SummaryMonochromatic light was provided by a continuous wave Argon ion laser. We chose to study the in vitro effects of light at 457.9, 465.8, 476.5, 488.0, 501.7, and 514.5 nm as representative of a reasonably evenly spaced samplig across the blue-green spectrum. The in vivo experiments were conducted at 457.9, 476.5, 488.0, and 514.5 nm.In vitro light at 488.0 nm appeared to be more effective than the others studied.After 24 h of irradiance, the in vivo decline in serum bilirubin concentration produced by light at 488.0 nm was one-and-one-half, two, and four times as effective as light at 457.9, 476.5 and 514.5 nm, respectively. By 48 h of exposure, the declines produced by light at 457.9 nm and 488.0 nm are significantly superior to that at 476.5 nm and 514.5 nm, but they do not differ from one another.The photon-induced chemical alteration of bilirubin has been demonstrated by various light sources both in vitro and in vivo. The clinical application of this phenomenon has been widely used as phototherapy in the treatment of neonatal hyperbilirubinemia. Investigations designed to delineate the effective wavelengths have employed broad spectrum light sources and have indicated that irradiance with light of wavelengths of 425-475 nm is maximally effective both in vitro (2,7,8,10, 13,25,31) and in vivo (1,11,17,24,29,33,36). But one study performed in vitro with a relatively narrow spectral source suggested wavelengths at 490 nm might also be efficacious (10). More recently, Lilien et al. (27) have performed experiments that also suggest that wavelengths of light beyond the 425475 nm range are efficacious in vitro.Radiant energies within the 400-500 nm range exhibit potential for inducing damage to tissues. Light from standard fluorescent lamps causes breaks in DNA strands in vitro (3, 35) and increases sister chromatid exchanges and other chromosomal alterations in cultured cells (4,18,21,23,32,35,37). An increased frequency of sister chromatid exchange has been reported in some infants after phototherapy (12). Although we know of no reports regarding any increase in sister chromatid exchange in vivo in response to monochromatic light, the occurrence seems likely; thus, the widespread use of phototherapy has generated concern regarding the potential for long-term mutagenic and carcinogenic effects. Inasmuch as most published data suggest that the offending wavelengths are principally in the ultraviolet range, some recent work has implicated light of wavelengths exceeding 300 nm (9) and, indeed, some alterations appear to occur maximally in response to wavelengths of light between 420-500 nrn (35). Although the magnitude of these latter risks has not been quantitated as they may relate to the clinical setting, it seems desirable to more precisely define the most efficacious wavelengths for the photoalteration of bilirubin that results in its enhanced excretion. This is particularly needed in the design of future phototherapy instruments to be used in the management of neonatal hyperbilirubinemia. Preliminary po...