Heparin interferes with the uptake of liposomes in glioma

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Thomas S. van Solinge , Kristina Pagh Friis , Killian O'Brien , Romy L. Verschoor , Jeroen van Aarle , Arnold Koekman , Xandra O. Breakefield , Pieter Vader , Raymond Schiffelers , Marike Broekman
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Abstract

In glioblastoma, a malignant primary brain tumor, liposomes have shown promise in pre-clinical and early phase clinical trials as delivery vehicles for therapeutics. However, external factors influencing cellular uptake of liposomes in glioma cells are poorly understood. Heparin and heparin analogues are commonly used in glioma patients to decrease the risk of thrombo-embolic events. Our results show that heparin inhibits pegylated liposome uptake by U87 glioma and GL261 cells in a dose dependent manner in vitro, and that heparin-mediated inhibition of uptake required presence of fetal bovine serum in the media. In a subcutaneous model of glioma, Cy5.5 labeled liposomes could be detected with in vivo imaging after direct intra-tumoral injection. Ex-vivo analysis with flow cytometry showed a decreased uptake of liposomes into tumor cells in mice treated systemically with heparin compared to those treated with vehicle only.

Abstract Image

肝素干扰胶质瘤中脂质体的摄取
在胶质母细胞瘤(一种恶性原发性脑肿瘤)中,脂质体在临床前和早期临床试验中显示出作为治疗递送载体的前景。然而,影响胶质瘤细胞摄取脂质体的外部因素尚不清楚。肝素和肝素类似物通常用于神经胶质瘤患者,以降低血栓栓塞事件的风险。我们的结果表明,肝素在体外以剂量依赖性方式抑制U87神经胶质瘤和GL261细胞对聚乙二醇化脂质体的摄取,并且肝素介导的摄取抑制需要在培养基中存在胎牛血清。在神经胶质瘤的皮下模型中,直接瘤内注射后,可以通过体内成像检测Cy5.5标记的脂质体。流式细胞术的离体分析显示,与仅用载体处理的小鼠相比,用肝素系统处理的小鼠中脂质体对肿瘤细胞的摄取减少。
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来源期刊
International Journal of Pharmaceutics: X
International Journal of Pharmaceutics: X Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.60
自引率
0.00%
发文量
32
审稿时长
24 days
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