TY - JOUR
T1 - Surface-Modified G4 PAMAM Dendrimers Cross the Blood-Brain Barrier following Multiple Tail-Vein Injections in C57BL/6J Mice
AU - Srinageshwar, Bhairavi
AU - Dils, Anthony
AU - Sturgis, John
AU - Wedster, Anna
AU - Kathirvelu, Balachandar
AU - Baiyasi, Stephanie
AU - Swanson, Douglas
AU - Sharma, Ajit
AU - Dunbar, Gary L.
AU - Rossignol, Julien
N1 - Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/9/18
Y1 - 2019/9/18
N2 - Intracranial injections are currently used to deliver drugs into the brain, as most drugs cannot cross the blood-brain barrier (BBB) following systemic injections. Moreover, multiple dosing is difficult with invasive techniques. Therefore, viable systemic techniques are necessary to facilitate treatment paradigms that require multiple dosing of therapeutics across the BBB. In this study, we show that mixed-surface fourth-generation poly(amidoamine) (PAMAM) dendrimers containing predominantly biocompatible hydroxyl groups and a few amine groups are taken up by cultured primary cortical neurons derived from mouse embryo. We also show that these dendrimers cross the BBB following their administration to healthy mice in multiple doses via tail-vein injections and are taken up by neurons and the glial cells as evidenced by appropriate staining methods. Besides the brain, the dendrimers were found mostly in the kidneys compared to other peripheral organs, such as liver, lungs, and spleen, implying that they may be readily excreted, thereby preventing potential toxic accumulation in the body. Our findings provide a proof-of-concept that appropriate surface modifications of dendrimers provide safe, biocompatible nanomaterial with the potential to deliver therapeutic cargo across the BBB into the brain via multiple tail-vein injections.
AB - Intracranial injections are currently used to deliver drugs into the brain, as most drugs cannot cross the blood-brain barrier (BBB) following systemic injections. Moreover, multiple dosing is difficult with invasive techniques. Therefore, viable systemic techniques are necessary to facilitate treatment paradigms that require multiple dosing of therapeutics across the BBB. In this study, we show that mixed-surface fourth-generation poly(amidoamine) (PAMAM) dendrimers containing predominantly biocompatible hydroxyl groups and a few amine groups are taken up by cultured primary cortical neurons derived from mouse embryo. We also show that these dendrimers cross the BBB following their administration to healthy mice in multiple doses via tail-vein injections and are taken up by neurons and the glial cells as evidenced by appropriate staining methods. Besides the brain, the dendrimers were found mostly in the kidneys compared to other peripheral organs, such as liver, lungs, and spleen, implying that they may be readily excreted, thereby preventing potential toxic accumulation in the body. Our findings provide a proof-of-concept that appropriate surface modifications of dendrimers provide safe, biocompatible nanomaterial with the potential to deliver therapeutic cargo across the BBB into the brain via multiple tail-vein injections.
KW - PAMAM dendrimer
KW - blood-brain barrier
KW - dendrimer surface
KW - multiple injections
KW - systemic injections
KW - tail-vein injections
UR - http://www.scopus.com/inward/record.url?scp=85071949104&partnerID=8YFLogxK
U2 - 10.1021/acschemneuro.9b00347
DO - 10.1021/acschemneuro.9b00347
M3 - Article
C2 - 31390175
AN - SCOPUS:85071949104
SN - 1948-7193
VL - 10
SP - 4145
EP - 4150
JO - ACS Chemical Neuroscience
JF - ACS Chemical Neuroscience
IS - 9
ER -