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dc.contributor.authorBennour, Ines
dc.contributor.authorNúria Ramos, M.
dc.contributor.authorNuez-Martínez, Miquel
dc.contributor.authorXavier, Jewel Ann Maria
dc.contributor.authorBuades, Ana B.
dc.contributor.authorSillanpää, Reijo
dc.contributor.authorTeixidor, Francesc
dc.contributor.authorChoquesillo-Lazarte, Duane
dc.contributor.authorRomero, Isabel
dc.contributor.authorMartinez-Medina, Margarita
dc.contributor.authorViñas, Clara
dc.date.accessioned2022-06-22T11:43:46Z
dc.date.available2022-06-22T11:43:46Z
dc.date.issued2022
dc.identifier.citationBennour, I., Núria Ramos, M., Nuez-Martínez, M., Xavier, J. A. M., Buades, A. B., Sillanpää, R., Teixidor, F., Choquesillo-Lazarte, D., Romero, I., Martinez-Medina, M., & Viñas, C. (2022). Water soluble organometallic small molecules as promising antibacterial agents : synthesis, physical–chemical properties and biological evaluation to tackle bacterial infections. <i>Dalton Transactions</i>, <i>51</i>(18), 7188-7209. <a href="https://doi.org/10.1039/D2DT01015A" target="_blank">https://doi.org/10.1039/D2DT01015A</a>
dc.identifier.otherCONVID_146533271
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/81983
dc.description.abstractThe Na[3,3′-Fe(8-I-1,2-C2B9H10)2] and Na[2,2′-M(1,7-C2B9H11)] (M = Co3+, Fe3+) small molecules are synthesized and the X-ray structures of [(H3O)(H2O)5][2,2′-Co(1,7-C2B9H11)2] and [Cs(MeCN)][8,8′-I2-Fe(1,2 C2B9H10)2], both displaying a transoid conformation of the [M(C2B9)2]− framework, are reported. Importantly, the supramolecular structure of [(H3O)(H2O)5][2,2′-Co(1,7-C2B9H11)2] presents 2D layers leading to a lamellar arrangement of the anions while the cation layers form polymeric water rings made of six- and four-membered rings of water molecules connected via OH⋯H hydrogen bonds; B–H⋯O contacts connect the cationic and anionic layers. Herein, we highlight the influence of the ligand isomers (ortho-/meta-), the metal effect (Co3+/Fe3+) on the same isomer, as well as the influence of the presence of the iodine atoms on the physical–chemical and biological properties of these molecules as antimicrobial agents to tackle antibiotic-resistant bacteria, which were tested with four Gram-positive bacteria, five Gram-negative bacteria, and three Candida albicans strains that have been responsible for human infections. We have demonstrated an antimicrobial effect against Candida species (MIC of 2 and 3 nM for Na[3,3′-Co(8-I-1,2-C2B9H10)2] and Na[2,2′-Co(1,7-C2B9H11)2], respectively), and against Gram-positive and Gram-negative bacteria, including multiresistant MRSA strains (MIC of 6 nM for Na[3,3′-Co(8-I-1,2-C2B9H10)2]). The selectivity index for antimicrobial activity of Na[3,3′-Co(1,2-C2B9H11)2] and Na[3,3′-Co(8-I-1,2-C2B9H10)2] compounds is very high (165 and 1180, respectively), which reveals that these small anionic metallacarborane molecules may be useful to tackle antibiotic-resistant bacteria. Moreover, we have demonstrated that the outer membrane of Gram-negative bacteria constitutes an impermeable barrier for the majority of these compounds. Nonetheless, the addition of two iodine groups in the structure of the parent Na[3,3′-Co(1,2-C2B9H11)2] had an improved effect (3–7 times) against Gram-negative bacteria. Possibly the changes in their physical–chemical properties make the meta-isomers and the ortho-di-iodinated small molecules more permeable for crossing this barrier. It should be emphasized that the most active metallabis(dicarbollide) small molecules are both transoid conformers in contrast to the ortho- [3,3′-Co(1,2-C2B9H11)2]− that is cisoid. The fact that these small molecules cross the mammalian membrane and have antimicrobial properties but low toxicity for mammalian cells (high selectivity index, SI) represents a promising tool to treat infectious intracellular bacteria. Since there is an urgent need for antibiotic discovery and development, this study represents a relevant advance in the field.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherRoyal Society of Chemistry (RSC)
dc.relation.ispartofseriesDalton Transactions
dc.rightsCC BY-NC 4.0
dc.titleWater soluble organometallic small molecules as promising antibacterial agents : synthesis, physical–chemical properties and biological evaluation to tackle bacterial infections
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202206223588
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineEpäorgaaninen kemiafi
dc.contributor.oppiaineEpäorgaaninen ja analyyttinen kemiafi
dc.contributor.oppiaineInorganic Chemistryen
dc.contributor.oppiaineInorganic and Analytical Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange7188-7209
dc.relation.issn1477-9226
dc.relation.numberinseries18
dc.relation.volume51
dc.type.versionpublishedVersion
dc.rights.copyright© 2022 Royal Society of Chemistry (RSC)
dc.rights.accesslevelopenAccessfi
dc.subject.ysokemiallinen synteesi
dc.subject.ysobioaktiiviset yhdisteet
dc.subject.ysoantimikrobiset yhdisteet
dc.subject.ysoorganometalliyhdisteet
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p8468
jyx.subject.urihttp://www.yso.fi/onto/yso/p28433
jyx.subject.urihttp://www.yso.fi/onto/yso/p21949
jyx.subject.urihttp://www.yso.fi/onto/yso/p28123
dc.rights.urlhttps://creativecommons.org/licenses/by-nc/4.0/
dc.relation.doi10.1039/D2DT01015A
jyx.fundinginformationThis work was supported by the Spanish Ministerio de Economía y Competitividad (PID2019-106832RB-100, and SAF2017-82261-P grant cofounded by the European Regional Development Fund) and the Generalitat de Catalunya (2017SGR1720). J. A. M. Xavier acknowledges DOC-FAM program under the Marie Sklodowska-Curie grant agreement N°754397. A. B. Buades, M. Nuez and J. A. M. Xavier are enrolled in the PhD program of the UAB.
dc.type.okmA1


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