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新型强效光敏剂氚标记苯并卟啉衍生物(3H-BPD-MA)在正常小鼠和荷瘤小鼠体内的生物分布。

Biodistribution of tritiated benzoporphyrin derivative (3H-BPD-MA), a new potent photosensitizer, in normal and tumor-bearing mice.

作者信息

Richter A M, Cerruti-Sola S, Sternberg E D, Dolphin D, Levy J G

机构信息

Quadra Logic Technologies, Vancouver, British Columbia, Canada.

出版信息

J Photochem Photobiol B. 1990 Apr 15;5(2):231-44. doi: 10.1016/1011-1344(90)80008-l.

DOI:10.1016/1011-1344(90)80008-l
PMID:2111398
Abstract

The biodistribution of a new and very potent photosensitizer, benzoporphyrin derivative-monoacid, ring A (BPD-MA), was determined in normal and P815 (mastocytoma) or M1 (rhabdomyosarcoma) tumor-bearing DBA/2J mice. A dose of 80 micrograms of 3H-BPD-MA was determined at 3, 24, 48, 72, 96 and 168 h post injection. The following tissues were tested: blood, brain, heart, intestine, kidney, lung, liver, muscle, skin, stomach, spleen, thymus and tumor. The biodistribution of 3H-BPD-MA in normal and tumor-bearing mice was comparable overall. 3H-BPD-MA localized in tumors better than in other tissues except kidney, liver and spleen. The tumor to tissue ratios were in the range 1.5-3 at 24 h post injection and increased further during the next 72 h. The highest levels of 3H-BPD-MA were observed in all tissues at 3 h post injection and decreased rapidly during the first 24 h. After 24 h the clearance from tissues was rather slow. The preliminary clearance data obtained in a group of five normal mice indicated that the majority of the injected dose (60%) cleared from the body via the bile and feces, while only about 4% cleared via kidneys and urine. Studies in which 3H-BPD-MA was extracted from tumor, kidney and liver 3 and 24 h after injection showed that, at 3 h, all the photosensitizing activity in tumor was retained. At 24 h only 39% of the activity was retained and considerably less active material was present in liver and kidney.

摘要

在正常以及荷P815(肥大细胞瘤)或M1(横纹肌肉瘤)的DBA/2J小鼠中,测定了一种新型强效光敏剂苯并卟啉衍生物单酸A环(BPD-MA)的生物分布。注射80微克³H-BPD-MA后,于3、24、48、72、96和168小时进行测定。检测了以下组织:血液、脑、心脏、肠道、肾脏、肺、肝脏、肌肉、皮肤、胃、脾脏、胸腺和肿瘤。³H-BPD-MA在正常小鼠和荷瘤小鼠中的总体生物分布具有可比性。³H-BPD-MA在肿瘤中的定位优于除肾脏、肝脏和脾脏之外的其他组织。注射后24小时,肿瘤与组织的比值在1.5至3之间,在接下来的72小时内进一步升高。注射后3小时,所有组织中³H-BPD-MA的水平最高,在最初24小时内迅速下降。24小时后,组织中的清除相当缓慢。在一组5只正常小鼠中获得的初步清除数据表明,注射剂量的大部分(60%)通过胆汁和粪便从体内清除,而只有约4%通过肾脏和尿液清除。注射后3小时和24小时从肿瘤、肾脏和肝脏中提取³H-BPD-MA的研究表明,在3小时时,肿瘤中的所有光敏活性均得以保留。在24小时时,仅保留了39%的活性,并且肝脏和肾脏中存在的活性物质明显减少。

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