journal article·2024-08-14Open access

Unilateral Administration of Surface-Modified G1 and G4 PAMAM Dendrimers in Healthy Mice to Assess Dendrimer Migration in the Brain

Bhairavi Srinageshwar, Cassandra Thompson, Paulina Otero, Darren T. Story, Anna E. Wedster, Bethany MacDonald, Nikolas Munro, Sindhuja Koneru, Riley Crandall, Douglas Swanson, Ajit Sharma, Gary L. Dunbar, Julien Rossignol

ACS Applied Materials & Interfaces· Volume 16· Issue 32

Abstract

High Resolution Image Download MS PowerPoint Slide Polyamidoamine (PAMAM) dendrimers are nanoparticles that have a wide scope in the field of biomedicine. Previous evidence shows that the generation 4 (G4) dendrimers with a 100% amine surface (G4-NH 2 ) are highly toxic to cells in vitro and in vivo due to their positively charged amine groups. To reduce the toxicity, we modified the surface of the dendrimers to have more neutral functional groups, with 10% of the surface covered with −NH 2 and 90% of the surface covered with hydroxyl groups (−OH; G4–90/10). Our previous in vitro data show that these modified dendrimers are taken up by cells, neurons, and different types of stem cells in vitro and neurons and glial cells in vivo . The toxicity assay shows that these modified dendrimers are less toxic compared with G4-NH2 dendrimers. Moreover, prolonged dendrimer exposure (G1–90/10 and G4–90/10), up to 3 weeks following unilateral intrastriatal injections into the striatum of mice, showed that dendrimers have the tendency to migrate within the brain via corpus callosum at different rates depending on their size. We also found that there is a difference in migration between the G1 and G4 dendrimers based on their size differences. The G4 dendrimers migrate in the anterior and posterior directions as well as more laterally from the site of injection in the striatum compared to the G1 dendrimers. Moreover, the G4 dendrimers have unique projections from the site of injection to the cortical areas.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Neurogenesis and neuroplasticity mechanisms · RNA Interference and Gene Delivery · Supramolecular Self-Assembly in Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

College of Medicine, Central Michigan University, Mount Pleasant, Michigan 48859, United States

Program of Neuroscience, Central Michigan University, Mount Pleasant, Michigan 48859, United States

Field Neurosciences Institute Laboratory for Restorative Neurology, Central Michigan University, Mount Pleasant, Michigan 48859, United States

Department of Psychology, Central Michigan University, Mount Pleasant, Michigan 48859, United States

Department of Psychology, Saginaw Valley State University, University Center, Michigan 48710, United States

Department of Chemistry and Biochemistry, Central Michigan University, Mount Pleasant, Michigan 48859, United States

Funding

National Institute of Neurological Disorders and Stroke · American Heart Association · Field Neurosciences Institute · Central Michigan University

References (12)

Show source-provided references
1. 10.3390/pharmaceutics1004026910.3390/pharmaceutics10040269 ↗
2. 10.3390/ijms22211165410.3390/ijms222111654 ↗
3. 10.1021/acsomega.0c0159210.1021/acsomega.0c01592 ↗
4. 10.1021/acs.molpharmaceut.3c0088010.1021/acs.molpharmaceut.3c00880 ↗
5. 10.3389/fnins.2023.112746010.3389/fnins.2023.1127460 ↗
6. 10.3390/ijms1803062810.3390/ijms18030628 ↗
7. 10.1021/acschemneuro.9b0034710.1021/acschemneuro.9b00347 ↗
8. 10.3390/pharmaceutics1207061910.3390/pharmaceutics12070619 ↗
9. 10.3389/fnana.2014.0000910.3389/fnana.2014.00009 ↗
10. 10.1038/s41467-018-07318-310.1038/s41467-018-07318-3 ↗
11. 10.1371/journal.pbio.300123310.1371/journal.pbio.3001233 ↗
12. 10.3389/fnmol.2023.117219710.3389/fnmol.2023.1172197 ↗