Evidence map›Paper›PMID 34420176›Full record

ArticleInflammopharmacology2021

Evaluating the mucoprotective effects of glycyrrhizic acid-loaded polymeric nanoparticles in a murine model of 5-fluorouracil-induced intestinal mucositis via suppression of inflammatory mediators and oxidative stress.

Mahira Zeeshan, Ayesha Atiq, Qurat Ul Ain, Jawad Ali, Salman Khan, Hussain Ali

Abstract read
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In one paragraph

Article in Inflammopharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.5field-weighted citation impact, top 6% of its field
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

12 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Application of nanoparticles in antibody drug delivery.Frontiers in bioengineering and biotechnology · 2026
    Review
  3. ModifiedWorld journal of gastroenterology · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Article
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  10. Recent Advances inMetabolites · 2022
    Review
  11. Article
  12. Review
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

6 authors at 1 institution in 1 country.

Mahira ZeeshanDepartment of Pharmacy, Quaid-I-Azam University, Islamabad, 45320, Pakistan.
Ayesha AtiqDepartment of Pharmacy, Quaid-I-Azam University, Islamabad, 45320, Pakistan.
Qurat Ul AinDepartment of Pharmacy, Quaid-I-Azam University, Islamabad, 45320, Pakistan.
Jawad AliDepartment of Pharmacy, Quaid-I-Azam University, Islamabad, 45320, Pakistan.
Salman KhanDepartment of Pharmacy, Quaid-I-Azam University, Islamabad, 45320, Pakistan.
Hussain AliDepartment of Pharmacy, Quaid-I-Azam University, Islamabad, 45320, Pakistan. h.ali@qau.edu.pk.ORCID http://orcid.org/0000-0001-5422-5916
Quaid-i-Azam University · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectives5-Fluorouracil (5-FU), a chemotherapeutic drug, has severe deteriorating effects on the intestine, leading to mucositis. Glycyrrhizic acid is a compound derived from a common herbal plant Glycyrrhiza glabra, with mucoprotective, antioxidant and anti-inflammatory actions, however, associated with poor pharmacokinetics. Owing to the remarkable therapeutic action of glycyrrhizic acid-loaded polymeric nanocarriers in inflammatory bowel disease, we explored their activity against 5-FU-induced intestinal mucositis in mice. Polymeric nanocarriers have proven to be efficient drug delivery vehicles for the long-term treatment of inflammatory diseases, but have not yet been explored for 5-FU-induced mucositis. Therefore, this study aimed to produce glycyrrhizic acid-loaded polylactic-co-glycolic acid (GA-PLGA) nanoparticles to evaluate their protective and therapeutic effects in a 5-FU-induced mucositis model.

methodsGA-PLGA nanoparticles were prepared using a modified double emulsion method, physicochemically characterized, and tested for in vitro drug release. Thereafter, mucositis was induced by 5-FU (50 mg/kg; IP) administration to the mice for the first 3 days (day 0, 1, 2), and mice were treated orally with GA-PLGA nanoparticles for 7 days (day 0-6).

resultsGA-PLGA nanoparticles significantly reduced mucositis severity measured by body weight, diarrhea score, distress, and anorexia. Further, 5-FU induced intestinal histopathological damage, altered villi-crypt length, reduced goblet cell count, elevated pro-inflammatory mediators, and suppressed antioxidant enzymes, all of which were reversed by GA-PLGA nanoparticles.

conclusionMorphological, behavioral, histological, and biochemical results suggested that GA-PLGA nanoparticles were efficient, biocompatible, targeted, and sustained release drug delivery nano-vehicle for enhanced mucoprotective, anti-inflammatory, and antioxidant effects in 5-FU-induced intestinal mucositis.

Indexed as

NanoparticlesAnimalsAnti-Inflammatory AgentsAntimetabolites, AntineoplasticAntioxidantsDrug CarriersFluorouracilGlycyrrhizic AcidInflammation MediatorsIntestinal MucosaMiceMice, Inbred BALB CMucositisOxidative StressPolylactic Acid-Polyglycolic Acid CopolymerAnti-Inflammatory AgentsAntimetabolites, AntineoplasticAntioxidantsDrug CarriersFluorouracilGlycyrrhizic AcidInflammation MediatorsPolylactic Acid-Polyglycolic Acid Copolymer5-FluorouracilGlycyrrhizic acidIntestinal mucositisOral drug deliveryOxidative stressPolymeric nanoparticles

Identifiers

PMID34420176
OpenAlexW3196257083

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Registered trials

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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.