Validation of a liquid chromatographic method for the pharmaceutical quality control of products containing elacridar$
- Author:
Sawicki Emilia
;
Hillebrand J. Michel
;
Rosing Hilde
;
Schellens H.M. Jan
;
Nuijen Bastiaan
;
Beijnen H. Jos
- Publication Type:Journal Article
- Keywords:
GF120918;
Solid dispersion;
Dissolution;
Hydroxylation;
HPLC-UV
- From:
Journal of Pharmaceutical Analysis
2016;6(4):268-275
- CountryChina
- Language:Chinese
-
Abstract:
Many anticancer drugs have an impaired bioavailability and poor brain penetration because they are sub-strates to drug efflux pumps such as P-glycoprotein and Breast Cancer Resistance Protein. Elacridar is a strong inhibitor of these two drug efflux pumps and therefore has great potential to improve oral absorption and brain penetration of many anticancer drugs. Currently, a clinical formulation of elacridar is unavailable and therefore the pharmaceutical development of a drug product is highly warranted. This also necessitates the availability of an analytical method for its quality control. A reverse-phase high-performance liquid chro-matographic method with ultraviolet detection was developed for the pharmaceutical quality control of products containing elacridar as the active pharmaceutical ingredient. The analytical method was validated for linearity, accuracy, precision, selectivity, carry-over, stability of stock and reference solutions, stability of the final extract, stability-indicating capability and impurity testing. We found that elacridar is unstable in aqueous solutions that are exposed to light because a hydroxylation product of elacridar is formed. Therefore, sample solutions with elacridar must be protected from light.
