Citation

Geng L, Han L, Huang L, Wu Z, Wu Z, et al. (2019) High Anti-Acid Omeprazole Lightweight Capsule for Gastro-Enteric System Acid-Related Disorders Treatment. J Clin Gastroenterol Treat 5:068. doi.org/10.23937/2469-584X/1510068

Copyright

© 2019 Geng L, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

RESEARCH ARTICLE | OPEN ACCESS DOI: 10.23937/2469-584X/1510068

High Anti-Acid Omeprazole Lightweight Capsule for Gastro-Enteric System Acid-Related Disorders Treatment

Longjian Geng1, Lidong Han1, Lulu Huang2, Ziheng Wu3, Zhenghong Wu1* and Xiaole Qi1*

1Key Laboratory of Modern Chinese Medicines, China Pharmaceutical University, Nanjing, PR China

2National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention; WHO Collaborating Centre for Tropical Diseases; National Center for International Research on Tropical Diseases, Ministry of Science and Technology; Key Laboratory of Parasite and Vector Biology, Ministry of Health, Shanghai, PR China

3Parkville campus, Monash University, Australia

Abstract

Background and aim

Utilization of diverse anti-acid materials is necessary for the preparation of compound omeprazole capsules. However, to gain the satisfied anti-acid effect, use of large amount of anti-acids is always difficult to swallow. This study aimed to develop a lightweight compound omeprazole capsule which could achieve immediately drug releasing with high anti-acid ability in stomach.

Methods

Omeprazole was encapsulated in β-cyclodextrin to improve the drug solubility and stability. The influence of different factors on the efficiency of the drug encapsulation was investigated. In addition, the omeprazole inclusions were assessed by Fourier transform-infrared spectroscopy, differential scanning calorimeter, and X-ray diffraction. Finally, anti-acids materials such as magnesium oxide (MgO) and sodium bicarbonate (NaHCO3) were used to reduce the weight of the capsule contents.

Results

Compared to the market omeprazole capsule (ENCHENG®), the omeprazole compound capsule demonstrated significantly improved drug dissolution (the maximum release ratio was 95.42 ± 2.51%) in simulated gastric environment. Moreover, rabbit pharmacokinetics showed that the area under the plasma concentration-time curve (AUC0-t) was significantly increased to 54180.11 ± 6483.16 min•ng•mL-1 (p < 0.05), compared with that (39011.55 ± 6637.08 min•ng•mL-1) of the currently used capsules (ENCHENG®).

Conclusions

The light compound omeprazole capsule could be an effective and swallowable oral delivering system for Acid-Related Disorders.