Frontiers in aging neuroscience · 2026
Solid lipid nanoparticles as carriers for Ulva rigida peptide extract with demonstrated anti-β-amyloid and antioxidant properties.
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.
Tavares Tânia G, Carvalho Iva, Ramalho Maria João, Andrade Stéphanie, Pereira Maria Carmo, Loureiro Joana A
Аннотация
INTRODUCTION: Alzheimer's disease (AD) remains one of the greatest challenges in neurodegenerative research, largely due to the toxic aggregation of the β-amyloid (Aβ) peptide and the difficulty of delivering therapeutic compounds across the blood-brain barrier (BBB).
METHODS: This work explored Ulva rigida (U. rigida), a green macroalga rich in bioactive peptides, as a natural source of anti-amyloidogenic and antioxidant agents.
RESULTS: First, the peptides extraction process was optimized by design of experiments (DoE). Peptides extracted and hydrolyzed under optimized conditions showed antioxidant capacity (2.51 ± 0.18 μmolTrolox equivalent/ mghydrolyzed protein), and the fraction of peptides with a molecular weight lower than 3 kDa was able to reduce the aggregation of Aβ 1-42 peptide in vitro by around 60%. To overcome the issue of limited bioavailability, we encapsulated these peptides in solid lipid nanoparticles (SLNs). The developed nanoformulation displayed a size of 158 ± 14 nm, narrow polydispersity, and near-neutral zeta potential (-4.7 ± 0.6 mV), with an encapsulation efficiency (EE) of 54.1 ± 0.1% and suitable stability under simulated gastrointestinal and storage conditions.
DISCUSSION: By combining biological activity with a delivery platform, this study highlights the potential of Ulva rigida as a source of bioactive peptides with the potential to delay the progression of AD.
METHODS: This work explored Ulva rigida (U. rigida), a green macroalga rich in bioactive peptides, as a natural source of anti-amyloidogenic and antioxidant agents.
RESULTS: First, the peptides extraction process was optimized by design of experiments (DoE). Peptides extracted and hydrolyzed under optimized conditions showed antioxidant capacity (2.51 ± 0.18 μmolTrolox equivalent/ mghydrolyzed protein), and the fraction of peptides with a molecular weight lower than 3 kDa was able to reduce the aggregation of Aβ 1-42 peptide in vitro by around 60%. To overcome the issue of limited bioavailability, we encapsulated these peptides in solid lipid nanoparticles (SLNs). The developed nanoformulation displayed a size of 158 ± 14 nm, narrow polydispersity, and near-neutral zeta potential (-4.7 ± 0.6 mV), with an encapsulation efficiency (EE) of 54.1 ± 0.1% and suitable stability under simulated gastrointestinal and storage conditions.
DISCUSSION: By combining biological activity with a delivery platform, this study highlights the potential of Ulva rigida as a source of bioactive peptides with the potential to delay the progression of AD.