Skin P-31 MRS measurements might detect metabolic damage from irradiat
ion, chemotherapy, or ischemia. Although rat and cadaver data have dem
onstrated this potential (C. D. Cuono, et al., Plast. Reconstr. Surg.
81, 1-11 (1988), H. W. Klein, ef al., Ann. Plast. Surg. 20, 547-551 (1
988)), few studies of in vivo phosphorus human skin spectra have been
published (A. Zemtsov, et al., J. Dermatol. Surg. Oncol. 15, 1207-1211
(1989), A Zemtsov, et al., J. Am. Acad. Dermatol. 30, 959-965 (1994))
, and those likely reflect underlying muscle as much as skin. To separ
ate P-31 Skin and muscle spectra, we have developed a unique two-layer
''flotation'' phantom for mapping coil sensitivity and an associated
semiempirical two-power RF depth-resolved technique. Phantom and metho
d have been applied in a study of 17 normal volunteers to obtain human
in vivo P-31 skin spectra uncompromised by muscle contamination and t
o quantitate ratios of major phosphometabolites. Skin results consiste
ntly showed low ratios of phosphocreatine (PCr) to adenosine triphosph
ate (ATP), high levels of phosphomonoester (PME), P-i, and phosphodies
ter (PDE) relative to PCr, and demonstrated a shift in pH toward great
er alkalinity, compared to that with simultaneous muscle results.