Antoniou Antonia I, Nordio Giulia, Di Paolo Maria Luisa, Colombo Eleonora, Gaffuri Beatrice, Polito Laura, Amenta Arianna, Seneci Pierfausto, Dalla Via Lisa, Perdicchia Dario, Passarella Daniele
Dipartimento di Chimica, Università degli Studi di Milano, Via Golgi 19, 20133 Milano, Italy.
Dipartimento di Scienze del Farmaco, Università degli Studi di Padova, Via F. Marzolo 5, 35131 Padova, Italy.
Pharmaceuticals (Basel). 2023 May 9;16(5):722. doi: 10.3390/ph16050722.
A potent nontoxic antitumor drug, 2-hydroxyoleic acid (, 2OHOA) used for membrane lipid therapy, was selected as a self-assembly inducer due to its ability to form nanoparticles (NPs) in water. For this purpose, it was conjugated with a series of anticancer drugs through a disulfide-containing linker to enhance cell penetration and to secure drug release inside the cell. The antiproliferative evaluation of the synthesized NP formulations against three human tumor cell lines (biphasic mesothelioma MSTO-211H, colorectal adenocarcinoma HT-29, and glioblastoma LN-229) showed that nanoassemblies - exhibit antiproliferative activity at micromolar and submicromolar concentrations. Furthermore, the ability of the disulfide-containing linker to promote cellular effects was confirmed for most nanoformulations. Finally, induced intracellular ROS increase in glioblastoma LN-229 cells similarly to free drug , and such elevated production was decreased by pretreatment with the antioxidant -acetylcysteine. Also, nanoformulations and confirmed the mechanism of action of the free drugs.
一种用于膜脂质治疗的高效无毒抗肿瘤药物2-羟基油酸(2OHOA),因其能够在水中形成纳米颗粒(NPs)而被选作自组装诱导剂。为此,它通过含二硫键的连接子与一系列抗癌药物偶联,以增强细胞穿透能力并确保药物在细胞内释放。对合成的纳米颗粒制剂针对三种人类肿瘤细胞系(双相性间皮瘤MSTO-211H、结肠直肠腺癌HT-29和胶质母细胞瘤LN-229)的抗增殖评估表明,纳米组装体在微摩尔和亚微摩尔浓度下表现出抗增殖活性。此外,对于大多数纳米制剂,含二硫键的连接子促进细胞效应的能力得到了证实。最后,与游离药物一样,在胶质母细胞瘤LN-229细胞中诱导细胞内活性氧增加,而用抗氧化剂N-乙酰半胱氨酸预处理可降低这种升高的产生。此外,纳米制剂和证实了游离药物的作用机制。