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Potential antimicrobial, antidiabetic, catalytic, antioxidant and ROS/RNS inhibitory activities of Silybum marianum mediated biosynthesized copper oxide nanoparticles.
Iqbal, Junaid; Andleeb, Anisa; Ashraf, Hajra; Meer, Bisma; Mehmood, Azra; Jan, Hasnain; Zaman, Gouhar; Nadeem, Muhammad; Drouet, Samantha; Fazal, Hina; Giglioli-Guivarc'h, Nathalie; Hano, Christophe; Abbasi, Bilal Haider.
Afiliación
  • Iqbal J; Department of Biotechnology, Quaid-i-Azam University Islamabad 45320 Pakistan juniqbal34@gmail.com anisaandleeb@bs.qau.edu.pk hajraashraf67@gmail.com bismameer786@gmail.com gzaman@bs.qau.edu.pk bhabbasi@qau.edu.pk.
  • Andleeb A; Department of Biotechnology, Quaid-i-Azam University Islamabad 45320 Pakistan juniqbal34@gmail.com anisaandleeb@bs.qau.edu.pk hajraashraf67@gmail.com bismameer786@gmail.com gzaman@bs.qau.edu.pk bhabbasi@qau.edu.pk.
  • Ashraf H; Department of Biotechnology, Quaid-i-Azam University Islamabad 45320 Pakistan juniqbal34@gmail.com anisaandleeb@bs.qau.edu.pk hajraashraf67@gmail.com bismameer786@gmail.com gzaman@bs.qau.edu.pk bhabbasi@qau.edu.pk.
  • Meer B; Department of Biotechnology, Quaid-i-Azam University Islamabad 45320 Pakistan juniqbal34@gmail.com anisaandleeb@bs.qau.edu.pk hajraashraf67@gmail.com bismameer786@gmail.com gzaman@bs.qau.edu.pk bhabbasi@qau.edu.pk.
  • Mehmood A; Stem Cell & Regenerative Medicine Lab, National Centre of Excellence in Molecular Biology, University of Punjab 87-West Canal Bank Road Lahore 53700 Pakistan azramehmood@cemb.edu.pk.
  • Jan H; Institute of Biochemical Sciences, National Taiwan University Taipei City 10617 Taiwan rhasnain849@gmail.com.
  • Zaman G; Department of Biotechnology, Quaid-i-Azam University Islamabad 45320 Pakistan juniqbal34@gmail.com anisaandleeb@bs.qau.edu.pk hajraashraf67@gmail.com bismameer786@gmail.com gzaman@bs.qau.edu.pk bhabbasi@qau.edu.pk.
  • Nadeem M; Institute of Integrative Biosciences, CECOS University Peshawar 25100 Pakistan m.nadeem@cecos.edu.pk.
  • Drouet S; Laboratoire de Biologie des Ligneux et des Grandes Cultures (LBLGC), INRAE USC1328, Université d'Orléans 45067 Orléans Cedex 2 France samantha.drouet@univ-orleans.fr hano@univ-orleans.fr.
  • Fazal H; Pakistan Council of Scientific and Industrial Research (PCSIR) Laboratories Complex Peshawar 25120 Pakistan hina_fazalso@yahoo.com.
  • Giglioli-Guivarc'h N; EA2106 Biomolécules et Biotechnologies Végétales, Université Francois-Rabelais de Tours Tours France nathalie.guivarch@univ-tours.fr.
  • Hano C; Laboratoire de Biologie des Ligneux et des Grandes Cultures (LBLGC), INRAE USC1328, Université d'Orléans 45067 Orléans Cedex 2 France samantha.drouet@univ-orleans.fr hano@univ-orleans.fr.
  • Abbasi BH; Department of Biotechnology, Quaid-i-Azam University Islamabad 45320 Pakistan juniqbal34@gmail.com anisaandleeb@bs.qau.edu.pk hajraashraf67@gmail.com bismameer786@gmail.com gzaman@bs.qau.edu.pk bhabbasi@qau.edu.pk.
RSC Adv ; 12(22): 14069-14083, 2022 May 05.
Article en En | MEDLINE | ID: mdl-35558860
ABSTRACT
Use of medicinal plants for the biosynthesis of nanoparticles offers several advantages over other synthesis approaches. Plants contain a variety of bioactive compounds that can participate in reduction and capping of nanoparticles. Plant mediated synthesis has the leverage of cost effectiveness, eco-friendly approach and sustained availability. In the current study Silybum marianum, a medicinally valuable plant rich in silymarin content, is used as a reducing and stabilizing agent for the fabrication of nanoparticles. Biosynthesized CuO-NPs were characterized using High Performance Liquid Chromatography (HPLC), Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and Dynamic Light Scattering (DLS) techniques. Characterization revealed that CuO-NPs having a crystalline structure showed spherical morphology with an average size of 15 nm. HPLC analysis demonstrated conjugation of various silymarin components, especially the presence of silybin A (705.06 ± 1.59 mg g-1 DW). CuO-NPs exhibited strong bactericidal potency against clinically important pathogenic bacterial strains e.g. Enterobacter aerogenes and Salmonella typhi with an inhibition zone of 18 ± 1.3 mm and 17 ± 1.2 mm, respectively. Synthesized nanoparticles indicated a dose dependent cytotoxic effect against fibroblast cells exhibiting a percentage cell viability of 83.60 ± 1.505% and 55.1 ± 1.80% at 25 µg mL-1 and 100 µg mL-1 concentration, respectively. Moreover, CuO-NPs displayed higher antioxidant potential in terms of (TAC 96.9 ± 0.26 µg AAE/mg), (TRP 68.8 ± 0.35 µg AAE/mg), (DPPH 55.5 ± 0.62%), (ABTS 332.34 µM) and a significant value for (FRAP 215.40 µM). Furthermore, enzyme inhibition assays also exhibited excellent enzyme inhibition potential against α-amylase (35.5 ± 1.54%), urease (78.4 ± 1.26%) and lipase (80.50.91%), respectively. Overall findings indicated that biosynthesized CuO-NPs possess immense in vitro biological and biomedical properties and could be used as a broad-spectrum agent for a wider range of biomedical applications.

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: RSC Adv Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: RSC Adv Año: 2022 Tipo del documento: Article