Evidence map›Paper›PMID 40606616›Full record

ArticleFrontiers in pharmacology2025

Innovative pH-responsive alginate-coated rosuvastatin-loaded chitosan nanoparticles: a targeted approach to inhibiting HMGB1-activated RAGE/TLR4-NFκB signaling in colonic inflammation in rats.

Elsayed A Elmorsy, Sameh Saber, Zubida M Al-Majdoub, Rabab S Hamad, Mustafa Ahmed Abdel-Reheim, Asmaa Ramadan, Norah Suliman Alsoqih, Mariam S Alharbi, Hamad Alsaykhan, Alshaimaa A Farrag and 7 more

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
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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

17 authors.

Elsayed A ElmorsyDepartment of Pharmacology and Toxicology, College of Pharmacy, Qassim University, Buraidah, Saudi Arabia.
Sameh SaberDepartment of Pharmacology, Faculty of Pharmacy, Delta University for Science and Technology, Gamasa, Egypt.
Zubida M Al-MajdoubCentre for Applied Pharmacokinetic Research, University of Manchester, Manchester, United Kingdom.
Rabab S HamadBiological Sciences Department, College of Science, King Faisal University, Al Ahsa, Saudi Arabia.
Mustafa Ahmed Abdel-ReheimDepartment of Pharmacology, College of Pharmacy, Shaqra University, Shaqra, Saudi Arabia.
Asmaa RamadanDepartment of Biochemistry, Faculty of Pharmacy, Delta University for Science and Technology, Gamasa, Egypt.
Norah Suliman AlsoqihDepartment of Pediatrics, College of Medicine, Qassim University, Buraidah, Saudi Arabia.
Mariam S AlharbiDepartment of Medicine, College of Medicine, Qassim University, Buraidah, Saudi Arabia.
Hamad AlsaykhanDepartment of Anatomy and Histology, College of Medicine, Qassim University, Buraidah, Saudi Arabia.
Alshaimaa A FarragDepartment of Anatomy, College of Medicine, University of Bisha, Bisha, Saudi Arabia.
Hanan EissaDepartment of Pharmacology, College of Medicine, University of Bisha, Bisha, Saudi Arabia.
Rasha AbdelhadyPharmacology and Toxicology Department, Faculty of Pharmacy, Fayoum University, Fayoum, Egypt.
Abousree T EllethyDepartment of Basic Oral Sciences and Dental Education, Biochemistry Division, College of Dentistry, Qassim University, Buraidah, Saudi Arabia.
Mostafa M KhodeirDepartment of Pathology, College of Medicine, Qassim University, Buraidah, Saudi Arabia.
Hossam A ElsisiDepartment of Pharmacology and Toxicology, College of Pharmacy, Qassim University, Buraidah, Saudi Arabia.
Syed Suhail AhmedDepartment of Microbiology and Immunology, College of Medicine, Qassim University, Buraidah, Saudi Arabia.
Ahmed Y KiraDepartment of Pharmaceutics, Faculty of Pharmacy, Delta University for Science and Technology, Gamasa, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study developed and optimized an innovative oral pH-dependent drug delivery system utilizing rosuvastatin-loaded chitosan nanoparticles (RSV-CSNPs) coated with sodium alginate (ALG). The goal was to protect RSV-CSNPs from degradation in the acidic gastric environment and facilitate targeted sustained release in the colon to address inflammatory bowel disease. Nanoparticles were initially prepared by ionic gelation. A subsequent ALG coating process was optimized using a 2

Indexed as

colonic delivery system/colitisDSS/Sprague-Dawley rat colitis modelHMGB1-RAGE/TLR4-NFκBinflammationrosuvastatin/pH-responsive nanoparticlessodium alginate/chitosan nanoparticles

Identifiers

PMID40606616
PMCPMC12213710

What Socratic 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 Socratic graph.