Dang Huan, Wang Ji, Cheng Jiang-Xue, Wang Peng-Yuan, Wang Ying, Cheng Li-Fei, Du Caigan, Wang Xiao-Juan
State Key Laboratory of Military Stomatology, Department of Pharmacy, School of Stomatology, The Fourth Military Medical University Xi'an, Shaanxi 710032, China.
Department of Pharmacy, Shaanxi University of Chinese Medicine Xianyang, Shaanxi 712046, China.
Am J Cancer Res. 2014 Dec 15;5(1):243-54. eCollection 2015.
Ardipusilloside I (ADS-I) is a natural compound that can be isolated from the Chinese medicinal herb Ardisiapusilla A.DC, and has been reported to inhibit the growth of glioblastoma cells in cultures. This study was designed to test its efficacy by the delivery using biodegradable implants against glioblastoma in vivo. ADS-I was incorporated into polymer microspheres, which were prepared by a mixture of poly (D, L-lactic acid) and poly (D, L-lactic-co-glycolic acid) polymers and then fabricated into wafers. The anti-glioma activities of ADS-I-loaded wafers were examined by methylthiazol tetrazolium (MTT) assay in cultured rat C6 glioma cells, and by magnetic resonance imaging (MRI) and survival monitoring in C6 glioma-bearing rats. Here, we showed that ADS-I-loaded wafers sustained ADS-I release in vitro for 36 days in Higuchi model of kinetics, and had the same cytotoxic activity as ADS-I in the solution against the growth of C6 glioma cells in cultures. In C6 glioma-bearing rats, ADS-I wafer implants inhibited tumor growth in a dose-dependent matter, and were more effective than the same dosage of ADS-I in the solution. The tumor suppression efficacies of ADS-I wafer implants were positively correlated with an increase in tumor cell apoptosis and prolonged animal survival, and were associated with a decrease in vascular endothelial growth factor, C-reactive protein, tumor necrosis factor-α and interleukin-6, and an increase in interleukin-2 expression. In conclusion, this study demonstrates significant efficacy of local delivery of ADS-I using polymer implants against glioma tumor growth in vivo, suggesting the potential of ADS-I-loaded wafers for glioma treatment.
紫金牛苷 I(ADS-I)是一种天然化合物,可从中国草药紫金牛中分离得到,据报道它能抑制培养的胶质母细胞瘤细胞的生长。本研究旨在通过使用可生物降解植入物在体内递送 ADS-I 来测试其疗效。将 ADS-I 掺入聚合物微球中,聚合物微球由聚(D,L-乳酸)和聚(D,L-乳酸-共-乙醇酸)聚合物的混合物制备,然后制成薄片。通过甲基噻唑基四氮唑(MTT)法在培养的大鼠 C6 胶质瘤细胞中检测负载 ADS-I 的薄片的抗胶质瘤活性,并通过磁共振成像(MRI)和对荷 C6 胶质瘤大鼠的生存监测来评估。在此,我们表明,在 Higuchi 动力学模型中,负载 ADS-I 的薄片在体外可持续释放 ADS-I 达 36 天,并且在溶液中与 ADS-I 对培养的 C6 胶质瘤细胞生长具有相同的细胞毒性活性。在荷 C6 胶质瘤大鼠中,负载 ADS-I 的薄片植入物以剂量依赖的方式抑制肿瘤生长,并且比相同剂量的溶液中的 ADS-I 更有效。负载 ADS-I 的薄片植入物的肿瘤抑制效果与肿瘤细胞凋亡增加和动物存活时间延长呈正相关,并且与血管内皮生长因子、C 反应蛋白、肿瘤坏死因子-α 和白细胞介素-6 的减少以及白细胞介素-2 表达的增加有关。总之,本研究证明了使用聚合物植入物局部递送 ADS-I 对体内胶质瘤肿瘤生长具有显著疗效,表明负载 ADS-I 的薄片在胶质瘤治疗方面具有潜力。