2019
DOI: 10.1016/j.foodhyd.2018.12.027
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Green synthesis, characterization and in vitro release of cinnamaldehyde/sodium alginate/chitosan nanoparticles

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Cited by 81 publications
(41 citation statements)
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“…An intense peak was observed at 23°indicating the presence of the Cs-Al NDs, which can be inferred that alginate is influencing the crystalline properties of chitosan through hydrogen bonding, and electrostatic interaction between negative and positive charges, confirming the formation of a polyelectrolyte complex using the ionic gelation method [14,23,42]. These results are in agreement with those reported in the literature, allowing to state that the Cs-Al NDs present high crystallinity, strong electrostatic International Journal of Polymer Science interaction, and good order of the crystallites [19]. The crystallite size for the Cs-Al NDs was calculated to be 1.6 nm from the peak with the strongest intensity at 23°, according to the following Debye-Scherrer equation (1):…”
Section: Resultssupporting
confidence: 90%
See 1 more Smart Citation
“…An intense peak was observed at 23°indicating the presence of the Cs-Al NDs, which can be inferred that alginate is influencing the crystalline properties of chitosan through hydrogen bonding, and electrostatic interaction between negative and positive charges, confirming the formation of a polyelectrolyte complex using the ionic gelation method [14,23,42]. These results are in agreement with those reported in the literature, allowing to state that the Cs-Al NDs present high crystallinity, strong electrostatic International Journal of Polymer Science interaction, and good order of the crystallites [19]. The crystallite size for the Cs-Al NDs was calculated to be 1.6 nm from the peak with the strongest intensity at 23°, according to the following Debye-Scherrer equation (1):…”
Section: Resultssupporting
confidence: 90%
“…Scanning electron microscopy (SEM) images shown in Figures 1(a) and 1(b) determine the morphological features of the as-synthesized Cs-Al NDs. Agglomeration can be observed since the nanodisks were lyophilized previously, but the shape of the disks can still be seen clearly as shown in the SEM image in Figure 1(b) [19]. The nanoparticles were successfully synthesized with a more disk shape than the usual spherical or common structures, presenting a regular and smooth surface but a wide size range, which can be attributed to many factors such as the biopolymer concentrations and electrostatic interaction that occurs during ionotropic gelation using sodium tripolyphosphate (STPP) as a highly charged compound [20,21].…”
Section: Resultsmentioning
confidence: 92%
“…The IR spectrum of both biopolymers can be assigned by analogy to the literature. 50,51 FTIR analysis of the hybrid-beads (non-calcined samples) indicated the appearance of the characteristic peaks of the biopolymers used with slight modications (enhanced intensities) related to cross-linking biopolymer. It must be emphasized that an additional peak at 1733 cm À1 was observed in all hybrid materials, attributed to carbonyl stretching (-C]O group).…”
Section: Resultsmentioning
confidence: 99%
“…DLS provides a hydrodynamic size and is more quantitative, while AFM and TEM offer both qualitative and quantitative information such as particle shape, surface morphology, and size of the NPs. Similarly, structural changes in the formation of ChNPs were reportedly observed employing TEM, AFM, SEM, Fourier-transform infrared spectroscopy (FTIR), and X-ray powder diffraction (XRD) [72,73,74,75,76].…”
Section: Synthesis and Characterizationmentioning
confidence: 99%