Department of Life and Nanomedcine, Kyunghee University, Seoul, Republic of Korea.
Eur J Pharm Biopharm. 2009 Sep;73(1):59-65. doi: 10.1016/j.ejpb.2009.04.010. Epub 2009 May 4.
Doxorubicin was chemically conjugated to acrylated chitosan in order to obtain sustained-release profiles of doxorubicin from thermo-responsive and photo-crosslinkable hydrogels. Chitooligosaccharide was acrylated with glycidyl methacrylate and subsequently conjugated to doxorubicin via an amide linkage. A mixture of doxorubicin-chitosan conjugates, acrylated Pluronic, and doxorubicin formed physical gels at 37 degrees C. Photo-irradiation was subsequently performed to chemically crosslink the physical hydrogel at 37 degrees C. Chitooligosaccharide-doxorubicin conjugates in the doxorubicin hydrogels significantly reduced burst release of free doxorubicin from doxorubicin hydrogels compared hydrogels without the conjugates. Upon incubating doxorubicin hydrogels at 37 degrees C, chitosan-doxorubicin conjugates were confirmed to be degraded into more hydrophilic oligomers by reversed-phase chromatography. In vitro cytotoxicity assay using released media from doxorubicin hydrogels showed that degraded chitosan-doxorubicin had cytotoxicity comparable to free doxorubicin. Athymic nude mice bearing human lung adenocarcinoma were subjected to intra-tumoral injections of physical hydrogels. After photo-crosslinking injected hydrogels using surgical catheters, tumor sizes, body weights, and survivals were measured for 1 month. Released media from doxorubicin hydrogels exerted similar cytotoxicities to free doxorubicin, and the tumor volume was significantly reduced for 1 month compared to other samples. Thus, doxorubicin hydrogels containing doxorubicin conjugates can be employed as a novel injectable anti-cancer drug aiming to achieve sustained release of doxorubicin for several weeks against solid tumors.
阿霉素通过化学方法与丙烯酰化壳聚糖偶联,以获得热敏和光交联水凝胶中阿霉素的持续释放曲线。壳寡糖与甲基丙烯酸缩水甘油酯反应,然后通过酰胺键与阿霉素偶联。阿霉素-壳聚糖缀合物、丙烯酰化泊洛沙姆和阿霉素的混合物在 37°C 下形成物理凝胶。随后在 37°C 下进行光照射,以化学交联物理水凝胶。与不含缀合物的水凝胶相比,水凝胶中的壳寡糖-阿霉素缀合物显著减少了游离阿霉素从阿霉素水凝胶中的爆发释放。在 37°C 下孵育阿霉素水凝胶后,通过反相色谱证实壳聚糖-阿霉素缀合物降解为更亲水的低聚物。使用从阿霉素水凝胶中释放的介质进行的体外细胞毒性测定表明,降解的壳聚糖-阿霉素具有与游离阿霉素相当的细胞毒性。荷人肺腺癌细胞的裸鼠接受肿瘤内注射物理水凝胶。用光导纤维导管对注射的水凝胶进行光交联后,测量肿瘤大小、体重和存活时间 1 个月。从阿霉素水凝胶中释放的介质对游离阿霉素具有相似的细胞毒性,与其他样品相比,肿瘤体积在 1 个月内显著减小。因此,含有阿霉素缀合物的阿霉素水凝胶可作为一种新型的可注射抗癌药物,旨在实现数周内对实体瘤的阿霉素持续释放。