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基于HPMA的纳米药物的构效关系:肿瘤球体渗透研究。

Structure-to-Efficacy Relationship of HPMA-Based Nanomedicines: The Tumor Spheroid Penetration Study.

作者信息

Kudláčová Júlia, Kotrchová Lenka, Kostka Libor, Randárová Eva, Filipová Marcela, Janoušková Olga, Fang Jun, Etrych Tomáš

机构信息

Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovskeho nam. 2, 162 06 Prague 6, Czech Republic.

Faculty of Pharmaceutical Science, Sojo University, Ikeda 4-22-1, Nishi-ku, Kumamoto 860-0082, Japan.

出版信息

Pharmaceutics. 2020 Dec 20;12(12):1242. doi: 10.3390/pharmaceutics12121242.

DOI:10.3390/pharmaceutics12121242
PMID:33419291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7766879/
Abstract

Nanomedicines are a novel class of therapeutics that benefit from the nano dimensions of the drug carrier. These nanosystems are highly advantageous mainly within cancer treatment due to their enhanced tumor accumulation. Monolayer tumor cells frequently used in routine preclinical assessment of nanotherapeutics do not have a spatial structural architecture that allows the investigation of the penetration of nanomedicines to predict their behavior in real tumor tissue. Therefore, tumor spheroids from colon carcinoma C26 cells and glioblastoma U87-MG cells were used as 3D in vitro models to analyze the effect of the inner structure, hydrodynamic size, dispersity, and biodegradability of -(2-hydroxypropyl)methacrylamide (HPMA) copolymer-based nanomedicines carrying anticancer drug pirarubicin (THP) on the penetration within spheroids. While almost identical penetration through spheroids of linear and star-like copolymers and also their conjugates with THP was observed, THP penetration after nanomedicines application was considerably deeper than for the free THP, thus proving the benefit of polymer carriers. The cytotoxicity of THP-polymer nanomedicines against tumor cell spheroids was almost identical as for the free THP, whereas the 2D cell cytotoxicity of these nanomedicines is usually lower. The nanomedicines thus proved the enhanced efficacy within the more realistic 3D tumor cell spheroid system.

摘要

纳米药物是一类新型治疗药物,受益于药物载体的纳米尺寸。这些纳米系统具有高度优势,主要体现在癌症治疗中,因为它们能增强肿瘤蓄积。在纳米治疗药物的常规临床前评估中常用的单层肿瘤细胞没有空间结构架构,无法用于研究纳米药物的渗透情况以预测其在真实肿瘤组织中的行为。因此,将来自结肠癌C26细胞和胶质母细胞瘤U87 - MG细胞的肿瘤球体用作三维体外模型,以分析携带抗癌药物吡柔比星(THP)的基于聚(2 - 羟丙基)甲基丙烯酰胺(HPMA)共聚物的纳米药物的内部结构、流体动力学尺寸、分散性和生物降解性对球体内部渗透的影响。虽然观察到线性和星状共聚物及其与THP的缀合物对球体的穿透几乎相同,但纳米药物应用后THP的穿透比游离THP深得多,从而证明了聚合物载体的益处。THP - 聚合物纳米药物对肿瘤细胞球体的细胞毒性与游离THP几乎相同,而这些纳米药物对二维细胞的细胞毒性通常较低。因此,纳米药物在更现实的三维肿瘤细胞球体系统中证明了其增强的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0fb/7766879/bd4c22237a9a/pharmaceutics-12-01242-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0fb/7766879/afe401848f66/pharmaceutics-12-01242-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0fb/7766879/a0a5cc946bb0/pharmaceutics-12-01242-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0fb/7766879/e4bf93bf9042/pharmaceutics-12-01242-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0fb/7766879/41c42c2e964e/pharmaceutics-12-01242-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0fb/7766879/bd4c22237a9a/pharmaceutics-12-01242-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0fb/7766879/afe401848f66/pharmaceutics-12-01242-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0fb/7766879/a0a5cc946bb0/pharmaceutics-12-01242-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0fb/7766879/e4bf93bf9042/pharmaceutics-12-01242-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0fb/7766879/41c42c2e964e/pharmaceutics-12-01242-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0fb/7766879/bd4c22237a9a/pharmaceutics-12-01242-g005.jpg

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