检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:郑玉婷 洪涛 徐柯卉 温明皓 杨吉雪 伍梦莹 杭太俊[1] 宋敏[1] ZHENG Yuting;HONG Tao;XU Kehui;WEN Minghao;YANG Jixue;WU Mengying;HANG Taijun;SONG Min(Department of Pharmaceutical Analysis,China Pharmaceutical University,Nanjing 210009,China)
出 处:《中国药科大学学报》2023年第6期743-748,共6页Journal of China Pharmaceutical University
摘 要:体外释放度是评价脂质体制剂质量的重要指标,目前各国药典中均未收载脂质体体外释放度评价方法,致使脂质体质量评价缺乏统一标准和无法提供安全性保障。本研究以自制类紫杉醇脂质体为例,通过优化外部释放条件建立的桨膜结合法模拟了在生理条件下类紫杉醇药物12 h的释放情况,结果表明以0.5%SDS-HEPES作为释放介质,采用截留分子量为1000 kD的透析袋对脂质体水溶液进行释放的结果满足要求,且具有区分能力,为载药脂质体体外释放方法开发提供参考。The in vitro release is an important index to evaluate the quality of liposome formulation.Currently,there is no evaluation method for the in vitro release of liposome in pharmacopoeia of various countries,which leads to the lack of unified standard and safety guarantee for the quality evaluation of liposome formulation.Taking the self-made paclitaxel derivative liposomes as an example,the paddle membrane binding method established by optimizing external release conditions was used to simulate the complete release of paclitaxel derivative drugs in 12 hours under physiological conditions.The results showed that using 0.5%SDS-HEPES as the release medium and a dialysis bag with a molecular weight cutoff of 1000 kD to release the liposome solution met the requirements and had discrimination ability,providing a reference for the development of drug-loaded liposomes release methods in vitro.
关 键 词:脂质体体外释放 透析法 类紫杉醇脂质体 桨膜结合法
分 类 号:R917[医药卫生—药物分析学]
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.33