Evidence map›Paper›PMID 40562287›Full record

ArticleInternational journal of pharmaceutics2025

Immunostimulatory Pickering emulsion for oral vaccine delivery.

Jin Xie, Xiaodi Li, Grahmm A Funk, Su Jeong Song, Udita Shah, Connor S Ahlquist, Hyunjoon Kim

Abstract read
In one paragraph

Article in International journal of pharmaceutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

7 authors.

Jin XieDepartment of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS 66047, USA.
Xiaodi LiDepartment of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS 66047, USA.
Grahmm A FunkDepartment of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS 66047, USA.
Su Jeong SongDepartment of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS 66047, USA.
Udita ShahDepartment of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS 66047, USA.
Connor S AhlquistDepartment of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS 66047, USA; Bioengineering Program, University of Kansas, Lawrence, KS 66047, USA.
Hyunjoon KimDepartment of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS 66047, USA; Bioengineering Program, University of Kansas, Lawrence, KS 66047, USA. Electronic address: kimx@ku.edu.

Funding

Synthetic Chemical Biology CoreP20GM113117 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI OROZCO, ROBIN C. · 2016 to 2025
$23.9M
NIGMS NIH HHS P20 GM113117
6 · The paper itself

Abstract

To overcome gastric acid degradation and ensure robust immune activation, a novel Pickering emulsion stabilized by poly(lactic-co-glycolic acid) (PLGA) nanoparticles was developed for the co-delivery of vaccine antigens and adjuvants via the oral route. Pickering emulsions, stabilized by solid particles, can enhance stability and protect antigens from gastric degradation. We encapsulated a TLR7/8 agonist R848 in PLGA nanoparticles and fabricated Pickering emulsions (R848-PLGA-NP@PE) to boost immune activation, and further prepared model antigen Ovalbumin (OVA) loaded Pickering emulsion formulation (R848-PLGA-NP@PE-OVA) to induce antigen-specific immune responses. R848-PLGA-NPs can improve vaccine efficacy by serving both as a stabilizer and an adjuvant, activating antigen-presenting cells (APCs). R848-PLGA-NP@PE-OVA exhibited a uniform particle size (245 nm), stable zeta potential (-40 mV), and high antigen encapsulation efficiency (>80 %), that were tested in Simulated Intestinal Fluid (SIF) and Simulated Gastric Fluid (SGF). R848-PLGA-NP@PE exhibited enhanced uptake by and activation of dendritic cells compared to control groups. In vivo, R848-PLGA-NP@PE significantly improved CD4 + T cell, CD8 + T cell, and NK cell activation. Notably, granzyme B expression in NK cells reached 2.1 times the level of the PBS group and 1.45 times that of the Free OVA + R848 group. The OVA-specific IgG level in the R848-PLGA-NP@PE-OVA group was approximately 3.9 times that of the PBS group and 2.5 times that of the free R848 + OVA group. Fecal OVA-specific IgA levels were significantly higher than control group. The combined data suggests that Pickering emulsions fabricated with PLGA-NPs are versatile oral vaccine delivery platforms to induce cellular and humoral immune responses.

Indexed as

Adjuvants, ImmunologicAdjuvants, VaccineImidazolesNanoparticlesOvalbuminVaccinesAdministration, OralAnimalsAntigensDendritic CellsEmulsionsFemaleImmunoglobulin GMiceMice, Inbred BALB CMice, Inbred C57BLAdjuvants, ImmunologicAdjuvants, VaccineAntigensEmulsionsImidazolesImmunoglobulin GOvalbuminPolylactic Acid-Polyglycolic Acid CopolymerresiquimodToll-Like Receptor 7Toll-Like Receptor 8VaccinesNanoparticleOral vaccinePickering Emulsion

Identifiers

PMID40562287
PMCPMC12646106

What OpenQuestion holds

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Read underepoch 390

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 OpenQuestion graph.