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Direct in vivo injection of 131I-GMS and its distribution and excretion in rabbit.

机译:直接体内注射131I-GMS及其在兔子中的分布和排泄。

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AIM: To explore the distribution and metabolism of (131)I-gelatin microspheres ((131)I-GMSs) in rabbits after direct injection into rabbits' livers. METHODS: Twenty-eight healthy New Zealand rabbits were divided into seven groups, with four rabbits per group. Each rabbit's hepatic lobes were directly injected with 41.336 +/- 5.106 MBq (131)I-GMSs. Each day after (131)I-GMSs administration, 4 rabbits were randomly selected, and 250 microL of serum was collected for gamma count. Hepatic and thyroid functions were tested on days 1, 4, 8, 16, 24, 32, 48 and 64 after (131)I-GMSs administration. Single-photon emission computed tomography (SPECT) was taken for each group on days 0, 1, 4, 8, 16, 24, 32, 48, 64 after (131)I-GMSs administration. A group of rabbits were sacrificed respectively on days 1, 4, 16, 24, 32, 48, 64 after (131)I-GMSs administration. Their livers were taken out for histological examination. RESULTS: After (131)I-GMSs administration, the nuclide was collected in the hepatic area with microspheres. The radiation could be detected on day 48 after (131)I-GMSs administration, and radiography could be seen in thyroid areas in SPECT on days 4, 8, 16 and 24. One day after (131)I-GMSs administration, the liver function was damaged but recovered 4 d later. Eight days after (131)I-GMSs administration, the levels of free triiodothyronine and free thyroxin were reduced, which restored to normal levels on day 16. Histological examination showed that the microspheres were degraded to different degrees at 24, 32 and 48 d after (131)I-GMSs administration. The surrounding parts of injection points were in fibrous sheathing. No microspheres were detected in histological examination on day 64 after (131)I-GMSs administration. CONCLUSION: Direct in vivo injection of (131)I-GMSs is safe in rabbits. It may be a promising method for treatment of malignant tumors.
机译:目的:探讨兔体内直接注射(131)I-明胶微球((131)I-GMSs)在兔体内的分布和代谢。方法:将28只健康的新西兰兔分为7组,每组4只。每只兔的肝叶直接注射41.336 +/- 5.106 MBq(131)I-GMS。每天(131)I-GMS给药后,每天随机选择4只兔子,并收集250微升血清进行γ计数。服用(131)I-GMS后第1、4、8、16、24、32、48和64天测试肝和甲状腺功能。在给予(131)I-GMS后第0、1、4、8、16、24、32、48、64天对每组进行单光子发射计算机断层扫描(SPECT)。 (131)I-GMS给药后第1、4、16、24、32、48、64天分别处死一组兔子。他们的肝脏被取出进行组织学检查。结果:(131)I-GMSs给药后,核素被收集在带有微球的肝区。可以在(131)I-GMSs给药后第48天检测到放射线,在SPECT的第4、8、16和24天在甲状腺区域可以看到放射线照相。(131)I-GMSs给药后一天,肝脏功能受损,但在4天后恢复。 (131)I-GMS给药八天后,游离三碘甲状腺素和游离甲状腺素水平降低,并在第16天恢复到正常水平。组织学检查显示,微球在第24、32和48 d降解程度不同(131)I-GMS管理。注射点周围的部分在纤维鞘中。 (131)I-GMSs给药后第64天,组织学检查未检测到微球。结论:直接体内注射(131)I-GMS对家兔是安全的。这可能是治疗恶性肿瘤的有前途的方法。

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