Esmailzadeh Arman, Shanei Ahmad, Attaran Neda, Hejazi Seyed Hossein, Hemati Simin
Department of Medical Physics, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Department of Medical Physics, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Ultrasound Med Biol. 2022 Jun;48(6):1131-1142. doi: 10.1016/j.ultrasmedbio.2022.02.015. Epub 2022 Mar 17.
The use of nanoparticles as a sonosensitizer in cancer sonodynamic therapy has been gaining attention because of their great advantages in drug delivery applications. By conjugating chemotherapy agents with nanoparticles, we can develop a drug delivery platform, control drug release and improve the outcome of treatments. The in-vitro study described here evaluates the combination of AuSiO nanoparticles and dacarbazine (DTIC@AuSiO) as a sonosensitizer for sonodynamic therapy of melanoma. 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and flow cytometry assays revealed that the viability of B16F10 melanoma cells was significantly inhibited by the increase in apoptosis induction in treatment with DTIC@AuSiO nanoparticles under ultrasound exposure compared with treatment with the free DTIC or AuSiO nanoparticles. The sonosensitization activity of AuSiO nanoparticles and greater uptake of DTIC by tumor cells after loading in DTIC@AuSiO nanoparticles inhibited the proliferation of melanoma tumor cells effectively. In conclusion, the DTIC@AuSiO nanoparticles established in this study could represent a good drug delivery and sonosensitizer platform for use in melanoma sonodynamic therapy.
由于纳米颗粒在药物递送应用中具有巨大优势,其作为癌症声动力疗法中的声敏剂正受到越来越多的关注。通过将化疗药物与纳米颗粒结合,我们可以开发一个药物递送平台,控制药物释放并改善治疗效果。本文所述的体外研究评估了AuSiO纳米颗粒与达卡巴嗪(DTIC@AuSiO)组合作为黑色素瘤声动力疗法声敏剂的效果。3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)和流式细胞术分析表明,与游离DTIC或AuSiO纳米颗粒处理相比,在超声照射下用DTIC@AuSiO纳米颗粒处理诱导的凋亡增加显著抑制了B16F10黑色素瘤细胞的活力。AuSiO纳米颗粒的声敏化活性以及在DTIC@AuSiO纳米颗粒中负载后肿瘤细胞对DTIC的更大摄取有效地抑制了黑色素瘤肿瘤细胞的增殖。总之,本研究中建立的DTIC@AuSiO纳米颗粒可成为用于黑色素瘤声动力疗法的良好药物递送和声敏剂平台。