摘要
将水难溶性药物吲哚美辛包埋于可降解聚(醚-酐)三维光交联网络凝胶中,使该凝胶具有较好的溶胀性能.X射线衍射测定结果表明,药物能以分子或无定形态分布,贮存2个月后药物仍无形态改变,溶出实验结果表明,包载在凝胶中的药物比原料药物具有更快的溶出速率和累积溶出量.采用该法能提高制剂中药物的物理稳定性,阻延药物析晶,有效地用于药物增溶.
PEG-based degradable gels and ch drug was embedded in macromers containing anhydride bonds were synthesized and photopolymerized to form aracterized via FTIR and ^1H NMR. Indomethacin as a model of poorly water-soluble the degradable poly(ether-anhydride) photocrosslinked network, which had good swelling properties. The drug was proved to be distributed in an amorphous or molecular state in the crosslinked network and the physical morphology of the drug remained stable after two months storage demostrated by employing X-ray diffraction. Dissolution tests showed that the drug in the network displayed a better dissolution rate and more cumulative drug release than the crystal raw indomethacin. This method could increase the dissolution rate and inhibit recrystallization of indomethacin in the degradable photocrosslinked gels.
出处
《高等学校化学学报》
SCIE
EI
CAS
CSCD
北大核心
2007年第5期987-991,共5页
Chemical Journal of Chinese Universities
基金
天津市自然科学基金(批准号:05YFJMJC11200)资助.
关键词
光交联
可降解聚(醚-酐)
凝胶
吲哚美辛
药物增溶
Photocrosslink
Degradable poly(ether-anhydride) Indomethacin
Increase dissolution rate