Liubchanskiĭ E R, Nifatov A P, Okolelova N M, Siniakov E G
Med Radiol (Mosk). 1985 Feb;30(2):35-9.
The effect of a complexon therapy scheme including early (in 1 h) administration of Na3Ca DTPA and subsequent (in 1 day) administration of Na3Zn DTPA or Na3Ca DTPA at a dose of 25 mu Cimol/kg/day by three 2-week courses (5 times a week) with 2-week interruptions was studied in experiments on 541 male rats after intraperitoneal administration of 239Pu citrate complex (95 kBq/kg). The treatment resulted in a 3-fold lessening of the content of 239Pu and absorbed doses in the skeleton, a significant prolongation of the mean survival time (MST) from 452 to 593 days (Na3Zn DTPA) and 643 days (Na3Ca DTPA), and in a decrease of the osteosarcoma incidence from 76.4 to 32.6-41.2%. The ratio of osteosarcomas per 1 Gy retained in rats (0.076-0.083%) did not differ from that in untreated animals (0.067%) and varied within the ranges of established values (0.072-0.119%). The involvement of Na3Zn DTPA in the therapeutic scheme prolongs the MST of rats to a somewhat lesser degree than Na3Ca DTPA. No negative effects of Zn DTPA therapy were revealed.
在541只雄性大鼠腹腔注射柠檬酸钚络合物(95 kBq/kg)后进行的实验中,研究了一种络合剂治疗方案的效果,该方案包括早期(1小时内)给予Na3Ca DTPA,随后(1天内)给予Na3Zn DTPA或Na3Ca DTPA,剂量为25 μCi/mol/kg/天,分三个2周疗程(每周5次),中间间隔2周。治疗使骨骼中239Pu的含量和吸收剂量减少了3倍,平均生存时间(MST)显著延长,从452天延长至593天(Na3Zn DTPA)和643天(Na3Ca DTPA),骨肉瘤发病率从76.4%降至32.6 - 41.2%。大鼠每1 Gy保留的骨肉瘤比例(0.076 - 0.083%)与未治疗动物(0.067%)无差异,且在既定值范围内(0.072 - 0.119%)变化。与Na3Ca DTPA相比,将Na3Zn DTPA纳入治疗方案使大鼠的MST延长程度稍小。未发现Zn DTPA治疗的负面影响。