2020
DOI: 10.1016/j.ijbiomac.2019.10.013
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Fluorescent carbon nanoparticles synthesized from bovine serum albumin nanoparticles

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Cited by 13 publications
(4 citation statements)
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“…In order to further understand the chemical composition and surface element state of E-GFs, BSA-GFs, BGGs, and BRNGs, XPS characterization was used, and the results are shown in Figure b–i. The full XPS pattern of E-GFs, BSA-GFs, and BGGs exhibits the existence of C, N, Si, and O elements, and the survey spectrum of BRNGs shows new elements such as Ni and P. In the high-resolution C 1s XPS spectra of E-GFs, characteristic peaks located at 288.3 and 284.5 eV are attributed to −CO and C–C, respectively (Figure c). , Compared with E-GFs, new peaks located at 286.2 and 285.3 eV are ascribed to C–O and C–N in the high-resolution C 1s XPS spectra of BSA-GFs, respectively (Figure d). , For narrow scans of E-GFs and BSA-GFs, the intensity of N 1s is significantly enhanced and peak of −N (399.8 eV) can be observed (Figure g,h) . The presence of C–O, C–N, and −N indicates that BSA is adhered on the surface of GFs.…”
Section: Resultsmentioning
confidence: 97%
See 1 more Smart Citation
“…In order to further understand the chemical composition and surface element state of E-GFs, BSA-GFs, BGGs, and BRNGs, XPS characterization was used, and the results are shown in Figure b–i. The full XPS pattern of E-GFs, BSA-GFs, and BGGs exhibits the existence of C, N, Si, and O elements, and the survey spectrum of BRNGs shows new elements such as Ni and P. In the high-resolution C 1s XPS spectra of E-GFs, characteristic peaks located at 288.3 and 284.5 eV are attributed to −CO and C–C, respectively (Figure c). , Compared with E-GFs, new peaks located at 286.2 and 285.3 eV are ascribed to C–O and C–N in the high-resolution C 1s XPS spectra of BSA-GFs, respectively (Figure d). , For narrow scans of E-GFs and BSA-GFs, the intensity of N 1s is significantly enhanced and peak of −N (399.8 eV) can be observed (Figure g,h) . The presence of C–O, C–N, and −N indicates that BSA is adhered on the surface of GFs.…”
Section: Resultsmentioning
confidence: 97%
“…17,21 Compared with E-GFs, new peaks located at 286.2 and 285.3 eV are ascribed to C−O and C−N in the high-resolution C 1s XPS spectra of BSA-GFs, respectively (Figure 3d). 17,30 For narrow scans of E-GFs and BSA-GFs, the intensity of N 1s is significantly enhanced and peak of −N (399.8 eV) can be observed (Figure 3g,h). 17 34 The Ni 2p peaks at 856.2, 873.7, 861.4, and 880.5 eV are attributed to the main and satellite peaks of Ni 2+ in BRNGs.…”
Section: ■ Introductionmentioning
confidence: 99%
“…BSA nanoparticles are known for their favorable safety profile, making them suitable for various clinical applications. Their typical size range of 10 to 200 nanometers facilitates efficient cellular uptake and effective delivery to targeted sites while also allowing them to evade rapid immune clearance, prolonging their circulation time in the body [ 128 , 129 ].…”
Section: Nanotechnology In Bone Tuberculosis Treatmentmentioning
confidence: 99%
“…Fluorescence spectroscopy is an important method to study the interactions of biological macromolecules with small molecules and ions. 28,29 The emission characteristics, fluorescence polarization, energy transfer and fluorescence lifetime obtained in the fluorescence tests provide useful information on the structure of the fluorescent chromophore and the microenvironment in which it is located. [30][31][32] Therefore, fluorescence spectroscopy is a simple and sensitive method, which requires only a small amount of sample, to quantitatively study the interactions between BSA and small molecules, to calculate the binding constants, binding sites, and many thermodynamic and kinetic parameters.…”
Section: Introductionmentioning
confidence: 99%