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Amoxicillin and Clarithromycin Mucoadhesive Delivery System for Helicobacter pylori Infection in a Mouse Model: Characterization, Pharmacokinetics, and Efficacy

Helicobacter pylori is the main pathogen responsible for gastric ulcers and a predisposing factor of stomach cancer. Although current treatment is usually successful, it requires high doses and frequent administration. An innovative mucoadhesive system (Mucolast(®)) loaded with amoxicillin and clari...

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Autores principales: Villegas, Isabel, Rosillo, María Ángeles, Alarcón-de-la-Lastra, Catalina, Vázquez-Román, Victoria, Llorente, Maria, Sánchez, Susana, Gil, Ana Gloria, Alcalde, Pilar, González, Esther, Rosell, Elisabet, Nieto, Carles, Fernandez-Campos, Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911155/
https://www.ncbi.nlm.nih.gov/pubmed/33498958
http://dx.doi.org/10.3390/pharmaceutics13020153
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author Villegas, Isabel
Rosillo, María Ángeles
Alarcón-de-la-Lastra, Catalina
Vázquez-Román, Victoria
Llorente, Maria
Sánchez, Susana
Gil, Ana Gloria
Alcalde, Pilar
González, Esther
Rosell, Elisabet
Nieto, Carles
Fernandez-Campos, Francisco
author_facet Villegas, Isabel
Rosillo, María Ángeles
Alarcón-de-la-Lastra, Catalina
Vázquez-Román, Victoria
Llorente, Maria
Sánchez, Susana
Gil, Ana Gloria
Alcalde, Pilar
González, Esther
Rosell, Elisabet
Nieto, Carles
Fernandez-Campos, Francisco
author_sort Villegas, Isabel
collection PubMed
description Helicobacter pylori is the main pathogen responsible for gastric ulcers and a predisposing factor of stomach cancer. Although current treatment is usually successful, it requires high doses and frequent administration. An innovative mucoadhesive system (Mucolast(®)) loaded with amoxicillin and clarithromycin is proposed to improve the efficacy of treatment against H. pylori. The drug product was optimized based on its viscoelastic properties to obtain long-term stability of the vehicle. The drug release mechanisms were different for both antibiotics based on their solubilization status. A systemic and stomach pharmacokinetic profile was obtained after three different doses were administered to mice, obtaining similar systemic exposure levels but an increase in drug concentration in the stomach. The efficacy results in mice infected with H. pylori also demonstrated the superiority of the antibiotics when administered in Mucolast(®), as shown by the bacterial count in stomach tissue and under histopathological and biochemical evaluation. The proposed treatment was efficacious and safe and is presented as a realistic alternative to current treatment options to improve patient compliance and to reduce bacterial resistance.
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spelling pubmed-79111552021-02-28 Amoxicillin and Clarithromycin Mucoadhesive Delivery System for Helicobacter pylori Infection in a Mouse Model: Characterization, Pharmacokinetics, and Efficacy Villegas, Isabel Rosillo, María Ángeles Alarcón-de-la-Lastra, Catalina Vázquez-Román, Victoria Llorente, Maria Sánchez, Susana Gil, Ana Gloria Alcalde, Pilar González, Esther Rosell, Elisabet Nieto, Carles Fernandez-Campos, Francisco Pharmaceutics Article Helicobacter pylori is the main pathogen responsible for gastric ulcers and a predisposing factor of stomach cancer. Although current treatment is usually successful, it requires high doses and frequent administration. An innovative mucoadhesive system (Mucolast(®)) loaded with amoxicillin and clarithromycin is proposed to improve the efficacy of treatment against H. pylori. The drug product was optimized based on its viscoelastic properties to obtain long-term stability of the vehicle. The drug release mechanisms were different for both antibiotics based on their solubilization status. A systemic and stomach pharmacokinetic profile was obtained after three different doses were administered to mice, obtaining similar systemic exposure levels but an increase in drug concentration in the stomach. The efficacy results in mice infected with H. pylori also demonstrated the superiority of the antibiotics when administered in Mucolast(®), as shown by the bacterial count in stomach tissue and under histopathological and biochemical evaluation. The proposed treatment was efficacious and safe and is presented as a realistic alternative to current treatment options to improve patient compliance and to reduce bacterial resistance. MDPI 2021-01-24 /pmc/articles/PMC7911155/ /pubmed/33498958 http://dx.doi.org/10.3390/pharmaceutics13020153 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Villegas, Isabel
Rosillo, María Ángeles
Alarcón-de-la-Lastra, Catalina
Vázquez-Román, Victoria
Llorente, Maria
Sánchez, Susana
Gil, Ana Gloria
Alcalde, Pilar
González, Esther
Rosell, Elisabet
Nieto, Carles
Fernandez-Campos, Francisco
Amoxicillin and Clarithromycin Mucoadhesive Delivery System for Helicobacter pylori Infection in a Mouse Model: Characterization, Pharmacokinetics, and Efficacy
title Amoxicillin and Clarithromycin Mucoadhesive Delivery System for Helicobacter pylori Infection in a Mouse Model: Characterization, Pharmacokinetics, and Efficacy
title_full Amoxicillin and Clarithromycin Mucoadhesive Delivery System for Helicobacter pylori Infection in a Mouse Model: Characterization, Pharmacokinetics, and Efficacy
title_fullStr Amoxicillin and Clarithromycin Mucoadhesive Delivery System for Helicobacter pylori Infection in a Mouse Model: Characterization, Pharmacokinetics, and Efficacy
title_full_unstemmed Amoxicillin and Clarithromycin Mucoadhesive Delivery System for Helicobacter pylori Infection in a Mouse Model: Characterization, Pharmacokinetics, and Efficacy
title_short Amoxicillin and Clarithromycin Mucoadhesive Delivery System for Helicobacter pylori Infection in a Mouse Model: Characterization, Pharmacokinetics, and Efficacy
title_sort amoxicillin and clarithromycin mucoadhesive delivery system for helicobacter pylori infection in a mouse model: characterization, pharmacokinetics, and efficacy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911155/
https://www.ncbi.nlm.nih.gov/pubmed/33498958
http://dx.doi.org/10.3390/pharmaceutics13020153
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