Technical Advances in the Chiral Separation of Anti-diabetic Drugs Using Analytical and Bio-analytical Methods: A Comprehensive Review

被引:3
作者
Spandana, Tatineni [1 ]
Beeraka, Narasimha Murthy [2 ,3 ]
Vikram, Poola R. Hemanth [1 ]
Goli, Veera Venkata Nishanth [1 ]
Sri, Chiriki Devi [1 ]
Gurupadayya, Bannimath [1 ]
机构
[1] JSS Acad Higher Educ & Res, JSS Coll Pharm, Dept Pharmaceut Chem, Mysuru 570015, Karnataka, India
[2] JSS Acad Higher Educ & Res, Ctr Excellence Regenerat Med & Mol Biol CEMR, Dept Biochem, Mysuru 570015, Karnataka, India
[3] IM Sechenov First Moscow State Med Univ, Sechenov Univ, Kashiwa, Moscow 119146, Russia
关键词
Antidiabetic drugs; chiral; capillary electrophoresis (CE); high-performance liquid chromatography (HPLC); micellarelectrokinetic capillary chromatography (MEKC); liquid chromatography-mass sp ectroMETRY (LC-MS); gas chromatography (GC); PREPARATIVE GAS-CHROMATOGRAPHY; COUNTERCURRENT CHROMATOGRAPHY; CAPILLARY-ELECTROPHORESIS; PHARMACEUTICAL FORMULATIONS; ENANTIOMERIC SEPARATION; LC METHOD; NATEGLINIDE; PHARMACOKINETICS; ROSIGLITAZONE; REPAGLINIDE;
D O I
10.2174/1573411018666220820101237
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Chirality seems to be a pivotal technique in the field of science. Research teams are quite well versed in empirical separation, however, at the same time, they are clueless about the evolution of chiral separation. As per the guidelines of the United States Food and Drug Administration (US FDA), chiral drugs must be unraveled before they are sold to the public. Stereogenic separation has gained prominence during the last 10 decades due to the disparate biological function of enantiomers in the stereogenic environment. Chiral drugs exhibit a wide range of bioavailability, distribution, and pharmacodynamic properties; concomitantly, they exert divergent pharmacological and toxicological properties. Enantiomeric chiral products could be considered safe and potent in combating various diseases, including metabolic diseases like diabetes. Several studies have delineated the development of a novel analytical and bioanalytical method to detect/segregate/quantify chiral chemical components in medicinal chemistry. The same physicochemical characteristics of enantiomers have been proven to be beneficial to the estrangement of stereogenic compounds. Furthermore, the advancement of bioanalytical methods is also critical to shedding light on the destiny of distinct enantiomers in the biological environment. HPLC (High-Performance Liquid Chromatography) and CE (Capillary Electrophoresis) have been the most commonly employed separation techniques. But the technical advances are required to enhance the efficiency of detection and quantification of chiral molecules on a large scale. With technical advances, the current review delineates the need for the chiral separation of stereogenic antidiabetic drug compounds. Furthermore, this research is focused on the enantioseparation of chiral antidiabetic drugs and a brief overview of the analytical and bioanalytical methods conducted on distant chiral antidiabetic drugs to improve the efficiency of chiral separation.
引用
收藏
页码:1057 / 1069
页数:13
相关论文
共 66 条
[1]  
Adachi K., UNDERSTANDING CONDIT
[2]  
Amer Diabet Assoc, 2005, DIABETES CARE, V28, pS37
[3]   Chiral separation of pharmaceuticals possessing a carboxy moiety [J].
Arai, T .
JOURNAL OF CHROMATOGRAPHY B, 1998, 717 (1-2) :295-311
[4]   Simultaneous Chiral Separation of Geometry Isomers and Enantiomers of Nateglinide by Capillary Electrophoresis with Mixture of CD Derivations as Chiral Selector [J].
Bao-hui, Li ;
Bao-juan, Tian ;
Yun-kai, Lv .
ANALYTICAL LETTERS, 2008, 41 (17) :3177-3186
[5]  
Bastaki S., 2005, Int J. Diabetes Metab., V13, P111, DOI DOI 10.1159/000497580
[6]   Countercurrent chromatography: People and applications [J].
Berthod, A. ;
Ruiz-Angel, M. J. ;
Carda-Broch, S. .
JOURNAL OF CHROMATOGRAPHY A, 2009, 1216 (19) :4206-4217
[7]   COUNTERCURRENT CHROMATOGRAPHY IN ANALYTICAL CHEMISTRY (IUPAC Technical Report) [J].
Berthod, Alain ;
Maryutina, Tatyana ;
Spivakov, Boris ;
Shpigun, Oleg ;
Sutherland, Ian A. .
PURE AND APPLIED CHEMISTRY, 2009, 81 (02) :355-387
[8]   What's new in chromatographic enantioseparations [J].
Bojarski, J ;
Aboul-Enein, HY ;
Ghanem, A .
CURRENT ANALYTICAL CHEMISTRY, 2005, 1 (01) :59-77
[9]   Drug disposition in three dimensions: An update on stereoselectivity in pharmacokinetics [J].
Brocks, Dion R. .
BIOPHARMACEUTICS & DRUG DISPOSITION, 2006, 27 (08) :387-406
[10]  
Brown T., 2015, 10 MOST PRESCRIBED T