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三氧化二砷洗脱CalliSpheres微球与碘油乳剂肝动脉化疗栓塞术:兔肝肿瘤模型中的药代动力学及瘤内浓度

Hepatic Arterial Chemoembolization With Arsenic Trioxide Eluting CalliSpheres Microspheres Versus Lipiodol Emulsion: Pharmacokinetics And Intratumoral Concentration In A Rabbit Liver Tumor Model.

作者信息

Duan Xu-Hua, Li Hao, Ren Jian-Zhuang, Han Xin-Wei, Chen Peng-Fei, Li Feng-Yao, Huang Guo-Hao, Ju Shu-Guang

机构信息

Department of Interventional Radiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, People's Republic of China.

出版信息

Cancer Manag Res. 2019 Nov 26;11:9979-9988. doi: 10.2147/CMAR.S199188. eCollection 2019.

DOI:10.2147/CMAR.S199188
PMID:32063723
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6884976/
Abstract

BACKGROUND

The objective of this study was to investigate the plasma pharmacokinetic profiles, intratumoral concentration and tissue distribution of arsenic trioxide (ATO) by drug-eluting beads (DEB)-transcatheter arterial chemoembolization (TACE) compared with conventional TACE (cTACE) in a rabbit liver tumor model.

METHODS

Sixty-four rabbits with VX2 liver tumor were established and randomly assigned to four groups equally. The calliSpheres microspheres (CSM)-ATO group received DEB-TACE treatment using ATO-loaded CSM; the cTACE-ATO group received cTACE treatment using ATO mixed with lipiodol; the CSM-normal control (NC) group received DEB-TACE treatment using blank CSM; the TAE-lipiodol group received cTACE treatment using saline mixed with lipiodol. ATO concentration in plasma, tumor and normal tissues, and liver and kidney function indexes were evaluated.

RESULTS

The CSM-ATO group exhibited lower plasma ATO concentrations at 10 minutes and 20 minutes post treatment compared with the cTACE-ATO group. Meanwhile, intratumoral ATO concentrations were higher in the CSM-ATO group compared with the cTACE-ATO group at 3-, 7- and 14-days post treatment. In normal liver tissue, heart and muscle tissues, ATO concentrations between the CSM-ATO and cTACE groups were similar at each time point; in kidney and lung tissues, ATO concentrations were lower in the CSM-ATO group at 1-day post treatment while they were similar at 3, 7 and 14 days post treatment. Also, liver or kidney function indexes were of no difference at each time point between CSM-ATO and cTACE-ATO groups.

CONCLUSION

Administration of ATO via DEB-TACE decreases systemic concentration while increasing intratumoral concentration of ATO without increasing liver or kidney toxicity compared with cTACE.

摘要

背景

本研究的目的是在兔肝肿瘤模型中,研究与传统经动脉化疗栓塞术(cTACE)相比,经药物洗脱微球(DEB)-经动脉化疗栓塞术(TACE)使用三氧化二砷(ATO)后的血浆药代动力学特征、瘤内浓度及组织分布。

方法

建立64只VX2肝肿瘤兔模型,并随机均分为四组。CalliSpheres微球(CSM)-ATO组采用载有ATO的CSM进行DEB-TACE治疗;cTACE-ATO组采用ATO与碘油混合进行cTACE治疗;CSM-正常对照(NC)组采用空白CSM进行DEB-TACE治疗;TAE-碘油组采用生理盐水与碘油混合进行cTACE治疗。评估血浆、肿瘤及正常组织中的ATO浓度以及肝肾功能指标。

结果

与cTACE-ATO组相比,CSM-ATO组在治疗后10分钟和20分钟时血浆ATO浓度较低。同时,与cTACE-ATO组相比,CSM-ATO组在治疗后3天、7天和14天时瘤内ATO浓度较高。在正常肝组织、心脏和肌肉组织中,CSM-ATO组和cTACE组在各时间点的ATO浓度相似;在肾脏和肺组织中,CSM-ATO组在治疗后1天时ATO浓度较低,而在治疗后3天、7天和14天时相似。此外,CSM-ATO组和cTACE-ATO组在各时间点的肝肾功能指标无差异。

结论

与cTACE相比,通过DEB-TACE给予ATO可降低全身浓度,同时增加瘤内ATO浓度,且不增加肝脏或肾脏毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8988/6884976/880b17e2fea9/CMAR-11-9979-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8988/6884976/11a3b7e152b7/CMAR-11-9979-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8988/6884976/a786cdf29034/CMAR-11-9979-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8988/6884976/32f63e3e2c7d/CMAR-11-9979-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8988/6884976/dc646607c7ee/CMAR-11-9979-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8988/6884976/0a97d72c1a8a/CMAR-11-9979-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8988/6884976/880b17e2fea9/CMAR-11-9979-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8988/6884976/11a3b7e152b7/CMAR-11-9979-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8988/6884976/a786cdf29034/CMAR-11-9979-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8988/6884976/32f63e3e2c7d/CMAR-11-9979-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8988/6884976/dc646607c7ee/CMAR-11-9979-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8988/6884976/0a97d72c1a8a/CMAR-11-9979-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8988/6884976/880b17e2fea9/CMAR-11-9979-g0006.jpg

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