2004
DOI: 10.1365/s10337-004-0290-0
|View full text |Cite
|
Sign up to set email alerts
|

Isolation of Chitin from a Variety of Raw Materials, Modification of the Material, and Interaction its Derivatives with Metal Ions

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
7
0

Year Published

2007
2007
2018
2018

Publication Types

Select...
5
2

Relationship

0
7

Authors

Journals

citations
Cited by 15 publications
(7 citation statements)
references
References 0 publications
0
7
0
Order By: Relevance
“…It is the second most abundant natural polymer on earth next to cellulose and is crystalline in nature [2]. The three polymorphic crystalline forms of chitin are ␣, ␤ and ␥ [3,4]. These forms of chitin differ from one another based on the arrangement of polymer chains.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…It is the second most abundant natural polymer on earth next to cellulose and is crystalline in nature [2]. The three polymorphic crystalline forms of chitin are ␣, ␤ and ␥ [3,4]. These forms of chitin differ from one another based on the arrangement of polymer chains.…”
Section: Introductionmentioning
confidence: 99%
“…The polymer chains are arranged antiparallel to each other in ␣-chitin, parallel to each other in ␤-chitin whereas randomly in ␥-chitin. These polymer chains are tightly held by intermolecular hydrogen bonding between N H and C O functional groups [4]. Chitin, from the biomedical point of view has several advantages like biodegradability [5], biocompatibility, non-toxicity, [6] promotes mineralization (calcification) [7], etc.…”
Section: Introductionmentioning
confidence: 99%
“…Chitosan Bombyx mori with a degree of deacetylation of 88–96% (eq 1 of Supporting Information) and a molecular mass M w of 151.8–418.0 kDa (Table S1 of Supporting Information) was synthesized from chitin Bombyx mori by heterogenic deacetylation . Poly(ethylene glycol) monomethyl ether (MPEG) ( M w 2000) was purchased from Sigma Aldrich or Fluka.…”
Section: Methodsmentioning
confidence: 99%
“…Chitosan Bombyx mori with a degree of deacetylation of 88−96% (eq 1 of Supporting Information) and a molecular mass M w of 151.8−418.0 kDa (Table S1 of Supporting Information) was synthesized from chitin Bombyx mori by heterogenic deacetylation. 35 Poly(ethylene glycol) monomethyl ether (MPEG) (M w 2000) was purchased from Sigma Aldrich or Fluka. Bodipy (Invitrogen; M w : 660.5 Da; E max = 630 nm), sodium fluorescein (Fluka Chemika; M w : 376.3 Da; E max = 514 nm), isothiocyanate conjugate of bovine albumin (BSA−FITC) (M w = 66 kDa), and all the solvents were used without further purification.…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
“…Therefore, a series of pretreatments are necessary to remove the impurities before isolation. There are four critical steps involves nanochitin isolation, that is i) remove residual proteins by alkaline or enzymatic hydrolysis; ii) remove inorganic salts by HCl aqueous solution; iii) extract astaxanthin pigments and lipids with organic solvents; iv) obtain white chitin products through treatment of residues. In this review, we introduced four typical methods to nanochitin isolation, that is, acid hydrolysis, TEMPO‐mediated oxidation, partial deacetylation and mechanical isolation.…”
Section: Top‐down Isolation Techniquesmentioning
confidence: 99%