A novel and economical staining method for quick identification and evaluation of FFPE sections in a histology laboratory (CROSBI ID 650120)
Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija
Podaci o odgovornosti
Rođak, Edi ; Lovrić, Ivana ; Bijelić, Nikola ; Belovari, Tatjana
engleski
A novel and economical staining method for quick identification and evaluation of FFPE sections in a histology laboratory
Histological procedures can be a complex and lengthy process. Staining of formalin-fixed, paraffin-embedded (FFPE) sections requires a lot of intermediate steps in which the consumption of chemicals can be extensive and time-consuming. Furthermore, an unknown tissue sample may occur, or a quick look at the tissue structure may be required for further planning. In order to avoid the numerous intermediate steps, we developed a quick method for staining of FFPE sections that takes about 10 to 15 minutes overall. Human liver, skin and small intestine FFPE samples from our department’s histological archive were used. 5µm sections were cut, placed on slides and dried for an hour on a thermal plate at 50 °C. Dry slides were left to cool down and 1.5 ml 3% (w/v) haematoxylin in 100% ethanol was added on slides using a micropipette. After 5 minutes, 1 ml of 2.3% iron (III) chloride solution was added to the already present haematoxylin solution. Mixed solution was left on slides for another 5 min, then slides were washed with dH2O. Slides were then immersed in same iron chloride solution to remove excess stain and rinsed with dH2O. The slides were examined and photographed within an hour after the staining was completed ; no cover slip was placed on the tissue. Blue nuances of haematoxylin were predominant, and paraffin crystals were visible. Characteristic details could be identified in all three examined tissues (e.g. central veins, hepatocytes, portal triads ; epidermis, hair follicles, sebaceous glands ; intestinal villi, crypts, goblet cells). Although the paraffin crystals distorted the image to an extent, the tissues could be easily identified, with characteristic tissue details visible enough for quick analysis. This method can be useful for quick identification or screening of FFPE samples. Apart from being fast, it is also valuable for economical reasons, since the usage of xylene, ethanol and other chemicals is reduced to minimum.
Histology, Methods, Staining
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Podaci o prilogu
93-94.
2017.
objavljeno
Podaci o matičnoj publikaciji
17th International European Light Microscopy Initiative Meeting Program and Abstract Book
Weber, Igor ; Tolić, Iva ; Kovačević, Goran ; Vidoš, Ana
Zagreb: Institut Ruđer Bošković
978-953-7941-16-1
Podaci o skupu
17th International European Light Microscopy Initiative Meeting
poster
23.05.2017-26.05.2017
Dubrovnik, Hrvatska