摘要
纳米技术对特定药物的有效分布和更低毒副作用提供了革新性的机遇。自其开始,运用纳米技术的目标是推进高效和可靠的抗肿瘤治疗和诊断。为实现这一目标,治疗药物纳米粒与单克隆抗体或类似物生物偶联战略,在体内和体外均已经显示为一种靶向的方法。在本综述中,我们主要关注原癌基因人类表皮生长因子受体2(HER2)过度表达肿瘤细胞中HER2受体特异识别,并评价抗HER2单克隆抗体,其为活性靶点的有效工具。当前,多种针对HER2阳性的乳腺癌纳米粒系统正处于临床前和临床研究,本文也综述了不同纳米技术拼接包括脂质体、胶束、树枝状聚合物、聚合物和无机纳米粒子,它们对于高分子合成具有较高的灵活性和多功能特性。抗-HER2功能纳米粒的进一步进展 对HER2阳性的乳腺癌纳米治疗技术的发展具有潜在推动作用。
关键词: 乳腺癌,树枝状大分子,原癌基因人类表皮生长因子受体2,脂质体,胶束,纳米粒,聚乳酸-羟基乙酸共聚物
图形摘要
Current Cancer Drug Targets
Title:Nano-pharmaceutical Formulations for Targeted Drug Delivery against HER2 in Breast Cancer
Volume: 15 Issue: 1
Author(s): Sams M.A. Sadat, Soodabeh Saeidnia, Adil J. Nazarali and Azita Haddadi
Affiliation:
关键词: 乳腺癌,树枝状大分子,原癌基因人类表皮生长因子受体2,脂质体,胶束,纳米粒,聚乳酸-羟基乙酸共聚物
摘要: Nanotechnology has revolutionized fundamental opportunities for higher specific drug delivery with minimum side effects. Since its inception, the goal of nanotechnology has been to advance effective and reliable systems for precise anti-cancer therapy and diagnosis. To accomplish this goal, bio-conjugation strategies of therapeutic agents loaded nanoparticles with monoclonal antibodies or their analogues have demonstrated a targeted approach both in vitro and in vivo. In this review, we primarily focus on the specific recognition of HER2 receptors of HER2 overexpressed tumor cells, and evaluate anti-HER2 monoclonal antibody as an effective tool for active targeting. Currently, a variety of nanoparticle systems are under both preclinical and clinical trials for targeting to HER2 positive breast cancer. Different nanotechnology scaffolds including liposomes, dendrimers, micelles, polymeric and inorganic nanoparticles that have higher flexibility for macromolecular synthesis and versatile functionalizing properties have been reviewed in this study. Continuing advances in anti-HER2 functionalized nanoparticles have good potential to lead to the development of nano-therapy against HER2 positive breast cancer.
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Cite this article as:
Sams M.A. Sadat, Soodabeh Saeidnia, Adil J. Nazarali and Azita Haddadi , Nano-pharmaceutical Formulations for Targeted Drug Delivery against HER2 in Breast Cancer, Current Cancer Drug Targets 2015; 15 (1) . https://dx.doi.org/10.2174/1568009615666150105115047
DOI https://dx.doi.org/10.2174/1568009615666150105115047 |
Print ISSN 1568-0096 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5576 |
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