In mice, intranasal VIP carried by nanoparticles raised the brain AUC of intact VIP by 3.5 to 4.7 fold versus VIP solution.
In plain wordsIn mice, VIP carried by nanoparticles reached the brain at 3.5 to 4.7 times the level of plain VIP solution.
- Outcome
- IncreaseBrain AUC of intact 125I-VIP with PEG-PLA nanoparticles
- Study
mousen: not reported in source
Intranasal dosing in mice- Comparator
- VIP solution
- Outcome group
- Pharmacokinetics · Pharmacology
- Studied dose
- Dose not stated · intranasalAs given in this study (mouse).
Measurements
- Brain AUC fold increase
- 3.5 to 4.7 fold
- nanoparticles versus solution
Source sentences
The area under the concentration-time curve of intact 125I-vasoactive intestinal peptide in brain of mice following the intranasal administration of 125I-vasoactive intestinal peptide carried by nanoparticles and wheat germ agglutinin-conjugated ones was significantly enlarged by 3.5 approximately 4.7 folds
2 context sentences(design, population, supporting numbers)
compared with that after intranasal application of 125I-vasoactive intestinal peptide solution.
In the present study, vasoactive intestinal peptide, a neuroprotective peptide, was efficiently incorporated into the poly (ethylene glycol)-poly (lactic acid) nanoparticles modified with wheat germ agglutinin and the biodistribution, brain uptake and neuroprotective effect of the formulation were assessed.