2019
DOI: 10.1016/j.foodhyd.2019.105217
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Physical and morphological properties of hydroxypropyl methylcellulose films with curcumin polymorphs

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Cited by 55 publications
(9 citation statements)
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“…Regarding EB, no effect was observed with the addition of free curcumin and curcumin-loaded nanohydrogels to CMC-based films, suggesting that the rigid properties of CMC were more prevalent than the elongation properties of the free curcumin and curcumin-loaded nanohydrogel in the films. The same behavior was observed by da Silva [31], who encapsulated treated curcumin (native curcumin treated using antisolvent precipitation) in hydroxypropyl methylcellulose.…”
Section: Mechanical Propertiessupporting
confidence: 77%
See 1 more Smart Citation
“…Regarding EB, no effect was observed with the addition of free curcumin and curcumin-loaded nanohydrogels to CMC-based films, suggesting that the rigid properties of CMC were more prevalent than the elongation properties of the free curcumin and curcumin-loaded nanohydrogel in the films. The same behavior was observed by da Silva [31], who encapsulated treated curcumin (native curcumin treated using antisolvent precipitation) in hydroxypropyl methylcellulose.…”
Section: Mechanical Propertiessupporting
confidence: 77%
“…Regarding color, the most significant change between films was observed for a* and b*, which was related to chromatic coordinates. As observed in Table 2, CMC-based films with curcumin-loaded nanohydrogels showed higher b* values compared to CMC-based films and CMC-based films with free curcumin, indicating a color transiting to yellowness (b* = 10.36), which was expected because of the curcumin color influence in these films [31]. These results can be confirmed visually in Figure 1.…”
Section: Color and Opacitysupporting
confidence: 71%
“…From 3600 to 3000 cm -1 the broad band corresponded to the characteristic stretching of O-H and N-H bonds (Božič et al, 2012b;Liu, You, Tarafder, Zou, & Fang 2019). It was possible to see two peaks on the curcumin spectrum, one at 3510 cm -1 and the other one at 1279 cm -1 corresponding to the stretching and the bending of the phenolic -OH groups, respectively (Božič et al, 2012b;Liu et al, Ying, Cai, & Le, 2017;Nascimento da Silva, de Matos Fonseca, Feldhaus, Soares, & Valencia, 2019). Peaks located at 1600 and 1508 cm -1 corresponded to the stretching of the C=C bonds of the cyclic alkenes (Božič et al, 2012b;Hasan et al, 2016;Poljanšek, Šebenik, & Krajnc 2006).…”
Section: Resultsmentioning
confidence: 95%
“…Pure HPMC shows a broad peak at 3488 cm −1 , which is attributable to the axial stretching of ‐OH groups and hydrogen bonds between polymeric chains. [ 39 ] The peak at 2930 cm −1 corresponds to the C–H symmetric stretching vibration of hydroxypropyl groups. [ 40 ] Noticed weak relative peaks at 1377 and 1458 cm −1 belong to ‐OH bending and –CH 2 scissoring stretching modes from methyl groups.…”
Section: Resultsmentioning
confidence: 99%