Quetiapine Nanoemulsion for Intranasal Drug Delivery: Evaluation of Brain-Targeting Efficiency
Abstract
To evaluate the possibility of improved drug delivery of quetiapine fumarate (QTP), a nanoemulsion system was developed for intranasal delivery. Effects of different HLBs of Emalex LWIS 10, PEG 400 and Transcutol P, as co-surfactants, were studied on isotropic region of pseudoternary-phase diagrams of nanoemulsion system composed of capmul MCM (CPM) as oil phase, Tween 80 as surfactant and water. Phase behaviour, globule size, transmission electron microscope (TEM) photographs and brain-targeting efficiency of quetiapine nanoemulsion were investigated. In vitro dissolution study of optimised nanoemulsion formulation, with mean diameter 144 ± 0.5 nm, showed more than twofold increase in drug release as compared with pure drug. According to results of in vivo tissue distribution study in Wistar rats, intranasal administration of QTP-loaded nanoemulsion had shorter T max compared with that of intravenous administration. Higher drug transport efficiency (DTE%) and direct nose-to-brain drug transport (DTP%) was achieved by nanoemulsion. The nanoemulsion system may be a promising strategy for brain-targeted delivery of QTP.
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Quetiapine is transported directly into the brain after nasal administration of quetiapine nanoemulsions.
“Brain distribution studies demonstrated that quetiapine is transported directly into the brain after the nasal administration of quetiapine NEs.”
From Nanoemulsions for “Nose-to-Brain” Drug Delivery (2019) · cites this paper as [70]
In male Wistar rats, nasal administration of quetiapine nanoemulsions containing Transcutol P and propylene glycol showed shorter Tmax and higher drug transport efficiency into the brain compared to intravenous administrations.
“In vivo studies carried out on male Wistar rats following the nasal administration of NEs containing Transcutol P and propylene glycol showed shorter Tmax compared with that of intravenous administrations, as well as higher drug transport efficiency into the brain.”
From Nanoemulsions for “Nose-to-Brain” Drug Delivery (2019) · cites this paper as [70]
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- Authors
- Boche, M., & Pokharkar, V.
- Affiliations
- Bharati Vidyapeeth (Deemed to be University) (IN)
- Corresponding author
- Pokharkar, Varsha
- ORCID
- Pokharkar, Varsha
- Venue
- AAPS PharmSciTech
- Published
- 2016-05-20
- Volume
- 18
- Issue
- 3
- Pages
- 686-696
- ISSN
- 1530-9932 (ISSN-L)
- OpenAlex
- W2405573244
- Cited by
- 109
- References
- 42
- Citations by year
- 2026: 7 · 2025: 6 · 2024: 23 · 2023: 14 · 2022: 14 · 2021: 11 · 2020: 9 · 2019: 14 · 2018: 8 · 2017: 3
- FWCI
- 4.75
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- AAPS PharmSciTech (publishedVersion)
- PubMed (publishedVersion)
- Funders
- All India Council for Technical Education
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advancements in Transdermal Drug Delivery
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Keywords
- quetiapine, nanoemulsions, intranasal drug delivery, brain drug delivery, nose-to-brain transport, pseudo-ternary phase diagram, cosurfactants, globule size, drug release, tissue distribution, antipsychotic drug delivery
- MeSH terms
- Quetiapine Fumarate, Administration, Intranasal, Animals, Brain, Chemistry, Pharmaceutical, Emulsions, Male, Particle Size, Polysorbates, Solubility, Surface-Active Agents, Tissue Distribution, Drug Delivery Systems, Rats, Wistar, Rats, Nanoparticles, Drug Liberation
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