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Pharmacological Basis of CD101 Efficacy: Exposure Shape Matters

CD101 is a novel echinocandin with concentration-dependent fungicidal activity in vitro and a long half-life (∼133 h in humans, ∼70 to 80 h in mice). Given these characteristics, it is likely that the shape of the CD101 exposure (i.e., the time course of CD101 concentrations) influences efficacy. To...

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Autores principales: Lakota, Elizabeth A., Bader, Justin C., Ong, Voon, Bartizal, Ken, Miesel, Lynn, Andes, David R., Bhavnani, Sujata M., Rubino, Christopher M., Ambrose, Paul G., Lepak, Alexander J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655053/
https://www.ncbi.nlm.nih.gov/pubmed/28848022
http://dx.doi.org/10.1128/AAC.00758-17
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author Lakota, Elizabeth A.
Bader, Justin C.
Ong, Voon
Bartizal, Ken
Miesel, Lynn
Andes, David R.
Bhavnani, Sujata M.
Rubino, Christopher M.
Ambrose, Paul G.
Lepak, Alexander J.
author_facet Lakota, Elizabeth A.
Bader, Justin C.
Ong, Voon
Bartizal, Ken
Miesel, Lynn
Andes, David R.
Bhavnani, Sujata M.
Rubino, Christopher M.
Ambrose, Paul G.
Lepak, Alexander J.
author_sort Lakota, Elizabeth A.
collection PubMed
description CD101 is a novel echinocandin with concentration-dependent fungicidal activity in vitro and a long half-life (∼133 h in humans, ∼70 to 80 h in mice). Given these characteristics, it is likely that the shape of the CD101 exposure (i.e., the time course of CD101 concentrations) influences efficacy. To test this hypothesis, doses which produce the same total area under the concentration-time curve (AUC) were administered to groups of neutropenic ICR mice infected with Candida albicans R303 using three different schedules. A total CD101 dose of 2 mg/kg was administered as a single intravenous (i.v.) dose or in equal divided doses of either 1 mg/kg twice weekly or 0.29 mg/kg/day over 7 days. The studies were performed using a murine disseminated candidiasis model. Animals were euthanized at 168 h following the start of treatment. Fungi grew well in the no-treatment control group and showed variable changes in fungal density in the treatment groups. When the CD101 AUC from 0 to 168 h (AUC(0–168)) was administered as a single dose, a >2 log(10) CFU reduction from the baseline at 168 h was observed. When twice-weekly and daily regimens with similar AUC values were administered, net fungal stasis and a >1 log(10) CFU increase from the baseline were observed, respectively. These data support the hypothesis that the shape of the CD101 AUC influences efficacy. Thus, CD101 administered once per week demonstrated a greater degree of fungal killing than the same dose divided into twice-weekly or daily regimens.
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spelling pubmed-56550532017-10-30 Pharmacological Basis of CD101 Efficacy: Exposure Shape Matters Lakota, Elizabeth A. Bader, Justin C. Ong, Voon Bartizal, Ken Miesel, Lynn Andes, David R. Bhavnani, Sujata M. Rubino, Christopher M. Ambrose, Paul G. Lepak, Alexander J. Antimicrob Agents Chemother Pharmacology CD101 is a novel echinocandin with concentration-dependent fungicidal activity in vitro and a long half-life (∼133 h in humans, ∼70 to 80 h in mice). Given these characteristics, it is likely that the shape of the CD101 exposure (i.e., the time course of CD101 concentrations) influences efficacy. To test this hypothesis, doses which produce the same total area under the concentration-time curve (AUC) were administered to groups of neutropenic ICR mice infected with Candida albicans R303 using three different schedules. A total CD101 dose of 2 mg/kg was administered as a single intravenous (i.v.) dose or in equal divided doses of either 1 mg/kg twice weekly or 0.29 mg/kg/day over 7 days. The studies were performed using a murine disseminated candidiasis model. Animals were euthanized at 168 h following the start of treatment. Fungi grew well in the no-treatment control group and showed variable changes in fungal density in the treatment groups. When the CD101 AUC from 0 to 168 h (AUC(0–168)) was administered as a single dose, a >2 log(10) CFU reduction from the baseline at 168 h was observed. When twice-weekly and daily regimens with similar AUC values were administered, net fungal stasis and a >1 log(10) CFU increase from the baseline were observed, respectively. These data support the hypothesis that the shape of the CD101 AUC influences efficacy. Thus, CD101 administered once per week demonstrated a greater degree of fungal killing than the same dose divided into twice-weekly or daily regimens. American Society for Microbiology 2017-10-24 /pmc/articles/PMC5655053/ /pubmed/28848022 http://dx.doi.org/10.1128/AAC.00758-17 Text en Copyright © 2017 Lakota et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Pharmacology
Lakota, Elizabeth A.
Bader, Justin C.
Ong, Voon
Bartizal, Ken
Miesel, Lynn
Andes, David R.
Bhavnani, Sujata M.
Rubino, Christopher M.
Ambrose, Paul G.
Lepak, Alexander J.
Pharmacological Basis of CD101 Efficacy: Exposure Shape Matters
title Pharmacological Basis of CD101 Efficacy: Exposure Shape Matters
title_full Pharmacological Basis of CD101 Efficacy: Exposure Shape Matters
title_fullStr Pharmacological Basis of CD101 Efficacy: Exposure Shape Matters
title_full_unstemmed Pharmacological Basis of CD101 Efficacy: Exposure Shape Matters
title_short Pharmacological Basis of CD101 Efficacy: Exposure Shape Matters
title_sort pharmacological basis of cd101 efficacy: exposure shape matters
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655053/
https://www.ncbi.nlm.nih.gov/pubmed/28848022
http://dx.doi.org/10.1128/AAC.00758-17
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