Nanoparticles and ultrasound for delivery of model macromolecular anti-cancer drugs in tumors

Y. Ivanova, B. Evers, R. Thomas, T.V. Ashitkov, R. Esenaliev
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引用次数: 4

Abstract

Penetration of macromolecular anti-cancer agents from blood into tumor cells is poor due to the physiological barriers: tumor capillary wall, interstitium, and cancer cell membrane. We proposed to use laser- or ultrasound-induced cavitation to enhance anti-cancer drug delivery through these barriers. Interaction of ultrasound with exogenous nanoparticles with certain acoustic properties may provide cavitation selectively in tumors and, therefore, may provide safe and efficient delivery of anti-cancer drugs in cancer cells without damage to normal tissues. In this paper, we studied enhanced delivery of model macromolecular anti-cancer drugs with ultrasound-induced cavitation in mice bearing human colon (KM20) and breast (MCF-7) tumors. Fluorescent rhodamine-dextrans of different molecular weight (10, 70, and 2,000 kDa) served as model drugs simulating antisense oligonucleotides, antibodies, and genes, respectively. Immunohistochemical staining of tumor vasculature with CD31 was used to visualize tumor blood vessels. Our studies demonstrated enhanced penetration of the drugs from blood vessels into tumor interstitium when ultrasound was applied in combination with polymer nanoparticle injections. Our results suggest that this drug delivery technique can potentially be used for efficient cancer chemo- and biotherapy.
纳米粒子和超声在肿瘤中传递模型大分子抗癌药物
由于肿瘤毛细血管壁、间质、肿瘤细胞膜等生理屏障的存在,大分子抗癌药物从血液进入肿瘤细胞的渗透能力较差。我们建议使用激光或超声诱导空化来增强抗癌药物通过这些屏障的递送。超声与具有一定声学特性的外源纳米粒子的相互作用可以在肿瘤中选择性地提供空化,因此可以在不损害正常组织的情况下安全有效地将抗癌药物输送到癌细胞中。在本文中,我们研究了超声诱导空化对人结肠癌(KM20)和乳腺癌(MCF-7)肿瘤小鼠模型大分子抗癌药物的增强传递。不同分子量(10,70和2,000 kDa)的荧光罗丹明-右旋糖酐分别作为模拟反义寡核苷酸、抗体和基因的模型药物。用CD31免疫组化染色法观察肿瘤血管。我们的研究表明,当超声与聚合物纳米颗粒注射结合使用时,药物从血管渗透到肿瘤间质。我们的研究结果表明,这种给药技术可以潜在地用于有效的癌症化疗和生物治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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