Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Department of Biotechnology, Faculty of Agricultural Science and Engineering, University of Tehran, Karaj, Iran.
BMC Pharmacol Toxicol. 2024 Oct 7;25(1):73. doi: 10.1186/s40360-024-00788-w.
Recently, the anti-tumor effects of cannabis extract on various cancers have attracted the attention of researchers. Here, we report a nanoemulsion (NE) composition designed to enhance the delivery of two active components in cannabis extracts (∆9-Tetrahydrocannabinol (THC) and Cannabidiol (CBD)) in an animal model of glioblastoma. The efficacy of the NE containing the two drugs (NED) was compared with the bulk drugs and carrier (NE without the drugs) using the C6 tumor model in rats. Hemocompatibility factors (RBC, MCV, MCH, MCHC, RDW, PPP, PT and PTT) were studied to determine the potential in vivo toxicity of NED. The optimized NED with mean ± SD diameter 29 ± 6 nm was obtained. It was shown that by administering the drugs in the form of NED, the hemocompatibility increased. Cytotoxicity studies indicated that the NE without the active components (i.e. mixture of surfactants and oil) was the most cytotoxic group, while the bulk group had no toxicity. From the in vivo MRI and survival studies, the NED group had maximum efficacy (with ~4 times smaller tumor volume on day 7 of treatment, compared with the control. Also, survival time of the control, bulk drug, NE and NED were 9, 4, 12.5 and 51 days, respectively) with no important adverse effects. In conclusion, the NE containing cannabis extract could be introduced as an effective treatment in reducing brain glioblastoma tumor progression.
最近,大麻提取物对各种癌症的抗肿瘤作用引起了研究人员的关注。在这里,我们报告了一种纳米乳液(NE)组合物,旨在增强大麻提取物中两种活性成分(∆9-四氢大麻酚(THC)和大麻二酚(CBD))在胶质母细胞瘤动物模型中的递送。使用大鼠 C6 肿瘤模型,将含有两种药物的 NE(NED)的功效与原料药和载体(不含药物的 NE)进行了比较。研究了血液相容性因素(RBC、MCV、MCH、MCHC、RDW、PPP、PT 和 PTT),以确定 NED 的潜在体内毒性。优化后的 NED 的平均直径为 29±6nm。结果表明,以 NED 的形式给药可提高血液相容性。细胞毒性研究表明,不含活性成分的 NE(即表面活性剂和油的混合物)是最具细胞毒性的组,而原料药组没有毒性。从体内 MRI 和存活研究来看,NED 组的疗效最大(与对照组相比,治疗第 7 天肿瘤体积缩小了约 4 倍。此外,对照组、原料药组、NE 组和 NED 组的存活时间分别为 9、4、12.5 和 51 天),没有重要的不良反应。总之,含有大麻提取物的 NE 可作为一种有效的治疗方法,用于减少脑胶质母细胞瘤肿瘤的进展。