K. R. Shylaja, Kalyan Raj, H. A. Deepa, Neelam Patil Radhika, S. Malini
{"title":"负载异康唑的纳米氧化铋配方的协同作用:结构表征的探索,增强的抗菌性能和动力学","authors":"K. R. Shylaja, Kalyan Raj, H. A. Deepa, Neelam Patil Radhika, S. Malini","doi":"10.1007/s11696-025-03998-6","DOIUrl":null,"url":null,"abstract":"<div><p>Drug-loaded nanoformulations exert numerous beneficial synergistic effects such as minimised toxicity and maximised bioavailability to combat drug resistance and achieve enhanced drug delivery. The current study explores the synthesis and enhanced antimicrobial behaviour of nano-Bi<sub>2</sub>O<sub>3</sub> loaded with Isoconazole. Bi<sub>2</sub>O<sub>3</sub> nanoparticles-Isoconazole formulation was characterised using XRD, FTIR in the range 500–4000 cm<sup>−1</sup>, SEM, EDX and UV analysis. The association of Bi<sub>2</sub>O<sub>3</sub> nanoparticles (Bi<sub>2</sub>O<sub>3</sub> NPs) with Isoconazole was revealed by XRD through peaks that match with tetragonal structure of β-Bi<sub>2</sub>O<sub>3</sub> for pure Bi<sub>2</sub>O<sub>3</sub> nanoparticles and altered dominant peaks after loading. Similarly, scanning electron microscopy conveyed detectable morphological changes along with average particle size elevating from 47.11 to 70.79 nm upon loading. Brunauer–Emmett–Teller curves indicated a reduced quantity of adsorbed nitrogen with surface area, pore volume and pore diameter of Bi<sub>2</sub>O<sub>3</sub> NPs decreasing from 7.23 m<sup>2</sup>/g, 6.98 × 10<sup>−3</sup> cm<sup>3</sup>/g and 22 nm to 4.11 m<sup>2</sup>/g, 4.94 × 10<sup>−3</sup> cm<sup>3</sup>/g and 18.011 nm, respectively. Also, significant changes in the signals of <sup>1</sup>H NMR upon loading Bi<sub>2</sub>O<sub>3</sub> NPs with Isoconazole were observed. UV analysis showed a bandgap of 2.6 eV, and the peak underwent red shift upon loading Isoconazole. An appreciable loading efficiency and loading capacity is reported along with release kinetics pattern following Higuchi plot based on Fickian diffusion. Enhanced planktonic antibacterial activity of Bi<sub>2</sub>O<sub>3</sub>-Isoconazole formulation as compared to pure Bi<sub>2</sub>O<sub>3</sub> and Isoconazole was found using zone inhibition. Also, antibiofilm activity by crystal violet assay was examined for minimum inhibitory concentration and minimum bactericidal concentration. Antifungal activity of 7.4–9.9 mm inhibition for concentrations of 5–75 μL with % growth inhibition of 98.3 and 95, respectively, was obtained by zone inhibition method and poison food technique. The antimicrobial studies based on the experimental evidences provide an insight into the behaviour of the new formulation that offers a cost-effective technique against new infections and works in a fairly suitable time frame.</p></div>","PeriodicalId":513,"journal":{"name":"Chemical Papers","volume":"79 5","pages":"3183 - 3203"},"PeriodicalIF":2.2000,"publicationDate":"2025-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synergism in isoconazole-loaded nano-bismuth oxide formulation: exploration of structural characterization, enhanced antimicrobial performance and kinetics\",\"authors\":\"K. R. Shylaja, Kalyan Raj, H. A. Deepa, Neelam Patil Radhika, S. Malini\",\"doi\":\"10.1007/s11696-025-03998-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Drug-loaded nanoformulations exert numerous beneficial synergistic effects such as minimised toxicity and maximised bioavailability to combat drug resistance and achieve enhanced drug delivery. The current study explores the synthesis and enhanced antimicrobial behaviour of nano-Bi<sub>2</sub>O<sub>3</sub> loaded with Isoconazole. Bi<sub>2</sub>O<sub>3</sub> nanoparticles-Isoconazole formulation was characterised using XRD, FTIR in the range 500–4000 cm<sup>−1</sup>, SEM, EDX and UV analysis. The association of Bi<sub>2</sub>O<sub>3</sub> nanoparticles (Bi<sub>2</sub>O<sub>3</sub> NPs) with Isoconazole was revealed by XRD through peaks that match with tetragonal structure of β-Bi<sub>2</sub>O<sub>3</sub> for pure Bi<sub>2</sub>O<sub>3</sub> nanoparticles and altered dominant peaks after loading. Similarly, scanning electron microscopy conveyed detectable morphological changes along with average particle size elevating from 47.11 to 70.79 nm upon loading. Brunauer–Emmett–Teller curves indicated a reduced quantity of adsorbed nitrogen with surface area, pore volume and pore diameter of Bi<sub>2</sub>O<sub>3</sub> NPs decreasing from 7.23 m<sup>2</sup>/g, 6.98 × 10<sup>−3</sup> cm<sup>3</sup>/g and 22 nm to 4.11 m<sup>2</sup>/g, 4.94 × 10<sup>−3</sup> cm<sup>3</sup>/g and 18.011 nm, respectively. Also, significant changes in the signals of <sup>1</sup>H NMR upon loading Bi<sub>2</sub>O<sub>3</sub> NPs with Isoconazole were observed. UV analysis showed a bandgap of 2.6 eV, and the peak underwent red shift upon loading Isoconazole. An appreciable loading efficiency and loading capacity is reported along with release kinetics pattern following Higuchi plot based on Fickian diffusion. Enhanced planktonic antibacterial activity of Bi<sub>2</sub>O<sub>3</sub>-Isoconazole formulation as compared to pure Bi<sub>2</sub>O<sub>3</sub> and Isoconazole was found using zone inhibition. Also, antibiofilm activity by crystal violet assay was examined for minimum inhibitory concentration and minimum bactericidal concentration. Antifungal activity of 7.4–9.9 mm inhibition for concentrations of 5–75 μL with % growth inhibition of 98.3 and 95, respectively, was obtained by zone inhibition method and poison food technique. 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Synergism in isoconazole-loaded nano-bismuth oxide formulation: exploration of structural characterization, enhanced antimicrobial performance and kinetics
Drug-loaded nanoformulations exert numerous beneficial synergistic effects such as minimised toxicity and maximised bioavailability to combat drug resistance and achieve enhanced drug delivery. The current study explores the synthesis and enhanced antimicrobial behaviour of nano-Bi2O3 loaded with Isoconazole. Bi2O3 nanoparticles-Isoconazole formulation was characterised using XRD, FTIR in the range 500–4000 cm−1, SEM, EDX and UV analysis. The association of Bi2O3 nanoparticles (Bi2O3 NPs) with Isoconazole was revealed by XRD through peaks that match with tetragonal structure of β-Bi2O3 for pure Bi2O3 nanoparticles and altered dominant peaks after loading. Similarly, scanning electron microscopy conveyed detectable morphological changes along with average particle size elevating from 47.11 to 70.79 nm upon loading. Brunauer–Emmett–Teller curves indicated a reduced quantity of adsorbed nitrogen with surface area, pore volume and pore diameter of Bi2O3 NPs decreasing from 7.23 m2/g, 6.98 × 10−3 cm3/g and 22 nm to 4.11 m2/g, 4.94 × 10−3 cm3/g and 18.011 nm, respectively. Also, significant changes in the signals of 1H NMR upon loading Bi2O3 NPs with Isoconazole were observed. UV analysis showed a bandgap of 2.6 eV, and the peak underwent red shift upon loading Isoconazole. An appreciable loading efficiency and loading capacity is reported along with release kinetics pattern following Higuchi plot based on Fickian diffusion. Enhanced planktonic antibacterial activity of Bi2O3-Isoconazole formulation as compared to pure Bi2O3 and Isoconazole was found using zone inhibition. Also, antibiofilm activity by crystal violet assay was examined for minimum inhibitory concentration and minimum bactericidal concentration. Antifungal activity of 7.4–9.9 mm inhibition for concentrations of 5–75 μL with % growth inhibition of 98.3 and 95, respectively, was obtained by zone inhibition method and poison food technique. The antimicrobial studies based on the experimental evidences provide an insight into the behaviour of the new formulation that offers a cost-effective technique against new infections and works in a fairly suitable time frame.
Chemical PapersChemical Engineering-General Chemical Engineering
CiteScore
3.30
自引率
4.50%
发文量
590
期刊介绍:
Chemical Papers is a peer-reviewed, international journal devoted to basic and applied chemical research. It has a broad scope covering the chemical sciences, but favors interdisciplinary research and studies that bring chemistry together with other disciplines.