Nanoparticle transport across in vitro olfactory cell monolayers
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, validační studie
PubMed
26721725
DOI
10.1016/j.ijpharm.2015.12.046
PII: S0378-5173(15)30444-0
Knihovny.cz E-zdroje
- Klíčová slova
- CPP, Lipid nanoparticles, NLC, Nanoparticles, Nose-to-brain delivery, Olfactory mucosa,
- MeSH
- aplikace intranazální MeSH
- biologický transport MeSH
- chitosan chemie MeSH
- čichová sliznice cytologie metabolismus MeSH
- farmaceutická chemie metody MeSH
- hematoencefalická bariéra metabolismus MeSH
- kopolymer kyseliny glykolové a mléčné MeSH
- krysa rodu Rattus MeSH
- kyselina mléčná chemie MeSH
- kyselina polyglykolová chemie MeSH
- lékové transportní systémy * MeSH
- lipidy chemie MeSH
- mozek metabolismus MeSH
- nanočástice * MeSH
- nosní sliznice metabolismus MeSH
- penetrační peptidy chemie MeSH
- polymery chemie MeSH
- potkani Wistar MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- validační studie MeSH
- Názvy látek
- chitosan MeSH
- kopolymer kyseliny glykolové a mléčné MeSH
- kyselina mléčná MeSH
- kyselina polyglykolová MeSH
- lipidy MeSH
- penetrační peptidy MeSH
- polymery MeSH
Drug access to the CNS is hindered by the presence of the blood-brain barrier (BBB), and the intranasal route has risen as a non-invasive route to transport drugs directly from nose-to-brain avoiding the BBB. In addition, nanoparticles (NPs) have been described as efficient shuttles for direct nose-to-brain delivery of drugs. Nevertheless, there are few studies describing NP nose-to-brain transport. Thus, the aim of this work was (i) to develop, characterize and validate in vitro olfactory cell monolayers and (ii) to study the transport of polymeric- and lipid-based NPs across these monolayers in order to estimate NP access into the brain using cell penetrating peptide (CPPs) moieties: Tat and Penetratin (Pen). All tested poly(d,l-lactide-co-glycolide) (PLGA) and nanostructured lipid carrier (NLC) formulations were stable in transport buffer and biocompatible with the olfactory mucosa cells. Nevertheless, 0.7% of PLGA NPs was able to cross the olfactory cell monolayers, whereas 8% and 22% of NLC and chitosan-coated NLC (CS-NLC) were transported across them, respectively. Moreover, the incorporation of CPPs to NLC surface significantly increased their transport, reaching 46% of transported NPs. We conclude that CPP-CS-NLC represent a promising brain shuttle via nose-to-brain for drug delivery.
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