Color Atlas of Chemical Peels 2011
DOI: 10.1007/978-3-642-20270-4_5
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Trichloroacetic Acid

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Cited by 4 publications
(3 citation statements)
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“…We hypothesize that because the penetration studies were run for 24 h, the TCA effectively acted as a powerful penetration enhancer, heavily or fully impairing the outermost stratum corneum of the skin barrier to allow L‐Lactic acid‐ 13 C 3 to be delivered unimpeded into the skin. TCA operates in part by diminishing corneocyte adhesion, 31,32 which would weaken or completely eliminate the chief barrier to active delivery into the skin 33 . 20% TCA in particular will cause significant levels of destruction to the skin barrier, resulting in the well‐known “frosting” effect seen in chemical peels with high levels of TCA 34,35 .…”
Section: Discussionmentioning
confidence: 99%
“…We hypothesize that because the penetration studies were run for 24 h, the TCA effectively acted as a powerful penetration enhancer, heavily or fully impairing the outermost stratum corneum of the skin barrier to allow L‐Lactic acid‐ 13 C 3 to be delivered unimpeded into the skin. TCA operates in part by diminishing corneocyte adhesion, 31,32 which would weaken or completely eliminate the chief barrier to active delivery into the skin 33 . 20% TCA in particular will cause significant levels of destruction to the skin barrier, resulting in the well‐known “frosting” effect seen in chemical peels with high levels of TCA 34,35 .…”
Section: Discussionmentioning
confidence: 99%
“…The higher the concentration or amount of TCA applied, the more intense the destructive effect is. Therefore, it may represent an alternative strategy for skin tumor [ 9 , 10 ]. Considering the location, number and size of the lesion, we chose 80% TCA as the treatment option in this case.…”
Section: Discussionmentioning
confidence: 99%
“…Trichloroacetic acid (TCA) is a common laboratory chemical which used to induce HCC in rats by increasing inflammation and oxidative stress (Fouad et al, 2013). TCA induces tumours in laboratory animals through potential mechanisms such as DNA hypomethylation, peroxisome proliferation, oncogene activation, cell proliferation, and inhibition of intercellular communication (Harmon et al, 2011). Systemic treatment options for liver cancer are limited, and only a few are available.…”
Section: Introductionmentioning
confidence: 99%