibon1, Anita Ankli2, Stefan Schwaiger1, Camille Magnenat3, Vasilik-Ioanna Boka4, Claudia Simões-Pires3, Naktarios Aligiannis4, Muriel Cuendet3, Alexios-Leandros Skaltsounis4, Eike Reich2, Hermann Stuppner1.
Abstract
A simple and rapid high-performance thin-layer chromatography-based autographic assay was established to screen plant extracts for the presence of tyrosinase-inhibiting substances. Three mobile phases were selected for the chromatographic separation of different types of extracts. After development, the plate was sprayed with the substrate solution Levodopa followed by a solution of the enzyme tyrosinase. Several known tyrosinase inhibitors were tested simultaneously as positive controls. They were detected as white spots with white light in remission from the plate as well as with white light transmitted through the plate. Some of the investigated extracts included spots showing a different behaviour; some lipophilic substances appeared as white spots in white light remission but were black in white light transmission. This behaviour, which could lead to false-positive results, was due to poor wettability of the corresponding spots. False-positive results were eliminated by adding Triton X-100 to the Levodopa solution and drying the plate after 10 minutes incubation with a molecular sieve. Tyrosinase inhibitors can be clearly identified as white spots against a dark background in white light remission as well as in white light transmitted through the plate. The established high-performance thin-layer chromatography autographic assay was validated and can be used as a standard method for the detection of tyrosinase inhibitors in plant extracts without causing false-positive results. Georg Thieme Verlag KG Stuttgart · New York.Entities:
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Year: 2015 PMID: 26218339 DOI: 10.1055/s-0035-1546250
Source DB: PubMed Journal: Planta Med ISSN: 0032-0943 Impact factor: 3.352