Spectroscopic studies of aqueous solutions of haematoporphyrin-type sensiti
sers reveal that photobleaching during eposure to light is followed by the
formation of stable red-absorbing photoproducts. Experiments in model syste
ms (sensitisers bound to human serum albumin or in a suspension of resealed
erythrocyte 'ghosts') and in tumour tissue show that similar photomodifica
tion takes place in all investigated environments. Loss of total absorption
and emission intensities is accompanied by an increase of absorption in th
e red spectral region (630-650 nm) which is used for the treatment of tumou
rs because of the deeper penetration of light into tissues. This should be
taken into account when the duration of illumination is chosen to reach an
appropriate photodynamic dose using Hp-type sensitisers in the photodynamic
treatment of tumours.