SPECTROPHOTOMETRIC CHARACTERIZATION OF EUMELANIN AND PHEOMELANIN IN HAIR
Citation
H. Ozeki et al., SPECTROPHOTOMETRIC CHARACTERIZATION OF EUMELANIN AND PHEOMELANIN IN HAIR, Pigment cell research, 9(5), 1996, pp. 265-270
Categorie Soggetti
Cell Biology
SICI code
0893-5785(1996)9:5<265:SCOEAP>2.0.ZU;2-E
Abstract
Mammalian melanins exist in two chemically distinct forms: the brown t
o black eumelanins and the yellow to reddish-brown pheomelanins. They
can be quantified by HPLC analysis of pyrrole-2,3,5-tricarboxylic acid
(PTCA) and aminohydroxyphenylalanine (AHP). We recently developed a s
pectrophotometric method for assaying the total amount of eu- and pheo
melanins by dissolving melanins in Soluene-350 plus water. In this stu
dy, we examined whether absorbance at 500 nm (A(500)) of the Soluene-3
50 solution reflects the total amount of melanins obtained by the HPLC
methods, and whether the ratio of absorbances between 650 and 500 nm
reflects the eumelanin/total melanin ratio in mouse hair, sheep wool,
and human hair. Our findings were as follows: (1) Total melanin levels
calculated from A(500) values correlate well with those obtained from
PTCA and AHP values by multiplying with the following factors: for mi
ce, PTCA x 45 + AHP x 2.5; for sheep, PTCA x 40 + AHP x 15; and for hu
mans, PTCA x 160 + AHP x 10. (2) The A(650)/A(500) ratios were higher
(0.25-0.33) in black to brown hair while they were significantly lower
(0.10-0.14) in yellow to red hair. These results indicate that (1) th
e A(500) value can be used to quantify the total combined amount of eu
- and pheomelanins, and (2) the A(650)/A(500) ratio can serve as a par
ameter to estimate the eumelanin/total melanin ratio. The present meth
od provides a convenient way to qualitatively characterize eu- and phe
omelanins in melanins produced in follicular melanocytes.