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不同大小分子在超声联合微泡下对浅层肿瘤模型的渗透。

Penetration of different molecule sizes upon ultrasound combined with microbubbles in a superficial tumour model.

机构信息

Department of Ultrasound, Guangdong Women and Children Hospital , Guangzhou , China.

Department of Medical Ultrasound, Guangzhou First People's Hospital , Guangzhou , China.

出版信息

J Drug Target. 2019 Dec;27(10):1068-1075. doi: 10.1080/1061186X.2019.1588279. Epub 2019 Mar 20.

Abstract

Ultrasound combined with microbubbles (USMB) has been extensively applied to enhance drug and gene targeting delivery. However, the accumulation and distribution of particle size in the range of 5-30 nm (nano drug) to the tumour and the effects of intratumoral vascular density on permeability have been rarely reported. This study investigated Evans blue (EB) and fluorescein isothiocyanate-labelled dextran (FITC-dextran) distribution in tumour tissue upon USMB with various molecular sizes (3.7 nm and 30.6 nm). USMB increased the penetration of molecules with sizes of 5-20 nm in the whole tumour tissue, especially on the rim. For a molecule with sizes of 30.6 nm, USMB only increased penetration around the rim of the tumour with minimal improvement in the central of tumour. USMB enhanced the permeability of tumour tissue and increased tumour cells dose exposure without affecting tumour blood perfusion or microvessel density. The current study served as the foundation of parameter preference for therapeutic USMB drug delivery.

摘要

超声联合微泡(USMB)已广泛应用于增强药物和基因靶向传递。然而,对于粒径在 5-30nm 范围内的纳米药物向肿瘤的积累和分布以及肿瘤内血管密度对通透性的影响,鲜有报道。本研究探讨了不同分子大小(3.7nm 和 30.6nm)的超声微泡联合对肿瘤组织中 Evans 蓝(EB)和异硫氰酸荧光素标记葡聚糖(FITC-dextran)分布的影响。USMB 增加了 5-20nm 大小分子在整个肿瘤组织中的穿透性,特别是在边缘。对于 30.6nm 大小的分子,USMB 仅增加了肿瘤边缘的穿透性,而对肿瘤中心的改善很小。USMB 增强了肿瘤组织的通透性,增加了肿瘤细胞的剂量暴露,而不影响肿瘤血液灌注或微血管密度。本研究为治疗性 USMB 药物输送的参数偏好提供了基础。

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