Veterinary drugs and feed additives (especially some coccidiostats) can be
absorbed by the digestive tract of laying hens and transferred to the egg.
Physicochemical characteristics of these compounds determine their pharmaco
kinetic behavior and distribution to and within the egg. Traditionally the
quite lipid soluble drugs and additives are expected to yield residues only
in the fat-rich yolk. However, the quite lipid soluble drug doxycycline -
as well as many other drugs - showed during long-term administration higher
residues in white than in yolk. In a model study with 11 sulfonamides diff
ering in pK(a) value and lipid solubility, their distribution in vivo betwe
en yolk and white was determined. Neither differences in pK(a) values nor t
hose in lipid solubility could explain the distributions found. Binding to
egg white macromolecules in vivo as an explanatory factor was tested with f
ive sulfonamides, and no correlation between binding and the distribution o
f sulfonamides between white and yolk was found. Literature-data on the dis
tribution of drugs between egg white and yolk showed a reasonable consisten
cy within drugs and a large variability among drugs (as could be expected).
This larger database also did not provide a clue as to what factor determi
nes the distribution of a drug between egg white and yolk when given to lay
ing hens.