Department of Chemistry, Purdue University, Multi-disciplinary Cancer Research Facility, 1203 W, State Street, West Lafayette, Indiana 47907, United States.
Boiler-Parseghian Center for Rare and Neglected Diseases, University of Notre Dame, Notre Dame, IN 46556, USA.
Sci Rep. 2017 Apr 28;7:46737. doi: 10.1038/srep46737.
Niemann-Pick Type C disease (NPC) is a rare metabolic disorder characterized by disruption of normal cholesterol trafficking within the cells of the body. There are no FDA approved treatments available for NPC patients. Recently, the cycloheptaglucoside 2-hydroxypropyl-β-cyclodextrin (HP-β-CD) has shown efficacy as a potential NPC therapeutic by extending lifetime in NPC mice, delaying neurodegeneration, and decreasing visceral and neurological cholesterol burden. Although promising, systemic HP-β-CD treatment is limited by a pharmacokinetic profile characterized by rapid loss through renal filtration. To address these shortcomings, we sought to design a family of HP-β-CD pro-drug delivery vehicles, known as polyrotaxanes (PR), capable of increasing the efficacy of a given injected dose by improving both pharmacokinetic profile and bioavailability of the HP-β-CD agent. PR can effectively diminish the cholesterol pool within the liver, spleen, and kidney at molar concentrations 10-to-100-fold lower than monomeric HP-β-CD. In addition to this proof-of-concept, use of PR scaffolds with differing physiochemical properties reveal structure-activity relationships in which PR characteristics, including hydrophobicity, threading efficiency and surface charge, were found to both decisively and subtly effect therapeutic efficacy. PR scaffolds exhibit absorption, pharmacokinetics, and biodistribution patterns that are significantly altered from monomeric HP-β-CD. In all, PR scaffolds hold great promise as potential treatments for visceral disease in NPC patients.
尼曼-匹克 C 型病(NPC)是一种罕见的代谢紊乱疾病,其特征是体内细胞中正常胆固醇转运受阻。目前尚无 FDA 批准的 NPC 治疗方法。最近,环己七葡糖苷 2-羟丙基-β-环糊精(HP-β-CD)已被证明是一种有希望的 NPC 治疗药物,可通过延长 NPC 小鼠的寿命、延缓神经退行性变以及降低内脏和神经胆固醇负荷来发挥作用。尽管前景广阔,但全身 HP-β-CD 治疗受到药代动力学特征的限制,其特点是通过肾脏过滤迅速丧失。为了解决这些缺点,我们试图设计一系列 HP-β-CD 前药输送载体,即聚轮烷(PR),通过改善 HP-β-CD 药物的药代动力学特征和生物利用度来提高给定注射剂量的疗效。PR 可以在摩尔浓度低 10-100 倍的情况下有效地减少肝脏、脾脏和肾脏中的胆固醇池。除了这一概念验证之外,使用具有不同物理化学性质的 PR 支架还揭示了结构-活性关系,其中 PR 的特性,包括疏水性、穿线效率和表面电荷,被发现对治疗效果具有决定性和微妙的影响。PR 支架表现出与单体 HP-β-CD 明显不同的吸收、药代动力学和生物分布模式。总之,PR 支架作为 NPC 患者内脏疾病潜在治疗方法具有很大的前景。