Analytical and semi‐preparative enantioresolution of (RS)‐ketorolac from pharmaceutical formulation and in human plasma by HPLC. (5th April 2016)

• Record Type: Journal Article
• Authors: Lal, Manohar; Bhushan, Ravi
• Is Part Of: Biomedical chromatography. Volume 30:Number 10(2016:Oct.)
• Page Start: 1526
• Page End: 1534
• Publication Date: 2016-04-05
• Subjects: (RS)‐ketorolac -- HPLC -- enantioresolution -- monochloro‐methylated cellulose and amylose CSP -- semi‐preparative; Chromatographic analysis -- Periodicals; Biology -- Periodicals; Medicine -- Periodicals; Biology -- Periodicals; Chromatography -- methods -- Periodicals; Medicine -- Periodicals; 543.089
• DOI: 10.1002/bmc.3716
• Languages: English
• ISSNs: 0269-3879

Abstract

Abstract: An efficient, simple, validated, analytical and semi‐preparative HPLC method has been developed for direct enantioresolution of ( RS )‐Ketorolac (Ket) using monochloro‐methylated derivatives of cellulose and amylose, i.e. cellulose (tris‐3‐chloro‐4‐methylphenylcarbamate) and amylose (tris‐5‐chloro‐2‐methylphenylcarbamate) as chiral stationary phases (CSPs) with photo diode array detection at 320 nm. Enantioresolution was carried out in samples of human plasma spiked with ( RS )‐Ket under normal and reversed‐phase elution modes with suitable mobile phase compositions. The effect of nature of alcohols (MeOH, EtOH, PrOH and n ‐BuOH) and other solvents (MeCN and MeOH) as organic modifiers in the mobile phase was investigated on the separation performance of two CSPs in terms of retention and separation of enantiomers. The best resolution was observed on cellulose‐based CSP using EtOH, while using 2‐PrOH (15%) and amylose‐based CSP obtained the highest retention. Under reversed‐phase elution mode the best enantioseparation was observed using 30% MeCN with ammonium formate buffer. The elution order of enantiomers was ascertained by determining specific rotations. The limit of detection and quantitation values were 5 and 15.5 ng/mL for each enantiomer of ( RS )‐Ket, respectively. Copyright © 2016 John Wiley & Sons, Ltd.