Determination of the stoichiometry between a drug and its counter-ion by supercritical fluid chromatography using ultra-violet and evaporative light scattering detections: Application to ondansetron hydrochloride

被引:9
作者
Bouchot, Pauline [1 ]
Foulon, Catherine [1 ]
Lecoeur, Marie [1 ]
机构
[1] Univ Lille, Grp Rech Formes Injectables & Technol Associees, GRITA, CHU Lille,ULR 7365, F-59000 Lille, France
关键词
Evaporative light scattering detector (ELSD); 2-Ethylpyridine stationary phase (2-EP); Ondansetron hydrochloride; Stoichiometry; Supercritical fluid chromatography (SFC); MASS-SPECTROMETRIC DETECTION; ULTRAVIOLET ABSORBENCY; SELECTION;
D O I
10.1016/j.talanta.2020.121166
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this paper, a supercritical fluid chromatography method using ultra-violet and evaporative light scattering detections (SFC-UV/ELSD) has been developed and validated for the stoichiometry determination of an anticmetic drug with its counter-ion i.e. ondansetron hydrochloride. Seven stationary phases were first screened using a CO2-methanol-diethylamine mobile phase. Best conditions were determined using Derringer's desirability functions regarding chromatographic separation: selectivity, resolution, peak shape and runtime. The influence of co-solvent composition on resolution was evaluated. After optimization, best chromatographic results were obtained using 2-ethylpyridine stationary phase and a co-solvent composed of 0.2% diethylamine and 2% water in methanol. While ondansetron was quantified using UV detection (214 nm) and an external calibration curve, the determination of chloride was carried out using ELSD and an internal calibration curve. Then, the method was validated using the accuracy profile approach with a total error included in the +/- 10%. Finally, the proposed method was applied for the determination of the molar ratio between ondansetron and chloride. A value of 1.001 +/- 0.003 demonstrated that the stoichiometry of this drug with its counter-ion was 1:1.
引用
收藏
页数:9
相关论文
共 23 条
[1]   QUANTITATIVE-DETERMINATION OF DRUG COUNTERION STOICHIOMETRY BY CAPILLARY ELECTROPHORESIS [J].
ALTRIA, KD ;
GOODALL, DM ;
ROGAN, MM .
CHROMATOGRAPHIA, 1994, 38 (9-10) :637-642
[2]  
[Anonymous], 1996, VAL AN PROC METH Q2B
[3]  
Bosch Maria Espinosa, 2009, Curr Drug Discov Technol, V6, P214
[4]   Emerging Analytical Separation Techniques with High Throughput Potential for Pharmaceutical Analysis, Part II: Novel Chromatographic Modes [J].
Dejaegher, Bieke ;
Pieters, Sigrid ;
Heyden, Yvan Vander .
COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING, 2010, 13 (06) :530-547
[5]   Evaluation of innovative stationary phase ligand chemistries and analytical conditions for the analysis of basic drugs by supercritical fluid chromatography [J].
Desfontaine, Vincent ;
Veuthey, Jean-Luc ;
Guillarme, Davy .
JOURNAL OF CHROMATOGRAPHY A, 2016, 1438 :244-253
[6]   Supercritical fluid chromatography in pharmaceutical analysis [J].
Desfontaine, Vincent ;
Guillarme, Davy ;
Francotte, Eric ;
Novakova, Lucie .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2015, 113 :56-71
[7]   Screening study of SFC critical method parameters for the determination of pharmaceutical compounds [J].
Dispas, Amandine ;
Lebrun, Pierre ;
Sacre, Pierre-Yves ;
Hubert, Philippe .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2016, 125 :339-354
[8]   Simultaneous determination of inorganic anions and cations by supercritical fluid chromatography using evaporative light scattering detection [J].
Foulon, Catherine ;
Di Giulio, Pauline ;
Lecoeur, Marie .
JOURNAL OF CHROMATOGRAPHY A, 2018, 1534 :139-149
[9]   A HILIC method for the analysis of tromethamine as the counter ion in an investigational pharmaceutical salt [J].
Guo, Y ;
Huang, AH .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2003, 31 (06) :1191-1201
[10]   The use of ammonium hydroxide as an additive in supercritical fluid chromatography for achiral and chiral separations and purifications of small, basic medicinal molecules [J].
Hamman, Chris ;
Schmidt, Donald E., Jr. ;
Wong, Mengling ;
Hayes, Michael .
JOURNAL OF CHROMATOGRAPHY A, 2011, 1218 (43) :7886-7894