Rugină Dumitriţa, Socaciu Mihai Adrian, Nistor Madalina, Diaconeasa Zorita, Cenariu Mihai, Tabaran Flaviu Alexandru, Socaciu Carmen
Faculty of Veterinary Medicine, University of Agricultural Sciences and Veterinary Medicine, 400372 Cluj-Napoca, Romania.
Faculty of Medicine, University of Medicine and Pharmacy "Iuliu Hatieganu", 400347 Cluj-Napoca, Romania.
Pharmaceuticals (Basel). 2024 Dec 4;17(12):1630. doi: 10.3390/ph17121630.
: Pentacyclic triterpenoids are increasingly studied as anticancer agents with many advantages compared to synthetic chemotherapeutics. The aim of this study was to prepare liposomal and nanostructured lipid formulations including a standardized extract of silver birch () outer bark (TTs) and to evaluate their potential as anticancer agents in vitro, using Melanoma B16-F10 and Walker carcinoma cells. : Appropriate solvents were selected for efficient TTs extraction, and original recipes were used to obtain Pegylated liposomes and nanolipid complexes with entrapped TTs, comparative to pure standards (betulinic acid and doxorubicin) in similar conditions. The composition, morphology, and sizes of all nanoformulations were checked by high-performance liquid chromatography/mass spectrometry, Transmission Electronic Microscopy, and Diffraction Light Scattering. The entrapment efficiency and its impact on cell viability, cell cycle arrest, and apoptosis by flow cytometry was also measured on both cancer cell lines. The standardized TTs, including betulin, lupeol, and betulinic acid, showed good stability and superior activity compared to pure betulinic acid. According to experimental data, TTs showed good entrapment in liposomal and NLC nanoformulations, both delivery systems including natural, biodegradable ingredients and enhanced bioavailability. The apoptosis and necrosis effects were more pronounced for TTs liposomal formulations in both types of cancer cells, with lower cytotoxicity compared to Doxorubicin, and can be correlated with their increased bioavailability.
五环三萜类化合物作为抗癌剂越来越受到研究,与合成化学疗法相比具有许多优势。本研究的目的是制备包含白桦()外皮标准化提取物(TTs)的脂质体和纳米结构脂质制剂,并使用黑色素瘤B16 - F10和沃克癌细胞在体外评估它们作为抗癌剂的潜力。:选择合适的溶剂以高效提取TTs,并使用原始配方获得包封有TTs的聚乙二醇化脂质体和纳米脂质复合物,与类似条件下的纯标准品(桦木酸和阿霉素)进行比较。通过高效液相色谱/质谱、透射电子显微镜和衍射光散射检查所有纳米制剂的组成、形态和大小。还通过流式细胞术测量了两种癌细胞系的包封效率及其对细胞活力、细胞周期阻滞和细胞凋亡的影响。标准化的TTs,包括桦木醇、羽扇豆醇和桦木酸,与纯桦木酸相比显示出良好的稳定性和优异的活性。根据实验数据,TTs在脂质体和NLC纳米制剂中显示出良好的包封效果,这两种递送系统都包含天然的、可生物降解的成分并提高了生物利用度。在两种类型的癌细胞中,TTs脂质体制剂的凋亡和坏死作用更为明显,与阿霉素相比细胞毒性较低,并且这可能与其提高的生物利用度相关。