Literature DB >> 16625655

Solid state interactions between the proton pump inhibitor omeprazole and various enteric coating polymers.

A Stroyer1, J W McGinity, C S Leopold.   

Abstract

The influence of the acidic film formers Eudragit L 100, HPMCAS-HF, HP-55, and shellac on the stability of the acid-labile proton pump inhibitor omeprazole in solid drug-polymer blends at accelerated storage conditions (40 degrees C/75% RH) was determined by fourier transform infrared spectroscopy (FTIR), modulated temperature differential scanning calorimetry (MTDSC), and high performance liquid chromatography (HPLC). As expected, acidic polymers caused a degradation of omeprazole which was manifested by discolorations and increasing amounts of degradation products. However, MTDSC curves and FTIR spectra did not show additional peaks resulting from the omeprazole degradation products. These methods appeared to be not sensitive enough to separate analytically the drug and polymer signals from those of the decomposition products. With HPLC a sufficient quantification of the degradation products was possible. HP-55 caused the highest degree of omeprazole degradation, followed by shellac, HPMCAS-HF, and Eudragit L 100. No correlation with the microenvironmental pH values generated by the acidic polymers at the applied storage conditions was found. The melting process and the dissolution of acidic impurities were figured out as possible reasons for the more pronounced decomposition of the drug in presence of HP-55 and shellac. (c) 2006 Wiley-Liss, Inc. and the American Pharmacists Association

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16625655     DOI: 10.1002/jps.20450

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  8 in total

1.  Solid-state interactions at the core-coat interface: physicochemical characterization of enteric-coated omeprazole pellets without a protective sub-coat.

Authors:  Vishnu Dutt Sharma; Suleyman Akocak; Marc A Ilies; Reza Fassihi
Journal:  AAPS PharmSciTech       Date:  2015-01-17       Impact factor: 3.246

Review 2.  Hot-Melt Extrusion: a Roadmap for Product Development.

Authors:  Marta F Simões; Rui M A Pinto; Sérgio Simões
Journal:  AAPS PharmSciTech       Date:  2021-06-17       Impact factor: 3.246

3.  A comprehensive development strategy in buccal drug delivery.

Authors:  Ana Figueiras; Alberto A C C Pais; Francisco J B Veiga
Journal:  AAPS PharmSciTech       Date:  2010-11-30       Impact factor: 3.246

4.  Influences of sodium carbonate on physicochemical properties of lansoprazole in designed multiple coating pellets.

Authors:  Wei He; Min Yang; Jun Hong Fan; Cai Xia Feng; Su Juan Zhang; Jin Xu Wang; Pei Pei Guan; Wei Wu
Journal:  AAPS PharmSciTech       Date:  2010-08-18       Impact factor: 3.246

5.  The role of L-arginine in inclusion complexes of omeprazole with cyclodextrins.

Authors:  Ana Figueiras; Jorge M G Sarraguça; Alberto A C C Pais; Rui A Carvalho; J Francisco Veiga
Journal:  AAPS PharmSciTech       Date:  2010-02-05       Impact factor: 3.246

6.  Enhanced dissolution and stability of lansoprazole by cyclodextrin inclusion complexation: preparation, characterization, and molecular modeling.

Authors:  Yi Lu; Tao Guo; Jianping Qi; Jiwen Zhang; Wei Wu
Journal:  AAPS PharmSciTech       Date:  2012-09-12       Impact factor: 3.246

7.  Eudragit L/HPMCAS blend enteric-coated lansoprazole pellets: enhanced drug stability and oral bioavailability.

Authors:  Yu Fang; Guozheng Wang; Rong Zhang; Zhihua Liu; Zhenghua Liu; Xiaohui Wu; Deying Cao
Journal:  AAPS PharmSciTech       Date:  2014-03-05       Impact factor: 3.246

Review 8.  Melt extrusion with poorly soluble drugs - An integrated review.

Authors:  Michael A Repka; Suresh Bandari; Venkata Raman Kallakunta; Anh Q Vo; Haley McFall; Manjeet B Pimparade; Ajinkya M Bhagurkar
Journal:  Int J Pharm       Date:  2017-11-02       Impact factor: 5.875

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.