Veronesi Michael C, Graner Brian D, Cheng Shih-Hsun, Zamora Marta, Zarrinmayeh Hamideh, Chen Chin-Tu, Das Sudip K, Vannier Michael W
The Department of Radiology and Imaging Sciences, School of Medicine, Indiana University Indianapolis, Indianapolis, IN 46202, USA.
The Department of Radiology, University of Chicago, Chicago, IL 60637, USA.
Pharmaceutics. 2021 Mar 15;13(3):391. doi: 10.3390/pharmaceutics13030391.
The fate of intranasal aerosolized radiolabeled polymeric micellar nanoparticles (LPNPs) was tracked with positron emission tomography/computer tomography (PET/CT) imaging in a rat model to measure nose-to-brain delivery. A quantitative temporal and spatial testing protocol for new radio-nanotheranostic agents was sought in vivo. LPNPs labeled with a zirconium 89 (Zr) PET tracer were administered via intranasal or intravenous delivery, followed by serial PET/CT imaging. After 2 h of continuous imaging, the animals were sacrificed, and the brain substructures (olfactory bulb, forebrain, and brainstem) were isolated. The activity in each brain region was measured for comparison with the corresponding PET/CT region of interest via activity measurements. Serial imaging of the LPNPs (100 nm PLA-PEG-DSPE+Zr) delivered intranasally via nasal tubing demonstrated increased activity in the brain after 1 and 2 h following intranasal drug delivery (INDD) compared to intravenous administration, which correlated with ex vivo gamma counting and autoradiography. Although assessment of delivery from nose to brain is a promising approach, the technology has several limitations that require further development. An experimental protocol for aerosolized intranasal delivery is presented herein, which may provide a platform for better targeting the olfactory epithelium.
在大鼠模型中,通过正电子发射断层扫描/计算机断层扫描(PET/CT)成像追踪鼻内雾化放射性标记的聚合物胶束纳米颗粒(LPNPs)的命运,以测量鼻到脑的递送。在体内寻找一种针对新型放射性纳米诊疗剂的定量时空测试方案。用锆89(Zr)PET示踪剂标记的LPNPs通过鼻内或静脉内给药,随后进行系列PET/CT成像。连续成像2小时后,处死动物,分离脑亚结构(嗅球、前脑和脑干)。通过活性测量来测量每个脑区的活性,以便与相应的PET/CT感兴趣区域进行比较。通过鼻管鼻内递送LPNPs(100nm PLA-PEG-DSPE+Zr)的系列成像显示,与静脉内给药相比,鼻内给药(INDD)后1小时和2小时脑内活性增加,这与离体γ计数和放射自显影相关。尽管评估从鼻到脑的递送是一种有前景的方法,但该技术有几个局限性,需要进一步发展。本文介绍了一种雾化鼻内递送的实验方案,该方案可能为更好地靶向嗅上皮提供一个平台。