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Taste, A New Incentive to Switch to (R)-Praziquantel in Schistosomiasis Treatment
BACKGROUND: Praziquantel (PZQ) is the drug compound of choice in the control and treatment of schistosomiasis. PZQ is administered as a racemate, i. e. 1∶1 mixture of enantiomers. The schistosomicidal activity arises from one PZQ-enantiomer, whereas the other enantiomer does not contribute to the ac...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614124/ https://www.ncbi.nlm.nih.gov/pubmed/19159015 http://dx.doi.org/10.1371/journal.pntd.0000357 |
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author | Meyer, Thorsten Sekljic, Harald Fuchs, Stefan Bothe, Heiko Schollmeyer, Dieter Miculka, Christian |
author_facet | Meyer, Thorsten Sekljic, Harald Fuchs, Stefan Bothe, Heiko Schollmeyer, Dieter Miculka, Christian |
author_sort | Meyer, Thorsten |
collection | PubMed |
description | BACKGROUND: Praziquantel (PZQ) is the drug compound of choice in the control and treatment of schistosomiasis. PZQ is administered as a racemate, i. e. 1∶1 mixture of enantiomers. The schistosomicidal activity arises from one PZQ-enantiomer, whereas the other enantiomer does not contribute to the activity. The WHO's Special Programme for Research and Training in Tropical Diseases (TDR) has assigned the low-cost preparation of pure schistosomicidal (−)-PZQ a key priority for future R&D on PZQ, but so far this transition has not happened. PZQ has two major administration drawbacks, the first being the high dose needed, and its well documented bitter and disgusting taste. Attempts of taste-masking by low-cost means have not been successful. We hypothesized that the non-schistosomicidal component in PZQ would be the main contributor to the unpleasant taste of the drug. If the hypothesis was confirmed, the two major administration drawbacks of PZQ, the high dose needed and its bitter taste, could be addressed in one go by removing the component contributing to the bitter taste. METHODS AND FINDINGS: PZQ was separated into its schistosomicidal and the non-schistosomicidal component, the absolute stereochemical configuration of (−)-PZQ was determined to be (R)-PZQ by X-ray crystallography, and the extent of bitterness was determined for regular racemic PZQ and the schistosomicidal component in a taste study in humans. Finding: The schistosomicidal component alone is significantly less bitter than regular, racemic PZQ. CONCLUSION: Our hypothesis is confirmed. We propose to use only the pure schistosomicidal component of PZQ, offering the advantage of halving the dose and expectedly improving the compliance due to the removal of the bitter taste. Therefore, (R)-PZQ should be specifically suitable for the treatment of school-age children against schistosomiasis. With this finding, we would like to offer an additional incentive to the TDR's recommendation to switch to the pure schistosomicidal (R)-PZQ. |
format | Text |
id | pubmed-2614124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26141242009-01-13 Taste, A New Incentive to Switch to (R)-Praziquantel in Schistosomiasis Treatment Meyer, Thorsten Sekljic, Harald Fuchs, Stefan Bothe, Heiko Schollmeyer, Dieter Miculka, Christian PLoS Negl Trop Dis Research Article BACKGROUND: Praziquantel (PZQ) is the drug compound of choice in the control and treatment of schistosomiasis. PZQ is administered as a racemate, i. e. 1∶1 mixture of enantiomers. The schistosomicidal activity arises from one PZQ-enantiomer, whereas the other enantiomer does not contribute to the activity. The WHO's Special Programme for Research and Training in Tropical Diseases (TDR) has assigned the low-cost preparation of pure schistosomicidal (−)-PZQ a key priority for future R&D on PZQ, but so far this transition has not happened. PZQ has two major administration drawbacks, the first being the high dose needed, and its well documented bitter and disgusting taste. Attempts of taste-masking by low-cost means have not been successful. We hypothesized that the non-schistosomicidal component in PZQ would be the main contributor to the unpleasant taste of the drug. If the hypothesis was confirmed, the two major administration drawbacks of PZQ, the high dose needed and its bitter taste, could be addressed in one go by removing the component contributing to the bitter taste. METHODS AND FINDINGS: PZQ was separated into its schistosomicidal and the non-schistosomicidal component, the absolute stereochemical configuration of (−)-PZQ was determined to be (R)-PZQ by X-ray crystallography, and the extent of bitterness was determined for regular racemic PZQ and the schistosomicidal component in a taste study in humans. Finding: The schistosomicidal component alone is significantly less bitter than regular, racemic PZQ. CONCLUSION: Our hypothesis is confirmed. We propose to use only the pure schistosomicidal component of PZQ, offering the advantage of halving the dose and expectedly improving the compliance due to the removal of the bitter taste. Therefore, (R)-PZQ should be specifically suitable for the treatment of school-age children against schistosomiasis. With this finding, we would like to offer an additional incentive to the TDR's recommendation to switch to the pure schistosomicidal (R)-PZQ. Public Library of Science 2009-01-13 /pmc/articles/PMC2614124/ /pubmed/19159015 http://dx.doi.org/10.1371/journal.pntd.0000357 Text en Meyer et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Meyer, Thorsten Sekljic, Harald Fuchs, Stefan Bothe, Heiko Schollmeyer, Dieter Miculka, Christian Taste, A New Incentive to Switch to (R)-Praziquantel in Schistosomiasis Treatment |
title | Taste, A New Incentive to Switch to (R)-Praziquantel in Schistosomiasis Treatment |
title_full | Taste, A New Incentive to Switch to (R)-Praziquantel in Schistosomiasis Treatment |
title_fullStr | Taste, A New Incentive to Switch to (R)-Praziquantel in Schistosomiasis Treatment |
title_full_unstemmed | Taste, A New Incentive to Switch to (R)-Praziquantel in Schistosomiasis Treatment |
title_short | Taste, A New Incentive to Switch to (R)-Praziquantel in Schistosomiasis Treatment |
title_sort | taste, a new incentive to switch to (r)-praziquantel in schistosomiasis treatment |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614124/ https://www.ncbi.nlm.nih.gov/pubmed/19159015 http://dx.doi.org/10.1371/journal.pntd.0000357 |
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