Suppr超能文献

配体纳米粒子偶联法用于靶向癌症治疗。

The ligand nanoparticle conjugation approach for targeted cancer therapy.

机构信息

Institute for Drug Research, The School of Pharmacy, The Hebrew University of Jerusalem, Jerusalem, Israel.

出版信息

Curr Drug Metab. 2012 Jan;13(1):22-41. doi: 10.2174/138920012798356899.

Abstract

Cancer therapy often requires frequent and high drug dosing. Yet, despite the significant progress in cancer research and the wide versatility of potent available drugs, treatment efficacy is still hurdled and often failed by the lack of pharmaco-selectivity to diseased cells, indiscriminate drug toxicities and poor patient compliance. Thus, innovative pharmaceutical solutions are needed to effectively deliver the cytotoxic drugs specifically to the tumor site while minimizing systemic exposure to frequent and high drug doses. Polymeric nanocarriers, particularly nanoparticles, have been extensively studied for improved oncological use. Such nanocarriers hold great potential in cancer treatment as they can be biocompatible, adapted to specific needs, tolerated and deliver high drug payloads while targeting tumors. Active targeting, as opposed to passive targeting, should add value to selective and site specific treatment. Active targeting of nanosized drug delivery systems is firmly rooted in the Magic Bullet Concept as was envisioned by Paul Ehrlich over 100 years ago. This targeting strategy is based on the molecular recognition of tumor biomarkers which are over-expressed on cancer cells, via specific vector molecules conjugated to the surface of the drug carrier. These vector molecules dictate the carrier's biodistribution and its biological affinity to the desired site of action. Many recent publications have shown encouraging results suggesting that targeting nanocarriers represent a highly-promising strategy for improved cancer treatment. This chapter will focus mainly on polymeric nanoparticles as the main drug carriers to be conjugated to various ligands able to deliver the drug to the specific desired pathological tissue.

摘要

癌症治疗通常需要频繁和高剂量的药物。然而,尽管癌症研究取得了重大进展,可用的强效药物种类繁多,但由于缺乏对病变细胞的药物选择性、药物的无差别毒性和患者的依从性差,治疗效果仍然受到阻碍,经常失败。因此,需要创新的药物制剂,以便将细胞毒性药物有效地专门递送到肿瘤部位,同时最大限度地减少频繁和高剂量药物的全身暴露。聚合物纳米载体,特别是纳米颗粒,已被广泛研究用于改善肿瘤学用途。这些纳米载体在癌症治疗中有很大的潜力,因为它们可以具有生物相容性,适应特定的需求,耐受并传递高药物载量,同时靶向肿瘤。与被动靶向相反,主动靶向应该为选择性和靶向治疗增加价值。纳米药物递送系统的主动靶向牢固地植根于 100 多年前 Paul Ehrlich 提出的“魔术子弹”概念。这种靶向策略基于对肿瘤标志物的分子识别,肿瘤标志物在癌细胞上过表达,通过与药物载体表面连接的特异性载体分子来实现。这些载体分子决定了载体的生物分布及其对所需作用部位的生物学亲和力。许多最近的出版物表明,靶向纳米载体代表了改善癌症治疗的一种极具前景的策略。本章将主要关注聚合物纳米颗粒作为主要的药物载体,与各种能够将药物递送到特定病理组织的配体结合。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验