Pongjanyakul T
Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen 40002, Thailand.
Pharmazie. 2007 Jul;62(7):493-8.
Diclofenac calcium alginate (DCA) beads containing microcrystalline cellulose (MCC) were prepared using ionotropic gelation method. The effect of MCC amounts on physicochemical characteristics of the DCA beads was examined. The particle size and entrapment efficiency of diclofenac sodium (DS) of the DCA beads increased with increasing amount of MCC. MCC could be involved in the calcium alginate formation to create a complex matrix in the DCA beads, which was revealed using FTIR spectroscopy. The MCC-DCA beads provided greater water uptake in distilled water, but retarded swelling rate in pH 6.8 phosphate buffer. A longer lag time and a similar drug release rate of the MCC-DCA beads in pH 6.8 phosphate buffer were found. The MCC-DCA beads also gave higher drug release rates in distilled water when compared with the DCA beads. However, the increase of MCC content over 0.5% in the DCA beads did not affect the drug release in distilled water. In conclusion, MCC could improve drug entrapment efficiency and modify drug release from the DCA beads.
采用离子凝胶法制备了含微晶纤维素(MCC)的双氯芬酸钙海藻酸盐(DCA)珠粒。考察了MCC用量对DCA珠粒理化性质的影响。DCA珠粒的粒径和双氯芬酸钠(DS)的包封率随MCC用量的增加而增大。MCC可能参与海藻酸钙的形成,在DCA珠粒中形成复合基质,傅里叶变换红外光谱(FTIR)证实了这一点。MCC-DCA珠粒在蒸馏水中的吸水量更大,但在pH 6.8的磷酸盐缓冲液中的溶胀速率较慢。发现MCC-DCA珠粒在pH 6.8的磷酸盐缓冲液中的滞后时间更长,药物释放速率相似。与DCA珠粒相比,MCC-DCA珠粒在蒸馏水中的药物释放速率也更高。然而,DCA珠粒中MCC含量超过0.5%时,对其在蒸馏水中的药物释放没有影响。总之,MCC可以提高药物包封率,并改变DCA珠粒的药物释放。