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Ground Calcium Carbonate as a Low Cost and Biosafety Excipient for Solubility and Dissolution Improvement of Praziquantel

Calcium carbonate is an abundant mineral with several advantages to be a successful carrier to improve oral bioavailability of poorly water-soluble drugs, such as praziquantel. Praziquantel is an antiparasitic drug classified in group II of the Biopharmaceutical Classification System hence character...

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Autores principales: Borrego-Sánchez, Ana, Sánchez-Espejo, Rita, Albertini, Beatrice, Passerini, Nadia, Cerezo, Pilar, Viseras, César, Sainz-Díaz, C. Ignacio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835254/
https://www.ncbi.nlm.nih.gov/pubmed/31615087
http://dx.doi.org/10.3390/pharmaceutics11100533
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author Borrego-Sánchez, Ana
Sánchez-Espejo, Rita
Albertini, Beatrice
Passerini, Nadia
Cerezo, Pilar
Viseras, César
Sainz-Díaz, C. Ignacio
author_facet Borrego-Sánchez, Ana
Sánchez-Espejo, Rita
Albertini, Beatrice
Passerini, Nadia
Cerezo, Pilar
Viseras, César
Sainz-Díaz, C. Ignacio
author_sort Borrego-Sánchez, Ana
collection PubMed
description Calcium carbonate is an abundant mineral with several advantages to be a successful carrier to improve oral bioavailability of poorly water-soluble drugs, such as praziquantel. Praziquantel is an antiparasitic drug classified in group II of the Biopharmaceutical Classification System hence characterized by high-permeability and low-solubility. Therefore, the dissolution rate is the limiting factor for the gastrointestinal absorption that contributes to the low bioavailability. Consequently, the therapeutic dose of the praziquantel must be high and big tablets and capsules are required, which are difficult to swallow, especially for pediatric and elderly patients. Mixtures of praziquantel and calcium carbonate using solid-solid physical mixtures and solid dispersions were prepared and characterized using several techniques (X-ray diffraction differential scanning calorimetry, thermogravimetric analysis, scanning electron microscopy, laser diffraction, Fourier transform infrared and Raman spectroscopies). Solubility of these formulations evidenced that the solubility of praziquantel-calcium carbonate interaction product increased in physiological media. In vitro dissolution tests showed that the interaction product increased the dissolution rate of the drug in acidic medium. Theoretical models were studied to understand this experimental behavior. Cytotoxicity and cell cycle studies were performed, showing that praziquantel-calcium carbonate physical mixture and interaction product were biocompatible with the HTC116 cells, because it did not produce a decrease in cell viability or alterations in the cell cycle.
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spelling pubmed-68352542019-11-25 Ground Calcium Carbonate as a Low Cost and Biosafety Excipient for Solubility and Dissolution Improvement of Praziquantel Borrego-Sánchez, Ana Sánchez-Espejo, Rita Albertini, Beatrice Passerini, Nadia Cerezo, Pilar Viseras, César Sainz-Díaz, C. Ignacio Pharmaceutics Article Calcium carbonate is an abundant mineral with several advantages to be a successful carrier to improve oral bioavailability of poorly water-soluble drugs, such as praziquantel. Praziquantel is an antiparasitic drug classified in group II of the Biopharmaceutical Classification System hence characterized by high-permeability and low-solubility. Therefore, the dissolution rate is the limiting factor for the gastrointestinal absorption that contributes to the low bioavailability. Consequently, the therapeutic dose of the praziquantel must be high and big tablets and capsules are required, which are difficult to swallow, especially for pediatric and elderly patients. Mixtures of praziquantel and calcium carbonate using solid-solid physical mixtures and solid dispersions were prepared and characterized using several techniques (X-ray diffraction differential scanning calorimetry, thermogravimetric analysis, scanning electron microscopy, laser diffraction, Fourier transform infrared and Raman spectroscopies). Solubility of these formulations evidenced that the solubility of praziquantel-calcium carbonate interaction product increased in physiological media. In vitro dissolution tests showed that the interaction product increased the dissolution rate of the drug in acidic medium. Theoretical models were studied to understand this experimental behavior. Cytotoxicity and cell cycle studies were performed, showing that praziquantel-calcium carbonate physical mixture and interaction product were biocompatible with the HTC116 cells, because it did not produce a decrease in cell viability or alterations in the cell cycle. MDPI 2019-10-14 /pmc/articles/PMC6835254/ /pubmed/31615087 http://dx.doi.org/10.3390/pharmaceutics11100533 Text en © 2019 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
Borrego-Sánchez, Ana
Sánchez-Espejo, Rita
Albertini, Beatrice
Passerini, Nadia
Cerezo, Pilar
Viseras, César
Sainz-Díaz, C. Ignacio
Ground Calcium Carbonate as a Low Cost and Biosafety Excipient for Solubility and Dissolution Improvement of Praziquantel
title Ground Calcium Carbonate as a Low Cost and Biosafety Excipient for Solubility and Dissolution Improvement of Praziquantel
title_full Ground Calcium Carbonate as a Low Cost and Biosafety Excipient for Solubility and Dissolution Improvement of Praziquantel
title_fullStr Ground Calcium Carbonate as a Low Cost and Biosafety Excipient for Solubility and Dissolution Improvement of Praziquantel
title_full_unstemmed Ground Calcium Carbonate as a Low Cost and Biosafety Excipient for Solubility and Dissolution Improvement of Praziquantel
title_short Ground Calcium Carbonate as a Low Cost and Biosafety Excipient for Solubility and Dissolution Improvement of Praziquantel
title_sort ground calcium carbonate as a low cost and biosafety excipient for solubility and dissolution improvement of praziquantel
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835254/
https://www.ncbi.nlm.nih.gov/pubmed/31615087
http://dx.doi.org/10.3390/pharmaceutics11100533
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