PRELIMINARY STUDY OF TRACE ELEMENTS IN HUMAN BRAIN TUMOUR TISSUES BY INAA  

PRELIMINARY STUDY OF TRACE ELEMENTS IN HUMAN BRAIN TUMOUR TISSUES BY INAA

在线阅读下载全文

作  者:庄圭荪 王荫淞 谈明光 支敏 王永吉 潘伟清 张福林 

机构地区:[1]Shanghai Institute of Nuclear Research, Academia Sinica, Shanghai 201800, China [2]Departments of Pathology and Neurology, Huashan Hospital, Shanghai 200040, China

出  处:《Nuclear Science and Techniques》1991年第2期100-105,共6页核技术(英文)

摘  要:Elemental profiles of brain tumour tissues from 15 male patients of astrocytomas (grade Ⅰ-Ⅲ) and normal human brain tissues of 23 male age matched autopsies as controls have been studied by INAA. A total of 18 elements Se, Na, K, Br, Cl, Mn, Mg. S, Ca, Cu, Hg, Cr, Fe, Rb, Zn, Co, Sc and P has been determined for this purpose. The analytical results showed that compared with the normal brain tissues, concentrations of Ca, Fe, Cu, Zn, Mn, Br and Sc were significantly higher in tumour tissues and that of Rb, K and P were lower while no differences for contents of Mg, S, Cr, Na and Cl were observed. A negative correlation between P and Ca in malignant and normal brain tissues was observed.Elemental profiles of brain tumour tissues from 15 male patients of astrocytomas (grade Ⅰ-Ⅲ) and normal human brain tissues of 23 male age matched autopsies as controls have been studied by INAA. A total of 18 elements Se, Na, K, Br, Cl, Mn, Mg. S, Ca, Cu, Hg, Cr, Fe, Rb, Zn, Co, Sc and P has been determined for this purpose. The analytical results showed that compared with the normal brain tissues, concentrations of Ca, Fe, Cu, Zn, Mn, Br and Sc were significantly higher in tumour tissues and that of Rb, K and P were lower while no differences for contents of Mg, S, Cr, Na and Cl were observed. A negative correlation between P and Ca in malignant and normal brain tissues was observed.

关 键 词:TRACE element Brain cancer NAA 

分 类 号:TL[核科学技术]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象