2022
DOI: 10.1016/j.ijpharm.2022.122142
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Mucoadhesive nanoemulsion enhances brain bioavailability of luteolin after intranasal administration and induces apoptosis to SH-SY5Y neuroblastoma cells

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Cited by 18 publications
(13 citation statements)
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“…Diedrich et al designed a chitosan-coated nanoemulsion loaded with Lu for potential brain-targeted delivery after intranasal administration. 90 The resulting NECh-LUT notably increased nasal mucosa permeability by nearly 6-fold, extended the half-life of Lu by about 10-fold, and enhanced the distribution of Lu in brain tissue by 4.4-fold. Remarkably, NECh-LUT effectively inhibited the growth of human neuroblastoma cell SH-SY5Y, highlighting its potential therapeutic value.…”
Section: Nanoemulsionsmentioning
confidence: 96%
See 1 more Smart Citation
“…Diedrich et al designed a chitosan-coated nanoemulsion loaded with Lu for potential brain-targeted delivery after intranasal administration. 90 The resulting NECh-LUT notably increased nasal mucosa permeability by nearly 6-fold, extended the half-life of Lu by about 10-fold, and enhanced the distribution of Lu in brain tissue by 4.4-fold. Remarkably, NECh-LUT effectively inhibited the growth of human neuroblastoma cell SH-SY5Y, highlighting its potential therapeutic value.…”
Section: Nanoemulsionsmentioning
confidence: 96%
“…Furthermore, intranasal drug delivery formulations, including chitosomes, nanoemulsions, and bilosomes, have been developed to facilitate brain-targeted drug delivery of Lu. 90,106,109 This approach increases bioavailability by facilitating the transport of drugs through the blood-brain barrier, offering an effective, non-invasive, and safe method of drug administration. This review also introduces the advancements and applications of Lu-loaded nano-scale drug delivery systems in the treatment of various diseases, as illustrated in Fig.…”
Section: Conclusion and Future Perspectivesmentioning
confidence: 99%
“…Therefore, the preparation of a mucoadhesive nasal preparation easily achieves this step. For example, rotigotine, asenapine maleate, luteolin, and teriflunomid are drugs that were formulated as intranasal mucoadhesive systems in a nanoemulsions form. The aim of all those preparations was to increase their retention time on the nasal mucosa, therefore increasing their brain availability.…”
Section: Strategies For Enhanced Brain Targetingmentioning
confidence: 99%
“…This provides a greater surface area for drug crossing through the membrane and into the brain [ 45 , 46 , 47 , 48 ]. For this reason, numerous chitosan-based nasal formulations have been proposed as drug delivery systems to the CNS, including chitosan-dopamine and chitosan-tyrosine conjugates for PD [ 49 ], chitosan hydrogels for drug delivery in AD [ 50 ], chitosan-poloxamer gel for anti-epileptic drug (AED) delivery [ 51 ], chitosan nanoemulsions for glioblastoma multiforme (GBM) therapies [ 52 ], and chitosan-poloxamer nanoemulsions for the treatment of cerebral ischemia [ 53 ]. While NPs can be synthesised from chitosan, it is commonly used as a surface coating to enhance mucoadhesion and particle transport across the nasal mucosa and into the brain.…”
Section: Nanotechnology For Bbb Crossingmentioning
confidence: 99%