Cargando…

Preparation of a Pt(II)–3-Hydroxy-2-tolyl-4H-chromen-4-one Complex Having Antimicrobial, Anticancerous, and Radical Scavenging Activities with Related Computational Studies

[Image: see text] A novel benzopyran-based platinum (II)–3-hydroxy-2-tolyl-4H-chromen-4-one (HToC) complex has been prepared and studied by UV–visible spectrophotometry. The study is based on the colored complexation between Pt(II) and HToC in the pH range of 8.92–9.21, resulting in the formation of...

Descripción completa

Detalles Bibliográficos
Autores principales: Mohmad, Masrat, Agnihotri, Nivedita, Kumar, Vikas, Azam, Mohammad, Kamal, Raj, Kumar, Ashish, Sharma, Ujjawal, Javed, Saleem, Muthu, Sambantham, Min, Kim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10483677/
https://www.ncbi.nlm.nih.gov/pubmed/37692249
http://dx.doi.org/10.1021/acsomega.3c01316
_version_ 1785102432140787712
author Mohmad, Masrat
Agnihotri, Nivedita
Kumar, Vikas
Azam, Mohammad
Kamal, Raj
Kumar, Ashish
Sharma, Ujjawal
Javed, Saleem
Muthu, Sambantham
Min, Kim
author_facet Mohmad, Masrat
Agnihotri, Nivedita
Kumar, Vikas
Azam, Mohammad
Kamal, Raj
Kumar, Ashish
Sharma, Ujjawal
Javed, Saleem
Muthu, Sambantham
Min, Kim
author_sort Mohmad, Masrat
collection PubMed
description [Image: see text] A novel benzopyran-based platinum (II)–3-hydroxy-2-tolyl-4H-chromen-4-one (HToC) complex has been prepared and studied by UV–visible spectrophotometry. The study is based on the colored complexation between Pt(II) and HToC in the pH range of 8.92–9.21, resulting in the formation of a stable binary yellow complex exhibiting λ(max) at 509–525 nm. The formed complex maintains linearity between 0.0 and 1.8 μg Pt(II) mL(–1). The well-known qualitative analytical methods, including Job’s method of continuous variations and the mole ratio approach, have both proven that the stoichiometry of the complex is 1:2 [Pt(II)/HToC]. Hence, the analytical results suggest that the formed platinum complex exhibits a square planar geometry. The values of various attributes corresponding to spectrophotometric studies and statistical calculations, such as the molar extinction coefficient (6.790 × 10(4) L mol(–1) cm(–1)), Sandell’s sensitivity (0.0029 μg Pt(II) cm(–2)), standard deviation (± 0.0011), RSD (0.317%), limit of detection (0.0147 μg mL(–1)) and correlation coefficient (0.9999), show that the performed study satisfies all of the criteria for good sensitivity, versatility, and cost-effectiveness. In order to have an apprehension of the molecular geometry and other structural specifics of the complex, DFT studies have been carried out. The in vitro anticancer potential of the ligand and its platinum complex in the human breast cancer cell line (T-27D), as determined by the MTT assay, reveals that the complex has better antiproliferative potential than the ligand. The antimicrobial potential of the complex has been successfully tested against both Gram-positive and -negative bacteria. Antioxidant capacity results suggest the better radical scavenging capacity of the complex than that of the ligand.
format Online
Article
Text
id pubmed-10483677
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-104836772023-09-08 Preparation of a Pt(II)–3-Hydroxy-2-tolyl-4H-chromen-4-one Complex Having Antimicrobial, Anticancerous, and Radical Scavenging Activities with Related Computational Studies Mohmad, Masrat Agnihotri, Nivedita Kumar, Vikas Azam, Mohammad Kamal, Raj Kumar, Ashish Sharma, Ujjawal Javed, Saleem Muthu, Sambantham Min, Kim ACS Omega [Image: see text] A novel benzopyran-based platinum (II)–3-hydroxy-2-tolyl-4H-chromen-4-one (HToC) complex has been prepared and studied by UV–visible spectrophotometry. The study is based on the colored complexation between Pt(II) and HToC in the pH range of 8.92–9.21, resulting in the formation of a stable binary yellow complex exhibiting λ(max) at 509–525 nm. The formed complex maintains linearity between 0.0 and 1.8 μg Pt(II) mL(–1). The well-known qualitative analytical methods, including Job’s method of continuous variations and the mole ratio approach, have both proven that the stoichiometry of the complex is 1:2 [Pt(II)/HToC]. Hence, the analytical results suggest that the formed platinum complex exhibits a square planar geometry. The values of various attributes corresponding to spectrophotometric studies and statistical calculations, such as the molar extinction coefficient (6.790 × 10(4) L mol(–1) cm(–1)), Sandell’s sensitivity (0.0029 μg Pt(II) cm(–2)), standard deviation (± 0.0011), RSD (0.317%), limit of detection (0.0147 μg mL(–1)) and correlation coefficient (0.9999), show that the performed study satisfies all of the criteria for good sensitivity, versatility, and cost-effectiveness. In order to have an apprehension of the molecular geometry and other structural specifics of the complex, DFT studies have been carried out. The in vitro anticancer potential of the ligand and its platinum complex in the human breast cancer cell line (T-27D), as determined by the MTT assay, reveals that the complex has better antiproliferative potential than the ligand. The antimicrobial potential of the complex has been successfully tested against both Gram-positive and -negative bacteria. Antioxidant capacity results suggest the better radical scavenging capacity of the complex than that of the ligand. American Chemical Society 2023-08-22 /pmc/articles/PMC10483677/ /pubmed/37692249 http://dx.doi.org/10.1021/acsomega.3c01316 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Mohmad, Masrat
Agnihotri, Nivedita
Kumar, Vikas
Azam, Mohammad
Kamal, Raj
Kumar, Ashish
Sharma, Ujjawal
Javed, Saleem
Muthu, Sambantham
Min, Kim
Preparation of a Pt(II)–3-Hydroxy-2-tolyl-4H-chromen-4-one Complex Having Antimicrobial, Anticancerous, and Radical Scavenging Activities with Related Computational Studies
title Preparation of a Pt(II)–3-Hydroxy-2-tolyl-4H-chromen-4-one Complex Having Antimicrobial, Anticancerous, and Radical Scavenging Activities with Related Computational Studies
title_full Preparation of a Pt(II)–3-Hydroxy-2-tolyl-4H-chromen-4-one Complex Having Antimicrobial, Anticancerous, and Radical Scavenging Activities with Related Computational Studies
title_fullStr Preparation of a Pt(II)–3-Hydroxy-2-tolyl-4H-chromen-4-one Complex Having Antimicrobial, Anticancerous, and Radical Scavenging Activities with Related Computational Studies
title_full_unstemmed Preparation of a Pt(II)–3-Hydroxy-2-tolyl-4H-chromen-4-one Complex Having Antimicrobial, Anticancerous, and Radical Scavenging Activities with Related Computational Studies
title_short Preparation of a Pt(II)–3-Hydroxy-2-tolyl-4H-chromen-4-one Complex Having Antimicrobial, Anticancerous, and Radical Scavenging Activities with Related Computational Studies
title_sort preparation of a pt(ii)–3-hydroxy-2-tolyl-4h-chromen-4-one complex having antimicrobial, anticancerous, and radical scavenging activities with related computational studies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10483677/
https://www.ncbi.nlm.nih.gov/pubmed/37692249
http://dx.doi.org/10.1021/acsomega.3c01316
work_keys_str_mv AT mohmadmasrat preparationofaptii3hydroxy2tolyl4hchromen4onecomplexhavingantimicrobialanticancerousandradicalscavengingactivitieswithrelatedcomputationalstudies
AT agnihotrinivedita preparationofaptii3hydroxy2tolyl4hchromen4onecomplexhavingantimicrobialanticancerousandradicalscavengingactivitieswithrelatedcomputationalstudies
AT kumarvikas preparationofaptii3hydroxy2tolyl4hchromen4onecomplexhavingantimicrobialanticancerousandradicalscavengingactivitieswithrelatedcomputationalstudies
AT azammohammad preparationofaptii3hydroxy2tolyl4hchromen4onecomplexhavingantimicrobialanticancerousandradicalscavengingactivitieswithrelatedcomputationalstudies
AT kamalraj preparationofaptii3hydroxy2tolyl4hchromen4onecomplexhavingantimicrobialanticancerousandradicalscavengingactivitieswithrelatedcomputationalstudies
AT kumarashish preparationofaptii3hydroxy2tolyl4hchromen4onecomplexhavingantimicrobialanticancerousandradicalscavengingactivitieswithrelatedcomputationalstudies
AT sharmaujjawal preparationofaptii3hydroxy2tolyl4hchromen4onecomplexhavingantimicrobialanticancerousandradicalscavengingactivitieswithrelatedcomputationalstudies
AT javedsaleem preparationofaptii3hydroxy2tolyl4hchromen4onecomplexhavingantimicrobialanticancerousandradicalscavengingactivitieswithrelatedcomputationalstudies
AT muthusambantham preparationofaptii3hydroxy2tolyl4hchromen4onecomplexhavingantimicrobialanticancerousandradicalscavengingactivitieswithrelatedcomputationalstudies
AT minkim preparationofaptii3hydroxy2tolyl4hchromen4onecomplexhavingantimicrobialanticancerousandradicalscavengingactivitieswithrelatedcomputationalstudies