Use of colloids of chromic [ 32P] phosphate in treatment of solid tumors

In order to evaluate the effectiveness of an intratumorally single dose of chromic [ 32P] phosphate for the treatment of solid tumors, studies of bioelimination, biodistribution, and therapeutic action were carried out. Only for comparative purposes were similar studies undertaken using a solution o...

Full description

Saved in:
Bibliographic Details
Published inNuclear medicine and biology Vol. 23; no. 7; pp. 907 - 910
Main Authors Zubillaga, M.B., Boccio, J.R., Nicolini, J.O., Ughetti, R., Lanari, E., Caro, R.A.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Inc 01.10.1996
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:In order to evaluate the effectiveness of an intratumorally single dose of chromic [ 32P] phosphate for the treatment of solid tumors, studies of bioelimination, biodistribution, and therapeutic action were carried out. Only for comparative purposes were similar studies undertaken using a solution of sodium [ 32P] orthophosphate-gelatin. Results show that when sodium [ 32P] orthophosphate-gelatin was intratumorally injected, the percentage of total elimination, after 32 days of treatment, was equal to 85.90 ± 8.70%, with a higher percentage in urine (64.50 ± 13.70%) than in feces (21.40 ± 4.50%). In biodistribution studies, the greater percentage was found in bone (15.54 ± 2.21%), whereas only 2.51 ± 0.39% remained in the tumor. When chromic [ 32P] phosphate was intratumorally injected, we found that the total elimination was equal to 51.70 ± 6.90%, with a higher amount in feces (32.70 ± 4.80%) than in urine (19.00 ± 3.60%). Biodistribution studies demonstrated that 28.93 ± 1.30% was still in the tumor and 19.01 ± 1.30% of the injected activity was found in the liver. On the other hand, when therapeutic action was evaluated, no tumoral regression was observed. These results demonstrate that the colloid of chromic [ 32P] phosphate cannot be used in the treatment of solid tumors as it mobilizes from the injection point, delivering a high dose to the entire organism.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0969-8051
1872-9614
DOI:10.1016/S0969-8051(96)00123-0