Medina Francisca J, Velasco Guillermo, Villamizar-Sarmiento María G, Torres Cristian G, Oyarzun-Ampuero Felipe A
PhD Program in Agriculture, Forestry, and Veterinary Sciences, Universidad de Chile, Santiago 8820808, Chile.
Centralized Laboratory for Veterinary Research (LACIV), Faculty of Veterinary and Animal Sciences, Universidad de Chile, Santiago 8320000, Chile.
Pharmaceutics. 2025 Jul 26;17(8):970. doi: 10.3390/pharmaceutics17080970.
: Mammary carcinoma is a common disease in female dogs. Cannabidiol (CBD) can inhibit cell proliferation and induce apoptosis in human cancer cells. However, its low solubility in aqueous media requires solvents such as ethanol or dimethylsulfoxide that limit their dosage. Incorporating CBD into oil-in-water nanoemulsions (Nem) can improve its aqueous dispersibility. This study aimed to develop a CBD-Nem formulation and evaluate its effects on canine mammary cancer cell lines (CF41.Mg and IPC366) and non-cancer cells (MDCK). : CBD-Nem was prepared with Miglyol 812 oil and Epikuron 145 V as the surfactant, and was characterized by analyzing size, morphology, zeta potential, release profile, and uptake/internalization. Moreover, the antitumor effects of CBD-Nem were evaluated in cancer cells through viability, proliferation, cell cycle, and migration-invasion assays. : CBD-Nem exhibited a monodisperse nanometric population (150 nm), spherical shape, and negative zeta potential (-50 mV). The in vitro release kinetics showed slow and sustained delivery at both pH 5.5 and pH 7.4. Rhodamine-Nem, as a fluorescent model of CBD-Nem, was taken up and homogenously internalized in CF41.Mg cells. CBD-Nem decreased the viability of cancer cells with a maximum effect at 50 µM and showed a lower toxicity in MDCK cells. Long-term efficacy (20 days) was evidenced by CBD-Nem at inhibiting colony formation in cancer cells. Furthermore, CBD-Nem reduced the proportion of cells in the G2-M phase, induced apoptosis, and inhibited the migration and invasion of CF41.Mg cells. : CBD-Nem exhibited an in vitro antitumor effect, which supports its study in dogs with mammary carcinoma.
乳腺癌是雌性犬类的常见疾病。大麻二酚(CBD)可抑制人类癌细胞的增殖并诱导其凋亡。然而,其在水性介质中的低溶解度需要使用乙醇或二甲基亚砜等溶剂,这限制了它们的用量。将CBD纳入水包油纳米乳剂(Nem)可改善其在水中的分散性。本研究旨在开发一种CBD-Nem制剂,并评估其对犬乳腺癌细胞系(CF41.Mg和IPC366)和非癌细胞(MDCK)的影响。:以Miglyol 812油和Epikuron 145 V作为表面活性剂制备CBD-Nem,并通过分析粒径、形态、zeta电位、释放曲线和摄取/内化进行表征。此外,通过活力、增殖、细胞周期和迁移侵袭试验评估了CBD-Nem在癌细胞中的抗肿瘤作用。:CBD-Nem呈现单分散纳米级群体(约150 nm)、球形形状和负zeta电位(约-50 mV)。体外释放动力学表明,在pH 5.5和pH 7.4时均有缓慢且持续的释放。罗丹明-Nem作为CBD-Nem的荧光模型,被CF41.Mg细胞摄取并均匀内化。CBD-Nem降低了癌细胞的活力,在50 μM时效果最佳,且对MDCK细胞的毒性较低。CBD-Nem在抑制癌细胞集落形成方面具有长期疗效(20天)。此外,CBD-Nem降低了G2-M期细胞的比例,诱导了细胞凋亡,并抑制了CF41.Mg细胞的迁移和侵袭。:CBD-Nem表现出体外抗肿瘤作用,这支持了其在患有乳腺癌的犬类中的研究。