A cascade targeting strategy for brain neuroglial cells employing nanoparticles modified with angiopep-2 peptide and EGFP-EGF1 protein

• Published in: Biomaterials Vol. 32; no. 33; pp. 8669 - 8675
• Main Authors: Huile, Gao, Shuaiqi, Pan, Zhi, Yang, Shijie, Cao, Chen, Chen, Xinguo, Jiang, Shun, Shen, Zhiqing, Pang, Yu, Hu
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Ltd 01.11.2011
• Subjects: Advanced Basic Science; adverse effects; Angiopep-2; Animals; Blood-brain barrier; brain; Brain - cytology; Brain neuroglial cells; Cascade targeting strategy; Dentistry; drugs; EGFP-EGF1; fluorescence in situ hybridization; Green Fluorescent Proteins - chemistry; image analysis; In Situ Hybridization, Fluorescence; in vitro studies; Male; Microscopy, Electron, Transmission; Nanoparticles; Neuroglia - cytology; Peptides - chemistry; Rats; Rats, Sprague-Dawley; therapeutics; transmission electron microscopy; utilities; Nanoparticles; Angiopep-2; EGFP-EGF1; Brain neuroglial cells; Cascade targeting strategy
• ISSN: 0142-9612; 1878-5905; 1878-5905
• DOI: 10.1016/j.biomaterials.2011.07.069

Targeted drug delivery to selected brain cell types is a crucial step in enhancing therapeutic effects while limiting side effects in non-target cells. Here we report on the development and evaluation of a new cascade targeting delivery system that employs PEG-PCL nanoparticles modified with both an angiopep-2 peptide and a EGFP-EGF1 protein for precise targeting of brain neuroglial cells. Angiopep-2 penetrates the blood–brain barrier and EGFP-EGF1 binds neuroglial cells, providing the system with two stages of targeting. In vitro studies demonstrated that both bEnd.3 cells and neuroglial cells had a higher uptake of angiopep-2 and EGFP-EGF1 conjugated nanoparticles (AENP) as compared to unmodified nanoparticles. Ex vivo imaging showed that AENP had higher accumulation in the brain over unmodified nanoparticles and EGFP-EGF1 modified nanoparticles. Fluorescent in situ hybridization of brain slides demonstrated that AENP co-localized with neuroglial cells. Transmission electron microscopy further showed that AENP could target and enter neuroglial cells. This newly developed cascade targeting delivery system that precisely targets neuroglial cells has great potential in the diagnosis and treatment of neuroglial related diseases. Replacing EGFP-EGF1 and angiopep-2 with other ligands may extend the utility of the system to diagnose and treat organ diseases beyond brain