Determination of maximum tolerated dose and toxicity of Inauhzin in mice

Reactivating the tumor suppressor p53 offers an attractive strategy for developing cancer therapy. We recently identified Inauhzin (INZ) as a novel non-genotoxic p53-activating compound. To develop INZ into a clinically applicable anticancer drug, we have initiated preclinical toxicity studies. Here...

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Main Authors: Qi Zhang, Shelya X. Zeng, Hua Lu
Format: Article
Language:English
Published: Elsevier 2015-01-01
Series:Toxicology Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S221475001500030X
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spelling doaj-c3b9df4747d24525854aa6b35c572a2b2020-11-24T22:58:31ZengElsevierToxicology Reports2214-75002015-01-012C54655410.1016/j.toxrep.2015.02.011Determination of maximum tolerated dose and toxicity of Inauhzin in miceQi ZhangShelya X. ZengHua LuReactivating the tumor suppressor p53 offers an attractive strategy for developing cancer therapy. We recently identified Inauhzin (INZ) as a novel non-genotoxic p53-activating compound. To develop INZ into a clinically applicable anticancer drug, we have initiated preclinical toxicity studies. Here, we report our study on determining the maximum tolerated dose (MTD) of INZ analog, Inauhzin-C (INZ (C)), following intraperitoneal (i.p.) administration (Phase A) and its toxicity following i.p. administration over a period of 5-day dosing plus 2-day recovery (Phase B) in CD-1 mice. The Phase A study showed that the MTD of INZ (C) is 200 mg/kg for female and 250 mg/kg for male, respectively. The Phase B study showed that the administration of INZ (C) via 5-day consecutive i.p. injection is tolerated by female CD-1 mice at all dose levels tested from 50 mg/kg to 120 mg/kg without significant changes in biochemical and pathological parameters in the animals. Together, these results indicate that our previously determined effective dose of INZ at 30–60 mg/kg via i.p. is quite safe to mice, and imply that this compound have the features worthy for further development into a clinically applicable drug.http://www.sciencedirect.com/science/article/pii/S221475001500030XInauhzinMouseToxicity studyDose range findingMaximum tolerated dose
collection DOAJ
language English
format Article
sources DOAJ
author Qi Zhang
Shelya X. Zeng
Hua Lu
spellingShingle Qi Zhang
Shelya X. Zeng
Hua Lu
Determination of maximum tolerated dose and toxicity of Inauhzin in mice
Toxicology Reports
Inauhzin
Mouse
Toxicity study
Dose range finding
Maximum tolerated dose
author_facet Qi Zhang
Shelya X. Zeng
Hua Lu
author_sort Qi Zhang
title Determination of maximum tolerated dose and toxicity of Inauhzin in mice
title_short Determination of maximum tolerated dose and toxicity of Inauhzin in mice
title_full Determination of maximum tolerated dose and toxicity of Inauhzin in mice
title_fullStr Determination of maximum tolerated dose and toxicity of Inauhzin in mice
title_full_unstemmed Determination of maximum tolerated dose and toxicity of Inauhzin in mice
title_sort determination of maximum tolerated dose and toxicity of inauhzin in mice
publisher Elsevier
series Toxicology Reports
issn 2214-7500
publishDate 2015-01-01
description Reactivating the tumor suppressor p53 offers an attractive strategy for developing cancer therapy. We recently identified Inauhzin (INZ) as a novel non-genotoxic p53-activating compound. To develop INZ into a clinically applicable anticancer drug, we have initiated preclinical toxicity studies. Here, we report our study on determining the maximum tolerated dose (MTD) of INZ analog, Inauhzin-C (INZ (C)), following intraperitoneal (i.p.) administration (Phase A) and its toxicity following i.p. administration over a period of 5-day dosing plus 2-day recovery (Phase B) in CD-1 mice. The Phase A study showed that the MTD of INZ (C) is 200 mg/kg for female and 250 mg/kg for male, respectively. The Phase B study showed that the administration of INZ (C) via 5-day consecutive i.p. injection is tolerated by female CD-1 mice at all dose levels tested from 50 mg/kg to 120 mg/kg without significant changes in biochemical and pathological parameters in the animals. Together, these results indicate that our previously determined effective dose of INZ at 30–60 mg/kg via i.p. is quite safe to mice, and imply that this compound have the features worthy for further development into a clinically applicable drug.
topic Inauhzin
Mouse
Toxicity study
Dose range finding
Maximum tolerated dose
url http://www.sciencedirect.com/science/article/pii/S221475001500030X
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