Fox Joseph, Batchelor Damien V B, Coletta Patricia Louise, Valleley Elizabeth M A, Evans Stephen D
Molecular and Nanoscale Physics Group, School of Physics and Astronomy, University of Leeds, Leeds LS2 9JT, U.K.
Leeds Institute of Medical Research, St James's University Hospital, Wellcome Trust Brenner Building, Leeds LS9 7TF, U.K.
ACS Omega. 2024 Oct 30;9(45):45270-45278. doi: 10.1021/acsomega.4c06779. eCollection 2024 Nov 12.
During chemotherapy treatment for cancer, often only a fraction of the administered dose reaches the tumor site, with the remaining drug spreading throughout the body, producing unwanted side-effects and restricting how much drug can be safely administered. A potential solution to reduce this problem is the use of microbubbles. The interaction between microbubbles and ultrasound generates pores in the tumor cells, permitting enhanced drug uptake. This study investigates the delivery of the ascorbic acid derivative, palmitoyl ascorbate, to KRAS-mutated colorectal cancer cells in vitro. Ultrasound-triggered microbubbles enhanced the efficacy of liposomal palmitoyl ascorbate treatments by 1.7- and 2.2-fold in LS174T and HCT116 CRC cell lines, respectively. This enhancement was achieved without increasing the drug dosage, and the therapeutic effect was shown to be localized to the area that received the ultrasound pulse, aiding in the reduction of off-site toxicity.
在癌症化疗期间,通常只有一小部分给药剂量能到达肿瘤部位,其余药物会扩散到全身,产生不良副作用并限制了安全给药的剂量。减少这一问题的一个潜在解决方案是使用微泡。微泡与超声之间的相互作用会在肿瘤细胞中产生孔隙,从而增强药物摄取。本研究在体外研究了抗坏血酸衍生物棕榈酰抗坏血酸向KRAS突变的结肠癌细胞的递送情况。超声触发的微泡分别使脂质体棕榈酰抗坏血酸治疗在LS174T和HCT116结肠癌细胞系中的疗效提高了1.7倍和2.2倍。这种增强是在不增加药物剂量的情况下实现的,并且治疗效果显示局限于接受超声脉冲的区域,有助于减少非靶向毒性。