Structure‐retention relationship for enantioseparation of selected fluoroquinolones. Issue 6 (6th April 2018)

• Record Type: Journal Article
• Authors: Hassan, Rasha M.; Yehia, Ali M.; Saleh, Ola A.; El‐Azzouny, Aida A.; Aboul‐Enein, Hassan Y.
• Is Part Of: Chirality. Volume 30:Issue 6(2018)
• Page Start: 828
• Page End: 836
• Publication Date: 2018-04-06
• Subjects: chiral chromatography -- experimental design -- fluoroquinolones -- structure‐retention relationship; Chirality -- Periodicals; Pharmaceutical chemistry -- Periodicals; 541.22
• DOI: 10.1002/chir.22861
• Languages: English
• ISSNs: 0899-0042

Abstract

Abstract: Fluoroquinolones are popular class of antibiotics with distinct chemical functionality. Most of them are ampholytes with one chiral center. Stereogeneic center is located either in the side ring of Gatifloxacin (GFLX) or in the quinolone core of Ofloxacin (OFLX). These two amphoteric fluoroquinolones have terminal amino groups in common. The unusual Nadifloxacin (NFLX) is an acidic fluoroquinolone with a core chiral center. Owing to chirality and functionality differences among GFLX, OFLX, and NFLX, we mapped these enantiomers onto structure‐retention relationship. Amount of acetic acid modifier was studied in screened mobile phase and cellulose tris(3‐chloro‐4‐methyl phenyl carbamate) (Lux cellulose‐2) stationary phase. Experimental design of acetic acid% along with column temperature have been applied. Resolution and enantioselectivity have been related to structural features of the studied enantiomers. High amount of acid (0.4%) was optimum for the separation of either side chirality with a proximate amino group (GFLX) or core chirality without basic functionality (NFLX), while low amount (0.2%) is optimum for core chiral center with distal amino group (OFLX). Temperature has no significant effect on resolution and retention of enantiomers except for OFLX. Enantio‐retention explains possible chiral selective and nonselective interactions. The proposed methods have been validated for pharmaceutical analyses. Abstract :