Evidence map›Paper›PMID 41888392›Full record

ArticleBioresources and bioprocessing2026

Development and evaluation of Sargassum polysaccharides-algal oil nanoemulsion for intranasal treatment of allergic rhinitis.

Shi-Yu Hung, Hsiang-Wen Chan, Hao-Hsiang Ku, Chung-Hsiung Huang

Abstract read
In one paragraph

Article in Bioresources and bioprocessing, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Shi-Yu HungDepartment of Food Science, National Taiwan Ocean University, Keelung, 202301, Taiwan.
Hsiang-Wen ChanDepartment of Food Science, National Taiwan Ocean University, Keelung, 202301, Taiwan.
Hao-Hsiang KuInstitute of Food Safety and Risk Management, National Taiwan Ocean University, Keelung, 20224, Taiwan. kuhh@mail.ntou.edu.tw.
Chung-Hsiung HuangDepartment of Food Science, National Taiwan Ocean University, Keelung, 202301, Taiwan. huangch@mail.ntou.edu.tw.ORCID http://orcid.org/0000-0002-2295-6412

Funding

National Science and Technology Council NSTC 113-2320-B019-004-MY3
6 · The paper itself

Abstract

Allergic rhinitis (AR) is a prevalent inflammatory disorder of the upper respiratory tract, affecting 20-40% of the global population and severely impairing quality of life. Given the limitations and adverse effects associated with conventional pharmacotherapy, naturally derived bioactives with low toxicity are gaining prominence as alternative interventions. In this study, we developed a bioresource-based nanoemulsion (NE) by integrating Sargassum polysaccharides (SP) into algal oil (AO) to enhance intranasal delivery and therapeutic efficacy against AR. Structural analysis confirmed that SP comprised sulfated polysaccharides enriched in fucose, glucose, and galactose. The optimized SP-AO NE, formulated with Tween 80 and prepared via ultrasonic emulsification, exhibited uniform spherical droplets (53.4 ± 1.8 nm), a low polydispersity index (0.3 ± 0.1), and a negative zeta potential (- 29.1 ± 2.8 mV), indicating high colloidal stability and effective oxidative protection of AO during refrigerated storage. In an ovalbumin-induced AR mouse model, intranasal administration of SP-AO NE significantly alleviated nasal rubbing, epithelial hypertrophy, goblet cell hyperplasia, mast cell infiltration, and pulmonary inflammation. Intranasal SP-AO NE treatment decreased IgE levels in serum, nasal lavage, and bronchoalveolar lavage fluids, while enhancing mucosal IgA. In addition, SP-AO NE downregulated IL-4 and TNF-α expression and upregulated TGF-β1, demonstrating a robust immunomodulatory effect. Overall, this work presents a stable, biocompatible, and functional NE that improves intranasal delivery of algal bioactives, offering a promising natural therapeutic strategy for the management of AR.

Indexed as

Algal oilAllergic rhinitisIntranasal deliveryNanoemulsionSargassum polysaccharides

Identifiers

PMID41888392
PMCPMC13022132

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.