TY - JOUR
T1 - Treatment of H. pylori infection and gastric ulcer
T2 - Need for novel Pharmaceutical formulation
AU - Gupta, Ashutosh
AU - Shetty, Shiran
AU - Mutalik, Srinivas
AU - Chandrashekar H, Raghu
AU - K, Nandakumar
AU - Mathew, Elizabeth Mary
AU - Jha, Abhishek
AU - Mishra, Brahmeshwar
AU - Rajpurohit, Siddheesh
AU - Ravi, Gundawar
AU - Saha, Moumita
AU - Moorkoth, Sudheer
N1 - Funding Information:
The work is funded by Indian Council of Medical Research , New Delhi, India. File no. 3/2/2/16/2022-NCD-III .
Funding Information:
The work is funded by Indian Council of Medical Research, New Delhi, India. File no. 3/2/2/16/2022-NCD-III.The authors are thankful to the Indian Council of Medical Research (ICMR) for the funding provided under the ICMR-SRF fellowship program. Authors are also grateful to Manipal Academy of Higher Education, Manipal, Karnataka for providing the facilities. The authors are thankful for Biorender.com, a figure-making tool.
Publisher Copyright:
© 2023
PY - 2023/10
Y1 - 2023/10
N2 - Peptic ulcer disease (PUD) is one of the most prevalent gastro intestinal disorder which often leads to painful sores in the stomach lining and intestinal bleeding. Untreated Helicobacter pylori (H. pylori) infection is one of the major reasons for chronic PUD which, if left untreated, may also result in gastric cancer. Treatment of H. pylori is always a challenge to the treating doctor because of the poor bioavailability of the drug at the inner layers of gastric mucosa where the bacteria resides. This results in ineffective therapy and antibiotic resistance. Current treatment regimens available for gastric ulcer and H. pylori infection uses a combination of multiple antimicrobial agents, proton pump inhibitors (PPIs), H2-receptor antagonists, dual therapy, triple therapy, quadruple therapy and sequential therapy. This polypharmacy approach leads to patient noncompliance during long term therapy. Management of H. pylori induced gastric ulcer is a burning issue that necessitates alternative treatment options. Novel formulation strategies such as extended-release gastro retentive drug delivery systems (GRDDS) and nanoformulations have the potential to overcome the current bioavailability challenges. This review discusses the current status of H. pylori treatment, their limitations and the formulation strategies to overcome these shortcomings. Authors propose here an innovative strategy to improve the H. pylori eradication efficiency.
AB - Peptic ulcer disease (PUD) is one of the most prevalent gastro intestinal disorder which often leads to painful sores in the stomach lining and intestinal bleeding. Untreated Helicobacter pylori (H. pylori) infection is one of the major reasons for chronic PUD which, if left untreated, may also result in gastric cancer. Treatment of H. pylori is always a challenge to the treating doctor because of the poor bioavailability of the drug at the inner layers of gastric mucosa where the bacteria resides. This results in ineffective therapy and antibiotic resistance. Current treatment regimens available for gastric ulcer and H. pylori infection uses a combination of multiple antimicrobial agents, proton pump inhibitors (PPIs), H2-receptor antagonists, dual therapy, triple therapy, quadruple therapy and sequential therapy. This polypharmacy approach leads to patient noncompliance during long term therapy. Management of H. pylori induced gastric ulcer is a burning issue that necessitates alternative treatment options. Novel formulation strategies such as extended-release gastro retentive drug delivery systems (GRDDS) and nanoformulations have the potential to overcome the current bioavailability challenges. This review discusses the current status of H. pylori treatment, their limitations and the formulation strategies to overcome these shortcomings. Authors propose here an innovative strategy to improve the H. pylori eradication efficiency.
UR - https://www.scopus.com/pages/publications/85172284805
UR - https://www.scopus.com/inward/citedby.url?scp=85172284805&partnerID=8YFLogxK
U2 - 10.1016/j.heliyon.2023.e20406
DO - 10.1016/j.heliyon.2023.e20406
M3 - Review article
AN - SCOPUS:85172284805
SN - 2405-8440
VL - 9
JO - Heliyon
JF - Heliyon
IS - 10
M1 - e20406
ER -