O-Methyl free N,N,N-trimethyl chitosan (TMC) was synthesized by treating chitosan with formic acid and formaldehyde firstly, followed by methylation with CH(3)l. TMC was further carboxymethylated by monochloroacetic acid to obtain N,N,N-trimethyl-O-carboxymethyl chitosan (TMCMC). The products were characterized by FTIR, H-1 NMR, EA and TGA. Their antibacterial activity was investigated against Staphylococcus aureus and Escherichia coli. The antibacterial activity of TMC decreased as the degree of substitution increased at pH 5.5. But the structure activity relationship was reversed at pH 7.2. TMCMC acted weaker than TMC, and its activity decreased as the degree of carboxymethylation increased. The experimental results showed that the activity of N,N,N-trimethyl amino group was weaker than other non-quaternized amino groups, and carboxymethylation did not enhance the antibacterial activity directly. (C) 2010 Elsevier Ltd. All rights reserved.
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Hacettepe Univ, Fac Pharm, Dept Pharmaceut Technol, TR-06100 Ankara, TurkeyHacettepe Univ, Fac Pharm, Dept Pharmaceut Technol, TR-06100 Ankara, Turkey
Sayin, B.
Somavarapu, S.
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Univ London, Sch Pharm, London WC1N 1AX, EnglandHacettepe Univ, Fac Pharm, Dept Pharmaceut Technol, TR-06100 Ankara, Turkey
Somavarapu, S.
Li, X. W.
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Univ London, Sch Pharm, London WC1N 1AX, EnglandHacettepe Univ, Fac Pharm, Dept Pharmaceut Technol, TR-06100 Ankara, Turkey
Li, X. W.
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Thanou, M.
Sesardic, D.
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Natl Inst Biol Stand & Controls, Div Bacteriol, Potters Bar EN6 3QG, Herts, EnglandHacettepe Univ, Fac Pharm, Dept Pharmaceut Technol, TR-06100 Ankara, Turkey
Sesardic, D.
Alpar, H. O.
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Univ London, Sch Pharm, London WC1N 1AX, EnglandHacettepe Univ, Fac Pharm, Dept Pharmaceut Technol, TR-06100 Ankara, Turkey
Alpar, H. O.
Senel, S.
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Hacettepe Univ, Fac Pharm, Dept Pharmaceut Technol, TR-06100 Ankara, TurkeyHacettepe Univ, Fac Pharm, Dept Pharmaceut Technol, TR-06100 Ankara, Turkey