Helicobacter pylori: past, current and future treatment strategies with gastroretentive drug delivery systems
Helicobacter pylori have been subject to intense investigation since its discovery from gastric biopsy in 1982. This gastropathogen has been regarded as serious public health problem due to its association with dyspepsia, gastritis, gastroduodenal ulcers, mucus-associated lymphoid tissue lymphoma an...
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Published in | Journal of drug targeting Vol. 24; no. 10; pp. 897 - 915 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Taylor & Francis
25.11.2016
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Abstract | Helicobacter pylori have been subject to intense investigation since its discovery from gastric biopsy in 1982. This gastropathogen has been regarded as serious public health problem due to its association with dyspepsia, gastritis, gastroduodenal ulcers, mucus-associated lymphoid tissue lymphoma and gastric carcinoma. In vivo eradication of established H. pylori infections is difficult due to several factors such as gastric niche, coccoid form due to sub-minimum inhibitory concentration of antimicrobials, bacterial load, primary antibiotic resistance, patient compliance and stability of therapeutics in gastric acid secretion. Considering these factors, a logical way to improve the outcome of the treatment is to develop dosage forms which are able to deliver the anti-helicobacter agents in the gastric niche for both local and systemic actions, simultaneously taking care of stability of therapeutics in acidic environment. Such dosage forms, which are popularly known as gastro retentive drug delivery systems (GRDDS), have the immense potential to effectively counter the problem of high bacterial load; prevent induction of coccoid bacteria thereby improving treatment outcome and compliance. This review describes efficacy of various therapeutic agents, treatment strategies and status of different GRDDS until now. |
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AbstractList | Helicobacter pylori have been subject to intense investigation since its discovery from gastric biopsy in 1982. This gastropathogen has been regarded as serious public health problem due to its association with dyspepsia, gastritis, gastroduodenal ulcers, mucus-associated lymphoid tissue lymphoma and gastric carcinoma. In vivo eradication of established H. pylori infections is difficult due to several factors such as gastric niche, coccoid form due to sub-minimum inhibitory concentration of antimicrobials, bacterial load, primary antibiotic resistance, patient compliance and stability of therapeutics in gastric acid secretion. Considering these factors, a logical way to improve the outcome of the treatment is to develop dosage forms which are able to deliver the anti-helicobacter agents in the gastric niche for both local and systemic actions, simultaneously taking care of stability of therapeutics in acidic environment. Such dosage forms, which are popularly known as gastro retentive drug delivery systems (GRDDS), have the immense potential to effectively counter the problem of high bacterial load; prevent induction of coccoid bacteria thereby improving treatment outcome and compliance. This review describes efficacy of various therapeutic agents, treatment strategies and status of different GRDDS until now. |
Author | Hegde, Rahul Rama Dubey, Juhi Verma, Anurag Rastogi, Vaibhav Pandit, J. K. |
Author_xml | – sequence: 1 givenname: Anurag surname: Verma fullname: Verma, Anurag email: anuragverma_iftm@yahoo.co.in, rahulhpharma@gmail.com organization: Department of Pharmaceutics, College of Pharmacy, IFTM – sequence: 2 givenname: Juhi surname: Dubey fullname: Dubey, Juhi organization: Department of Pharmaceutics, College of Pharmacy, IFTM – sequence: 3 givenname: Rahul Rama surname: Hegde fullname: Hegde, Rahul Rama email: anuragverma_iftm@yahoo.co.in, rahulhpharma@gmail.com organization: Department of Quality Assurance, Lupin Ltd, Verna – sequence: 4 givenname: Vaibhav surname: Rastogi fullname: Rastogi, Vaibhav organization: Department of Pharmaceutics, College of Pharmacy, IFTM – sequence: 5 givenname: J. K. surname: Pandit fullname: Pandit, J. K. organization: Department of Pharmaceutics, Institute of Technology, Banaras Hindu University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27027827$$D View this record in MEDLINE/PubMed |
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Snippet | Helicobacter pylori have been subject to intense investigation since its discovery from gastric biopsy in 1982. This gastropathogen has been regarded as... |
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SubjectTerms | Adhesive systems Antacids - administration & dosage Antacids - pharmacokinetics Antacids - therapeutic use Anti-Bacterial Agents - administration & dosage Anti-Bacterial Agents - pharmacokinetics Anti-Bacterial Agents - therapeutic use Drug Delivery Systems - methods Drug Resistance, Multiple, Bacterial Drug Therapy, Combination Gastric Mucosa - drug effects Gastric Mucosa - metabolism Gastric Mucosa - microbiology GRDDS H. pylori Helicobacter Infections - drug therapy Helicobacter Infections - microbiology Helicobacter pylori - drug effects Humans in situ gelling systems polymeric rafts Proton Pump Inhibitors - administration & dosage Proton Pump Inhibitors - pharmacokinetics Proton Pump Inhibitors - therapeutic use |
Title | Helicobacter pylori: past, current and future treatment strategies with gastroretentive drug delivery systems |
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