Clinical Implications of Proton Pump Inhibitors and Vonoprazan Micro/Nano Drug Delivery Systems for Gastric Acid-Related Disorders and Imaging

Nanotheranostics. 2024 Sep 30;8(4):535-560. doi: 10.7150/ntno.100727. eCollection 2024.

Abstract

Excessive stomach acid or bacterial infection are the root causes of gastric acid-related disorders, such as peptic ulcer disease and gastroesophageal reflux disease. Proton pump inhibitors including lansoprazole, omeprazole, esomeprazole, rabeprazole, etc. are medications used to treat gastric acid-related diseases. One of the most effective drugs for treating gastroesophageal reflux disease is vonoprazan, owing to its ability to strongly inhibit gastric acid. Proton pump inhibitors and vonoprazan work in distinct ways to prevent the production of stomach acid. Vonoprazan inhibits acid secretion by blocking the potassium-competitive acid blocker receptor, whereas proton pump inhibitors function by irreversibly blocking the proton pump in the parietal cells of the stomach. Delayed release tablets, delayed release capsules, minitablets, pellets, bilayer, floating, mucoadhesive tablets and nanoparticles, are some of the methods used in the development of micro/nano formulations with proton pump inhibitors and vonoprazan. Diagnosis and therapy of gastric acid-related illnesses, particularly those treated with drugs such as vonoprazan and proton pump inhibitors, rely heavily on imaging modalities such as CT scans, X-rays, endoscopy, fluorescence and HRM imaging. This review provides a comprehensive update on various micro/nanoformulations of proton pump inhibitors and vonoprazan. Moreover, we provide an outlook on clinical imaging of proton pump inhibitors and vonoprazan formulation for gastric acid related diseases. We have limited our discussion to case studies and clinical trials on proton pump inhibitors and vonoprazan for gastric acid related disease.

Keywords: Gastric acid related disease; case studies; clinical trials; imaging; proton pump inhibitors; vonoprazan.

Publication types

  • Review

MeSH terms

  • Animals
  • Drug Delivery Systems / methods
  • Gastric Acid* / metabolism
  • Gastroesophageal Reflux / drug therapy
  • Humans
  • Proton Pump Inhibitors* / chemistry
  • Proton Pump Inhibitors* / pharmacology
  • Pyrroles* / chemistry
  • Pyrroles* / pharmacology
  • Sulfonamides* / chemistry
  • Sulfonamides* / pharmacology

Substances

  • Proton Pump Inhibitors
  • Pyrroles
  • 1-(5-(2-fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl)-N-methylmethanamine
  • Sulfonamides