CavitoMod-UTMDNet: A Mechanistic Cavitation-Diffusion Framework for Ultrasound-Targeted Microbubble Destruction-Enhanced Liposomal Doxorubicin Delivery in Pancreatic Cancer.

IF 1.7 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Yazeed Alashban, Ghada Moh Samir Elhessewi, Mohammed Maray, Ali M Al-Sharafi, Hanadi Alkhudhayr, Rana Alabdan, Nujud Aloshban, Shouki A Ebad
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引用次数: 0

Abstract

Background: Pancreatic ductal adenocarcinoma (PDAC) has one of the poorest treatment responses since it contains desmoplastic stroma, lacks good vascularity, and has high interstitial fluid pressures, which are the most damaging factors depriving chemotherapy. Liposomal doxorubicin is much better in terms of systemic pharmacokinetics but is not efficient in PDAC due to the significant barrier of nanoparticles-stromal and vascular barriers.Purpose/Hypothesis: In a bid to eliminate these shortcomings, this paper presents CavitoMod-UTMDNet, which is an integrated mechanistic and experimental platform capable of utilizing ultrasound-targeted masterpiece unaffiliating (UTMD) as a means of temporarily improving vascular and stromal permeability and better intratumoral delivery of liposomal doxorubicin.Population/Subjects: The model combines Rayleigh-Plesset cavitation modeling and Fickian diffusion analysis with a two-compartment pharmacokinetic model and systematic in vitro and in vivo validation.Assessment: Passive cavitation detection was used to establish stable cavitation exposure windows within FDA-acceptable mechanical index limits.Statistical Tests: UTMD increased intracellular drug uptake 3.2-3.8fold and reduced IC 0 in PANC-1 and BxPC-3 pancreatic cancer cell lines by around 50% in the presence of a stable cavitation (MI 1.2). UTMD progressively improved the level of intratumor drug delivery in the orthotopic immunodeficient mouse models (NU/NU strain) (2.4-fold) and led to a 54% decrease in tumor volume 21 days later without any trace of hepatic, renal, and cardiac toxicity.Results: There were strong links between cavitation energy density and drug uptake and diffusion depth and therapeutic response as evidence that there is a mechanistic character to UTMD-enhanced actions. It will support the drug development in a better way. CavitoMod-UTMDNet is a combined strategy to maximize ultrasound-enhanced nanocarrier (nanoparticles) delivery using a physics-based reproducible plan to optimize ultrasound-enhanced nanocarrier delivery in PDAC that will see improvement in future translation to image-guided therapeutic strategies.

CavitoMod-UTMDNet:超声靶向微泡破坏增强脂质体输注胰腺癌阿霉素的空化扩散机制框架。
背景:胰腺导管腺癌(Pancreatic ductal adencarcinoma, PDAC)是治疗效果最差的肿瘤之一,因为它含有间质增生基质,缺乏良好的血管性,且间质液压力高,这些都是导致化疗无效的最具破坏性的因素。阿霉素脂质体在系统药代动力学方面要好得多,但由于纳米颗粒-基质和血管屏障的显著屏障,在PDAC中效率不高。目的/假设:为了消除这些缺点,本文提出了CavitoMod-UTMDNet,这是一个综合的机制和实验平台,能够利用超声靶向杰作分离(UTMD)作为暂时改善血管和基质通透性的手段,更好地在肿瘤内递送阿霉素脂质体。人群/受试者:该模型结合了瑞利-普莱塞空化模型和菲克斯扩散分析,采用两室药代动力学模型,并进行了系统的体外和体内验证。评估:被动空化检测用于在fda可接受的机械指标限制范围内建立稳定的空化暴露窗口。统计试验:在稳定空化的情况下,UTMD使PANC-1和BxPC-3胰腺癌细胞系的细胞内药物摄取增加3.2-3.8倍,IC 0降低约50% (MI 1.2)。UTMD逐渐提高了原位免疫缺陷小鼠模型(NU/NU株)的肿瘤内药物递送水平(2.4倍),并导致21天后肿瘤体积减少54%,没有任何肝脏,肾脏和心脏毒性痕迹。结果:空化能密度与药物摄取和扩散深度以及治疗反应之间存在密切联系,这表明utmd增强作用具有机制特征。它将更好地支持药物开发。CavitoMod-UTMDNet是一种组合策略,利用基于物理的可重复计划最大化超声增强纳米载体(纳米颗粒)的递送,以优化超声增强纳米载体在PDAC中的递送,这将在未来转化为图像引导的治疗策略中得到改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.80
自引率
2.90%
发文量
87
审稿时长
3 months
期刊介绍: Cancer Biotherapy and Radiopharmaceuticals is the established peer-reviewed journal, with over 25 years of cutting-edge content on innovative therapeutic investigations to ultimately improve cancer management. It is the only journal with the specific focus of cancer biotherapy and is inclusive of monoclonal antibodies, cytokine therapy, cancer gene therapy, cell-based therapies, and other forms of immunotherapies. The Journal includes extensive reporting on advancements in radioimmunotherapy, and the use of radiopharmaceuticals and radiolabeled peptides for the development of new cancer treatments.
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