Ghiulai Roxana, Mioc Alexandra, Racoviceanu Roxana, Mioc Marius, Milan Andreea, Prodea Alexandra, Semenescu Alexandra, Dehelean Cristina, Barbu Tudoran Lucian, Avram Ștefana, Trandafirescu Cristina, Șoica Codruța
Department of Pharmacology-Pharmacotherapy, Faculty of Pharmacy, "Victor Babes" University of Medicine and Pharmacy, Eftimie Murgu Square No. 2, 300041 Timişoara, Romania.
Research Centre for Pharmaco-Toxicological Evaluation, "Victor Babes" University of Medicine and Pharmacy, Eftimie Murgu Square, No. 2, 300041 Timișoara, Romania.
Pharmaceuticals (Basel). 2022 Nov 5;15(11):1362. doi: 10.3390/ph15111362.
Implementing metallic nanoparticles as research instruments for the transport of therapeutically active compounds remains a fundamentally vital work direction that can still potentially generate novelties in the field of drug formulation development. Gold nanoparticles (GNP) are easily tunable carriers for active phytocompounds like pentacyclic triterpenes. These formulations can boost the bioavailability of a lipophilic structure and, in some instances, can also enhance its therapeutic efficacy. In our work, we proposed a biological in vitro assessment of betulinic acid (BA)-functionalized GNP. BA-GNP were obtained by grafting BA onto previously synthesized citrate-capped GNP through the use of cysteamine as a linker. The nanoformulation was tested in HaCaT human keratinocytes and RPMI-7951 human melanoma cells, revealing selective cytotoxic properties and stronger antiproliferative effects compared to free BA. Further examinations revealed a pro-apoptotic effect, as evidenced by morphological changes in melanoma cells and supported by western blot data showing the downregulation of anti-apoptotic Bcl-2 expression coupled with the upregulation of pro-apoptotic Bax. GNP also significantly inhibited mitochondrial respiration, confirming its mitochondrial-targeted activity.
将金属纳米颗粒用作治疗活性化合物运输的研究工具,仍然是一个至关重要的基础工作方向,在药物制剂开发领域仍有可能产生新成果。金纳米颗粒(GNP)是五环三萜等活性植物化合物的易于调节的载体。这些制剂可以提高亲脂性结构的生物利用度,在某些情况下,还可以增强其治疗效果。在我们的工作中,我们提出了对桦木酸(BA)功能化的GNP进行体外生物学评估。通过使用半胱胺作为连接剂,将BA接枝到先前合成的柠檬酸盐封端的GNP上,从而获得BA-GNP。该纳米制剂在HaCaT人角质形成细胞和RPMI-7951人黑色素瘤细胞中进行了测试,结果显示与游离BA相比,具有选择性细胞毒性特性和更强的抗增殖作用。进一步的研究揭示了促凋亡作用,黑色素瘤细胞的形态变化证明了这一点,蛋白质印迹数据也支持这一点,该数据显示抗凋亡Bcl-2表达下调,同时促凋亡Bax表达上调。GNP还显著抑制线粒体呼吸,证实了其线粒体靶向活性。