Sanderson C, Radley K, Mayton L
Bone and Joint Research Laboratory, Veteran Affairs Medical Center, Salt Lake City, Utah 84148, USA.
Biotech Histochem. 1995 Jan;70(1):12-8. doi: 10.3109/10520299509108310.
Ethylenediaminetetraacetic acid (EDTA) solution is used to decalcify bone specimens for histological examination. Sodium hydroxide (NaOH) has been used to dissolve EDTA and to bring EDTA solutions to neutral pH. This solution, however, requires several weeks to decalcify bone specimens. We investigated a new decalcification fluid using concentrated ammonium hydroxide (NH4OH) to dissolve EDTA and to adjust the pH to neutral. Decalcification was performed using a magnetic stirrer with and without vacuum, or with a sonic cleaner. Decalcification end point was confirmed using both the weight loss and X-ray methods. After decalcification, specimens were processed through paraffin and sections were stained with hematoxylin and eosin. Decalcification employing NH4OH required an average of six days. Light microscopy indicated good retention of cellular detail.
乙二胺四乙酸(EDTA)溶液用于对骨标本进行脱钙以便进行组织学检查。氢氧化钠(NaOH)已被用于溶解EDTA并将EDTA溶液调至中性pH值。然而,这种溶液需要数周时间来对骨标本进行脱钙。我们研究了一种新的脱钙液,使用浓氢氧化铵(NH4OH)来溶解EDTA并将pH值调至中性。脱钙过程使用磁力搅拌器,有或没有真空条件,或者使用超声波清洗器。使用失重法和X射线法来确认脱钙终点。脱钙后,标本经过石蜡处理,切片用苏木精和伊红染色。使用NH4OH进行脱钙平均需要六天。光学显微镜检查显示细胞细节保留良好。