Evidence mapPaperPMID 42198217Full record

ReviewPharmaceutics2026

Astaxanthin Delivery Across Administration Routes: Recent Advances to Improve Stability and Bioavailability.

Laetitia Novelli, Marco Cespi, Diego Romano Perinelli, Giulia Bonacucina

Abstract readReview
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Laetitia NovelliChemistry Interdisciplinary Project (ChIP), School of Pharmacy, University of Camerino, via Madonna delle Carceri, 62032 Camerino, Italy.ORCID 0009-0005-0208-6535
Marco CespiChemistry Interdisciplinary Project (ChIP), School of Pharmacy, University of Camerino, via Madonna delle Carceri, 62032 Camerino, Italy.ORCID 0000-0001-6916-7915
Diego Romano PerinelliChemistry Interdisciplinary Project (ChIP), School of Pharmacy, University of Camerino, via Madonna delle Carceri, 62032 Camerino, Italy.ORCID 0000-0002-7686-4150
Giulia BonacucinaChemistry Interdisciplinary Project (ChIP), School of Pharmacy, University of Camerino, via Madonna delle Carceri, 62032 Camerino, Italy.ORCID 0000-0002-8528-4166

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Astaxanthin (ASX) is a xanthophyll carotenoid widely studied for its beneficial properties in humans, mainly related to its local or systemic antioxidant, cytoprotective and immunomodulatory effects. Particularly, ASX can donate electrons to neutralize reactive oxygen species (ROS), thereby mitigating oxidative stress, a key factor in the onset of several chronic and degenerative diseases. Thanks to these valuable properties, ASX has attracted considerable interest in the pharmaceutical, nutraceutical and cosmetic sectors. Despite its promising biological potential, the application of ASX is limited by several physicochemical factors. It is a highly lipophilic molecule, unstable when exposed to light, heat and oxygen, which leads to rapid degradation, and is characterized by low bioavailability. To overcome these limitations, various formulation strategies have been developed, particularly encapsulation-based approaches aimed at improving stability, solubility and therapeutic applications. This review provides an overview of the conventional and innovative dosage forms of ASX developed to enhance bioavailability and preserve the chemical and biological properties of this powerful antioxidant, by focusing on the different administration routes. Special attention is given to the advantages and limitations of the different formulation strategies and their implications for human health according to the different administration routes. Although oral administration remains the most explored route, further studies are needed to develop formulations suitable for alternative routes of administration.

Indexed as

anti-agingchemical instabilitycosmeticsencapsulationnatural antioxidantsnutraceuticalsoralparenteralroutes of administrationtopical

Identifiers

PMID42198217
PMCPMC13210799

What Socratic holds

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Registered trials

None linked

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 Socratic graph.