• Journal of Biomedical Engineering Research
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• v.16 no.3
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• pp.257-264
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• 1995

The $\beta$-chitin derivatives were synthesized by reacting $\beta$-chitin with chloropropane, propyleneoxide and chloropropane diol to form propyl chitin (PPC), hydroxypropyl chitin (HPC) and dihydroxypropyl chitin (DHPC), respectively. Cast films from $\beta$-chitin and $\beta$-chitin derivatives solutions degraded by Iyrozyme in pseudo-extrra cellular fluid (PECF) solutions, at pH1.2, pH6.7 and pH8.2. Chitin derivatives rapidly degraded compared with virgin $\beta$-chitin within the first week. DHPC showed the best biodegradation among these derivatives.

• Journal of Biomedical Engineering Research
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• v.15 no.1
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• pp.89-96
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• 1994

The ether-type chitin derivatives were synthesized by reacting chitin with chloropropane, propylene oxide and chloropropane diol to form propyl chitin(PPC), hydroxypropyl chitin(HPC) and dihydroxypropyl chitin(DHPC). These derivatives formed a lyotropic cholesteric liquid crystallinity in concentrations over 30 wt% solution in formic acid (99%). Cast films from liquid crystalline solutions were degraded by lysozyme in pseudo-extra cellular tluid(PECF)solutions, at pH 1.2, pH 6.7 and pH 8.2. Three ether-type chitin derivatives rapidly degraded within the first week, and showed a decreased mechanical strength in neutral pH range. Dihydroxypropyl chitin showed the best biodegradation among these derivatives.

• Korean Journal of Food Science and Technology
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• v.36 no.1
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• pp.92-96
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• 2004

Chitin and its derivatives (chitosan and glucosamine) were studied for their effects on ethanol production using YPD (yeast extract 10%, peptone 20%, glucose 20%, agar 20%) medium. All chitin derivatives, particularly chitin, increased ethanol production compared with control. In non-steamed alcohol fermentation of tapioca, addition of 0.9% chitin yielded higher ethanol production (13.6%) with lower acetaldehyde (21.91 ppm) and methanol (65.49 ppm) contents than those (12.7%, 35.05 ppm, 84.31 ppm, respectively) of control after fermentation for 120 hr at $30^{\circ}C$. Results indicate that chitin can be used to increase ethanol production in non-steamed alcohol fermentation of tapioca.

• Applied Biological Chemistry
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• v.35 no.4
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• pp.265-271
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• 1992

Derivatives (microcrystalline chitin, carboxymethylchitin, acetylchitin, N-acetylchitosan, ethylchitosan and chitosansulfate) of chitin and chitosan were synthesized, and the physicochemical properties of the derivatives were compared with those of chitin and chitosan. Carboxymethylchitin was soluble in water or acetic acid, whereas chitosan and ethylchitosan were soluble in acetic acid alone. The water binding capacity of N-acetylchitosan was two fold higher than that of chitin. Lipid binding capacity of carboxymethylchitin was the highest, holding 1800%, and that of chitin was the lowest, holding 511% among the derivatives. Carboxymethylchitin among the derivatives showed the highest emulsifying capacity, however chitin and chitosan didn't produce emulsions. Dye binding capacity of acetylchitin was the highest, holding 0.93 mg dye/g sample (Blue R-250) and 0.96 mg dye/g sample (Red No. 2). It was concluded that carboxymethylchitin is a good emulsifier and N-acetylchitosan, chitosansulfate and chitosan are suitable for use as dye absorbents.

• Journal of Environmental Health Sciences
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• v.24 no.3
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• pp.11-17
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• 1998

Chitin is known as biodegradable natural polymer. In spite of various application of chitin derivatives from waste marine sources, commercial use of chitin has been limited due to high resistance to chemicals and the absense of proper solvents. We chitin prepared through the decalcification, bleaching and deproteination from Protunus trituberculatus shells by change of Hackman's method. Also, Microcrystalline chitin made by hydrolysis that was reduce made of resistance solvents used by dilute hydrochloric acid, ultrasonic and hydrogen peroxide. Crosslinked chitin derivatives were preparaed from chitin with crosslink agents(epichlorohydrin, 1,3-dichloropropanol) follwed by crosslinkage at 6C position. The effects of these parameters on chitin dervatives were invastigated by IR, DSC, XRD, BET, PSA and SEM. SEM analysis showed that both chitin and crosslinked chitin had a particle shaped morphology.

• Applied Chemistry for Engineering
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• v.4 no.4
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• pp.785-790
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• 1993

Three ester-type chitin derivatives were synthesized by reacting chitin with acetic anhydride, propionic anhydride and n-butyric anhydride to form acetyl chitin(AC), propionyl chitin(PC) and n-butyryl chitin(BC). Methanesulfonic acid was used as a catalyst. FT-IR spectra and solid state CP/MAS $^{13}C-NMR$ spectra of three chitin derivatives showed that the substituents were mainly incorporated in the $C_6$ position of chitin. The ester-type chititn derivatives were dissolved well in formic acid and swollen in aqueous acidic solution.

• Proceedings of the Korean Fiber Society Conference
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• 1996.10a
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• pp.53-58
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• 1996

The Chitin Thiocarbonate-Fe(II)-H2O2 redox initiator system was investigated for the graft copolymerization of acrylonitrile(AN) and acrylic acid(AA) monomers onto chitin powder. The reactions with vinyl monomers onto chitin were carried out under various the graft copolymerization conditions to elucidate the polymerization behavior in terms of graft yield. Reactions of chitin-acrylonitrile graft copolymer with hydroxyl amine hydrochloride and those with sodium hydroxide were conducted in order to obtain chitin-(amidoxime-co-acrylonitrile) and chitin-(acrylate-co-acrylamide) graft copolymers, respectively. The reaction efficiency was observed to depend on the alkali concentration, time, temperature, and the reactant concentrations. The prepared chitin derivatives were evaluated to find potential applications for use in wastewater treatments for adsorption and desorption of heavy metal ions as well as acidic and basic dyes.

• Applied Chemistry for Engineering
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• v.8 no.2
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• pp.237-245
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• 1997

A DEAE-chitin was prepared with DEAE HCl in an aqueous alkali-chitin solution. The resulting DEAE-chitin exhibited a highly improved affinity to water and organic solvents, It was N-deacetylated by heating in aqueous 10% sodium hydroxide containing sodium borohydride for 9h at $80^{\circ}C$ to produce DEAE-chitosan. These conditions were milder than those for the N-deacetylation of chitin. In order to increase its cationic character, the DEAE-chitin was treated with ethyl halide to give TEAE-chitin. The structural changes in the chitin derivatives were confirmed by using both FT-IR and $^1H$ NMR, and their flocculating behavior, in kaoline suspension showed the optimum property at a weak alkaline pH and 8 ppm concentration of resin conditions.

• Applied Biological Chemistry
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• v.47 no.3
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• pp.361-365
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• 2004

Chitin and its derivatives have been introduced to tomato seedlings by direct mixing of chitin, chitosan, or chitooligosaccharides (CO) with soils, watering of chitosan or CO solutions to soils, or chitosan-coating of tomato seeds as a biomodulator of plant growth, and the growth of tomato plants was measured 30- and 45-day after seeding in the pots. The treatment of chitin and its derivatives promoted the growth of tomato plants in plant heights, shoot weight, maximum leaf length and number of leaves. By comparison in the contents of cellular inorganic nutrients in the plants, it was found out that chitin or chitosan treatments accelerated nitrogen and potassium uptake but inhibit calcium uptake, suggesting that chitin and its derivatives modulate absorption of inorganic nutrients through plant roots from environment.

• Journal of Life Science
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• v.7 no.2
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• pp.149-159
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• 1997

Chitin, a linked polysaccharide composed of 2-acetamido-2-deoxy-$\beta$-D-glucopytanose residues, is distributed widely in nature. It has been utilized on various application field due to the development of chitin derivatives such as chitosan, partial deacetylated chitin, carboxylmethyl chitin, sulfated chitin, and so on. Chitin and chitosan have been recently interested in antitumor and antimicrobial activities, because of a powerful tumor inhibitory effect against experimental mouse tumors. Especially, the oligosaccharides obtained by partial degradation of them exhibited a remarkable antitumor effect against sarcoma 180, MM 48 and Meth Asolid tumors and antimetastatic effect against Lewis lung carcinoma in mice. This review describes on antitumor effects of chitin, chitosan and their oligosaccharides by their mechanism of action involving enhancement of immunological system.