2012
DOI: 10.1590/s1984-82502012000300006
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Mushroom tyrosinase inhibitory activity and major fatty acid constituents of Amazonian native flora oils

Abstract: In order to treat hyperpigmentation-related problems, there has been a global trend in developing cosmetics claiming to have skin-whitening properties, which act by inhibiting melanin biosynthesis. The objective of this work was to evaluate the in vitro mushroom tyrosinase inhibitory activity of five Amazonian native flora oils, and so to verify the possibility of their incorporation into cosmetic products. In addition, the fatty acid composition of the essential oils was determined by gas chromatography-flame… Show more

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Cited by 24 publications
(19 citation statements)
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“…An additional incubation period of 60 min at 30 ± 1 °C was performed, after which a new spectrophotometric reading was taken (T2). The inhibitory percentages at the two time points (T1 and T2) were obtained according to the formula: 𝐼𝐼𝐼𝐼% = 𝑐𝑐 − 𝑆𝑆 × 𝑐𝑐 100, where IA% = inhibitory activity; C = negative control absorbance; S = sample or positive control absorbance (absorbance at time T1 or T2 minus the absorbance at time T0) [ 44 ].…”
Section: Methodsmentioning
confidence: 99%
“…An additional incubation period of 60 min at 30 ± 1 °C was performed, after which a new spectrophotometric reading was taken (T2). The inhibitory percentages at the two time points (T1 and T2) were obtained according to the formula: 𝐼𝐼𝐼𝐼% = 𝑐𝑐 − 𝑆𝑆 × 𝑐𝑐 100, where IA% = inhibitory activity; C = negative control absorbance; S = sample or positive control absorbance (absorbance at time T1 or T2 minus the absorbance at time T0) [ 44 ].…”
Section: Methodsmentioning
confidence: 99%
“…Plant seed oils continue to receive growing interest from researchers working in a variety of different fields, including chemists, pharmacists, and physicians because of their potential applications in the pharmaceutical, cosmetics, and food industries [ 26 ]. Torreya grandis cv.…”
Section: Resultsmentioning
confidence: 99%
“…Tyrosinase inhibitory activity was carried out in accordance with Teixera et al (2012) with slight modifications. 25 μL of sample was reacted with 80 μL phosphate buffer, 125 μL L-tyrosine and 20 μL tyrosinase enzymes, and then incubated for 30 min at room temperature (Teixeira et al 2012). The absorbance was then recorded using a Multiscan (Nanoquant, Infinite M2000 Pro, TECAN) at 475 nm.…”
Section: Tyrosinase Inhibitory Activitymentioning
confidence: 99%