Cheung, A., Struble, E., He, J., Yang, C., Wang, E., Thurston, D.E. and Liu, P. (2005) Direct liquid chromatography determination of the reactive imine SJG-136 (NSC 694501). Journal of Chromatography B, 822 (1-2). pp. 10-20. 10.1016/j.jchromb.2005.04.027.
Full text not available from this repository.
SJG-136 (NSC 694501), 8,8′-[[(propane-1,3-diyl)dioxy]bis[(11aS)-7- methoxy-2-methylidene-1,2,3,11a-tetrahydro-5H-pyrrolo[2,1-c][1,4] benzodiazepin-5-one], which is being developed as a DNA-interactive antitumor agent, contains highly reactive imines in the diazepinone portions of the molecule. Water or alcohol adds readily to the imino moiety to form the corresponding carbinolamine or its alkyl ether, respectively. This sensitivity to protic substances poses a formidable challenge to the formulation and HPLC assay development for the compound. After studying the solution chemistry of SJG-136 and its potential interaction with various stationary phases, two reversed-phase liquid chromatographic assays for the compound have been developed. A direct assay that separates SJG-136 from its water or methanol adducts and an indirect assay that quantifies SJG-136 as its dihydrate adduct are reported. The latter method, which is more practical for drug development, has been validated. It is reproducible (R.S.D. < 2%), linear (r2 = 0.9999) and accurate (within 98-102% recovery), with a lower detection limit of 2.5 ng.
|Uncontrolled Keywords:||Benzodiazepine; Development; HPLC assay; NMR; NSC 694501; SJG-136; Validation; Water adducts|
|Departments, units and centres:||Department of Pharmaceutical and Biological Chemistry > Department of Pharmaceutical and Biological Chemistry|
|Journal or Publication Title:||Journal of Chromatography B|
|Deposited By:||Library Staff|
|Deposited On:||08 Mar 2012 10:42|
|Last Modified:||08 Mar 2012 10:42|
Item downloaded times since 08 Mar 2012 10:42.
Repository Staff Only: Item control page
School of Pharmacy Staff Only: Edit a copy to replace this item