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K Juliano

Publications and source records attributed to K Juliano.

2 recordsLinked to original sources

Development and validation of a cholate binding capacity method for DMP 504, a bile acid sequestrant.

DMP 504, a highly cross-linked insoluble polymer, is a bile acid sequestrant developed by the DuPont Pharmaceuticals Company for serum cholesterol reduction. Since DMP 504 is insoluble, it was necessary to develop unique specific analytical methods to measure and control the quality of different lots of the drug. Since the mechanism of action of DMP 504 is believed to be by sequestration of bile acids, the in-vitro binding capacity of the polymer for cholic acid was chosen as a surrogate of in-vivo performance and used to assess potency of the compound. In this method, individual aliquots of DMP 504 at three different levels were incubated with a cholate solution of known concentration. The residual cholate solution was filtered and analyzed by a reversed-phase HPLC method using refractive index detection. When the bound cholate was plotted versus the mass of DMP 504, the resulting curve was linear. The slope of this curve is the cholate binding capacity of DMP 504. This method has been shown to be precise and robust. Precision of the method was shown to have an RSD of 2.0% with injection precision of 0.4% and stability of cholate solutions up to 73 h. It is also a unique binding capacity method due to its multi-point determination, and it has been shown to be a suitable quality control method for ensuring lot-to-lot consistency of drug substance.

Cholates↗

Quantitation and determination of molecular weight distribution of residual water soluble extractable polyamines in DMP 504, a poly-alkylamine bile acid sequestrant, by aqueous high performance size exclusion chromatography.

A high performance size exclusion chromatography (HPSEC) method with refractive index detection for quantitation and molecular weight determination of extractable water soluble polyamines (SPA) in a novel proprietary polymeric pharmaceutical compound (DMP 504) is described. The extracted polyamines are synthetic impurities as well as potential degradation products of the polymer. Data for calibration, precision, solution stability, and limits of detection and quantitation are presented to validate the suitability of this method for its intended purpose. Response linearity for the poly(2-vinylpyridine) standard is demonstrated between 10 and 1000 micrograms ml-1, equivalent to 0.005% and 0.5% (w/w) in DMP 504. Molecular weight distributions of SPA extracted from DMP 504 are presented. No increase in SPA is detected in DMP 504 over 6 months storage at room temperature.

Calibration↗