Ajay Gupta’s scientific contributions

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Publications (1)


Figure 1: Dual delayed-release mechanism of dexlansoprazole facilitates sequential release of drug in 2 distinct phases. 33
Figure 2 (A and B): Results obtained on 5 th day subsequent to daily oral administrations of dexlansoprazole at a dosage of 60 mg, administered 30 min before meals/evening snack, are depicted. Panel A showcases average linear plasma concentration-time profiles, while panel B exhibits average intragastric pH measurements. In context of 24-hour temporal scale, x-axis delineates the interval spanning from 8:00 AM on morning of day 5 to 8:00 AM on day 6. Commencement and cessation of monitoring periods for each respective regimen are indicated by upward and downward-pointing arrows, respectively. For lunch, dinner, and snack regimens, data post 8:00 AM on day 6 have been transposed to the initial segment of the graphical representation. This alignment facilitates juxtaposition of mean 24-hour pH profiles of all four distinct regimens within a unified 24-hour visualization, thereby affording insight into diurnal influence of treatment on pH levels. 31
Summary of some important studies of dexlansoprazole.
Efficacy and safety of dexlansoprazole: a comprehensive review
  • Article
  • Full-text available

November 2023

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363 Reads

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2 Citations

International Journal of Research in Medical Sciences

C. C. Chaubal

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Sujit Chaudhury

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Dinesh Patil

Gastroesophageal reflux disease (GERD) remains prevalent in medical practice. Proton pump inhibitors (PPIs) are the primary treatment, yet limitations exist. Dexlansoprazole modified release (MR), an R-enantiomer of lansoprazole, offers high efficacy. Its dual release in the duodenum and small intestine yields two peak concentrations at different times (2- and 5-hours post-administration), ensuring the longest maintenance of drug concentration and proton pump inhibitory effect among all PPIs. Dexlansoprazole MR effectively heals erosive esophagitis, maintains healed esophageal mucosa, and controls NERD symptoms. It also improves nocturnal heartburn, GERD-related sleep disturbances, and bothersome regurgitation. Importantly, it maintains good plasma concentration regardless of food intake, enabling flexible dosing. Furthermore, it does not significantly affect clopidogrel metabolism or platelet inhibition, eliminating the need for dose adjustments when co-prescribed. This review highlights dexlansoprazole's unique attributes, pharmacokinetics, advantages, and safety in comparison to traditional PPIs.

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Citations (1)


... In contrast to other PPIs, dexlansoprazole is available in capsule form with a dual delayed-release mechanism [25,26]. Dexlansoprazole possesses a distinctive capability to release its active ingredient in both the duodenum and the small intestine, rendering it a dual-release agent [27]. After consumption, dexlansoprazole is released twice: first within one to two hours and again four to five hours later [28]. ...

Reference:

Comparative Efficacy of Dexlansoprazole, Pantoprazole, Esomeprazole, and Rabeprazole in Achieving Optimal 24-Hour Intragastric pH Control: A Randomized Crossover Study Using Ambulatory pH Monitoring
Efficacy and safety of dexlansoprazole: a comprehensive review

International Journal of Research in Medical Sciences