Investigation of astaxanthin-loaded hollow gold nanoparticles in mitigating the EAE mice model of multiple sclerosis

AIMS: Multiple sclerosis (MS) is a progressive neurological autoimmune disorder that affects the central nervous system. Current therapies lack the disease-modifying potential and precision. Astaxanthin is a naturally derived marine compound with potent biological properties and has been reported to mitigate the effects of multiple sclerosis. Herein, we aimed to develop astaxanthin-loaded gold nanoparticles to enhance precision in delivery to the brain by the efficient carrier properties of the gold nanoparticles. METHODS: In this study, we employed an experimental autoimmune encephalomyelitis (EAE) mouse model of multiple sclerosis and treated for 3 weeks with free astaxanthin (6 mg/kg) and astaxanthin-loaded hollow gold nanoparticles (0.6 mg/kg), a 10-fold lower dose of the drug. The outcomes were evaluated by biochemical, pathological, histological, and hematological parameters. RESULTS: Our findings indicate that astaxanthin-loaded gold nanoparticles significantly improved the disease outcomes. Our findings suggest that astaxanthin-loaded hollow gold nanoparticles improved oxidative-stress indicators and motor deficits and imparted significant cellular protection in the disease condition. CONCLUSION: Overall, this study highlights the potential of astaxanthin-loaded hollow gold nanoparticles to improve neurological outcomes in the EAE mice model.

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Publication Details

Journal
Therapeutic Delivery
Published
2026-11-09
DOI
https://doi.org/10.1080/20415990.2026.2755238
Primary Topic
Multiple Sclerosis Research Studies
Type
article
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article

Investigation of astaxanthin-loaded hollow gold nanoparticles in mitigating the EAE mice model of multiple sclerosis

Shyum Naqvi, Saba Naqvi, Aishwarya Mhatre
Therapeutic Delivery
Multiple Sclerosis Research Studies
article

Investigation of astaxanthin-loaded hollow gold nanoparticles in mitigating the EAE mice model of multiple sclerosis

Shyum Naqvi, Saba Naqvi, Aishwarya Mhatre
article en

Abstract

AIMS: Multiple sclerosis (MS) is a progressive neurological autoimmune disorder that affects the central nervous system. Current therapies lack the disease-modifying potential and precision. Astaxanthin is a naturally derived marine compound with potent biological properties and has been reported to mitigate the effects of multiple sclerosis. Herein, we aimed to develop astaxanthin-loaded gold nanoparticles to enhance precision in delivery to the brain by the efficient carrier properties of the gold nanoparticles. METHODS: In this study, we employed an experimental autoimmune encephalomyelitis (EAE) mouse model of multiple sclerosis and treated for 3 weeks with free astaxanthin (6 mg/kg) and astaxanthin-loaded hollow gold nanoparticles (0.6 mg/kg), a 10-fold lower dose of the drug. The outcomes were evaluated by biochemical, pathological, histological, and hematological parameters. RESULTS: Our findings indicate that astaxanthin-loaded gold nanoparticles significantly improved the disease outcomes. Our findings suggest that astaxanthin-loaded hollow gold nanoparticles improved oxidative-stress indicators and motor deficits and imparted significant cellular protection in the disease condition. CONCLUSION: Overall, this study highlights the potential of astaxanthin-loaded hollow gold nanoparticles to improve neurological outcomes in the EAE mice model.

Therapeutic Delivery
National Institute of Pharmaceutical Education and Research (IN), National Institute of Pharmaceutical Education and Research (IN), National Institute of Pharmaceutical Education and Research (IN), National Institute of Pharmaceutical Education and Research (IN), National Institute of Pharmaceutical Education and Research (IN), National Institute of Pharmaceutical Education and Research (IN)
Multiple Sclerosis Research Studies
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Investigation of astaxanthin-loaded hollow gold nanoparticles in mitigating the EAE mice model of multiple sclerosis — Shyum Naqvi, Saba Naqvi, et al. · Therapeutic Delivery (2026) | TGRS Research Map | TGRS