Posting this under the heading it deserves: Buffers, pH and why a formulation is a formulation Everything below is what sits behind that.
A formulation question rather than a pharmacological one, though the two keep getting merged in this category.
Solubility, buffer, pH and container all change what happens to a molecule, and none of them change what the molecule does at a receptor. The published stability data covers a designed formulation; a home preparation is not one.
How far does the published work actually carry?