Film-forming process and biocide assessment of high-molecular-weight chitosan as determined by combined ATR-FTIR spectroscopy and antimicrobial assays

被引:30
作者
Fernandez-Saiz, P.
Ocio, M. J.
Lagaron, J. M.
机构
[1] CSIC, Inst Agrochem & Food Technol, Burjassot 46100, Spain
[2] Univ Valencia, Dept Prevent Med, Fac Pharm, Burjassot 46100, Spain
关键词
chitosan; antimicrobial properties; FT-IR; film forming;
D O I
10.1002/bip.20589
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
This pioneering study reported about the film-forming properties of high-molecular-weight chitosan as followed in situ by attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, and has implications in fields such as biomedical, pharmaceutical, packaging, and coating applications. From the results, it was observed that immediately after dissolution in an acetic acid aqueous solution and subsequent casting over the ATR crystal, the formed carboxylate antimicrobial (-NH3+ -OOCH) species are not stable in the film formulation and become reduced over time; further assays confirmed previous research, which suggested that the presence and stability of these groups is strongly dependent, among other factors, on storage conditions. As-received chitosan and chitosan neutralized in NaOH films did not exhibit biocide performance towards Staphylococcus aureus. The antimicrobial tests were also found to strongly relate the presence of a sufficient quantity of these carboxylate groups to the chitosan activity as a biocide agent. Moreover, a novel methodology based on the use of a normalized infrared band centered at 1405 cm(-1) is proposed which can be correlated with the antimicrobial character of the biopolymer. (c) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:577 / 583
页数:7
相关论文
共 26 条
[1]
[Anonymous], CHITIN NATURE TECHNO
[2]
Visualisation of the heterogeneous water sorption in a pharmaceutical formulation under controlled humidity via FT-IR imaging [J].
Chan, KLA ;
Kazarian, SG .
VIBRATIONAL SPECTROSCOPY, 2004, 35 (1-2) :45-49
[3]
Deacetylation of β-chitin.: I.: Influence of the deacetylation conditions [J].
Chen, CH ;
Wang, FY ;
Ou, ZP .
JOURNAL OF APPLIED POLYMER SCIENCE, 2004, 93 (05) :2416-2422
[4]
Chung YC, 2004, ACTA PHARMACOL SIN, V25, P932
[5]
N-CARBOXYMETHYLCHITOSAN INHIBITION OF AFLATOXIN PRODUCTION - ROLE OF ZINC [J].
CUERO, RG ;
OSUJI, G ;
WASHINGTON, A .
BIOTECHNOLOGY LETTERS, 1991, 13 (06) :441-444
[6]
CHITOSAN CARBOXYLIC-ACID SALTS IN SOLUTION AND IN THE SOLID-STATE [J].
DEMARGERANDRE, S ;
DOMARD, A .
CARBOHYDRATE POLYMERS, 1994, 23 (03) :211-219
[7]
ANTIFUNGAL ACTIVITY OF CHITOSAN ON POSTHARVEST PATHOGENS - INDUCTION OF MORPHOLOGICAL AND CYTOLOGICAL ALTERATIONS IN RHIZOPUS-STOLONIFER [J].
ELGHAOUTH, A ;
ARUL, J ;
ASSELIN, A ;
BENHAMOU, N .
MYCOLOGICAL RESEARCH, 1992, 96 :769-779
[8]
FERNANDEZCERVER.M, 2004, J CARBOHYDR POLYM, V58, P401
[9]
THE USE OF FTIR-ATR SPECTROSCOPY TO CHARACTERIZE PENETRANT DIFFUSION IN POLYMERS [J].
FIELDSON, GT ;
BARBARI, TA .
POLYMER, 1993, 34 (06) :1146-1153
[10]
Hanh BD, 2000, INT J PHARMACEUT, V204, P145