New in vitro highly cytotoxic platinum and palladium cyanoximates with minimal side effects in vivo

Several biologically active bivalent Pd and Pt complexes with two structurally similar cyanoxime ligands abbreviated as H(DECO): 2-oximino-2-cyano-N,N′-diethylacetamide, and H(PyrCO): 2-oximino-2-cyan-N-pyrrolidine acetamide were synthesized and characterized using spectroscopic methods, thermal ana...

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Veröffentlicht in:Journal of inorganic biochemistry 2020-07, Vol.208, p.111082-111082, Article 111082
Hauptverfasser: Dannen, Stephanie D., Cornelison, Lauren, Durham, Paul, Morley, John E., Shahverdi, Kiana, Du, Junwei, Zhou, Haiying, Sudlow, Leland C., Hunter, Daniel, Wood, Matthew D., Berezin, Mikhail Y., Gerasimchuk, Nikolay
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container_title Journal of inorganic biochemistry
container_volume 208
creator Dannen, Stephanie D.
Cornelison, Lauren
Durham, Paul
Morley, John E.
Shahverdi, Kiana
Du, Junwei
Zhou, Haiying
Sudlow, Leland C.
Hunter, Daniel
Wood, Matthew D.
Berezin, Mikhail Y.
Gerasimchuk, Nikolay
description Several biologically active bivalent Pd and Pt complexes with two structurally similar cyanoxime ligands abbreviated as H(DECO): 2-oximino-2-cyano-N,N′-diethylacetamide, and H(PyrCO): 2-oximino-2-cyan-N-pyrrolidine acetamide were synthesized and characterized using spectroscopic methods, thermal analysis and X-ray crystallography. Structures revealed planar cis-geometry of studied complexes. Freshly obtained Pt(DECO)2, Pd(DECO)2, Pt(PyrCO)2 and Pd(PyrCO)2 complexes were used in for in vitro cytotoxicity assays using two different etiology human cancer cell lines HeLa and WiDr cells. Investigated compounds showed cytotoxicity levels at or above cisplatin. Pt(DECO)2 was also tested in vivo in healthy C57BL/6 mice. The complex was administered at three different dosage (0, 7.5, 15 mg/kg, i.p. once/week), over a total period of 8 weeks. No changes were observed in the animal weight in the treated mice compared to the control dextrose-treated group. The levels of erythrocytes, leukocytes, and hemoglobin were within the normal level suggesting low myelotoxicity. Negligible cardiotoxicity was observed from the histological evaluation of the hearts from the treated animals. Results from the tail nerve conduction velocity (NCV) and nerve histomorphometry suggested no impact of Pt(DECO)2 on peripheral nerves. The complex, however, induced certain hepatotoxicity and lead to the elevation of IL-6, a pro-inflammatory cytokine. Overall, Pt(DECO)2 showed minimal in vivo toxicity, thus presenting a promising candidate for future testing in animal models of cancer. [Display omitted] •Four new planar cis-geometry Pt(II) and Pd(II) amide-cyanoximes were synthesized.•In vitro cytotoxicity of the complexes against cancer cell was comparable to cisplatin.•Pt(II)-DECO complex was tested in vivo in healthy C57BL/6 mice.•Minimum in vivo toxicity of the lead Pt complex was observed in the treated animals
doi_str_mv 10.1016/j.jinorgbio.2020.111082
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Structures revealed planar cis-geometry of studied complexes. Freshly obtained Pt(DECO)2, Pd(DECO)2, Pt(PyrCO)2 and Pd(PyrCO)2 complexes were used in for in vitro cytotoxicity assays using two different etiology human cancer cell lines HeLa and WiDr cells. Investigated compounds showed cytotoxicity levels at or above cisplatin. Pt(DECO)2 was also tested in vivo in healthy C57BL/6 mice. The complex was administered at three different dosage (0, 7.5, 15 mg/kg, i.p. once/week), over a total period of 8 weeks. No changes were observed in the animal weight in the treated mice compared to the control dextrose-treated group. The levels of erythrocytes, leukocytes, and hemoglobin were within the normal level suggesting low myelotoxicity. Negligible cardiotoxicity was observed from the histological evaluation of the hearts from the treated animals. Results from the tail nerve conduction velocity (NCV) and nerve histomorphometry suggested no impact of Pt(DECO)2 on peripheral nerves. The complex, however, induced certain hepatotoxicity and lead to the elevation of IL-6, a pro-inflammatory cytokine. Overall, Pt(DECO)2 showed minimal in vivo toxicity, thus presenting a promising candidate for future testing in animal models of cancer. [Display omitted] •Four new planar cis-geometry Pt(II) and Pd(II) amide-cyanoximes were synthesized.•In vitro cytotoxicity of the complexes against cancer cell was comparable to cisplatin.•Pt(II)-DECO complex was tested in vivo in healthy C57BL/6 mice.•Minimum in vivo toxicity of the lead Pt complex was observed in the treated animals</description><identifier>ISSN: 0162-0134</identifier><identifier>ISSN: 1873-3344</identifier><identifier>EISSN: 1873-3344</identifier><identifier>DOI: 10.1016/j.jinorgbio.2020.111082</identifier><identifier>PMID: 32413634</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animal model ; Animals ; Coordination Complexes - adverse effects ; Coordination Complexes - chemical synthesis ; Coordination Complexes - chemistry ; Coordination Complexes - pharmacology ; Crystal structures ; Cytotoxins - adverse effects ; Cytotoxins - chemical synthesis ; Cytotoxins - chemistry ; Cytotoxins - pharmacology ; Drug Screening Assays, Antitumor ; HeLa Cells ; Human cancer cells ; Humans ; in vitro studies ; in vivo studies ; Male ; Mice ; Neoplasms - drug therapy ; Neoplasms - metabolism ; Neoplasms - pathology ; Palladium - adverse effects ; Palladium - chemistry ; Palladium - pharmacology ; Pd/Pt-cyanoximates ; Platinum - adverse effects ; Platinum - chemistry ; Platinum - pharmacology</subject><ispartof>Journal of inorganic biochemistry, 2020-07, Vol.208, p.111082-111082, Article 111082</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. 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Structures revealed planar cis-geometry of studied complexes. Freshly obtained Pt(DECO)2, Pd(DECO)2, Pt(PyrCO)2 and Pd(PyrCO)2 complexes were used in for in vitro cytotoxicity assays using two different etiology human cancer cell lines HeLa and WiDr cells. Investigated compounds showed cytotoxicity levels at or above cisplatin. Pt(DECO)2 was also tested in vivo in healthy C57BL/6 mice. The complex was administered at three different dosage (0, 7.5, 15 mg/kg, i.p. once/week), over a total period of 8 weeks. No changes were observed in the animal weight in the treated mice compared to the control dextrose-treated group. The levels of erythrocytes, leukocytes, and hemoglobin were within the normal level suggesting low myelotoxicity. Negligible cardiotoxicity was observed from the histological evaluation of the hearts from the treated animals. Results from the tail nerve conduction velocity (NCV) and nerve histomorphometry suggested no impact of Pt(DECO)2 on peripheral nerves. The complex, however, induced certain hepatotoxicity and lead to the elevation of IL-6, a pro-inflammatory cytokine. Overall, Pt(DECO)2 showed minimal in vivo toxicity, thus presenting a promising candidate for future testing in animal models of cancer. [Display omitted] •Four new planar cis-geometry Pt(II) and Pd(II) amide-cyanoximes were synthesized.•In vitro cytotoxicity of the complexes against cancer cell was comparable to cisplatin.•Pt(II)-DECO complex was tested in vivo in healthy C57BL/6 mice.•Minimum in vivo toxicity of the lead Pt complex was observed in the treated animals</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>32413634</pmid><doi>10.1016/j.jinorgbio.2020.111082</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Animal model
Animals
Coordination Complexes - adverse effects
Coordination Complexes - chemical synthesis
Coordination Complexes - chemistry
Coordination Complexes - pharmacology
Crystal structures
Cytotoxins - adverse effects
Cytotoxins - chemical synthesis
Cytotoxins - chemistry
Cytotoxins - pharmacology
Drug Screening Assays, Antitumor
HeLa Cells
Human cancer cells
Humans
in vitro studies
in vivo studies
Male
Mice
Neoplasms - drug therapy
Neoplasms - metabolism
Neoplasms - pathology
Palladium - adverse effects
Palladium - chemistry
Palladium - pharmacology
Pd/Pt-cyanoximates
Platinum - adverse effects
Platinum - chemistry
Platinum - pharmacology
title New in vitro highly cytotoxic platinum and palladium cyanoximates with minimal side effects in vivo
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