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TMZ-BioShuttle – a reformulated Temozolomide

There is a large number of effective cytotoxic drugs whose side effect profile, efficacy, and long-term use in man are well understood and documented over decades of use in clinical routine e.g. in the treatment of recurrent glioblastoma multiforme (GBM) and the hormone-refractory prostate cancer (H...

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Autores principales: Waldeck, Waldemar, Wiessler, Manfred, Ehemann, Volker, Pipkorn, Ruediger, Spring, Herbert, Debus, Juergen, Didinger, Bernd, Mueller, Gabriele, Langowski, Joerg, Braun, Klaus
Formato: Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2536715/
https://www.ncbi.nlm.nih.gov/pubmed/18797509
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author Waldeck, Waldemar
Wiessler, Manfred
Ehemann, Volker
Pipkorn, Ruediger
Spring, Herbert
Debus, Juergen
Didinger, Bernd
Mueller, Gabriele
Langowski, Joerg
Braun, Klaus
author_facet Waldeck, Waldemar
Wiessler, Manfred
Ehemann, Volker
Pipkorn, Ruediger
Spring, Herbert
Debus, Juergen
Didinger, Bernd
Mueller, Gabriele
Langowski, Joerg
Braun, Klaus
author_sort Waldeck, Waldemar
collection PubMed
description There is a large number of effective cytotoxic drugs whose side effect profile, efficacy, and long-term use in man are well understood and documented over decades of use in clinical routine e.g. in the treatment of recurrent glioblastoma multiforme (GBM) and the hormone-refractory prostate cancer (HRPC). Both cancers are insensitive against most chemotherapeutic interventions; they have low response rates and poor prognoses. Some cytotoxic agents can be significantly improved by using modern technology of drug delivery or formulation. We succeeded to enhance the pharmacologic potency with simultaneous reduction of unwanted adverse reactions of the highly efficient chemotherapeutic temozolomide (TMZ) as an example. The TMZ connection to transporter molecules (TMZ-BioShuttle) resulted in a much higher pharmacological effect in glioma cell lines while using reduced doses. This permits the conclusion that a suitable chemistry could realize the ligation of pharmacologically active, but sensitive and highly unstable pharmaceutical ingredients without functional deprivation. The re-formulation of TMZ to TMZ-BioShuttle achieved a nearly 10-fold potential of the established pharmaceutic TMZ far beyond the treatment of brain tumors cells and results in an attractive reformulated drug with enhanced therapeutic index.
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spelling pubmed-25367152008-09-16 TMZ-BioShuttle – a reformulated Temozolomide Waldeck, Waldemar Wiessler, Manfred Ehemann, Volker Pipkorn, Ruediger Spring, Herbert Debus, Juergen Didinger, Bernd Mueller, Gabriele Langowski, Joerg Braun, Klaus Int J Med Sci Research Paper There is a large number of effective cytotoxic drugs whose side effect profile, efficacy, and long-term use in man are well understood and documented over decades of use in clinical routine e.g. in the treatment of recurrent glioblastoma multiforme (GBM) and the hormone-refractory prostate cancer (HRPC). Both cancers are insensitive against most chemotherapeutic interventions; they have low response rates and poor prognoses. Some cytotoxic agents can be significantly improved by using modern technology of drug delivery or formulation. We succeeded to enhance the pharmacologic potency with simultaneous reduction of unwanted adverse reactions of the highly efficient chemotherapeutic temozolomide (TMZ) as an example. The TMZ connection to transporter molecules (TMZ-BioShuttle) resulted in a much higher pharmacological effect in glioma cell lines while using reduced doses. This permits the conclusion that a suitable chemistry could realize the ligation of pharmacologically active, but sensitive and highly unstable pharmaceutical ingredients without functional deprivation. The re-formulation of TMZ to TMZ-BioShuttle achieved a nearly 10-fold potential of the established pharmaceutic TMZ far beyond the treatment of brain tumors cells and results in an attractive reformulated drug with enhanced therapeutic index. Ivyspring International Publisher 2008-09-15 /pmc/articles/PMC2536715/ /pubmed/18797509 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Research Paper
Waldeck, Waldemar
Wiessler, Manfred
Ehemann, Volker
Pipkorn, Ruediger
Spring, Herbert
Debus, Juergen
Didinger, Bernd
Mueller, Gabriele
Langowski, Joerg
Braun, Klaus
TMZ-BioShuttle – a reformulated Temozolomide
title TMZ-BioShuttle – a reformulated Temozolomide
title_full TMZ-BioShuttle – a reformulated Temozolomide
title_fullStr TMZ-BioShuttle – a reformulated Temozolomide
title_full_unstemmed TMZ-BioShuttle – a reformulated Temozolomide
title_short TMZ-BioShuttle – a reformulated Temozolomide
title_sort tmz-bioshuttle – a reformulated temozolomide
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2536715/
https://www.ncbi.nlm.nih.gov/pubmed/18797509
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