Literature DB >> 15080761

Single-isomer drugs: true therapeutic advances.

Tommy Andersson1.   

Abstract

Chirality is one of the main features of biology, and many of the processes essential for life are stereospecific, meaning that one out of two or more isomers may work best in a particular physiological situation. Could this be used in drug development and result in any clinical relevance and true therapeutic advance? There are occasions when the development of one of the isomers might be expected to be advantageous: for example, only one of the isomers may be active, only one of the isomers may cause adverse effects, or one of the isomers may have more advantageous pharmacological properties. As an example of the last, the successful development of esomeprazole will be described. Before the introduction of esomeprazole, the proton pump inhibitor omeprazole was the standard treatment for gastric acid-related diseases, such as gastro-oesophageal reflux disease. A serious type of gastro-oesophageal reflux disease is erosive oesophagitis, an increasingly common condition that may lead to life-threatening complications. Doubling the standard dose of omeprazole from 20 to 40 mg did not improve healing rates (74% versus 75%), and thus a substantial proportion of patients remained unhealed with standard treatment. The (S)-isomer of omeprazole, esomeprazole, was shown to heal more patients than omeprazole as a result of unique metabolic properties that clearly differentiates esomeprazole from omeprazole, the racemate. At comparable doses, these properties lead to several clinical advantages: higher bioavailability in extensive metabolisers (the majority of patients), lower exposure in poor metabolisers, less interindividual variation and a steeper dose-response curve at steady state resulting in a more pronounced inhibition of gastric acid secretion. Esomeprazole has been studied clinically for a variety of acid-related conditions, showing that the compound is as well tolerated and more effective with regard to healing and symptom relief than the recommended treatment with omeprazole. Thus, from this example it is clear that the exploration and development of single-isomer drugs may bring significant advances in treatment options.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15080761     DOI: 10.2165/00003088-200443050-00001

Source DB:  PubMed          Journal:  Clin Pharmacokinet        ISSN: 0312-5963            Impact factor:   6.447


  25 in total

1.  Effect of omeprazole treatment on diazepam plasma levels in slow versus normal rapid metabolizers of omeprazole.

Authors:  T Andersson; C Cederberg; G Edvardsson; A Heggelund; P Lundborg
Journal:  Clin Pharmacol Ther       Date:  1990-01       Impact factor: 6.875

2.  Double-blind comparison [correction of Double-blind, placebo-controlled comparison] of rabeprazole 20 mg vs. omeprazole 20 mg in the treatment of erosive or ulcerative gastro-oesophageal reflux disease. The European Rabeprazole Study Group.

Authors:  C P Dekkers; J A Beker; B Thjodleifsson; A Gabryelewicz; N E Bell; T J Humphries
Journal:  Aliment Pharmacol Ther       Date:  1999-01       Impact factor: 8.171

3.  Opposing time trends of peptic ulcer and reflux disease.

Authors:  H B el-Serag; A Sonnenberg
Journal:  Gut       Date:  1998-09       Impact factor: 23.059

4.  Esomeprazole improves healing and symptom resolution as compared with omeprazole in reflux oesophagitis patients: a randomized controlled trial. The Esomeprazole Study Investigators.

Authors:  P J Kahrilas; G W Falk; D A Johnson; C Schmitt; D W Collins; J Whipple; D D'Amico; B Hamelin; B Joelsson
Journal:  Aliment Pharmacol Ther       Date:  2000-10       Impact factor: 8.171

5.  Efficacy and safety of esomeprazole compared with omeprazole in GERD patients with erosive esophagitis: a randomized controlled trial.

Authors:  J E Richter; P J Kahrilas; J Johanson; P Maton; J R Breiter; C Hwang; V Marino; B Hamelin; J G Levine
Journal:  Am J Gastroenterol       Date:  2001-03       Impact factor: 10.864

Review 6.  Pharmacokinetics, metabolism and interactions of acid pump inhibitors. Focus on omeprazole, lansoprazole and pantoprazole.

Authors:  T Andersson
Journal:  Clin Pharmacokinet       Date:  1996-07       Impact factor: 6.447

7.  Appropriate acid suppression for the management of gastro-oesophageal reflux disease.

Authors:  N J Bell; D Burget; C W Howden; J Wilkinson; R H Hunt
Journal:  Digestion       Date:  1992       Impact factor: 3.216

8.  A double-blind study of pantoprazole and omeprazole in the treatment of reflux oesophagitis: a multicentre trial.

Authors:  J Mössner; A H Hölscher; R Herz; A Schneider
Journal:  Aliment Pharmacol Ther       Date:  1995-06       Impact factor: 8.171

9.  Efficacy and safety of lansoprazole in the treatment of erosive reflux esophagitis. The Lansoprazole Group.

Authors:  D O Castell; J E Richter; M Robinson; S J Sontag; M M Haber
Journal:  Am J Gastroenterol       Date:  1996-09       Impact factor: 10.864

10.  Identification of human liver cytochrome P450 isoforms mediating omeprazole metabolism.

Authors:  T Andersson; J O Miners; M E Veronese; W Tassaneeyakul; W Tassaneeyakul; U A Meyer; D J Birkett
Journal:  Br J Clin Pharmacol       Date:  1993-12       Impact factor: 4.335

View more
  10 in total

Review 1.  Optimising acid inhibition treatment.

Authors:  Fernando Gomollón; Xavier Calvet
Journal:  Drugs       Date:  2005       Impact factor: 9.546

Review 2.  Pharmacokinetics of proton pump inhibitors in children.

Authors:  Catherine Litalien; Yves Théorêt; Christophe Faure
Journal:  Clin Pharmacokinet       Date:  2005       Impact factor: 6.447

3.  Enantiomeric impurity analysis using circular dichroism spectroscopy with United States Pharmacopeia liquid chromatographic methods.

Authors:  Douglas Kirkpatrick; Margaret Fain; Jingyue Yang; Michael Trehy
Journal:  J Pharm Biomed Anal       Date:  2018-04-24       Impact factor: 3.935

Review 4.  Stereoselective disposition of proton pump inhibitors.

Authors:  Tommy Andersson; Lars Weidolf
Journal:  Clin Drug Investig       Date:  2008       Impact factor: 2.859

5.  Comparison of reversed-phase enantioselective HPLC methods for determining the enantiomeric purity of (S)-omeprazole in the presence of its related substances.

Authors:  Bruno Gallinella; Rosella Ferretti; Leo Zanitti; Isabella Sestili; Antonina Mosca; Roberto Cirilli
Journal:  J Pharm Anal       Date:  2015-11-06

6.  Pharmacokinetics of esomeprazole following intravenous and oral administration in healthy dogs.

Authors:  Emily K Cook; Nana Satake; Ben W Sykes; Emma L Bennett; Paul C Mills
Journal:  Vet Med (Auckl)       Date:  2016-08-31

7.  Design and efficient synthesis of pyrazoline and isoxazole bridged indole C-glycoside hybrids as potential anticancer agents.

Authors:  Priti Kumari; Vishnu S Mishra; Chintam Narayana; Ashish Khanna; Anindita Chakrabarty; Ram Sagar
Journal:  Sci Rep       Date:  2020-04-20       Impact factor: 4.379

8.  Engineering Saccharomyces cerevisiae for the production of dihydroquercetin from naringenin.

Authors:  Shiqin Yu; Mingjia Li; Song Gao; Jingwen Zhou
Journal:  Microb Cell Fact       Date:  2022-10-15       Impact factor: 6.352

9.  Unusual retention behavior of omeprazole and its chiral impurities B and E on the amylose tris (3-chloro-5-methylphenylcarbamate) chiral stationary phase in polar organic mode.

Authors:  Rosella Ferretti; Leo Zanitti; Adriano Casulli; Roberto Cirilli
Journal:  J Pharm Anal       Date:  2018-04-20

10.  Cyclic RGD-Decorated Liposomal Gossypol AT-101 Targeting for Enhanced Antitumor Effect.

Authors:  Hao Liu; Ruirui Zhang; Dan Zhang; Chun Zhang; Zhuo Zhang; Xiujuan Fu; Yu Luo; Siwei Chen; Ailing Wu; Weiling Zeng; Kunyan Qu; Hao Zhang; Sijiao Wang; Houyin Shi
Journal:  Int J Nanomedicine       Date:  2022-01-14
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.