Liu Yu, Zhu Yi-ying, Wei Gang, Lu Wei-yue
Department of Pharmaceutics, School of Pharmacy, Fudan University, Shanghai, PR China.
Eur J Pharm Sci. 2009 Jun 28;37(3-4):306-12. doi: 10.1016/j.ejps.2009.02.022. Epub 2009 Mar 14.
The aim of this work is to explore effects of carrageenan on sustained-release properties of poloxamer 407-based vaginal in situ gel. After formulation of composite gel systems composed of carrageenan and poloxamer 407, in vitro release profiles and in vivo local drug residence after vaginal administration in mice was investigated using acyclovir as the model drug. Rheological experiment was conducted to investigate effects of carrageenan on temperature-dependent viscoelasticity of poloxamer 407-based gels. It appeared that carrageenan and poloxamer 407 could form composite gel systems with good thermosensitity similar to gels containing only poloxamer 407. In the in vitro release experiment, carrageenan significantly decreased the release rate of acyclovir, retarded the dissolution of poloxamer 407 and slowed the gel erosion (weight loss) in a concentration-dependent manner. In vivo local drug residence experiment indicated that carrageenan significantly prolonged local residence of acyclovir and further showed a synergistic bioadhesive effect with acrylic acid polymers (Carbopol). In conclusion, carrageenan was able to improve the sustained-release properties of poloxamer 407-based in situ gel, indicating that the combination of carrageenan and poloxamer 407 may find use in the development of vaginal in situ gel drug delivery systems with prolonged local residence and thus better clinical outcome.
本研究旨在探讨卡拉胶对泊洛沙姆407基阴道原位凝胶缓释性能的影响。在制备了由卡拉胶和泊洛沙姆407组成的复合凝胶体系后,以阿昔洛韦为模型药物,研究了小鼠阴道给药后的体外释放曲线和体内局部药物滞留情况。进行流变学实验以研究卡拉胶对泊洛沙姆407基凝胶温度依赖性粘弹性的影响。结果表明,卡拉胶和泊洛沙姆407可以形成具有良好热敏性的复合凝胶体系,类似于仅含泊洛沙姆407的凝胶。在体外释放实验中,卡拉胶显著降低了阿昔洛韦的释放速率,延缓了泊洛沙姆407的溶解,并以浓度依赖的方式减缓了凝胶侵蚀(失重)。体内局部药物滞留实验表明,卡拉胶显著延长了阿昔洛韦的局部滞留时间,并进一步显示出与丙烯酸聚合物(卡波姆)的协同生物粘附作用。总之,卡拉胶能够改善泊洛沙姆407基原位凝胶的缓释性能,表明卡拉胶与泊洛沙姆407的组合可能用于开发具有延长局部滞留时间从而获得更好临床效果的阴道原位凝胶药物递送系统。