Kinetic studies of glutaraldehyde binding in liver

被引:5
|
作者
Helander, KG
Widéhn, S
Helander, HF
机构
[1] Univ Calif Los Angeles, W Los Angeles VA Hosp, Lab Membrane Biol, Los Angeles, CA 90073 USA
[2] Gothenburg Univ, Dept Biomed Lab Sci, S-41345 Gothenburg, Sweden
[3] Gothenburg Univ, Dept Pathol, S-41345 Gothenburg, Sweden
关键词
electron microscopy; fixation; glutaraldehyde; immunohistochemistry; kinetics; light microscopy; liver;
D O I
10.1080/714028200
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To study the kinetics of glutaraldehyde fixation, fresh rabbit liver cubes were immersed in 3% buffered H-3-glutaraldehyde for various periods of time. Following weighing and a brief rinse in water, the tissues were solubilized, and the radioactivity was measured in a scintillation counter. Binding of the isotope was half-maximal after approximately 4 h and a plateau was reached after approximately 20 h. We also investigated the reversibility of glutaraldehyde fixation. Fixed liver cubes were weighed and immersed in water for various periods of time, and after solubilization, the radioactivity was determined. After rinsing for 48 h, approximately 95% of the radioactivity was lost from the tissue specimens, indicating that fixation with glutaraldehyde is largely reversible. Light and electron microscopy of specimens rinsed for 1 and 48 h showed essentially similar morphology. Rinsing for 48 h restored some of the immunoreactivity that was absent after rinsing for only 1 h.
引用
收藏
页码:207 / 212
页数:6
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