黄培林,童冠圣,刘璐,等.32P胶体局部给药防治H22移植瘤淋巴道转移的实验研究[J].中华放射医学与防护杂志,2004,24(4):324-327.HUANG Pei-lin,TONG Guan-sheng,LIU Lu,et al.An experimental study on effect of 32P colloid on lymphatic metastasis of transplanted H22 hepatoma in mices[J].Chin J Radiol Med Prot,2004,24(4):324-327 |
32P胶体局部给药防治H22移植瘤淋巴道转移的实验研究 |
An experimental study on effect of 32P colloid on lymphatic metastasis of transplanted H22 hepatoma in mices |
投稿时间:2004-01-08 |
DOI: |
中文关键词: 32P磷酸铬胶体 小鼠 H22腹水型肝癌 淋巴道转移 体内分布 |
英文关键词:Chromic 32P phosphate colloid Mouse Ascitic hepatoma Lymph metastasis Biodistribution |
基金项目:江苏省社会发展基金资助项目(BS2000062);铁道部医学科研基金资助项目 |
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中文摘要: |
目的 探讨不同剂量的32P胶体局部注射对小鼠H22移植瘤和区域淋巴结转移灶的治疗作用。方法 应用小鼠H22腹水型肝癌淋巴道转移模型,通过肿瘤组织局部给药,观察32P胶体在模型小鼠移植瘤、区域淋巴结及全身各器官、组织内的分布。结果 32P胶体局部给药后主要聚集在瘤体注射局部和区域淋巴结内,而在肝、脾、肺等脏器分布的活度较低。区域淋巴结聚集的活度随给药剂量增高而递增。治疗早期瘤体和窝淋巴结转移灶呈现局灶性坏死。后期移植瘤和区域淋巴结转移灶的瘤组织呈现出血、坏死。结论 32P胶体瘤体给药可在局部富集,并可经淋巴道转运、聚集于区域淋巴结,对肿瘤组织和邻近的淋巴结转移灶具有明显的杀伤作用。 |
英文摘要: |
Objective To study the anticancer effects and biodistribution of chromic 32 P phosphate colloid in mice with lymphatic metastasis of hepatoma after intratumoral injection. Methods Forty-eight Km mice with H22 ascites hepatoma were injected with 32 P colloid intratumorally.The distribution of 32 P in regional lymph nodes and other organs was observed dynamically, and its anticancer effectiveness was investigated in the tumor and regional lymph nodes. Results 32 P mainly remained in the tumor and regional lymph nodes, while the of 32 P organs, such as liver, spleen, lung, only retained a mild activity. By histopathologic observation, neoplamic focis could be found in pad, right popliteal lymph node and groin lymph node, and necrosis was seen in the tumor and its metastatic foci in right popliteal lymph node. On day 17 after 32 P treatment, the transplanted tumor focis necrosed thoroughly, and normal structure of regional lymph nodes disappeared, which was replaced by necrotic tissue and hemorrhage. Conclusion The intratumoral administration of chromic [ 32 P] colloid could be used for treatment of the primary tumor, and lymphatic metastatic focus as well, in order to produce obvious anticancer effects. |
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