2020
DOI: 10.3390/polym12071445
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Antioxidant and Moisturizing Properties of Carboxymethyl Chitosan with Different Molecular Weights

Abstract: This research aimed to synthesize carboxymethyl chitosan (CMCH) from different molecular weights of chitosan including low MW (L, 50–190 kDa), medium MW (M, 210–300 kDa) and high MW (H, 310–375 kDa) on the antioxidant and moisturizing properties. The L-CMCH, M-CMCH and H-CMCH improved the water solubility by about 96%, 90% and 89%, respectively when compared to native chitosan. Higher MW resulted in more viscous of CMCH. For antioxidant properties, IC50 values of DPPH and ABTS radical scavenging activi… Show more

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Cited by 71 publications
(46 citation statements)
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“…The FTIR spectra of chitosan films ( Figure 7 a) and the infrared spectra of chitosan incorporated with 0.16 mg/mL of curcumin extract ( Figure 7 b) should be obtained at peaks between 3500 and 3000 cm −1 . The characteristic peaks of chitosan are at 3455 cm −1 (O–H stretching), 2867 cm −1 (C–H stretching) [ 29 , 30 ], 1647 cm −1 (N–H bending), 1319 cm −1 (C–N stretching or amide II) [ 31 , 32 ], and 1023 cm −1 (C–O stretching) [ 17 , 33 ]. This shows that the stretching vibration of free hydroxyl and the symmetric stretching of the N–H bonds (amide A) [ 34 ] in an amino group are stronger in the control films when compared to the chitosan incorporated with curcumin extract [ 30 ].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The FTIR spectra of chitosan films ( Figure 7 a) and the infrared spectra of chitosan incorporated with 0.16 mg/mL of curcumin extract ( Figure 7 b) should be obtained at peaks between 3500 and 3000 cm −1 . The characteristic peaks of chitosan are at 3455 cm −1 (O–H stretching), 2867 cm −1 (C–H stretching) [ 29 , 30 ], 1647 cm −1 (N–H bending), 1319 cm −1 (C–N stretching or amide II) [ 31 , 32 ], and 1023 cm −1 (C–O stretching) [ 17 , 33 ]. This shows that the stretching vibration of free hydroxyl and the symmetric stretching of the N–H bonds (amide A) [ 34 ] in an amino group are stronger in the control films when compared to the chitosan incorporated with curcumin extract [ 30 ].…”
Section: Resultsmentioning
confidence: 99%
“…The total radical scavenging capacity of curcumin extract was determined by using the DPPH with a modified method of Chaiwong et al [ 17 ].…”
Section: Methodsmentioning
confidence: 99%
“…When thermal manifestation (50 to 650 °C) was applied to chitosan after γ-irradiation, it was discovered that degradation and decomposition occurred first, before the residue remained ( Figure 4 ). In this sense, heating chitosan at 100 °C causes water evaporation and proceeds with endothermic dehydration [ 41 ].…”
Section: Resultsmentioning
confidence: 99%
“…Interestingly, chitosan oligosaccharide recovered aging-induced liver dysfunction via the upregulation of Nrf2 antioxidant signaling [ 202 ]. Chitosan-gallic acid, synthetic carboxymethyl chitosan, chitosan-ellagic acid and selenide chitosan sulfate have also been demonstrated to have an antioxidant activity [ 203 , 204 , 205 , 206 ].…”
Section: Potential Applications Of Chitin and Chitosan Oligosacchamentioning
confidence: 99%