2002
DOI: 10.1016/s0142-9612(02)00071-6
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis and characterization of chitosan–poly(acrylic acid) nanoparticles

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

16
279
1
2

Year Published

2003
2003
2024
2024

Publication Types

Select...
6
3
1

Relationship

0
10

Authors

Journals

citations
Cited by 485 publications
(303 citation statements)
references
References 28 publications
16
279
1
2
Order By: Relevance
“…The very intense characteristic band at 1560 cm −1 is due to the C(O asymmetric stretching of the carboxylate anion from poly(AA) grafted onto M3 and M4 chitosan membranes. This is reconfirmed by other sharp peak at 1405 cm −1 , which is related to the symmetric stretching mode of the carboxylate anion (Hu et al, 2002;Mahdavinia et al, 2004). The salt form of the free carboxylic group is expected since the membranes were neutralized with sodium hydroxide solution to remove them from the plates.…”
Section: Resultsmentioning
confidence: 69%
“…The very intense characteristic band at 1560 cm −1 is due to the C(O asymmetric stretching of the carboxylate anion from poly(AA) grafted onto M3 and M4 chitosan membranes. This is reconfirmed by other sharp peak at 1405 cm −1 , which is related to the symmetric stretching mode of the carboxylate anion (Hu et al, 2002;Mahdavinia et al, 2004). The salt form of the free carboxylic group is expected since the membranes were neutralized with sodium hydroxide solution to remove them from the plates.…”
Section: Resultsmentioning
confidence: 69%
“…The direct acid-base reaction between COOH and NH 2 groups leading to ionic bonds is also very probable [35].…”
Section: Discussion Characteristics Of Obtained Materials By Uv-vis mentioning
confidence: 99%
“…In this work, a non-toxic hydrophilic polymer, poly(acrylic acid) (PAA), with a low molecular weight, was employed as the crosslinker due to its chain mobility and carboxyl groups that react with the hydroxyl groups in PVA to form an ester [24,25]. Similar to PVA, PAA also displays excellent biocompatibility and has been used in applications such as sitespecific drug delivery systems [26,27], wound dressing materials [28] and partially degradable bone cements [29]. It has also been used in conjunction with PVA to form hydrogel fibres where the degree of swelling can be easily controlled by the degree of crosslinking [30].…”
Section: Accepted M Manuscriptmentioning
confidence: 99%