S. Gronlund-pakkanen et al., Effect of photodynamic therapy on urinary bladder function: an experimental study with rats, UROL RES, 29(3), 2001, pp. 205-209
Photodynamic therapy (PDT) produces localized necrosis with light after pri
or administration of a photosensitizing drug. The problems with laser light
dosimetry and complications relating to bladder function appear to be impo
rtant limiting factors of PDT in urology. Photodynamic therapy on urinary b
ladder with normal epithelium of rats was performed using an argon ion lase
r as an energy source, with aminolevulinic acid (ALA)-induced protoporphyri
n IX (PpIX) photosensitizer. Four hours after ALA intravenous administratio
n, the bladders were intravesically radiated with light doses 20, 40, or 80
J/cm(2). Animals in the control group did not receive ALA and were radiate
d with 20 J/cm(2) light dose. Three weeks prior to PDT, the bladder capacit
y and pressure changes during filling cystometry were assessed. Cystometric
s were repeated 1, 3, 7, or 21 days after laser therapy. The light dose 20
J/cm(2) and 40 J/cm(2) together with the used ALA dose caused no reduction
in bladder capacity, whereas 80 J/cm(2) light dose produced up to 50% reduc
tion in the capacity at 3 weeks postoperatively. In control group without A
LA, the animals did not regain more than 34% of the capacity of their contr
ol values at 3 weeks. The light dose of 20 J/cm(2) and 40 J/cm(2) with ALA
induced functional changes that subsided after day 1. Our results indicate
that with proper dosing of photosensitizing drug and light energy, the func
tional impairment of urinary bladder may be reduced as transient. These fin
dings support the use of PDT as safe therapy of superficial bladder cancer.