TY - JOUR
T1 - Preparation, characterization and application of a novel biodegradable macromolecule
T2 - Carboxymethyl zein
AU - Yin, Huayue
AU - Lu, Tao
AU - Liu, Li
AU - Lu, Chuanhua
N1 - Publisher Copyright:
© 2014 Elsevier B.V.
PY - 2014/8/27
Y1 - 2014/8/27
N2 - Zein, a naturally biocompatible and biodegradable macromolecule, is widely used as plastic film material; however, the poor water solubility limits its other applications. In this study, we aimed to obtain carboxymethyl zein (CM-zein) by modifying it with sodium monochloroacetate in weakly basic environment. CM-zein showed a new FTIR peak of C-O-C bond at 1080cm-1, with a new signal region appearing at 4.0-4.05ppm that assigned to the protons of the CH2 group from a carboxymethyl on 1H NMR and a Tg of 168.0°C by thermal analysis. Compared with the -12.3mV of zeta potential of unmodified zein, CM-zein increased it significantly to -23.9mV as a consequence of carboxymethylation. 5-Fluorouracil (5-FU), a model drug used in CM-zein-based tablet, was rarely detected in 0.1mol/L HCl (pH 1.0) but it was released massively and quickly in phosphates buffer (pH 6.8) in vitro assays. The unmodified zein-based tablet illustrated much lower release level in these two fluids. Furthermore, the pharmacokinetic study of rats showed that CM-zein released 5-FU in intestine but not in stomach after dissolving. These findings indicated that CM-zein has the potential to be used for enteric preparation as a novel pH-selective biomaterial.
AB - Zein, a naturally biocompatible and biodegradable macromolecule, is widely used as plastic film material; however, the poor water solubility limits its other applications. In this study, we aimed to obtain carboxymethyl zein (CM-zein) by modifying it with sodium monochloroacetate in weakly basic environment. CM-zein showed a new FTIR peak of C-O-C bond at 1080cm-1, with a new signal region appearing at 4.0-4.05ppm that assigned to the protons of the CH2 group from a carboxymethyl on 1H NMR and a Tg of 168.0°C by thermal analysis. Compared with the -12.3mV of zeta potential of unmodified zein, CM-zein increased it significantly to -23.9mV as a consequence of carboxymethylation. 5-Fluorouracil (5-FU), a model drug used in CM-zein-based tablet, was rarely detected in 0.1mol/L HCl (pH 1.0) but it was released massively and quickly in phosphates buffer (pH 6.8) in vitro assays. The unmodified zein-based tablet illustrated much lower release level in these two fluids. Furthermore, the pharmacokinetic study of rats showed that CM-zein released 5-FU in intestine but not in stomach after dissolving. These findings indicated that CM-zein has the potential to be used for enteric preparation as a novel pH-selective biomaterial.
KW - 5-Fluorouracil
KW - Biomaterial
KW - Carboxymethyl zein
UR - http://www.scopus.com/inward/record.url?scp=84926138545&partnerID=8YFLogxK
U2 - 10.1016/j.ijbiomac.2014.08.025
DO - 10.1016/j.ijbiomac.2014.08.025
M3 - Article
C2 - 25173708
AN - SCOPUS:84926138545
SN - 0141-8130
VL - 72
SP - 480
EP - 486
JO - International Journal of Biological Macromolecules
JF - International Journal of Biological Macromolecules
ER -