Greattings,
My apologies, my fault.
I am working with Pamidronate Disodium. 
I'm making tests with the method of U.S. Pharmacopoeia 35 Official Monographs page 4200 (Assay).
"Mobile phase— To 2500 mL of water, add 0.47 mL of anhydrous formic acid, adjust with 2 N sodium hydroxide solution to a pH of 3.5, filter, and degas. Make adjustments if necessary (see System Suitability under Chromatography 621). [note—The small amounts of formic acid have a strong influence on the retention times. ] 
Standard preparation— Dissolve an accurately weighed quantity of USP Pamidronate Disodium RS in water, and dilute quantitatively, and stepwise if necessary, with water to obtain a solution having a known concentration of about 2 mg per mL. Chromatographic system (see Chromatography 621)— The liquid chromatograph is equipped with a refractive index detector and a 4.6-mm ×10-cm column that contains packing L23. The flow rate is about 1.0 mL per minute. The column temperature is maintained at 35.  Chromatograph the Standard preparation, and record the peak responses as directed for Procedure: the tailing factor is not less than 0.3 and not more than 1.2; and the relative standard deviation for replicate injections is not more than 2.0%."
Att,
Rodolfo