Near infrared spectroscopy in large animals: Optical pathlength and influence of hair covering and epidermal pigmentation

Citation
J. Pringle et al., Near infrared spectroscopy in large animals: Optical pathlength and influence of hair covering and epidermal pigmentation, VET J, 158(1), 1999, pp. 48-52
Citations number
18
Categorie Soggetti
Veterinary Medicine/Animal Health
Journal title
VETERINARY JOURNAL
ISSN journal
10900233 → ACNP
Volume
158
Issue
1
Year of publication
1999
Pages
48 - 52
Database
ISI
SICI code
1090-0233(199907)158:1<48:NISILA>2.0.ZU;2-K
Abstract
The effects of epidermal pigmentation and hair covering on the relative tra nsparency of various animal tissues to near infrared (NIR) light were exami ned, and the pathlengths of NIR light through tissues at four wavelengths i n the NIR range were subsequently determined. Black hair covering and black or dark-coloured hooves prevented NIR light from penetration sufficient fo r conduction of pathlength or NIR spectroscopy measurements. Non-pigmented hair covering of the head did not appear to be a barrier to successful NIR light transmission. Tissues sufficiently transparent to NIR light had the d ifferential path length factor (DPF, i.e. the ratio of the observed light p athlength and the geometric light source-detector separation) of NIR light determined by intensity modulated spectroscopy at the wavelengths 744, 806, 834 and 860 nm. Horse gluteal muscles had DPFs of 6.2, 6.2, 6.0, and 5.6, whereas forelimb muscles had DPF of 4.7, 4.4, 4.5 and 3.9 at the respective wavelengths. She ep heads had DPF of 7.2 +/- 0.3, 5.8 +/- 0.5, 5.5 +/- 0.4 and 4.4 +/- 0.6 ( +/- SEM) for the above respective wavelengths, of which the pathlengths all differed significantly from the other, except for between 806 and 834 nm, and 834 and 860 nm. The DPF of horse hooves were 4.8 +/- 0.1, 4.8 +/- 0.1, 4.7 +/- 0.1 and 4.4 +/- 0.1 (SEM) for the above noted wavelengths, of which the pathlength at 744 and 806 nm differed from the pathlength at 860 nm (P >0.05). These results show that NIRS is possible through lighter pigmented hair and epidermal tissues, and provide DPFs of horse feet and muscle and t he sheep head that enables quantitative NIRS in these species.