Physiochemical, Optical and Biological Activity of Chitosan-Chromone Derivative for Biomedical Applications

被引:334
作者
Kumar, Santosh [1 ]
Koh, Joonseok [1 ]
机构
[1] Konkuk Univ, Dept Text Engn, Seoul 143701, South Korea
关键词
chitosan; chitosan-chromone derivative; characterization; biomaterial; CONTROLLED-RELEASE; ANALOGS; AGENTS; DRUG; FLAVONOIDS; PROPERTY; ADHESION; DESIGN; CHITIN;
D O I
10.3390/ijms13056102
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This paper describes the physiochemical, optical and biological activity of chitosan-chromone derivative. The chitosan-chromone derivative gels were prepared by reacting chitosan with chromone-3-carbaldehyde, followed by solvent exchange, filtration and drying by evaporation. The identity of Schiff base was confirmed by UV-Vis absorption spectroscopy and Fourier-transform infrared (FTIR) spectroscopy. The chitosan-chromone derivative was evaluated by X-ray diffraction (XRD), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), scanning electron microscopy (SEM), photoluminescence (PL) and circular dichroism (CD). The CD spectrum showed the chitosan-chromone derivative had a secondary helical structure. Microbiological screening results demonstrated the chitosan-chromone derivative had antimicrobial activity against Escherichia coli bacteria. The chitosan-chromone derivative did not have any adverse effect on the cellular proliferation of mouse embryonic fibroblasts (MEF) and did not lead to cellular toxicity in MEFs. These results suggest that the chitosan-chromone derivative gels may open a new perspective in biomedical applications.
引用
收藏
页码:6102 / 6116
页数:15
相关论文
共 50 条
[1]   Synthesis, characterization, cytotoxicity and antibacterial studies of chitosan, O-carboxymethyl and N,O-carboxymethyl chitosan nanoparticles [J].
Anitha, A. ;
Rani, V. V. Divya ;
Krishna, R. ;
Sreeja, V. ;
Selvamurugan, N. ;
Nair, S. V. ;
Tamura, H. ;
Jayakumar, R. .
CARBOHYDRATE POLYMERS, 2009, 78 (04) :672-677
[2]  
[Anonymous], MAT SCI TECHNOL
[3]   Hierarchical transfer of stereochemical information in synthetic macromolecules [J].
Cornelissen, JJLM .
PURE AND APPLIED CHEMISTRY, 2002, 74 (11) :2021-2030
[4]   New antimicrobial flavanones from Physena madagascariensis [J].
Deng, YH ;
Lee, JP ;
Tianasoa-Ramamonjy, M ;
Snyder, JK ;
Des Etages, SA ;
Kanada, D ;
Snyder, MP ;
Turner, CJ .
JOURNAL OF NATURAL PRODUCTS, 2000, 63 (08) :1082-1089
[5]   Controlled release of drug from folate-decorated and graphene mediated drug delivery system: Synthesis, loading efficiency, and drug release response [J].
Depan, D. ;
Shah, J. ;
Misra, R. D. K. .
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2011, 31 (07) :1305-1312
[6]   Structure-process-property relationship of the polar graphene oxide-mediated cellular response and stimulated growth of osteoblasts on hybrid chitosan network structure nanocomposite scaffolds [J].
Depan, D. ;
Girase, B. ;
Shah, J. S. ;
Misra, R. D. K. .
ACTA BIOMATERIALIA, 2011, 7 (09) :3432-3445
[7]   Organic/inorganic hybrid network structure nanocomposite scaffolds based on grafted chitosan for tissue engineering [J].
Depan, D. ;
Surya, P. K. C. Venkata ;
Girase, B. ;
Misra, R. D. K. .
ACTA BIOMATERIALIA, 2011, 7 (05) :2163-2175
[8]   Synthesis and characterization of Schiff bases from chitosan and salicylaldehyde derivatives [J].
dos Santos, JE ;
Dockal, ER ;
Cavalheiro, ÉTG .
CARBOHYDRATE POLYMERS, 2005, 60 (03) :277-282
[9]   Chemical modification of chitosan: synthesis and biological activity of new heterocyclic chitosan derivatives [J].
El Badawy, Mohamed .
POLYMER INTERNATIONAL, 2008, 57 (02) :254-261
[10]  
Fradet G., 1986, CHITIN NATURE TECHNO, P443