Evidence map›Paper›PMID 42286842›Full record

ArticleDrug delivery2026

Oral self-assembly nanoemulsion drives

Xinjing Shen, Jie Deng, Aijiao Jiang, Qianqi Cai, Deyong Tian, Linlin Zhao, Jing Ye, Lie Zhang, Yucheng Xiang, Quan Zhang

Abstract read
In one paragraph

Article in Drug delivery, 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

10 authors.

Xinjing ShenDepartment of Neurosurgery, The First Affiliated Hospital of Chengdu Medical College, Chengdu, China.
Jie DengKey Laboratory of Structure-Specific Small Molecule Drugs at Chengdu Medical College of Sichuan Province, School of Pharmacy, Chengdu Medical College, Chengdu, China.
Aijiao JiangKey Laboratory of Structure-Specific Small Molecule Drugs at Chengdu Medical College of Sichuan Province, School of Pharmacy, Chengdu Medical College, Chengdu, China.
Qianqi CaiKey Laboratory of Structure-Specific Small Molecule Drugs at Chengdu Medical College of Sichuan Province, School of Pharmacy, Chengdu Medical College, Chengdu, China.
Deyong TianKey Laboratory of Structure-Specific Small Molecule Drugs at Chengdu Medical College of Sichuan Province, School of Pharmacy, Chengdu Medical College, Chengdu, China.
Linlin ZhaoKey Laboratory of Structure-Specific Small Molecule Drugs at Chengdu Medical College of Sichuan Province, School of Pharmacy, Chengdu Medical College, Chengdu, China.
Jing YeKey Laboratory of Structure-Specific Small Molecule Drugs at Chengdu Medical College of Sichuan Province, School of Pharmacy, Chengdu Medical College, Chengdu, China.
Lie ZhangDepartment of Neurosurgery, The First Affiliated Hospital of Chengdu Medical College, Chengdu, China.
Yucheng XiangKey Laboratory of Structure-Specific Small Molecule Drugs at Chengdu Medical College of Sichuan Province, School of Pharmacy, Chengdu Medical College, Chengdu, China.
Quan ZhangDepartment of Neurosurgery, The First Affiliated Hospital of Chengdu Medical College, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatic fibrosis is a chronic liver disease that requires long-term treatment and is characterized by the excessive accumulation of extracellular matrix (ECM), which is produced primarily by activated hepatic stellate cells (aHSCs). Oral medication represents a non-invasive and crucial strategy for prolonged therapy. However, achieving targeted drug delivery to aHSCs through oral administration remains a significant challenge because of the susceptibility of nanoparticles to structural disruption during intestinal transit. To address this, an oral vitamin A (VA)-functionalized self-nanoemulsifying drug delivery system (termed VA-SNEDDS) was fabricated for the precise delivery of morin (MOR) to aHSCs for the treatment of liver fibrosis. After oral administration, the designed VA-SNEDDS successfully translocated across the intestinal epithelium while maintaining the structural integrity of the nanoemulsion, entered the systemic circulation

Indexed as

FlavonoidsHepatic Stellate CellsLiver CirrhosisNanoparticlesAdministration, OralAnimalsCarbon TetrachlorideDrug Delivery SystemsEmulsionsFlavonesLiverMaleRatsRats, Sprague-DawleyTransforming Growth Factor beta1Vitamin ACarbon TetrachlorideEmulsionsFlavonesFlavonoidsTransforming Growth Factor beta1Vitamin Ahepatic stellate cellliver fibrosisOral deliveryself-nanoemulsifying drug delivery systemVitamin A

Identifiers

PMID42286842
PMCPMC13267024

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.