2017
DOI: 10.1016/j.matdes.2017.07.014
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Antibacterial activity of PLAL synthesized nanocinnamon

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Cited by 42 publications
(17 citation statements)
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“…Furthermore, the absorption peaks were located at 1414 cm −1 assigned to carbon-hydroxyl groups (C-O) of aromatic amines that conjugates from aromatic ring in the Cin [25]. All these peaks confirmed the absorption of the cinnamon molecules and amide linkages of proteins attached on the surface of the NCs by different functional groups as reported earlier [9,25]. The observed shift was due to the presence of the cinnamaldehyde (main compound of cinnamon) and enlargement in the particle size.…”
Section: Resultssupporting
confidence: 83%
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“…Furthermore, the absorption peaks were located at 1414 cm −1 assigned to carbon-hydroxyl groups (C-O) of aromatic amines that conjugates from aromatic ring in the Cin [25]. All these peaks confirmed the absorption of the cinnamon molecules and amide linkages of proteins attached on the surface of the NCs by different functional groups as reported earlier [9,25]. The observed shift was due to the presence of the cinnamaldehyde (main compound of cinnamon) and enlargement in the particle size.…”
Section: Resultssupporting
confidence: 83%
“…1a). This was due to the existence of the polyphenols, heterocyclic and cinnamaldehyde compounds in the Cin [9]. Furthermore, the absorption peaks were located at 1414 cm −1 assigned to carbon-hydroxyl groups (C-O) of aromatic amines that conjugates from aromatic ring in the Cin [25].…”
Section: Resultsmentioning
confidence: 98%
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