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Safety assessments of subcutaneous doses of aragonite calcium carbonate nanocrystals in rats
Calcium carbonate nanoparticles have shown promising potentials in the delivery of drugs and metabolites. There is however, a paucity of information on the safety of their intentional or accidental over exposures to biological systems and general health safety. To this end, this study aims at docume...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427138/ https://www.ncbi.nlm.nih.gov/pubmed/28553160 http://dx.doi.org/10.1007/s11051-017-3849-z |
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author | Jaji, Alhaji Zubair Zakaria, Zuki Abu Bakar Mahmud, Rozi Loqman, Mohamad Yusof Hezmee, Mohamad Noor Mohamad Abba, Yusuf Isa, Tijani Mahmood, Saffanah Khuder |
author_facet | Jaji, Alhaji Zubair Zakaria, Zuki Abu Bakar Mahmud, Rozi Loqman, Mohamad Yusof Hezmee, Mohamad Noor Mohamad Abba, Yusuf Isa, Tijani Mahmood, Saffanah Khuder |
author_sort | Jaji, Alhaji Zubair |
collection | PubMed |
description | Calcium carbonate nanoparticles have shown promising potentials in the delivery of drugs and metabolites. There is however, a paucity of information on the safety of their intentional or accidental over exposures to biological systems and general health safety. To this end, this study aims at documenting information on the safety of subcutaneous doses of biogenic nanocrystals of aragonite polymorph of calcium carbonate derived from cockle shells (ANC) in Sprague-Dawley (SD) rats. ANC was synthesized using the top-down method, characterized using the transmission electron microscopy and field emission scanning electron microscope and its acute and repeated dose 28-day trial toxicities were evaluated in SD rats. The results showed that the homogenous 30 ± 5 nm-sized spherical pure aragonite nanocrystals were not associated with mortality in the rats. Severe clinical signs and gross and histopathological lesions, indicating organ toxicities, were recorded in the acute toxicity (29,500 mg/m(2)) group and the high dose (5900 mg/m(2)) group of the repeated dose 28-day trial. However, the medium- (590 mg/m(2) body weight) and low (59 mg/m(2))-dose groups showed moderate to mild lesions. The relatively mild lesions observed in the low toxicity dosage group marked the safety margin of ANC in SD rats. It was concluded from this study that the toxicity of CaCO(3) was dependent on the particulate size (30 ± 5 nm) and concentration and the route of administration used. |
format | Online Article Text |
id | pubmed-5427138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-54271382017-05-26 Safety assessments of subcutaneous doses of aragonite calcium carbonate nanocrystals in rats Jaji, Alhaji Zubair Zakaria, Zuki Abu Bakar Mahmud, Rozi Loqman, Mohamad Yusof Hezmee, Mohamad Noor Mohamad Abba, Yusuf Isa, Tijani Mahmood, Saffanah Khuder J Nanopart Res Research Paper Calcium carbonate nanoparticles have shown promising potentials in the delivery of drugs and metabolites. There is however, a paucity of information on the safety of their intentional or accidental over exposures to biological systems and general health safety. To this end, this study aims at documenting information on the safety of subcutaneous doses of biogenic nanocrystals of aragonite polymorph of calcium carbonate derived from cockle shells (ANC) in Sprague-Dawley (SD) rats. ANC was synthesized using the top-down method, characterized using the transmission electron microscopy and field emission scanning electron microscope and its acute and repeated dose 28-day trial toxicities were evaluated in SD rats. The results showed that the homogenous 30 ± 5 nm-sized spherical pure aragonite nanocrystals were not associated with mortality in the rats. Severe clinical signs and gross and histopathological lesions, indicating organ toxicities, were recorded in the acute toxicity (29,500 mg/m(2)) group and the high dose (5900 mg/m(2)) group of the repeated dose 28-day trial. However, the medium- (590 mg/m(2) body weight) and low (59 mg/m(2))-dose groups showed moderate to mild lesions. The relatively mild lesions observed in the low toxicity dosage group marked the safety margin of ANC in SD rats. It was concluded from this study that the toxicity of CaCO(3) was dependent on the particulate size (30 ± 5 nm) and concentration and the route of administration used. Springer Netherlands 2017-05-11 2017 /pmc/articles/PMC5427138/ /pubmed/28553160 http://dx.doi.org/10.1007/s11051-017-3849-z Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Paper Jaji, Alhaji Zubair Zakaria, Zuki Abu Bakar Mahmud, Rozi Loqman, Mohamad Yusof Hezmee, Mohamad Noor Mohamad Abba, Yusuf Isa, Tijani Mahmood, Saffanah Khuder Safety assessments of subcutaneous doses of aragonite calcium carbonate nanocrystals in rats |
title | Safety assessments of subcutaneous doses of aragonite calcium carbonate nanocrystals in rats |
title_full | Safety assessments of subcutaneous doses of aragonite calcium carbonate nanocrystals in rats |
title_fullStr | Safety assessments of subcutaneous doses of aragonite calcium carbonate nanocrystals in rats |
title_full_unstemmed | Safety assessments of subcutaneous doses of aragonite calcium carbonate nanocrystals in rats |
title_short | Safety assessments of subcutaneous doses of aragonite calcium carbonate nanocrystals in rats |
title_sort | safety assessments of subcutaneous doses of aragonite calcium carbonate nanocrystals in rats |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427138/ https://www.ncbi.nlm.nih.gov/pubmed/28553160 http://dx.doi.org/10.1007/s11051-017-3849-z |
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