2003
DOI: 10.1016/s0168-3659(03)00327-4
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N-acylated chitosan: hydrophobic matrices for controlled drug release

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Cited by 289 publications
(194 citation statements)
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“…The two new peaks at 1720 and 1710 cm -1 were due to C=O of -NCOR group and C=O of -OCOR group of stearoyl chitosan, which were resulted from the acylation reaction between stearoyl chloride and -NH 2 and -OH groups of chitosan [15,21]. Presence of both 1720 and 1700 cm -1 peaks confirmed that the substitution took place at both -NH2 and -OH groups in stearoyl chitosan starting from chitosan.…”
Section: Structure Characterization 321 Ft-ir Data Analysismentioning
confidence: 79%
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“…The two new peaks at 1720 and 1710 cm -1 were due to C=O of -NCOR group and C=O of -OCOR group of stearoyl chitosan, which were resulted from the acylation reaction between stearoyl chloride and -NH 2 and -OH groups of chitosan [15,21]. Presence of both 1720 and 1700 cm -1 peaks confirmed that the substitution took place at both -NH2 and -OH groups in stearoyl chitosan starting from chitosan.…”
Section: Structure Characterization 321 Ft-ir Data Analysismentioning
confidence: 79%
“…The other two prominent peaks around 2920 and 2850 cm -1 were due to asymmetrical and symmetrical bending vibrations of methylene groups of long alkyl chain of stearoyl chitosan [15]. The absorption intensity was higher in stearoyl chitosan starting from deacetylated chitosan than that in stearoyl chitosan starting from chitosan.…”
Section: Structure Characterization 321 Ft-ir Data Analysismentioning
confidence: 92%
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“…The film-forming property of chitosan has found many applications in tissue engineering and drug delivery, packaging by virtue of its mechanical strength and rather slow biodegradation [5]. Some drug-loaded chitosan films are emerging as novel drug delivery systems, and films appear to have potential for local sustained delivery of cancer chemotherapeutic agents.…”
Section: Introductionmentioning
confidence: 99%