The Phosphotungstic Acid-Hematoxylin (PTAH) staining method relies on acid-base chemistry to stain collagen and muscle fibers. These fibers are demonstrated using a tungsten mordant provided by the phosphotungstic acid. This mordant binds hematin and stains selective tissue components blue, while the phosphotungstic acid is believed to stain other tissue components red-brown.
Traditionally, tissue sections intended for PTAH staining were preferably fixed in Zenker's solution containing mercuric chloride. However, due to regulatory initiatives to remove all mercury from laboratories, Zenker's is no longer readily used. Fixation in 10% neutral buffered formalin is acceptable.
A section of skeletal muscle tissue can be used for quality control.
The amount of phosphotungstic acid in the staining solution is far more significant than that of hematein. Tungsten is believed to bind all available components blue, while phosphotungstic acid is thought to stain the red-brown components. This stain has been referred to as a polychrome stain because one solution gives two significant colors. The red-brown components will lose this color with water or prolonged alcohol washes. Therefore, dehydration of the tissue section following staining must be rapid.
