Claßen Rebecca, Pouokam Ervice, Wickleder Matthias, Diener Martin, Mattern Annabelle
Institute for Veterinary Physiology and Biochemistry, Justus Liebig University Giessen, Frankfurter Strasse 100, 35392 Giessen, Germany.
Institute of Inorganic Chemistry, University of Cologne, Greinstrasse 6, 50939 Cologne, Germany.
R Soc Open Sci. 2022 Oct 5;9(10):220244. doi: 10.1098/rsos.220244. eCollection 2022 Oct.
Gold nanoparticles have a high potential to be a treatment of diseases by their specific drug delivery properties and multivalent receptor stimulation. For the present project, spherical gold nanoparticles were synthesized and functionalized with the muscarinic receptor antagonist atropine (Au-MUDA-AT NPs). The diameter of the gold core could precisely be controlled by using different synthetic methods and reducing agents resulting in functionalized gold nanoparticles with diameters ranging from 8 to 16 nm. The ability to interact with intestinal muscarinic receptors is size-dependent. When using intestinal chloride secretion induced by the stable acetylcholine derivative, carbachol, as read-out, the strongest inhibition, i.e. the most efficient blockade of muscarinic receptors, was observed with 13 nm sized Au-MUDA-AT NPs. Functional experiments indicate that Au-MUDA-AT NPs with a diameter of 14 nm are able to pass the intestinal mucosa in a time-dependent manner after administration to the intestinal lumen. For example, luminally administered Au-MUDA-AT NPs inhibited contractions of the small intestinal longitudinal muscle layer induced by electrical stimulation of myenteric neurons. A similar inhibition of basolateral epithelial receptors was observed after luminal administration of Au-MUDA-AT NPs when using carbachol-induced chloride secretion across the intestinal epithelium as a test system. Thus, Au-MUDA-AT NPs might be a therapeutic tool for the modulation of intestinal secretion and motility after oral application in the future.
金纳米颗粒因其特定的药物递送特性和多价受体刺激作用,在疾病治疗方面具有很高的潜力。对于本项目,合成了球形金纳米颗粒并用毒蕈碱受体拮抗剂阿托品进行功能化修饰(Au-MUDA-AT NPs)。通过使用不同的合成方法和还原剂,可以精确控制金核的直径,从而得到直径范围为8至16纳米的功能化金纳米颗粒。与肠道毒蕈碱受体相互作用的能力取决于颗粒大小。当使用稳定的乙酰胆碱衍生物卡巴胆碱诱导的肠道氯化物分泌作为检测指标时,观察到13纳米大小的Au-MUDA-AT NPs具有最强的抑制作用,即对毒蕈碱受体的阻断最为有效。功能实验表明,直径为14纳米的Au-MUDA-AT NPs在给予肠腔后能够以时间依赖的方式穿过肠黏膜。例如,经肠腔给予的Au-MUDA-AT NPs抑制了由肠肌间神经元电刺激诱导的小肠纵肌层收缩。当使用卡巴胆碱诱导的氯化物跨肠上皮分泌作为测试系统时,经肠腔给予Au-MUDA-AT NPs后,对基底外侧上皮受体也观察到了类似的抑制作用。因此,Au-MUDA-AT NPs未来可能成为口服后调节肠道分泌和运动的治疗工具。