2010
DOI: 10.1590/s1516-89132010000300016
|View full text |Cite
|
Sign up to set email alerts
|

Antibacterial activity of chitosan and the interpolyelectrolyte complexes of poly(acrylic acid)-chitosan

Abstract: ABSTRACT

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

1
17
0

Year Published

2013
2013
2023
2023

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 31 publications
(18 citation statements)
references
References 21 publications
(19 reference statements)
1
17
0
Order By: Relevance
“…The structure of the MWCNTs, activated-MWCNTs, and CTSNPs-aMWCNTs were studied utilizing Fourier-transform infrared (FT-IR) spectroscopy as exhibited in Figure 2 e. Feature peaks at wave numbers 3275 cm −1 , 1643 cm −1 , and 1322 cm −1 equivalent to (–N–H, –O–H), (C=O), and (C–N), respectively, confirmed the realization of CTSNPs-aMWCNTs composites [ 34 , 35 ]. The peak with wave number 2940 cm −1 indicates the presence of C-H bonds, a dominating bond in Pristine-MWCNTs while peaks with wave numbers 1755 cm −1 , 3176 cm −1 , and 1113 cm −1 corresponding to (C=O), (-O-H), and (-C-O), respectively, suggest the carboxylation of the pristine-MWCNTs.…”
Section: Resultsmentioning
confidence: 99%
“…The structure of the MWCNTs, activated-MWCNTs, and CTSNPs-aMWCNTs were studied utilizing Fourier-transform infrared (FT-IR) spectroscopy as exhibited in Figure 2 e. Feature peaks at wave numbers 3275 cm −1 , 1643 cm −1 , and 1322 cm −1 equivalent to (–N–H, –O–H), (C=O), and (C–N), respectively, confirmed the realization of CTSNPs-aMWCNTs composites [ 34 , 35 ]. The peak with wave number 2940 cm −1 indicates the presence of C-H bonds, a dominating bond in Pristine-MWCNTs while peaks with wave numbers 1755 cm −1 , 3176 cm −1 , and 1113 cm −1 corresponding to (C=O), (-O-H), and (-C-O), respectively, suggest the carboxylation of the pristine-MWCNTs.…”
Section: Resultsmentioning
confidence: 99%
“…Chitosan has excellent biocompatibility and biodegradability, being a nontoxic natural biological material. It can interact with negatively charged proteins and polymers because of its positive charges and the ─NH 2 group terminals and has, therefore, been widely used in the pharmaceutical industry in recent years (Ortega‐Ortiz, Gutiérrez‐Rodríguez, Cadenas‐Pliego, & Ibarra Jimenez, ; Venkatesan & Kim, ). BMP‐2 was shown to be continuously released for up to 6 weeks from a silica xerogel–chitosan hybrid coating layer on a porous HA scaffold and promoted the repair of bone defects (Jun et al, ).…”
Section: Discussionmentioning
confidence: 99%
“…Once inside the cell, where the pH is maintained near 7, the acid will dissociate and pH will decrease, thus disturbing and finally killing the microorganism (31) . The secondary action is the anionic part of the organic acids (carboxylic groups) that cannot escape the bacteria in its dissociated form will accumulate within the bacteria and disrupt many metabolic functions, leading to osmotic pressure increase, incompatible with the survival of the bacteria (32)(33)(34) .…”
Section: Inhibition Mechanism Of Chitosan Solutionsmentioning
confidence: 99%