2014
DOI: 10.1016/j.ijbiomac.2014.01.064
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Protection of 4-hydroxybenzyl-chitooligomers against inflammatory responses in Chang liver cells

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Cited by 13 publications
(5 citation statements)
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“…From the 1 H-NMR spectra, 4-hydroxybenzyl-CHOS showed peaks at 8-6.9 ppm belonging to the protons of the aromatic ring of 4-hydroxybenzaldehyde along with characteristic peaks of CHOS. Thus, the spectroscopic results elucidated the successful link between 4-hydroxybenzaldehyde and CHOS [63].…”
Section: N-aryl Chosmentioning
confidence: 88%
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“…From the 1 H-NMR spectra, 4-hydroxybenzyl-CHOS showed peaks at 8-6.9 ppm belonging to the protons of the aromatic ring of 4-hydroxybenzaldehyde along with characteristic peaks of CHOS. Thus, the spectroscopic results elucidated the successful link between 4-hydroxybenzaldehyde and CHOS [63].…”
Section: N-aryl Chosmentioning
confidence: 88%
“…To eliminate the free aldehyde, the dialysate was precipitated in acetone and rinsed with diethyl ether. The final step was to dry the product at room temperature to produce 4-hydroxybenzyl-CHOS [63].…”
Section: N-aryl Chosmentioning
confidence: 99%
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“…The RAW264.7 cells were incubated with COS or CA‐COS (10–100 μg/mL) for 1 h and added LPS (1 μg/mL) for 24 h while a blank sample was not incubated with both sample and LPS. The NO content in the growth medium for 24 h was determined by the Griess method (Trinh et al., 2014). After 24 h, 50 μL of Griess reagent (1% sulfanilamide and 0.1% naphthyl ethylenediamine dihydrochloride in 2.5% phosphoric acid) was mixed with 50 μL of the culture medium and incubated for 20 min at the room temperature.…”
Section: Methodsmentioning
confidence: 99%