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Acute Toxicity Study of Zerumbone-Loaded Nanostructured Lipid Carrier on BALB/c Mice Model
Zerumbone- (ZER-) loaded nanostructure lipid carrier (NLC) (ZER-NLC) prepared for its antileukemia effect in vitro was evaluated for its toxicological effects by observing changes in the liver, kidney, spleen, lung, heart, and brain tissues, serum biochemical parameters, total haemogram, and bone ma...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4172924/ https://www.ncbi.nlm.nih.gov/pubmed/25276798 http://dx.doi.org/10.1155/2014/563930 |
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author | Rahman, Heshu Sulaiman Rasedee, Abdullah Othman, Hemn Hassan Chartrand, Max Stanley Namvar, Farideh Yeap, Swee Keong Abdul Samad, Nozlena Andas, Reena Joys Muhammad Nadzri, Nabilah Anasamy, Theebaa Ng, Kuan Beng How, Chee Wun |
author_facet | Rahman, Heshu Sulaiman Rasedee, Abdullah Othman, Hemn Hassan Chartrand, Max Stanley Namvar, Farideh Yeap, Swee Keong Abdul Samad, Nozlena Andas, Reena Joys Muhammad Nadzri, Nabilah Anasamy, Theebaa Ng, Kuan Beng How, Chee Wun |
author_sort | Rahman, Heshu Sulaiman |
collection | PubMed |
description | Zerumbone- (ZER-) loaded nanostructure lipid carrier (NLC) (ZER-NLC) prepared for its antileukemia effect in vitro was evaluated for its toxicological effects by observing changes in the liver, kidney, spleen, lung, heart, and brain tissues, serum biochemical parameters, total haemogram, and bone marrow stem cells. The acute toxicity study for ZER-NLC was conducted by orally treating BALB/c mice with a single dose with either water, olive oil, ZER, NLC, or ZER-NLC for 14 days. The animals were observed for clinical and behavioral abnormalities, toxicological symptoms, feed consumption, and gross appearance. The liver, kidney, heart, lung, spleen, and brain tissues were assessed histologically. Total haemogram was counted by hemocytometry and microhematocrit reader. Bone marrow examination in terms of cellular morphology was done by Wright staining with bone marrow smear. Furthermore, serum biochemical parameters were determined spectrophotometrically. Grossly all treated mice, their investigated tissues, serum biochemical parameters, total haemogram, and bone marrow were normal. At oral doses of 100 and 200 mg/kg ZER-NLC there was no sign of toxicity or mortality in BALB/c mice. This study suggests that the 50% lethal dose (LD(50)) of ZER-NLC is higher than 200 mg/kg, thus, safe by oral administration. |
format | Online Article Text |
id | pubmed-4172924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-41729242014-09-30 Acute Toxicity Study of Zerumbone-Loaded Nanostructured Lipid Carrier on BALB/c Mice Model Rahman, Heshu Sulaiman Rasedee, Abdullah Othman, Hemn Hassan Chartrand, Max Stanley Namvar, Farideh Yeap, Swee Keong Abdul Samad, Nozlena Andas, Reena Joys Muhammad Nadzri, Nabilah Anasamy, Theebaa Ng, Kuan Beng How, Chee Wun Biomed Res Int Research Article Zerumbone- (ZER-) loaded nanostructure lipid carrier (NLC) (ZER-NLC) prepared for its antileukemia effect in vitro was evaluated for its toxicological effects by observing changes in the liver, kidney, spleen, lung, heart, and brain tissues, serum biochemical parameters, total haemogram, and bone marrow stem cells. The acute toxicity study for ZER-NLC was conducted by orally treating BALB/c mice with a single dose with either water, olive oil, ZER, NLC, or ZER-NLC for 14 days. The animals were observed for clinical and behavioral abnormalities, toxicological symptoms, feed consumption, and gross appearance. The liver, kidney, heart, lung, spleen, and brain tissues were assessed histologically. Total haemogram was counted by hemocytometry and microhematocrit reader. Bone marrow examination in terms of cellular morphology was done by Wright staining with bone marrow smear. Furthermore, serum biochemical parameters were determined spectrophotometrically. Grossly all treated mice, their investigated tissues, serum biochemical parameters, total haemogram, and bone marrow were normal. At oral doses of 100 and 200 mg/kg ZER-NLC there was no sign of toxicity or mortality in BALB/c mice. This study suggests that the 50% lethal dose (LD(50)) of ZER-NLC is higher than 200 mg/kg, thus, safe by oral administration. Hindawi Publishing Corporation 2014 2014-09-08 /pmc/articles/PMC4172924/ /pubmed/25276798 http://dx.doi.org/10.1155/2014/563930 Text en Copyright © 2014 Heshu Sulaiman Rahman et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Rahman, Heshu Sulaiman Rasedee, Abdullah Othman, Hemn Hassan Chartrand, Max Stanley Namvar, Farideh Yeap, Swee Keong Abdul Samad, Nozlena Andas, Reena Joys Muhammad Nadzri, Nabilah Anasamy, Theebaa Ng, Kuan Beng How, Chee Wun Acute Toxicity Study of Zerumbone-Loaded Nanostructured Lipid Carrier on BALB/c Mice Model |
title | Acute Toxicity Study of Zerumbone-Loaded Nanostructured Lipid Carrier on BALB/c Mice Model |
title_full | Acute Toxicity Study of Zerumbone-Loaded Nanostructured Lipid Carrier on BALB/c Mice Model |
title_fullStr | Acute Toxicity Study of Zerumbone-Loaded Nanostructured Lipid Carrier on BALB/c Mice Model |
title_full_unstemmed | Acute Toxicity Study of Zerumbone-Loaded Nanostructured Lipid Carrier on BALB/c Mice Model |
title_short | Acute Toxicity Study of Zerumbone-Loaded Nanostructured Lipid Carrier on BALB/c Mice Model |
title_sort | acute toxicity study of zerumbone-loaded nanostructured lipid carrier on balb/c mice model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4172924/ https://www.ncbi.nlm.nih.gov/pubmed/25276798 http://dx.doi.org/10.1155/2014/563930 |
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