Synthesis, crystal structure and leishmanicidal activity of new trimethoprim Ru(III), Cu(II) and Pt(II) metal complexes

Leishmaniasis is a parasitic disease caused by protozoa of the genus Leishmania, which has very limited treatment options and affects poor and underdeveloped populations. The current treatment is plagued by many complications, such as high toxicity, high cost and resistance to parasites; therefore,...

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Veröffentlicht in:Journal of inorganic biochemistry 2020-04, Vol.205, p.111002-111002, Article 111002
Hauptverfasser: Silva, Giovani Lindolfo, Dias, Júlia Scaff Moreira, Silva, Henrique Vieira Reis, Teixeira, Jessica Da Silva, De Souza, Ijaiel Rian Brito, Guimarães, Elisalva Teixeira, de Magalhães Moreira, Diogo Rodrigo, Soares, Milena Botelho Pereira, Barbosa, Marília Imaculada Frazão, Doriguetto, Antônio Carlos
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container_title Journal of inorganic biochemistry
container_volume 205
creator Silva, Giovani Lindolfo
Dias, Júlia Scaff Moreira
Silva, Henrique Vieira Reis
Teixeira, Jessica Da Silva
De Souza, Ijaiel Rian Brito
Guimarães, Elisalva Teixeira
de Magalhães Moreira, Diogo Rodrigo
Soares, Milena Botelho Pereira
Barbosa, Marília Imaculada Frazão
Doriguetto, Antônio Carlos
description Leishmaniasis is a parasitic disease caused by protozoa of the genus Leishmania, which has very limited treatment options and affects poor and underdeveloped populations. The current treatment is plagued by many complications, such as high toxicity, high cost and resistance to parasites; therefore, novel therapeutic agents are urgently needed. Herein, the synthesis, characterization and in vitro leishmanicidal potential of new complexes with the general formula [RuCl3(TMP)(dppb)] (1), [PtCl(TMP)(PPh3)2]PF6 (2) and [Cu(CH3COO)2(TMP)2]·DMF (3) (dppb = 1,4-bis(diphenylphosphino)butane, PPH3 = triphenylphosphine and TMP = trimethoprim) were evaluated. The complexes were characterized by infrared, UV–vis, cyclic voltammetry, molar conductance measurements, elemental analysis and NMR experiments. Also, the geometry of (2) and (3) were determined by single crystal X-ray diffraction. Despite being less potent against promastigote L. amazonensis proliferation than amphotericin B reference drug (IC50 = 0.09 ± 0.02 μM), complex (2) (IC50 = 3.6 ± 1.5 μM) was several times less cytotoxic (CC50 = 17.8 μM, SI = 4.9) in comparison with amphotericin B (CC50 = 3.3 μM, SI = 36.6) and gentian violet control (CC50 = 0.8 μM). Additionally, complex (2) inhibited J774 macrophage infection and amastigote number by macrophages (IC50 = 6.6 and SI = 2.7). Outstandingly, complex (2) was shown to be a promising candidate for a new leishmanicidal therapeutic agent, considering its biological power combined with low toxicity. Trimethoprim complexes with ruthenium(III), platinum(II) and cooper(II) were synthesized and characterized and their leishmanicidal activity evaluated. The platinum complex exhibited promising leishmanicidal activity and low toxicity. [Display omitted] •New trimethoprim Ru(III), Cu(II) and Pt(II) complexes are reported.•The crystal structure of the Cu(II) and Pt(II) complexes are determined.•The Pt(II) complex is a promising candidate for a leishmanicidal therapeutic agent.
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The current treatment is plagued by many complications, such as high toxicity, high cost and resistance to parasites; therefore, novel therapeutic agents are urgently needed. Herein, the synthesis, characterization and in vitro leishmanicidal potential of new complexes with the general formula [RuCl3(TMP)(dppb)] (1), [PtCl(TMP)(PPh3)2]PF6 (2) and [Cu(CH3COO)2(TMP)2]·DMF (3) (dppb = 1,4-bis(diphenylphosphino)butane, PPH3 = triphenylphosphine and TMP = trimethoprim) were evaluated. The complexes were characterized by infrared, UV–vis, cyclic voltammetry, molar conductance measurements, elemental analysis and NMR experiments. Also, the geometry of (2) and (3) were determined by single crystal X-ray diffraction. Despite being less potent against promastigote L. amazonensis proliferation than amphotericin B reference drug (IC50 = 0.09 ± 0.02 μM), complex (2) (IC50 = 3.6 ± 1.5 μM) was several times less cytotoxic (CC50 = 17.8 μM, SI = 4.9) in comparison with amphotericin B (CC50 = 3.3 μM, SI = 36.6) and gentian violet control (CC50 = 0.8 μM). Additionally, complex (2) inhibited J774 macrophage infection and amastigote number by macrophages (IC50 = 6.6 and SI = 2.7). Outstandingly, complex (2) was shown to be a promising candidate for a new leishmanicidal therapeutic agent, considering its biological power combined with low toxicity. Trimethoprim complexes with ruthenium(III), platinum(II) and cooper(II) were synthesized and characterized and their leishmanicidal activity evaluated. The platinum complex exhibited promising leishmanicidal activity and low toxicity. [Display omitted] •New trimethoprim Ru(III), Cu(II) and Pt(II) complexes are reported.•The crystal structure of the Cu(II) and Pt(II) complexes are determined.•The Pt(II) complex is a promising candidate for a leishmanicidal therapeutic agent.</description><identifier>ISSN: 0162-0134</identifier><identifier>EISSN: 1873-3344</identifier><identifier>DOI: 10.1016/j.jinorgbio.2020.111002</identifier><identifier>PMID: 32007697</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Antiprotozoal Agents - chemical synthesis ; Antiprotozoal Agents - chemistry ; Antiprotozoal Agents - pharmacology ; Cell Line ; Coordination Complexes - chemical synthesis ; Coordination Complexes - chemistry ; Coordination Complexes - pharmacology ; Copper - chemistry ; Copper - pharmacology ; Crystallography, X-Ray ; L. amazonensis ; Leishmania - growth &amp; development ; Leishmaniasis - drug therapy ; Leishmaniasis - metabolism ; Leishmaniasis - pathology ; Leishmanicidal activity ; Mice ; Molecular Structure ; Platinum - chemistry ; Platinum - pharmacology ; Ru(III), Pt(II), Cu(II) complexes ; Rubidium - chemistry ; Rubidium - pharmacology ; Selectivity ; Trimethoprim ; Trimethoprim - chemistry ; Trimethoprim - pharmacology</subject><ispartof>Journal of inorganic biochemistry, 2020-04, Vol.205, p.111002-111002, Article 111002</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. 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The current treatment is plagued by many complications, such as high toxicity, high cost and resistance to parasites; therefore, novel therapeutic agents are urgently needed. Herein, the synthesis, characterization and in vitro leishmanicidal potential of new complexes with the general formula [RuCl3(TMP)(dppb)] (1), [PtCl(TMP)(PPh3)2]PF6 (2) and [Cu(CH3COO)2(TMP)2]·DMF (3) (dppb = 1,4-bis(diphenylphosphino)butane, PPH3 = triphenylphosphine and TMP = trimethoprim) were evaluated. The complexes were characterized by infrared, UV–vis, cyclic voltammetry, molar conductance measurements, elemental analysis and NMR experiments. Also, the geometry of (2) and (3) were determined by single crystal X-ray diffraction. Despite being less potent against promastigote L. amazonensis proliferation than amphotericin B reference drug (IC50 = 0.09 ± 0.02 μM), complex (2) (IC50 = 3.6 ± 1.5 μM) was several times less cytotoxic (CC50 = 17.8 μM, SI = 4.9) in comparison with amphotericin B (CC50 = 3.3 μM, SI = 36.6) and gentian violet control (CC50 = 0.8 μM). Additionally, complex (2) inhibited J774 macrophage infection and amastigote number by macrophages (IC50 = 6.6 and SI = 2.7). Outstandingly, complex (2) was shown to be a promising candidate for a new leishmanicidal therapeutic agent, considering its biological power combined with low toxicity. Trimethoprim complexes with ruthenium(III), platinum(II) and cooper(II) were synthesized and characterized and their leishmanicidal activity evaluated. The platinum complex exhibited promising leishmanicidal activity and low toxicity. [Display omitted] •New trimethoprim Ru(III), Cu(II) and Pt(II) complexes are reported.•The crystal structure of the Cu(II) and Pt(II) complexes are determined.•The Pt(II) complex is a promising candidate for a leishmanicidal therapeutic agent.</description><subject>Animals</subject><subject>Antiprotozoal Agents - chemical synthesis</subject><subject>Antiprotozoal Agents - chemistry</subject><subject>Antiprotozoal Agents - pharmacology</subject><subject>Cell Line</subject><subject>Coordination Complexes - chemical synthesis</subject><subject>Coordination Complexes - chemistry</subject><subject>Coordination Complexes - pharmacology</subject><subject>Copper - chemistry</subject><subject>Copper - pharmacology</subject><subject>Crystallography, X-Ray</subject><subject>L. amazonensis</subject><subject>Leishmania - growth &amp; development</subject><subject>Leishmaniasis - drug therapy</subject><subject>Leishmaniasis - metabolism</subject><subject>Leishmaniasis - pathology</subject><subject>Leishmanicidal activity</subject><subject>Mice</subject><subject>Molecular Structure</subject><subject>Platinum - chemistry</subject><subject>Platinum - pharmacology</subject><subject>Ru(III), Pt(II), Cu(II) complexes</subject><subject>Rubidium - chemistry</subject><subject>Rubidium - pharmacology</subject><subject>Selectivity</subject><subject>Trimethoprim</subject><subject>Trimethoprim - chemistry</subject><subject>Trimethoprim - pharmacology</subject><issn>0162-0134</issn><issn>1873-3344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE9PGzEQxS1EVQLtV6A-gsQG_4sdH1FUIBJSK6Bny-udbRztroPthebb4xDg2tOMZn5vRu8h9IOSKSVUXq6naz-E-Lf2YcoIK1NKCWEHaELnilecC3GIJoVkFaFcHKHjlNaEkNlMqK_oiDNClNRqgl4etkNeQfLpAru4Tdl2OOU4ujxGwHZocAc-rXo7eOebsrQu-2eftzi0eIAXnKPvIa_CplR8P54tl8vzC7zYNedv-t_5rS1QUbvQbzr4B-kb-tLaLsH393qC_lz_fFzcVne_bpaLq7vKcUVzpTVtlarnknHF61qIRmvHWzevnSC6LqYlm1mmGkGV1kowKWwtqZNzrUGC5ifobH93E8PTCCmb3icHXWcHCGMyjM8I55pIWVC1R10MKUVozc6TjVtDidmlbtbmM3WzS93sUy_K0_cnY91D86n7iLkAV3sAitVnD9Ek52Fw0PgILpsm-P8-eQV_A5Zo</recordid><startdate>202004</startdate><enddate>202004</enddate><creator>Silva, Giovani Lindolfo</creator><creator>Dias, Júlia Scaff Moreira</creator><creator>Silva, Henrique Vieira Reis</creator><creator>Teixeira, Jessica Da Silva</creator><creator>De Souza, Ijaiel Rian Brito</creator><creator>Guimarães, Elisalva Teixeira</creator><creator>de Magalhães Moreira, Diogo Rodrigo</creator><creator>Soares, Milena Botelho Pereira</creator><creator>Barbosa, Marília Imaculada Frazão</creator><creator>Doriguetto, Antônio Carlos</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>202004</creationdate><title>Synthesis, crystal structure and leishmanicidal activity of new trimethoprim Ru(III), Cu(II) and Pt(II) metal complexes</title><author>Silva, Giovani Lindolfo ; Dias, Júlia Scaff Moreira ; Silva, Henrique Vieira Reis ; Teixeira, Jessica Da Silva ; De Souza, Ijaiel Rian Brito ; Guimarães, Elisalva Teixeira ; de Magalhães Moreira, Diogo Rodrigo ; Soares, Milena Botelho Pereira ; Barbosa, Marília Imaculada Frazão ; Doriguetto, Antônio Carlos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-991f77b862373bb44d99c3fc8bc409b110625a27d4179974264ab61c6899e6e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Antiprotozoal Agents - chemical synthesis</topic><topic>Antiprotozoal Agents - chemistry</topic><topic>Antiprotozoal Agents - pharmacology</topic><topic>Cell Line</topic><topic>Coordination Complexes - chemical synthesis</topic><topic>Coordination Complexes - chemistry</topic><topic>Coordination Complexes - pharmacology</topic><topic>Copper - chemistry</topic><topic>Copper - pharmacology</topic><topic>Crystallography, X-Ray</topic><topic>L. amazonensis</topic><topic>Leishmania - growth &amp; development</topic><topic>Leishmaniasis - drug therapy</topic><topic>Leishmaniasis - metabolism</topic><topic>Leishmaniasis - pathology</topic><topic>Leishmanicidal activity</topic><topic>Mice</topic><topic>Molecular Structure</topic><topic>Platinum - chemistry</topic><topic>Platinum - pharmacology</topic><topic>Ru(III), Pt(II), Cu(II) complexes</topic><topic>Rubidium - chemistry</topic><topic>Rubidium - pharmacology</topic><topic>Selectivity</topic><topic>Trimethoprim</topic><topic>Trimethoprim - chemistry</topic><topic>Trimethoprim - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Silva, Giovani Lindolfo</creatorcontrib><creatorcontrib>Dias, Júlia Scaff Moreira</creatorcontrib><creatorcontrib>Silva, Henrique Vieira Reis</creatorcontrib><creatorcontrib>Teixeira, Jessica Da Silva</creatorcontrib><creatorcontrib>De Souza, Ijaiel Rian Brito</creatorcontrib><creatorcontrib>Guimarães, Elisalva Teixeira</creatorcontrib><creatorcontrib>de Magalhães Moreira, Diogo Rodrigo</creatorcontrib><creatorcontrib>Soares, Milena Botelho Pereira</creatorcontrib><creatorcontrib>Barbosa, Marília Imaculada Frazão</creatorcontrib><creatorcontrib>Doriguetto, Antônio Carlos</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of inorganic biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Silva, Giovani Lindolfo</au><au>Dias, Júlia Scaff Moreira</au><au>Silva, Henrique Vieira Reis</au><au>Teixeira, Jessica Da Silva</au><au>De Souza, Ijaiel Rian Brito</au><au>Guimarães, Elisalva Teixeira</au><au>de Magalhães Moreira, Diogo Rodrigo</au><au>Soares, Milena Botelho Pereira</au><au>Barbosa, Marília Imaculada Frazão</au><au>Doriguetto, Antônio Carlos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, crystal structure and leishmanicidal activity of new trimethoprim Ru(III), Cu(II) and Pt(II) metal complexes</atitle><jtitle>Journal of inorganic biochemistry</jtitle><addtitle>J Inorg Biochem</addtitle><date>2020-04</date><risdate>2020</risdate><volume>205</volume><spage>111002</spage><epage>111002</epage><pages>111002-111002</pages><artnum>111002</artnum><issn>0162-0134</issn><eissn>1873-3344</eissn><abstract>Leishmaniasis is a parasitic disease caused by protozoa of the genus Leishmania, which has very limited treatment options and affects poor and underdeveloped populations. The current treatment is plagued by many complications, such as high toxicity, high cost and resistance to parasites; therefore, novel therapeutic agents are urgently needed. Herein, the synthesis, characterization and in vitro leishmanicidal potential of new complexes with the general formula [RuCl3(TMP)(dppb)] (1), [PtCl(TMP)(PPh3)2]PF6 (2) and [Cu(CH3COO)2(TMP)2]·DMF (3) (dppb = 1,4-bis(diphenylphosphino)butane, PPH3 = triphenylphosphine and TMP = trimethoprim) were evaluated. The complexes were characterized by infrared, UV–vis, cyclic voltammetry, molar conductance measurements, elemental analysis and NMR experiments. Also, the geometry of (2) and (3) were determined by single crystal X-ray diffraction. Despite being less potent against promastigote L. amazonensis proliferation than amphotericin B reference drug (IC50 = 0.09 ± 0.02 μM), complex (2) (IC50 = 3.6 ± 1.5 μM) was several times less cytotoxic (CC50 = 17.8 μM, SI = 4.9) in comparison with amphotericin B (CC50 = 3.3 μM, SI = 36.6) and gentian violet control (CC50 = 0.8 μM). Additionally, complex (2) inhibited J774 macrophage infection and amastigote number by macrophages (IC50 = 6.6 and SI = 2.7). Outstandingly, complex (2) was shown to be a promising candidate for a new leishmanicidal therapeutic agent, considering its biological power combined with low toxicity. Trimethoprim complexes with ruthenium(III), platinum(II) and cooper(II) were synthesized and characterized and their leishmanicidal activity evaluated. The platinum complex exhibited promising leishmanicidal activity and low toxicity. [Display omitted] •New trimethoprim Ru(III), Cu(II) and Pt(II) complexes are reported.•The crystal structure of the Cu(II) and Pt(II) complexes are determined.•The Pt(II) complex is a promising candidate for a leishmanicidal therapeutic agent.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>32007697</pmid><doi>10.1016/j.jinorgbio.2020.111002</doi><tpages>1</tpages></addata></record>
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subjects Animals
Antiprotozoal Agents - chemical synthesis
Antiprotozoal Agents - chemistry
Antiprotozoal Agents - pharmacology
Cell Line
Coordination Complexes - chemical synthesis
Coordination Complexes - chemistry
Coordination Complexes - pharmacology
Copper - chemistry
Copper - pharmacology
Crystallography, X-Ray
L. amazonensis
Leishmania - growth & development
Leishmaniasis - drug therapy
Leishmaniasis - metabolism
Leishmaniasis - pathology
Leishmanicidal activity
Mice
Molecular Structure
Platinum - chemistry
Platinum - pharmacology
Ru(III), Pt(II), Cu(II) complexes
Rubidium - chemistry
Rubidium - pharmacology
Selectivity
Trimethoprim
Trimethoprim - chemistry
Trimethoprim - pharmacology
title Synthesis, crystal structure and leishmanicidal activity of new trimethoprim Ru(III), Cu(II) and Pt(II) metal complexes
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