The blood-brain barrier (BBB) is a semipermeable barrier that protects the brain
from potential pathogens. Despite its protective nature, BBB prevents the passage
of any medication into the brain, except for those with a low molecular weight
(below 500 Da) and lipophilic compounds. In this research, we developed
PEGylated curcumin loaded mesoporous silica nanoparticles (P/CRM@MSNs)
that were fabricated to target the brain by either bypassing or crossing the BBB
intranasally (in) and intravenously (iv), respectively. Various techniques were
employed to characterize the P/CRM@MSNs. In vivo experiments demonstrated
that intranasal administration of P/CRM@MSNs improved cellular uptake and
reduced clearance from brain tissues, showing a three-fold increase compared to
intravenous administration at one-hour post-injection. Pharmacokinetic analysis
revealed a higher AUC_(0-1h) value (324 ± 75 ng. h/ml; P ˂ 0.05) following
intranasal administration than intravenous administration (195 ± 55 ng. h/ml).
Intranasal administration of P/CRM@MSNs significantly reduced drug clearance
from the brain (0.2 ± 0.05 ml/h) compared to intravenous administration (0.4 ±
0.06 ml/h). These findings suggest that P/CRM@MSNs could be a promising
nanocarrier system for treating brain disorders.
Keywords: Curcumin, Mesoporous silica nanoparticles, Blood-brain barrier,
Intranasal, Intravenous
