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使用5-氨基乙酰丙酸(5-ALA)和替莫唑胺(TMZ)声敏剂的高通量3D胶质母细胞瘤球体模型进行体外声动力治疗

In Vitro Sonodynamic Therapy Using a High Throughput 3D Glioblastoma Spheroid Model with 5-ALA and TMZ Sonosensitizers.

作者信息

Datta Priyankan, Lee Nan Sook, Moolayadukkam Sreejesh, Sahu Rakesh P, Yu Xi, Guo Tianze, Zhou Qifa, Wang Y, Puri Ishwar K

机构信息

Department of Aerospace and Mechanical Engineering, University of Southern California, Los Angeles, CA, 90089, USA.

Alfred E. Mann Department of Biomedical Engineering, University of Southern California, Los Angeles, CA, 90089, USA.

出版信息

Adv Healthc Mater. 2024 Dec;13(32):e2402877. doi: 10.1002/adhm.202402877. Epub 2024 Oct 21.

Abstract

Sonodynamic therapy (SDT) administered using low-intensity pulsed ultrasound and sonosensitizers is an emerging, minimally invasive, targeted deep-tissue therapy for solid tumors such as glioblastoma multiforme (GBM). Initial clinical trials show promising outcomes for SDT treatments of GBM. A crucial aspect of SDT is the sonosensitizer that interacts with ultrasound, facilitating energy transfer to the tumor, thus inducing therapeutic efficacy. Current in vitro methods for determining the therapeutic efficacies of sonosensitizers are time-consuming and expensive. A novel high-throughput magnetically printed 3D GBM model is used to overcome this challenge. The hypothesis is that the use of two sonosensitizers, one a chemotherapeutic drug, enhances SDT efficacy through their additive chemical interactions. The GBM model is used to evaluate the effectiveness of two sonosensitizer molecules, 5-aminolevulinic acid (5-ALA) and theU.S. Food and Drug Administration (FDA)-approved chemotherapeutic drug Temozolomide (TMZ). It is confirmed that implement high-throughput GBM models to evaluate sonosensitizer combinations and their efficacies is feasible and, for the first time, show that the combined effect of both sensitizers, 5-ALA and TMZ, is superior for preventing spheroid growth than employing each molecule separately. This finding is relevant for future clinical trials of GBM treatment with SDT.

摘要

使用低强度脉冲超声和超声敏化剂进行的声动力疗法(SDT)是一种新兴的、微创的、针对实体瘤(如多形性胶质母细胞瘤,GBM)的深部组织靶向治疗方法。初步临床试验表明,SDT治疗GBM的效果很有前景。SDT的一个关键方面是与超声相互作用的超声敏化剂,它促进能量向肿瘤转移,从而产生治疗效果。目前用于确定超声敏化剂治疗效果的体外方法既耗时又昂贵。一种新型的高通量磁性打印3D GBM模型被用于克服这一挑战。其假设是,使用两种超声敏化剂,其中一种是化疗药物,通过它们的加成化学相互作用提高SDT疗效。该GBM模型用于评估两种超声敏化剂分子——5-氨基乙酰丙酸(5-ALA)和美国食品药品监督管理局(FDA)批准的化疗药物替莫唑胺(TMZ)的有效性。研究证实,采用高通量GBM模型评估超声敏化剂组合及其疗效是可行的,并且首次表明,5-ALA和TMZ这两种敏化剂的联合效果在防止球体生长方面优于单独使用每种分子。这一发现与未来GBM的SDT治疗临床试验相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcf4/11670275/a49275f1d93f/ADHM-13-0-g004.jpg

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