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压力驱动药物递送显著增加猪模型中肝肿瘤的动脉内栓塞微球递送量。

Pressure-Enabled Drug Delivery Significantly Increases Intra-Arterial Delivery of Embolic Microspheres to Liver Tumors in a Porcine Model.

作者信息

Jaroch David B, Liu Yujia, Kim Alexander Y, Katz Steven C, Cox Bryan F, Hullinger Thomas G

机构信息

TriSalus Life Sciences, Westminster, Colorado.

TriSalus Life Sciences, Westminster, Colorado.

出版信息

J Vasc Interv Radiol. 2025 Mar;36(3):499-504.e1. doi: 10.1016/j.jvir.2024.11.014. Epub 2024 Nov 23.

Abstract

This study aimed to test the hypothesis that pressure-enabled drug delivery (PEDD) with a pressure-modulating microcatheter device (TriNav; TriSalus Life Sciences, Westminster, Colorado) would increase delivery of microspheres via hepatic arterial infusion to liver tumors in an Oncopig model (Sus Clinicals, Chicago, Illinois) when compared with a conventional end-hole microcatheter. Trisacryl gelatin microspheres (100-300 μm in size) were fluorescently labeled and infused into porcine liver tumors using conventional technique (n = 8) or by PEDD (n = 8). Liver tissue was harvested, and images were analyzed with a custom deep learning algorithm (Visiopharm, Hørsholm, Denmark) to quantitate signal intensity. PEDD increased microsphere penetration into the tumor by 227% (P = .029) when compared with conventional methodology and improved the tumor-to-normal tissue ratio from 2.7 to 4.2. These data demonstrate improved delivery into tumor tissue using PEDD, along with improved selectivity by minimizing relative off-target deposition.

摘要

本研究旨在验证以下假设

与传统端孔微导管相比,使用压力调节微导管装置(TriNav;TriSalus生命科学公司,科罗拉多州威斯敏斯特)进行压力驱动药物递送(PEDD),可通过肝动脉灌注增加微球在Oncopig模型(Sus Clinicals,伊利诺伊州芝加哥)中向肝肿瘤的递送。将尺寸为100 - 300μm的三丙烯酸明胶微球进行荧光标记,并使用传统技术(n = 8)或通过PEDD(n = 8)注入猪肝肿瘤。采集肝组织,并用定制的深度学习算法(Visiopharm,丹麦霍斯霍尔姆)分析图像以定量信号强度。与传统方法相比,PEDD使微球向肿瘤内的渗透增加了227%(P = .029),并将肿瘤与正常组织的比率从2.7提高到4.2。这些数据表明,使用PEDD可改善向肿瘤组织的递送,同时通过最小化相对非靶向沉积提高了选择性。

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