Bantfu:Motsa0615/Kukhanyisa sikhumba

Kukhanyisa sikhumba[notes 1] ngumkhuba wekusebentisa timonyu, emakhatsakhatsa, kumbe letinye tindlela tekwenta sikhumba sibe mhlophe. Imitsi yekukhanyisa sikhumba isebenta ngekwehlisa linani  melanin yesikhumba. Imitsi leminyenti ikhonjisiswe kutsi inemandla ekukhanyiseni sikhumba, leminye inemitselela lenemvuzo (sib..: ema-antioxidant,[1] tondlamtimba, kumbe yehlise bungoti betinhlobo tsite temdlavuza); leminye yalemitsi inebungoti lobukhulu emphilweni (sibonelo, timonyo letinemekhuri).

Umsebenti

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Tindzawo letitsite letishe kakhulu tinebumnyama lobendlulele njengemabla e-lentigo , tinsumpe nemkhango tingakhanyiswa kute umbala wato uhambisane newesikhumba lesimadvutane. Mayelana nekucateka, sikhumba lesingakacateki singakhanyiswa kwentelwe kutsi kube nekufanana kwesikhumba sonkhe.[2]

Discovery and design

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Melanogenesis inhibitors have been discovered and developed through several methods, including: screening of synthetic chemical libraries (high throughput screening is occasionally used), screening of plant extracts,[3] computational (in silico) search,[4][5] found as a side effect of previously known drugs[6][7][8][9] and exploration of structural analogues of previously known tyrosinase inhibitors[10][11] based on knowledge (in varying degrees) of their structure-activity relationship. Thus, the development and discovery of melanogenesis inhibitors illustrates many of the methods used in drug design. Some of the most potent competitive reversible tyrosinase inhibitors are synthetic compounds with a potency hundreds of times that of kojic acid.

Mechanisms of action

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  1. Instead of "whitening", the terms "lightening", "brightening", "depigmentation" and "bleaching" are also used.

References

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  1. Empty citation (help)  No-cost access and free license (CC BY 4.0).
  2. skin-lightening uses
  3. Chang, Te-Sheng (2009). "An Updated Review of Tyrosinase Inhibitors". Int. J. Mol. Sci. 10 (6): 2440–2475. PMC 2705500. PMID 19582213. doi:10.3390/ijms10062440.  iThempleti:Lref
  4. Empty citation (help)  Restricted access.
  5. Empty citation (help)  No-cost access and free license (CC BY 4.0).
  6. Empty citation (help)  No-cost access but non-free license.
  7. Empty citation (help)  No-cost access and free license (CC BY 4.0).
  8. Empty citation (help)  Restricted access.
  9. Espín, Juan Carlos; Wichers, Harry J. (2001). "Effect of captopril on mushroom tyrosinase activity in vitro". Biochim. Biophys. Acta 1544 (1-2): 289–300. PMID 11341938. doi:10.1016/s0167-4838(00)00230-2.  iThempleti:Lref
  10. Empty citation (help)  No-cost access and free license (CC BY 4.0).
  11. Empty citation (help)  No-cost access and free license (CC BY 3.0).

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