dc.contributor.author | Bennour, Ines | |
dc.contributor.author | Núria Ramos, M. | |
dc.contributor.author | Nuez-Martínez, Miquel | |
dc.contributor.author | Xavier, Jewel Ann Maria | |
dc.contributor.author | Buades, Ana B. | |
dc.contributor.author | Sillanpää, Reijo | |
dc.contributor.author | Teixidor, Francesc | |
dc.contributor.author | Choquesillo-Lazarte, Duane | |
dc.contributor.author | Romero, Isabel | |
dc.contributor.author | Martinez-Medina, Margarita | |
dc.contributor.author | Viñas, Clara | |
dc.date.accessioned | 2022-06-22T11:43:46Z | |
dc.date.available | 2022-06-22T11:43:46Z | |
dc.date.issued | 2022 | |
dc.identifier.citation | Bennour, 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.other | CONVID_146533271 | |
dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/81983 | |
dc.description.abstract | The 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.mimetype | application/pdf | |
dc.language.iso | eng | |
dc.publisher | Royal Society of Chemistry (RSC) | |
dc.relation.ispartofseries | Dalton Transactions | |
dc.rights | CC BY-NC 4.0 | |
dc.title | Water soluble organometallic small molecules as promising antibacterial agents : synthesis, physical–chemical properties and biological evaluation to tackle bacterial infections | |
dc.type | research article | |
dc.identifier.urn | URN:NBN:fi:jyu-202206223588 | |
dc.contributor.laitos | Kemian laitos | fi |
dc.contributor.laitos | Department of Chemistry | en |
dc.contributor.oppiaine | Epäorgaaninen kemia | fi |
dc.contributor.oppiaine | Epäorgaaninen ja analyyttinen kemia | fi |
dc.contributor.oppiaine | Inorganic Chemistry | en |
dc.contributor.oppiaine | Inorganic and Analytical Chemistry | en |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
dc.description.reviewstatus | peerReviewed | |
dc.format.pagerange | 7188-7209 | |
dc.relation.issn | 1477-9226 | |
dc.relation.numberinseries | 18 | |
dc.relation.volume | 51 | |
dc.type.version | publishedVersion | |
dc.rights.copyright | © 2022 Royal Society of Chemistry (RSC) | |
dc.rights.accesslevel | openAccess | fi |
dc.type.publication | article | |
dc.subject.yso | kemiallinen synteesi | |
dc.subject.yso | bioaktiiviset yhdisteet | |
dc.subject.yso | antimikrobiset yhdisteet | |
dc.subject.yso | organometalliyhdisteet | |
dc.format.content | fulltext | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p8468 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p28433 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p21949 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p28123 | |
dc.rights.url | https://creativecommons.org/licenses/by-nc/4.0/ | |
dc.relation.doi | 10.1039/D2DT01015A | |
jyx.fundinginformation | This 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.okm | A1 | |