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J Pharm Biomed Anal ; 174: 348-359, 2019 Sep 10.
Article in English | MEDLINE | ID: mdl-31202877

ABSTRACT

A simple, rapid and accurate ultra-high performance liquid chromatographic (UHPLC) method with a UV detection for the determination of the chemical purity and assay of bimatoprost (BT-1) was developed. The chromatographic separation was achieved with the use of an Acquity BEH C8, 150 × 2.1 mm, 1.7 µm reversed phase analytical column. The mobile phase consisted of 0.01% H3PO4: acetonitrile (initial conditions 80 : 20, v/v) was passed through the column at the flow rate of 0.7 mL min-1. The separation was carried out in the gradient elution mode. The presented method allows to separate ten potential impurities of BT-1. The full validation according to the ICH Q2 (R1) guidelines was carried out for five of the potential impurities while limit tests were performed for four BT-1 related substances. The performed validation tests proved the suitability of the method for its intended purposes. An additional LC/MS method was utilized for the identification of the unknown impurities in bimatoprost as well as the degradation impurities generated during the forced degradation studies.


Subject(s)
Bimatoprost/analysis , Chemistry, Pharmaceutical/methods , Chromatography, High Pressure Liquid/methods , Chromatography, Reverse-Phase/methods , Drug Contamination , Drug Stability , Acetonitriles/chemistry , Limit of Detection , Linear Models , Mass Spectrometry , Quality Control , Reproducibility of Results
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