HPLC enantio-separation and chiral recognition mechanism of quinolones on vancomycin CSP

被引:17
作者
ALOthman, Zeid A. [1 ]
ALanazi, Abdullah G. [1 ]
Suhail, Mohd [2 ]
Ali, Imran [2 ,3 ]
机构
[1] King Saud Univ, Coll Sci, Dept Chem, POB 2455, Riyadh 11451, Saudi Arabia
[2] Jamia Millia Islamia, Dept Chem, New Delhi 110025, India
[3] Taibah Univ, Coll Sci, Dept Chem, Al Medina Al Munawara 41477, Saudi Arabia
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2020年 / 1157卷
关键词
Chiral recognition mechanism; Enantio-separation; Quinolones; Vancomycin; PERFORMANCE LIQUID-CHROMATOGRAPHY; STATIONARY PHASES; CAPILLARY-ELECTROPHORESIS; DRUGS; RESOLUTION; OFLOXACIN; ENANTIOSEPARATION; SULCONAZOLE; MICONAZOLE; NEBIVOLOL;
D O I
10.1016/j.jchromb.2020.122335
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new HPLC method was developed for the enantio-separation and chiral recognition mechanism of quinolones (lomefloxacine, ofloxacine, primaquine and quinacrine) on Vancomycin CSP. The column used was Chirabiotic V column (150 x 4.6 mm, 5.0 mu m) with two mobile phases i.e. (I) MeOH:ACN:H2O:TEA (50:30:20:0.1%) and (II) MeOH:ACN: H2O:TEA (70:10:20:0.1%) at 1.0 mL/minute flow rate with various UV detection. The values of retention, separation and resolution factors in a solvent system I were ranged from 2.20 to 5.05, 1.70 to 1.96 and 1.75 to 2.20 while these values were 1.93 to 6.85, 1.62 & 2.01 and 2.30 & 2.40 in solvent system II. The limits of detection and quantification were ranged from 8.0 to 10.5 mu g and 24.4 to 33.5 mu g. The resolution was controlled mainly by pi-pi interactions along with other forces like hydrogen bonding, van der Waal's forces, steric effects, etc. The determination of the chiral recognition mechanism may be beneficial to separate other racemates successfully. The method is fast precise and efficient and may be utilized to analyze enantiomers of the reported quinolones.
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页数:7
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