Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 480-486 |
| Number of pages | 7 |
| Journal | International Journal of Biological Macromolecules |
| Volume | 72 |
| DOIs | |
| Publication status | Published - 27 Aug 2014 |
| Externally published | Yes |
Keywords
- 5-Fluorouracil
- Biomaterial
- Carboxymethyl zein
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