2013
DOI: 10.1016/j.foodchem.2013.03.098
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Physicochemical characterisation of β-chitosan from Sepioteuthis lessoniana gladius

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Cited by 49 publications
(21 citation statements)
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“…Stretching of the C-O-C was appeared around band 1152 cm -1 which agreed with Dong et al (2001); Zvezdova (2010); Liu et al (2013); Subhapradha et al (2013);Hafsa et al (2014) and Kaya et al (2015). According to the results of Dong et al (2001); Zvezdova (2010); Zhang et al (2011); Liu et al (2013) and Kaya et al (2015), the stretching of hydroxyl groups of C-OH was observed at bands around 1091cm -1 and 1035 cm -1 .…”
Section: Dynamic Light Scattering (Dls) Analysissupporting
confidence: 82%
See 1 more Smart Citation
“…Stretching of the C-O-C was appeared around band 1152 cm -1 which agreed with Dong et al (2001); Zvezdova (2010); Liu et al (2013); Subhapradha et al (2013);Hafsa et al (2014) and Kaya et al (2015). According to the results of Dong et al (2001); Zvezdova (2010); Zhang et al (2011); Liu et al (2013) and Kaya et al (2015), the stretching of hydroxyl groups of C-OH was observed at bands around 1091cm -1 and 1035 cm -1 .…”
Section: Dynamic Light Scattering (Dls) Analysissupporting
confidence: 82%
“…The asymmetric stretching vibration of CH (-CH 2 ) was observed at peak around 2922 cm -1 , this result agreed with Dong et al (2001); Gylienë et al (2003); Zvezdova (2010); Liu et al (2013); Song et al (2013); Wanule et al (2014) and Kaya et al (2015). The detection of the bending vibration for NH (R-NH 2 ) at beak around peak 1596 cm -1 was matched with Jia and Xu (2001); Gylienë et al (2003); Liu et al (2013); Song et al (2013); Subhapradha et al (2013) and Kaya et al (2015). Corresponding with Dong et al (2001); Gylienë et al (2003); Zvezdova (2010); Liu et al (2013) and Kaya et al (2015), the bending vibration of CH (-CH 2 ) was represented at bands around 1424 cm -1 and 1381cm -1 .…”
Section: Dynamic Light Scattering (Dls) Analysissupporting
confidence: 80%
“…Three polymorphic forms (α, β and γ) of chitin have been discovered, which differ in the arrangement of the chains in the crystalline regions; that is, α-chitin has antiparallel chains, while β-chitin has parallel chains for, and γ-chitin is a combination of αand β-chitin [1,2]. α-Chitosan has been commercially manufactured from shrimp and crab shells and has been widely applied in various fields, whereas β-chitosan has been commonly obtained from squid pens and has a limited number of studies and applications, primarily due to its limited availability [5][6][7][8]. It was reported that the β-chitin crystalline structure was more modified than that of α-chitin after deacetylation, resulting in better properties such as degree of solubility, and swelling capacitity [1,7], which consequently…”
Section: Introductionmentioning
confidence: 99%
“…The existence of free amino (−NH 2 ) groups in its structure makes chitosan a highly functional polysaccharide that can interact with many anionic polymers [7]. Some of the excellent features of chitosan are non-toxicity, homeostasis, antibacterial, biocompatibility and biodegradability [8,9]. These advantageous qualities make chitosan suitable for a variety of biomedical purposes such as wound healing [10][11][12][13], tissue engineering scaffolds [14][15][16][17], drug delivery systems [18] and biosensors [19].…”
Section: Introductionmentioning
confidence: 99%