Abstract

The purpose of this investigation was to develop a rapid, simple titrimetric method which could be used to replace the more expensive and time consuming Warburg method for the assay of milk arylesterase (A-esterase) activity. A titrimetric method was selected on the basis of preliminary experimentation. Optimum conditions (e.g., temp, pH, substrate concentration, and time) for the assay of milk A-esterase activity were then investigated. On the basis of these results a standard titrimetric method was suggested. This procedure was then compared with the Warburg method (r = 0.97, n = 182). The coefficients of variation between duplicate samples were 2.6 and 5.2%, respectively, for the Warburg and titrimetric methods. The precision of the titrimetric procedure was increased (approximately fourfold) by titrating to a constant pH, using a potentiometer instead of phenolphthalein.

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