Literature DB >> 34159427

Effect of Elevated pH on the Commercial Enteric-Coated Omeprazole Pellets Resistance: Patent Review and Multisource Generics Comparison.

Valentyn Mohylyuk1, Anna Yerkhova2, Marina Katynska2, Vitaliy Sirko3, Kavil Patel4.   

Abstract

Omeprazole is a widely used over-the-counter (20 mg) proton pump inhibitor, usually supplied as oral enteric-coated pellets intended to release at pH 5.5 and higher; however, it is sensitive to acidic pH. The likelihood of elevated gastric pH in practice is very high for patients; thus, the aim of this study was to investigate the effect of elevated pH on the performance of commercial omeprazole pellets. Commercial enteric-coated delayed-release pellets were tested with water uptake-weight loss (WU-WL) test at pH range between 1.2 and 4.5 in addition to "gastric" (pH 1.2 or 4.5) and "intestinal" (pH 7.4) phase dissolution tests. The range of physical characteristics of pellets was determined with a single pellet size and sedimentation time measurement, followed by the application of modified Stokes' Law equation. The coefficient of variation of pellet size and density, and volume-density determination coefficient (R2) as descriptors of coating thickness and microstructure variability, degree of ionisation of enteric polymers, aqueous solubility and molecular weight of plasticisers have been found useful to explain commercial delayed-release pellets behaviour during WU-WL and dissolution test. Investigated commercial delayed-release pellets demonstrated pH-dependent WU-WL results. "Gastric phase" dissolution testing of pellets at pH 4.5 showed the highest omeprazole degradation (48.1%) for Nosch Labs, intermediate values of dose loss (23.4% and 17.1%) for Teva and UQUIFA delayed-release pellets, respectively. Lab Liconsa pellets have been found as the least susceptible (3.2% of dose loss). Additionally, "gastric phase" dissolution test at pH 4.5 significantly influenced omeprazole release during the "intestinal phase". The risk of inadequate therapy associated with intake of investigated enteric-coated delayed-release pellets at elevated gastric pH has been found as minimal for Lab Liconsa and has increased from UQUIFA and Teva to Nosh Labs pellets.

Entities:  

Keywords:  delayed-release; enteric-coated; generic; microstructure; omeprazole; pellets

Mesh:

Substances:

Year:  2021        PMID: 34159427     DOI: 10.1208/s12249-021-02038-2

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   3.246


  23 in total

1.  Dissolution of omeprazole from delayed-release solid oral dosage forms.

Authors:  A Farinha; A Bica; J M Martins; J P Pais
Journal:  Drug Dev Ind Pharm       Date:  2000-07       Impact factor: 3.225

2.  Generic omeprazole delayed-release capsules: in vitro performance evaluations.

Authors:  Terry Moore; Anjanette Smith; Wei Ye; Duckhee Y Toler; Benjamin J Westenberger; Robert Lionberger; Andre Raw; Lawrence Yu; Lucinda F Buhse
Journal:  Drug Dev Ind Pharm       Date:  2009-08       Impact factor: 3.225

3.  In vitro evaluation of dissolution properties and degradation products of omeprazole in enteric-coated pellets.

Authors:  S Storpirtis; D Rodrigues
Journal:  Drug Dev Ind Pharm       Date:  1998-11       Impact factor: 3.225

4.  Acid-suppressive efficacy of a reduced dosage of rabeprazole: comparison of 10 mg twice daily rabeprazole with 20 mg twice daily rabeprazole, 30 mg twice daily lansoprazole, and 20 mg twice daily omeprazole by 24-hr intragastric pH-metry.

Authors:  Tomohiko Shimatani; Masaki Inoue; Tomoko Kuroiwa; Jing Xu; Susumu Tazuma; Yoko Horikawa; Masuo Nakamura
Journal:  Dig Dis Sci       Date:  2005-07       Impact factor: 3.199

5.  Stereoselective metabolism of omeprazole by human cytochrome P450 enzymes.

Authors:  A Abelö; T B Andersson; M Antonsson; A K Naudot; I Skånberg; L Weidolf
Journal:  Drug Metab Dispos       Date:  2000-08       Impact factor: 3.922

6.  Degradation of omeprazole induced by enteric polymer solutions and aqueous dispersions: HPLC investigations.

Authors:  A Riedel; C S Leopold
Journal:  Drug Dev Ind Pharm       Date:  2005-01       Impact factor: 3.225

7.  Quantification of omeprazole degradation by enteric coating polymers: an UV-VIS spectroscopy study.

Authors:  A Riedel; C S Leopold
Journal:  Pharmazie       Date:  2005-02       Impact factor: 1.267

8.  Toward Biopredictive Dissolution for Enteric Coated Dosage Forms.

Authors:  J Al-Gousous; G L Amidon; P Langguth
Journal:  Mol Pharm       Date:  2016-05-10       Impact factor: 4.939

9.  Development of a pH-responsive drug delivery system for enantioselective-controlled delivery of racemic drugs.

Authors:  Roongnapa Suedee; Chutima Jantarat; Wolfgang Lindner; Helmut Viernstein; Sarunyoo Songkro; Teerapol Srichana
Journal:  J Control Release       Date:  2009-10-23       Impact factor: 9.776

Review 10.  Pharmacokinetics of intravenous omeprazole in critically ill paediatric patients.

Authors:  Maria Jose Solana; Jesús López-Herce
Journal:  Eur J Clin Pharmacol       Date:  2009-12-30       Impact factor: 2.953

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  1 in total

1.  Somatostatin plus Gastroscopic Administration of Omeprazole for the Treatment of Acute Upper Gastrointestinal Bleeding: An Exploration of a Promising Alternative.

Authors:  Lu Feng; Jing Fu
Journal:  Evid Based Complement Alternat Med       Date:  2022-07-04       Impact factor: 2.650

  1 in total

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