Kibler Elina, Lavrinenko Anastasia, Kolesnik Ilya, Stankevich Ksenia, Bolbasov Evgeny, Kudryavtseva Valeriya, Leonov Andrey, Schepetkin Igor, Khlebnikov Andrei, Quinn Mark T, Tverdokhlebov Sergei
National Research Tomsk Polytechnic University, Tomsk 634050, Russia.
Department of Microbiology and Immunology, Montana State University, Bozeman, MT 59717, USA.
Eur Polym J. 2020 Mar 15;127. doi: 10.1016/j.eurpolymj.2020.109598. Epub 2020 Mar 4.
Mitogen-activated protein kinases (MAPKs), including c-Jun N-terminal kinase (JNK), play important role in the regulation of pro-inflammatory cytokine secretion and signaling cascades. Therefore, JNKs are key targets for the treatment of cytokine/JNK-driven diseases. Herein, we developed electrospray poly(lactic-co-glycolic acid) (PLGA) microparticles doped with novel JNK inhibitor 11-indeno[1,2-]quinoxalin-11-one oxime (IQ-1). Optimized electrospray parameters allowed us to produce IQ-1-doped microparticles with round shape, smooth and non-porous surface, and mean diameter of 0.9-1.3 μm. We have shown that IQ-1 was well integrated into the polymer matrix and had a prolonged release in two steps via non-Fickian release. The fabricated particles doped with IQ-1 exhibited anti-inflammatory effects, as indicated by inhibited neutrophil activation and cytokine secretion by human monocytic MonoMac-6 cells. Overall, our study demonstrates that PLGA microparticles doped with a novel JNK inhibitor (IQ-1) could be a promising delivery system for treatment of JNK-mediated diseases.
丝裂原活化蛋白激酶(MAPK),包括c-Jun氨基末端激酶(JNK),在促炎细胞因子分泌和信号级联反应的调节中起重要作用。因此,JNK是治疗细胞因子/JNK驱动疾病的关键靶点。在此,我们开发了掺杂新型JNK抑制剂11-茚并[1,2-]喹喔啉-11-酮肟(IQ-1)的电喷雾聚乳酸-乙醇酸共聚物(PLGA)微粒。优化的电喷雾参数使我们能够制备出形状为圆形、表面光滑且无孔、平均直径为0.9-1.3μm的掺杂IQ-1的微粒。我们已经表明,IQ-1很好地整合到聚合物基质中,并通过非菲克释放分两步进行延长释放。掺杂IQ-1的制成颗粒表现出抗炎作用,这通过抑制人单核细胞MonoMac-6细胞的中性粒细胞活化和细胞因子分泌得以体现。总体而言,我们的研究表明,掺杂新型JNK抑制剂(IQ-1)的PLGA微粒可能是治疗JNK介导疾病的一种有前景的递送系统。