to-BBB technologies BV, Niels Bohrweg 11, Leiden, Netherlands.
Curr Pharm Biotechnol. 2012 Sep;13(12):2328-39. doi: 10.2174/138920112803341815.
Drug delivery to the brain remains challenging due to the presence of the blood-brain barrier. In this review, 10 key development criteria are presented that are important for successful drug development to treat CNS diseases by targeted drug delivery systems. Although several routes of delivery are being investigated, such as intranasal delivery, direct injections into the brain or CSF, and transient opening of the blood-brain barrier, the focus of this review is on physiological strategies aiming to target endogenous transport mechanisms. Examples from literature, focusing on targeted drug delivery systems that are being commercially developed, will be discussed to illustrate the 10 key development criteria. The first four criteria apply to the targeting of the blood-brain barrier: (1) a proven inherently safe receptor biology, (2) a safe and human applicable ligand, (3) receptor specific binding, and (4) applicable for acute and chronic indications. Next to an efficient and safe targeting strategy, as captured in key criteria 1 to 4, a favorable pharmacokinetic profile is also important (key criterion 5). With regard to the drug carriers, two criteria are important: (6) no modification of active ingredient and (7) able to carry various classes of molecules. The final three criteria apply to the development of a drug from lab to clinic: (8) low costs and straightforward manufacturing, (9) activity in all animal models, and (10) strong intellectual property (IP) protection. Adhering to these 10 key development criteria will allow for a successful brain drug development.
由于血脑屏障的存在,药物向大脑的输送仍然具有挑战性。在这篇综述中,提出了 10 个关键的开发标准,这些标准对于通过靶向药物传递系统治疗中枢神经系统疾病的药物开发成功非常重要。尽管正在研究几种给药途径,如鼻腔给药、直接向脑或 CSF 注射以及血脑屏障的短暂开放,但本综述的重点是针对旨在靶向内源性转运机制的生理策略。将讨论文献中的示例,重点介绍正在商业化开发的靶向药物传递系统,以说明这 10 个关键开发标准。前四个标准适用于血脑屏障的靶向:(1)已证明具有固有安全性的受体生物学,(2)安全且适用于人类的配体,(3)受体特异性结合,以及(4)适用于急性和慢性适应症。除了高效和安全的靶向策略(关键标准 1 至 4)外,良好的药代动力学特征也很重要(关键标准 5)。就药物载体而言,有两个标准很重要:(6)不改变有效成分,以及(7)能够携带各种类别的分子。最后三个标准适用于从实验室到临床的药物开发:(8)低成本和简单的制造,(9)在所有动物模型中的活性,以及(10)强大的知识产权(IP)保护。遵守这 10 个关键开发标准将有助于成功开发脑部药物。