基于超声的血脑屏障打开后卡铂和荧光素脑保留的药动学分析。

IF 10.2 1区 医学 Q1 ONCOLOGY
Karl J Habashy, Timothy W Synold, Ye Feng, Cristal Gomez, Christina Amidei, Rachel Ward, Sarah VanderMolen, Ashkan Zarrieneh, Kwang-Soo Kim, Mateo Gomez, Victor A Arrieta, Jawad Fares, Kirsten B Burdett, Hui Zhang, Crismita Dmello, Li Chen, John F Bebawy, Michael Canney, Roger Stupp, Behnam Badie, Jana Portnow, Adam M Sonabend
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引用次数: 0

摘要

背景:血脑屏障(BBB)阻碍大多数循环药物进入大脑。低强度脉冲超声微泡(LIPU/MB)瞬时打开血脑屏障,改善实质药物渗透。短期血脑屏障打开后的实质药物潴留尚不清楚。我们研究了LIPU/MB随时间对卡铂和荧光素浓度的影响,并比较了替莫唑胺、卡铂和荧光素在非超声脑中的实质保留。方法:在NCT04528680临床试验中,我们分析了4例接受术中LIPU/MB并静脉给予卡铂和荧光素的患者。将微透析导管植入超声和非超声脑内,并在24小时内测量药物水平。采用已发表的替莫唑胺无LIPU/MB微透析数据进行比较。结果:LIPU/MB导致脑实质药物浓度持续升高,卡铂和荧光素脑-血浆AUC增加3.1倍(P = 0.03)。在非超声脑中,替莫唑胺浓度仍低于其血浆水平,因为实质药物清除反映了血浆清除。相反,不渗透血脑屏障的药物如卡铂和荧光素表现出延迟的实质清除,导致随着时间的推移,脑内药物水平高于血浆药物水平。超声不影响卡铂和荧光素的实质药物清除率。结论:LIPU/MB后,血脑屏障不渗透药物的实质浓度持续升高,超过其血浆水平,突出了血脑屏障对药物通过的双向限制。未来的研究需要探索药物捕获和持续暴露于细胞毒性药物治疗脑浸润性肿瘤的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacokinetic Analysis of Carboplatin and Fluorescein Brain Retention following Ultrasound-Based Blood-Brain Barrier Opening.

Purpose: The blood-brain barrier (BBB) impedes the passage of most circulating drugs into the brain. Low-intensity pulsed ultrasound with microbubbles (LIPU/MB) transiently opens the BBB, improving parenchymal drug penetration. Parenchymal drug retention following short-lived BBB opening is unknown. We investigated the effect of LIPU/MB on the concentration of carboplatin and fluorescein over time and compared the parenchymal retention of temozolomide (TMZ), carboplatin, and fluorescein in the nonsonicated brain.

Experimental design: We analyzed four patients who underwent intraoperative LIPU/MB with intravenous administration of carboplatin and fluorescein in the NCT04528680 clinical trial. Microdialysis catheters were implanted into sonicated and nonsonicated brain regions, and drug levels were measured over 24 hours. Published microdialysis data of TMZ without LIPU/MB were used for comparison.

Results: LIPU/MB led to sustained elevated parenchymal drug concentrations, achieving a 3.1-fold increase in brain-to-plasma AUC for carboplatin and fluorescein (P = 0.03). In the nonsonicated brain, TMZ concentrations remained below their plasma levels, as parenchymal drug clearance mirrored plasma clearance. In contrast, BBB-impermeable drugs such as carboplatin and fluorescein exhibited delayed parenchymal clearance, resulting in higher brain than plasma drug levels over time. Parenchymal drug clearance of carboplatin and fluorescein was not affected by sonication.

Conclusions: Following LIPU/MB, BBB-impermeable drugs exhibit sustained elevated parenchymal concentrations surpassing their plasma levels, highlighting the bidirectional restriction of drug passage by the BBB. Future studies are warranted to explore drug trapping and the efficacy of sustained exposure to cytotoxic drugs for the treatment of brain-infiltrating tumors.

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来源期刊
Clinical Cancer Research
Clinical Cancer Research 医学-肿瘤学
CiteScore
20.10
自引率
1.70%
发文量
1207
审稿时长
2.1 months
期刊介绍: Clinical Cancer Research is a journal focusing on groundbreaking research in cancer, specifically in the areas where the laboratory and the clinic intersect. Our primary interest lies in clinical trials that investigate novel treatments, accompanied by research on pharmacology, molecular alterations, and biomarkers that can predict response or resistance to these treatments. Furthermore, we prioritize laboratory and animal studies that explore new drugs and targeted agents with the potential to advance to clinical trials. We also encourage research on targetable mechanisms of cancer development, progression, and metastasis.
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