Kollath Vinayaraj Ozhukil, Pulakazhi Venu Vivek Krishna, Saifeddine Mahmoud, Mihara Koichiro, Hirota Simon A, Hollenberg Morley D, Karan Kunal
Department of Chemical and Petroleum Engineering, University of Calgary Calgary AB Canada
Department of Physiology & Pharmacology, Inflammation Research Network-Snyder Institute for Chronic Disease, University of Calgary Cumming School of Medicine Calgary AB Canada
Nanoscale Adv. 2024 Nov 18;7(3):830-839. doi: 10.1039/d4na00481g. eCollection 2025 Jan 28.
Biocompatible polymeric nanoparticles (NPs) as carriers for therapeutic agents with multifunctional activities have received unprecedented attention for a variety of bio-pharmaceutical applications. We describe the synthesis, the fluorescence properties, the bio-compatible nature and the alpha-1 adrenergic receptor bio-activity of engineered quantum dot-like polynorepinephrine (PNE) NPs. The spherical PNE NPs, which are internalized in smooth muscle cells a receptor-selective mechanism, activate alpha-1-adrenoceptors in intact mouse aorta and aorta-derived cultured smooth muscle cells, leading to the activation of calcium signaling/contraction and stimulation of mitogen-activated protein kinase (MAPK), thereby displaying receptor-triggering biological activity, possibly acting both extracellularly and intracellularly. Our data indicate that NPs generated by the polymerization of pharmacologically active compounds like norepinephrine can retain receptor-selective biological activity coupled to inherent fluorescence.
具有多功能活性的生物相容性聚合物纳米颗粒(NPs)作为治疗剂的载体,在各种生物制药应用中受到了前所未有的关注。我们描述了工程化的量子点样聚去甲肾上腺素(PNE)纳米颗粒的合成、荧光特性、生物相容性以及α-1肾上腺素能受体生物活性。球形的PNE纳米颗粒通过受体选择性机制内化于平滑肌细胞中,在完整的小鼠主动脉和主动脉来源的培养平滑肌细胞中激活α-1肾上腺素能受体,导致钙信号/收缩的激活和丝裂原活化蛋白激酶(MAPK)的刺激,从而显示出受体触发的生物活性,可能在细胞外和细胞内都发挥作用。我们的数据表明,由去甲肾上腺素等药理活性化合物聚合产生的纳米颗粒可以保留与固有荧光相关的受体选择性生物活性。