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机构地区:[1]华侨大学材料科学与工程学院环境友好功能材料教育部工程中心,福建厦门361021
出 处:《化工进展》2015年第5期1365-1370,共6页Chemical Industry and Engineering Progress
基 金:福建省重点科技项目(2009H0030);福建省自然科学基金(2012J01396和2011J01312);科技部科技人员服务企业项目(2009GJC40030)
摘 要:制备了具有良好油溶性的O-磺化-N,N-双十二烷基壳聚糖(HSDLCS)和O-季铵化-N,N-双十二烷基壳聚糖(QADLCS),研究了HSDLCS/QADLCS混合单分子膜和自组装囊泡性质的关系。结果表明,混合单分子膜的崩溃压(46.14m N/m)和最大压缩模量(Cs,max-1,98.85m N/m)较相应的单组分大;自组装形成球形囊泡的粒径在200~400nm;以维生素B12为模型药物制备HSDLCS/QADLCS复合囊泡的载药量为0.1987mg/mg,包封率为38.25%,药物平衡释放率为23.68%。静电作用使得混合单分子膜的凝聚性和抗形变能力更强,复合囊泡药物通透性降低,结构更紧密。单分子膜的Cs,max-1与其相应载药囊泡药物平衡释放率呈一定的线性关系。Oil-soluble O-sulfonated-N,N-dilauryl chitosan(HSDLCS) and O-quaternized-N,N-dilauryl chitosan(QADLCS) with similar substitution were synthesized. The properties of mixed monolayers and self-assembly vesicles of HSDLCS and QADLCS were studied. The mixed monolayers had larger collapse pressure(πc) larger maximum compression modulus(Cs,max-1) and limited molecular area(Aex) compared with HSDLCS and QADLCS monolayers. Spherical self-assembly vesicles were formed in diameter 200—400nm. Using Vitamin B12 as model drug,drug loading and encapsulation efficiency of complex vesicles were 0.1987 mg/mg and 38.25%,and equilibrium rates of Vitamin B12 release was 23.68%. Electrostatic attraction existing between the hydrophilic groups of HSDLCS and QADLCS resulted in stronger anti-deformation ability and cohesion of the mixed monolayers,decreased drug permeability of complex vesicles,and more tight structure of vesicles. Therer was a linear relationship between the Cs,max-1 of monolayers and equilibrium drug-release rate of the vesicles.
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