1. In the current project, we intend to generate the toxicological profile of nanomaterials (NM) of medical importance newly synthesized in our institute.
2. NM will be characterized as their physicochemical properties that may be important in understanding the toxic effects of the test materials include particle size and size distribution, agglomeration state, and porosity.
3. The nanomaterials would be Hydroxyapatite(HAP -10 and 20 nm) and Iron oxide (Fe2O3-10 and 20nm). For comparison, bulk materials of Hydroxyapatite and Iron oxide will be used. The Toxicity will be compared based on size and composition of nanomaterials.
4. The in vivo toxicity will be carried out in rats by oral/dermal/inhalation routes of exposure using OECD Guidelines.
5. Genotoxicity will be studied utilizing Micronucleus Test (MNT)/Comet Test in rats and invitro studies chromosome aberration(CA) test.
6. Toxicokinetic studies will be performed to investigate kinetics of nanomaterials using oral/dermal/inhalation routes of exposure.
7. The histopathology of rat organs will be investigated to examine the extent of tissue damage caused by nanomaterials after acute and toxicokinetic studies.
8. The mode of action of nanomaterials after oral/dermal/inhalation treatment will also be studied using biochemical and molecular end point related to oxidative stress and genotoxicity.
9. The in vitro toxicity will be evaluated with the rat liver cell line eg.BRL 3A.
10. The results originating from these studies will be useful in predicting the possible toxic hazards that may arise from the introduction of the nanomaterials into the environment.
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NM have unique properties that are highly desirable for application within the medical sector. The innovation properties of NM have already found their first commercial and emerging biomedical applictions. If the NM of the current study are found to be toxicologically safe two new of medical importance will emerge for the benefit of mankind.
Summary of The Knowledge Outcome.
1. In the current project, we intend to generate the toxicological profile of nanomaterials (NM) of medical importance newly synthesized in our institute.
2. NM will be characterized as their physicochemical properties that may be important in understanding the toxic effects of the test materials include particle size and size distribution, agglomeration state, and porosity.
3. The nanomaterials would be Hydroxyapatite(HAP -10 and 20 nm) and Iron oxide (Fe2O3-10 and 20nm). For comparison, bulk materials of Hydroxyapatite and Iron oxide will be used. The Toxicity will be compared based on size and composition of nanomaterials.
4. The in vivo toxicity will be carried out in rats by oral/dermal/inhalation routes of exposure using OECD Guidelines.
5. Genotoxicity will be studied utilizing Micronucleus Test (MNT)/Comet Test in rats and invitro studies chromosome aberration(CA) test.
6. Toxicokinetic studies will be performed to investigate kinetics of nanomaterials using oral/dermal/inhalation routes of exposure.
7. The histopathology of rat organs will be investigated to examine the extent of tissue damage caused by nanomaterials after acute and toxicokinetic studies.
8. The mode of action of nanomaterials after oral/dermal/inhalation treatment will also be studied using biochemical and molecular end point related to oxidative stress and genotoxicity.
9. The in vitro toxicity will be evaluated with the rat liver cell line eg.BRL 3A.
10. The results originating from these studies will be useful in predicting the possible toxic hazards that may arise from the introduction of the nanomaterials into the environment.
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Publication.
1 Monika Kumari, Sheik Rajak, Shailendra P. Singh, Upadhyayula S. N. Murty, Mohammed Mahboob, Paramjit Grover and Mohammed F. Rahman Biochemical alterations induced by acute oral doses of iron oxide nanoparticles in Wistar rats Drug and Chemical Toxicology 2013, 36, 296-305
2 Monika Kumari, Sheik Rajak, Shailendra Pratap singh, Srinivas indu kumari, Uday Kumar Putcha, Upadhyayula S. N. Murty, Mohammed Mahboob, Paramjit Grover and Mohammed F. Rahman Repeated Oral Dose Toxicity of Iron Oxide Nanoparticles: Biochemical and Histopathological Alterations in Different Tissues of Rats Journal of Nanoscience and Nanotechnology 2012, 12, 2149-2159
3 P. V. Prabhakar, Utkarsh A. Reddy, S. P. Singh, A. Balasubramanyam, M. F. Rahman, S. Indu Kumari, Sachin B. Agawane, U. S. N. Murty, Paramjit Grover and Mohammed Mahboob Oxidative stress induced by aluminum oxide nanomaterials after acute oral treatment in Wistar rats Journal of Applied Toxicology 2012, 32, 436-445
4 Shailendra Pratap Singh, M. F. Rahman, U. S. N. Murty, M. Mahboob and Paramjit Grover Comparative study of genotoxicity and tissue distribution of nano and micron sized iron oxide in rats after acute oral treatment Toxicology and Applied Pharmacology 2013, 266, 56-66
5 Shailendra Pratap Singh, Monika Kumari, Srinivas I. Kumari, Mohammed F. Rahman, M. Mahboob and Paramjit Grover Toxicity assessment of manganese oxide micro and nanoparticles in Wistar rats after 28 days of repeated oral exposure Journal of Applied Toxicology 2013, 33, 1165 - 1179
6 Shailendra Pratap Singh, Monika Kumari, Srinivas I. Kumari, Mohammed F. Rahman, S. S. Kalyan Kamal, M. Mahboob and Paramjit Grover Genotoxicity of nano- and micron-sized manganese oxide in rats after acute oral treatment Mutation Research/Genetic Toxicology and Environmental Mutagenesis 2013, 754, 39 - 50
Patent.
Technology Transferred..
Human Resources.
3 JRF