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通过靶向微泡的脉冲超声增强治疗性表皮生长因子受体(EGFR)抗体递送用于胶质瘤治疗

Enhanced Therapeutic Epidermal Growth Factor Receptor (EGFR) Antibody Delivery via Pulsed Ultrasound with Targeting Microbubbles for Glioma Treatment.

作者信息

Liao Ai-Ho, Chou Hsin-Yi, Hsieh Yi-Lei, Hsu Sheng-Chieh, Wei Kuo-Chen, Liu Hao-Li

机构信息

Graduate Institute of Biomedical Engineering, National Taiwan University of Science and Technology, Taipei, 106 Taiwan.

Department of Electrical Engineering, Chang Gung University, Taoyuan, 333 Taiwan.

出版信息

J Med Biol Eng. 2015;35(2):156-164. doi: 10.1007/s40846-015-0032-9. Epub 2015 Apr 10.

Abstract

Pulsed-mode ultrasound (pUS) in combination with intravenously (IV) administered microbubbles (MBs) can enhance local drug delivery by temporarily enhancing capillary permeability. This study evaluates the use of epidermal growth factor receptor (EGFR)-targeting MBs after pUS treatment to enhance the effects of therapeutic-EGFR antibody delivery to glioma tumor cells in mice. Three animal groups were compared: (1) IV-injected non-targeting MBs, (2) IV-injected targeting MBs, and (3) IV-injected targeting MBs combined with pUS treatment. All animals were analyzed using high-frequency small-animal US imaging. The mean halftime of circulating targeting MBs was significantly increased from 3.13 min of targeting bubble alone to 5.86 min by targeting MBs combined with pUS treatment, compared to 2.34 min for non-targeting MBs. Compared to targeting bubble administration alone, pUS exposure prior to injection of targeting MBs was also significantly better at suppressing tumor growth when monitored for up to 35 days ( < 0.05). The final relative tumor volumes were 2664, 700, and 188 mm for non-targeting MBs, targeting MBs, and targeting MBs combined with pUS treatment, respectively. pUS treatment prolonged the mean circulatory halftime of targeting MBs and enhanced the anti-tumor effect of EGFR antibodies in a human glioma model in mice. Targeting MBs combined with pUS treatment thus has potential for enhanced therapeutic antibody delivery for facilitating anti-glioma treatment.

摘要

脉冲模式超声(pUS)与静脉注射微泡(MBs)相结合,可通过暂时增强毛细血管通透性来提高局部药物递送效率。本研究评估了在pUS治疗后使用靶向表皮生长因子受体(EGFR)的微泡,以增强治疗性EGFR抗体对小鼠胶质瘤肿瘤细胞的递送效果。比较了三个动物组:(1)静脉注射非靶向微泡;(2)静脉注射靶向微泡;(3)静脉注射靶向微泡并结合pUS治疗。所有动物均使用高频小动物超声成像进行分析。与非靶向微泡的2.34分钟相比,联合pUS治疗的靶向微泡使循环靶向微泡的平均半衰期从单独靶向微泡的3.13分钟显著增加至5.86分钟。在长达35天的监测期内,与单独给予靶向微泡相比,在注射靶向微泡前进行pUS照射在抑制肿瘤生长方面也显著更好(<0.05)。非靶向微泡、靶向微泡和联合pUS治疗的靶向微泡的最终相对肿瘤体积分别为2664、700和188立方毫米。pUS治疗延长了靶向微泡的平均循环半衰期,并增强了EGFR抗体在小鼠人胶质瘤模型中的抗肿瘤作用。因此,靶向微泡联合pUS治疗在增强治疗性抗体递送以促进抗胶质瘤治疗方面具有潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b82c/4414932/9a37869ec1fb/40846_2015_32_Fig1_HTML.jpg

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