摘要
当今,药物的传递通过静脉注射纳米药物载体—高分子药物聚合物、脂质体和微胶粒,在技术上是可行的。这些传递系统主要用于肿瘤治疗,和通过众所周知的EPR效应来被动的积累其在肿瘤中的浓度。靶向纳米载体,其额外地包含了细胞表面上受体的配体表达,也被广泛的研究,但是这种产品还没有上市销售,只有少数应用于临床试验中。聚合纳米粒子能够向中枢神经系统传递药物在1995年首次被发现。大量的论述用聚合纳米粒子能够穿过血脑屏障的大脑靶向药物递质的文献已经被发表了,主要是脑肿瘤的治疗。但是目前,这些纳米粒子的转化潜能似乎超过了靶向脂质体,靶向脂质体是一种基于成熟技术的平台。这种药物传递系统在被发现后很快就被应用于临床试验,然而在配方、特性和具有大脑靶向的聚合纳米粒子的生产方面的挑战可能成为阻碍其发展的因素。一个关键的问题是他几乎不可能定义体内实际作用的聚合物,尤其是在脑内,这是一个常规的要求;也许这就是为什么这项研究没有进展。最先进的治疗脑肿瘤的纳米粒子在这里将与已发表的中枢神经系统以外的肿瘤的临床试验研究相关的数据进行比较,值得强调的是,这些知识空白依旧使得这些传递系统处于不利地位。目前,出现了治疗脑部肿瘤的新方法,例如脂质纳米粒子或者避免使用聚合物的单克隆抗体药物复合物的使用。聚合纳米粒子在临床试验审批的成功或失败将一定程度的影响这个领域。目前,它们得到批准的可能性似乎非常低。
关键词: 血脑屏障,载体,中枢神经系统,药物传递,胶质瘤,脂质体,纳米粒子,靶向,肿瘤
Current Medicinal Chemistry
Title:Challenges in the Design of Clinically Useful Brain-targeted Drug Nanocarriers
Volume: 21 Issue: 37
Author(s): L. Costantino, D. Boraschi and M. Eaton
Affiliation:
关键词: 血脑屏障,载体,中枢神经系统,药物传递,胶质瘤,脂质体,纳米粒子,靶向,肿瘤
摘要: Nowadays, the delivery of drugs by means of intravenously administered nanosized drug carriers - polymerdrug conjugates, liposomes and micelles, is technically possible. These delivery systems are mainly designed for tumour therapy, and accumulate passively into tumours by means of the well known EPR effect. Targeted nanocarriers, that additionally contain ligands for receptors expressed on cell surfaces, are also widely studied but products of this kind are not marketed, and only a few are in clinical trial. Polymeric nanoparticles (Np) able to deliver drugs to the CNS were pioneered in 1995; a number of papers have been published dealing with brain-targeted drug delivery using polymeric Np able to cross the BBB, mainly for the treatment of brain tumours. At present, however, the translation potential of these Np seems to have been exceeded by targeted liposomes, a platform based on a proven technology. This drug delivery system entered clinical trials soon after its discovery, while the challenges in formulation, characterization and manufacturing of brain-targeted polymeric Np and the cost/benefit ratio could be the factors that have prevented their development. A key issue is that it is virtually impossible to define the in vivo fate of polymers, especially in the brain, which is a regulatory requirement; perhaps this is why no progress has been made. The most advanced Np for brain tumours treatment will be compared here with the published data available for those in clinical trial for tumours outside the CNS, to highlight the knowledge gaps that still penalise these delivery systems. At present, new approaches for brain tumours are emerging, such as lipid Np or the use of monoclonal antibody (mAb)-drug conjugates, which avoid polymers. The success or failure in the approval of the polymeric Np currently in clinical trials will certainly affect the field. At present, the chances of their approval appear to be very low.
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Cite this article as:
Costantino L., Boraschi D. and Eaton M., Challenges in the Design of Clinically Useful Brain-targeted Drug Nanocarriers, Current Medicinal Chemistry 2014; 21 (37) . https://dx.doi.org/10.2174/0929867321666140716101921
DOI https://dx.doi.org/10.2174/0929867321666140716101921 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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