Expert opinion on drug delivery · 2025
Lipid carrier-based intranasal delivery of calcium channel blockers for Alzheimer's disease.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Jog Sunil, Dighe Sayali, Nathani Khushali, Waghmare Akanksha, Mangrulkar Shubhada V, Sawarkar Sujata P, Omri Abdelwahab
Аннотация
BACKGROUND: Felodipine (FLD) is an L-type calcium channel blocker with pronounced neuroprotection against Alzheimer's disease (AD). Unfortunately, the efficacy of FLD has been impeded by limited solubility, poor bioavailability, and sub-optimal accumulation. Thus, the current study unfolds the potential of nanostructured lipid carriers based on in-situ gel of FLD (FLD-NLCs gel) to ameliorate dementia.
METHODS: The FLD-contained NLCs were prepared using the microemulsion-sonication method and further integrated into thermosensitive gel comprised poloxamer 407 and HPMC K4M. The formulation was evaluated by ex-vivo permeation study, cell culture studies, and in-vivo efficacy study. The toxicity of formulation was assessed by HET-CAM assay, and nasal cilitoxicity study.
RESULTS: The optimized FLD-NLCs had nanoscaled dimension, spherical shape, and augmented %EE (~96%). The FLD-NLCs gel displayed biphasic release, with ~1.3-fold higher permeation as relative to free FLD. The HET-CAM assay and cell culture study revealed compatible nature of formulation. The in-vivo biochemical, neurotransmitter, and inflammatory marker determination revealed neuroprotective and restorative potential of the FLD-NLCs gel.
CONCLUSIONS: The repurposing tactic of FLD presents a viable concept to combat AD. Also, the NLC-based temperature responsive intranasal gel exemplifies a practical approach to augment the efficacy of FLD.
METHODS: The FLD-contained NLCs were prepared using the microemulsion-sonication method and further integrated into thermosensitive gel comprised poloxamer 407 and HPMC K4M. The formulation was evaluated by ex-vivo permeation study, cell culture studies, and in-vivo efficacy study. The toxicity of formulation was assessed by HET-CAM assay, and nasal cilitoxicity study.
RESULTS: The optimized FLD-NLCs had nanoscaled dimension, spherical shape, and augmented %EE (~96%). The FLD-NLCs gel displayed biphasic release, with ~1.3-fold higher permeation as relative to free FLD. The HET-CAM assay and cell culture study revealed compatible nature of formulation. The in-vivo biochemical, neurotransmitter, and inflammatory marker determination revealed neuroprotective and restorative potential of the FLD-NLCs gel.
CONCLUSIONS: The repurposing tactic of FLD presents a viable concept to combat AD. Also, the NLC-based temperature responsive intranasal gel exemplifies a practical approach to augment the efficacy of FLD.