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Ketal 连接的帕利哌酮前药的微晶用于长效抗精神病药物。

Microcrystals of Ketal-Linked Paliperidone Prodrugs for Long-Acting Antipsychotics.

机构信息

Key Laboratory of Functional Polymer Materials of Ministry of Education, State Key Laboratory of Medicinal Chemical Biology, Institute of Polymer Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China.

Translational Medicine Center, Key Laboratory of Molecular Target and Clinical Pharmacology, School of Pharmaceutical Sciences, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou 510260, China.

出版信息

Mol Pharm. 2022 Nov 7;19(11):3846-3857. doi: 10.1021/acs.molpharmaceut.2c00348. Epub 2022 Sep 1.

Abstract

Intramuscularly injectable long-acting prodrug-based microcrystals (MCs) are of particular interest for chronic disease management. Nevertheless, current prevalently used linkers degraded by enzymes have the potential drawback of substantial differences in enzyme levels between individuals. Here, we reported the synthesis of a stearyl-modified paliperidone prodrug (SKP) with an acid-sensitive ketal linker for developing long-acting MC antipsychotics. SKP-MCs of three different sizes were prepared and systematically examined. We found that paliperidone exposure in SKP-MC-treated rats was prolonged compared with that in rats treated with the commercial antipsychotic Invega Sustenna and that the drug release rate decreased with increasing MC size. In inflammation-inhibition-model rats, paliperidone release from the SKP-MCs was considerably decreased, indicating that the immune-mediated foreign-body response after intramuscular administration boosted paliperidone release. Our findings will provide valuable insights into in vivo drug release from prodrug-based MC formulations. The ketal-linked prodrug strategy might be a new solution for developing long-acting prodrug formulations of hydroxyl-group-bearing drugs.

摘要

肌内注射长效前药微晶体(MCs)特别适用于慢性疾病管理。然而,目前广泛使用的酶降解连接物存在个体间酶水平存在显著差异的潜在缺点。在这里,我们报道了一种具有酸敏感缩酮连接物的棕榈酰修饰帕利哌酮前药(SKP)的合成,用于开发长效 MC 抗精神病药。制备了三种不同粒径的 SKP-MC 并进行了系统研究。我们发现,与商业抗精神病药 Invega Sustenna 治疗的大鼠相比,SKP-MC 治疗的大鼠中帕利哌酮的暴露时间延长,并且随着 MC 粒径的增加,药物释放速率降低。在抑制炎症模型大鼠中,SKP-MC 中的帕利哌酮释放明显减少,表明肌肉内给药后的免疫介导的异物反应促进了帕利哌酮的释放。我们的研究结果将为基于前药的 MC 制剂的体内药物释放提供有价值的见解。缩酮连接的前药策略可能是开发含羟基药物长效前药制剂的新解决方案。

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