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Acute oral toxicity evaluations of some zinc(II) complexes derived from 1-(2-salicylaldiminoethyl)piperazine Schiff bases in rats
The current study described the synthesis and the in vivo acute oral toxicity evaluations in Sprague Dawley rats. The compounds were characterized by elemental analyses, LC-MS, FTIR, (1)H NMR, (13)C NMR and UV-visible spectroscopy. In the acute toxicity study, a single administration of the compound...
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Published in: | International journal of molecular sciences 2012-02, Vol.13 (2), p.1393-1404 |
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description | The current study described the synthesis and the in vivo acute oral toxicity evaluations in Sprague Dawley rats. The compounds were characterized by elemental analyses, LC-MS, FTIR, (1)H NMR, (13)C NMR and UV-visible spectroscopy. In the acute toxicity study, a single administration of the compounds was performed orally to the rats at the single doses of 2000 mg/kg and they were then monitored for possible side effects, mortality or behavioral changes up to 14 days. The serum level of aspartate (AST), alanine aminotransferases (ALT), alkaline phosphate (ALP), triglyceride, high density lipoprotein (HDL), immunoglobulins (GAM) and the C-reactive proteins did not significantly change. The hematological indices white blood cells (WBC), haematocrit (HCT), red blood cells (RBC), mean corpuscular volume (MCV), mean corpuscular haemoglobin concentration (MCHC), and mean corpuscular hemoglobin (MCH) were within the normal range. The renal function indices examined were also within the reference range. Generally, the compounds exhibited low toxic effects as required for further in vivo therapeutic studies. |
doi_str_mv | 10.3390/ijms13021393 |
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The compounds were characterized by elemental analyses, LC-MS, FTIR, (1)H NMR, (13)C NMR and UV-visible spectroscopy. In the acute toxicity study, a single administration of the compounds was performed orally to the rats at the single doses of 2000 mg/kg and they were then monitored for possible side effects, mortality or behavioral changes up to 14 days. The serum level of aspartate (AST), alanine aminotransferases (ALT), alkaline phosphate (ALP), triglyceride, high density lipoprotein (HDL), immunoglobulins (GAM) and the C-reactive proteins did not significantly change. The hematological indices white blood cells (WBC), haematocrit (HCT), red blood cells (RBC), mean corpuscular volume (MCV), mean corpuscular haemoglobin concentration (MCHC), and mean corpuscular hemoglobin (MCH) were within the normal range. The renal function indices examined were also within the reference range. Generally, the compounds exhibited low toxic effects as required for further in vivo therapeutic studies.</description><subject>Administration, Oral</subject><subject>Alanine Transaminase - blood</subject><subject>Alkaline Phosphatase - blood</subject><subject>Animals</subject><subject>Aspartic Acid - blood</subject><subject>C-Reactive Protein - metabolism</subject><subject>Dose-Response Relationship, Drug</subject><subject>Erythrocyte Indices</subject><subject>Female</subject><subject>Immunoglobulins - blood</subject><subject>Inorganic chemistry</subject><subject>Ligands</subject><subject>Lipoproteins, HDL - blood</subject><subject>Male</subject><subject>Phenols</subject><subject>Piperazines - toxicity</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Schiff Bases - toxicity</subject><subject>Time Factors</subject><subject>Toxicity</subject><subject>Triglycerides - blood</subject><subject>Zinc</subject><subject>Zinc - toxicity</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpdUUFrFDEYDaLYunrzLAEvW3A0-TKbzFwKpahdKPSgnkM2842bJTMZk8zS9dZ_bqS1rL183wffe4_3eIS85eyjEC375HZD4oIBF614Rk55DVAxJtXzo_uEvEppxxgIWLUvyQlAzRrRqlNyd2HnjDRE42kOt866fKC4N3422YUx0dDTFAakv91ol-v1GbVhmDzeYqIdRrfHjvYxDJRXS6iS8c4evPGdG9wYMG8P_mxyE0ZT-Ei_2a3re7oxqdDdSKPJ6TV50Ruf8M3DXpAfXz5_v7yqrm--ri8vritb13WupAG5Mp1kXDYNNIA9Z0Kh2ijEMhshlGxrBSu1kaBUI1GC7GowqgVlhRULcn6vO82bATuLYy6h9RTdYOJBB-P0_5_RbfXPsNcCWt5KWQSWDwIx_JoxZT24ZNF7M2KYk-ZCqrrhbfG1IO-fQHdhjmOJp_kKSgamShcL8uEeZWNIKWL_aIYz_bdbfdxtgb87DvAI_lem-ANH36Cd</recordid><startdate>20120201</startdate><enddate>20120201</enddate><creator>Salga, Muhammad Saleh</creator><creator>Ali, Hapipah Mohd</creator><creator>Abdulla, Mahmood Ameen</creator><creator>Abdelwahab, Siddig Ibrahim</creator><general>MDPI AG</general><general>Molecular Diversity Preservation International (MDPI)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7U7</scope><scope>C1K</scope><scope>5PM</scope></search><sort><creationdate>20120201</creationdate><title>Acute oral toxicity evaluations of some zinc(II) complexes derived from 1-(2-salicylaldiminoethyl)piperazine Schiff bases in rats</title><author>Salga, Muhammad Saleh ; Ali, Hapipah Mohd ; Abdulla, Mahmood Ameen ; Abdelwahab, Siddig Ibrahim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c444t-6a265ad601688282ef1037e7b7eee7b83376947257b627786e626d42a7927c3c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Administration, Oral</topic><topic>Alanine Transaminase - blood</topic><topic>Alkaline Phosphatase - blood</topic><topic>Animals</topic><topic>Aspartic Acid - blood</topic><topic>C-Reactive Protein - metabolism</topic><topic>Dose-Response Relationship, Drug</topic><topic>Erythrocyte Indices</topic><topic>Female</topic><topic>Immunoglobulins - blood</topic><topic>Inorganic chemistry</topic><topic>Ligands</topic><topic>Lipoproteins, HDL - blood</topic><topic>Male</topic><topic>Phenols</topic><topic>Piperazines - toxicity</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Schiff Bases - toxicity</topic><topic>Time Factors</topic><topic>Toxicity</topic><topic>Triglycerides - blood</topic><topic>Zinc</topic><topic>Zinc - toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Salga, Muhammad Saleh</creatorcontrib><creatorcontrib>Ali, Hapipah Mohd</creatorcontrib><creatorcontrib>Abdulla, Mahmood Ameen</creatorcontrib><creatorcontrib>Abdelwahab, Siddig Ibrahim</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Databases</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Salga, Muhammad Saleh</au><au>Ali, Hapipah Mohd</au><au>Abdulla, Mahmood Ameen</au><au>Abdelwahab, Siddig Ibrahim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute oral toxicity evaluations of some zinc(II) complexes derived from 1-(2-salicylaldiminoethyl)piperazine Schiff bases in rats</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2012-02-01</date><risdate>2012</risdate><volume>13</volume><issue>2</issue><spage>1393</spage><epage>1404</epage><pages>1393-1404</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>The current study described the synthesis and the in vivo acute oral toxicity evaluations in Sprague Dawley rats. The compounds were characterized by elemental analyses, LC-MS, FTIR, (1)H NMR, (13)C NMR and UV-visible spectroscopy. In the acute toxicity study, a single administration of the compounds was performed orally to the rats at the single doses of 2000 mg/kg and they were then monitored for possible side effects, mortality or behavioral changes up to 14 days. The serum level of aspartate (AST), alanine aminotransferases (ALT), alkaline phosphate (ALP), triglyceride, high density lipoprotein (HDL), immunoglobulins (GAM) and the C-reactive proteins did not significantly change. The hematological indices white blood cells (WBC), haematocrit (HCT), red blood cells (RBC), mean corpuscular volume (MCV), mean corpuscular haemoglobin concentration (MCHC), and mean corpuscular hemoglobin (MCH) were within the normal range. The renal function indices examined were also within the reference range. Generally, the compounds exhibited low toxic effects as required for further in vivo therapeutic studies.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>22408397</pmid><doi>10.3390/ijms13021393</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Oral Alanine Transaminase - blood Alkaline Phosphatase - blood Animals Aspartic Acid - blood C-Reactive Protein - metabolism Dose-Response Relationship, Drug Erythrocyte Indices Female Immunoglobulins - blood Inorganic chemistry Ligands Lipoproteins, HDL - blood Male Phenols Piperazines - toxicity Rats Rats, Sprague-Dawley Schiff Bases - toxicity Time Factors Toxicity Triglycerides - blood Zinc Zinc - toxicity |
title | Acute oral toxicity evaluations of some zinc(II) complexes derived from 1-(2-salicylaldiminoethyl)piperazine Schiff bases in rats |
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