Optimization of carboxymethyl chitosan synthesis using response surface methodology and desirability function

被引:173
作者
Bukzem, Andrea L. [1 ]
Signini, Roberta [1 ]
dos Santos, Danilo M. [1 ]
Liao, Luciano M. [2 ]
Ascheri, Diego Palmiro R. [1 ]
机构
[1] Univ Estadual de Goias, Campus Anapolis Ciencias Exatas & Tecnol Henrique, BR-75132903 Anapolis, Go, Brazil
[2] Univ Fed Goias, Inst Quim, Campus Samambaia,POB 131, BR-74001970 Goiania, Go, Brazil
关键词
Carboxymethylation of chitosan; Response surface methodology; Desirability function; DRUG-DELIVERY; DERIVATIVES; DEGRADATION; SOLUBILITY; CHITIN;
D O I
10.1016/j.ijbiomac.2016.01.017
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
In this paper, chitosan was reacted with monochloroacetic acid under alkaline conditions to prepare carboxymethyl chitosan. A 23 full-factorial central composite design was applied to evaluate the effect of molar ratio sodium hydroxide (NaOH)/Chitosan (Ch), time and molar ratio monochloroacetic acid (MCA)/Chitosan (Ch) on the reaction yield and on the characteristics of carboxymethyl chitosan such as average degree of substitution ((DS) over bar) and solubility. An optimization strategy based on response surface methodology was used together with the desirability function approach to optimize this process. The occurrence of carboxymethylation was evidenced by FUR and H-1 NMR spectroscopy. The optimum conditions for carboxymethylation process were found to be 12.4, 10.6 h and 5 for molar ratio sodium hydroxide (NaOH)/Chitosan (Ch), time and molar ratio monochloroacetic acid (MCA)/Chitosan (Ch), respectively. Under these optimal conditions, it was possible to obtain carboxymethyl chitosan with (DS) over bar of 1.86 and solubility of 99.6%. X-ray diffraction and thermogravimetry analysis showed that crystallinity and thermal stability of derivatives was lower than chitosan and decreased with increase of (DS) over bar. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:615 / 624
页数:10
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