Evidence map›Paper›PMID 37017879›Full record

ArticleDrug delivery and translational research2023

Response surface optimization of a cardioprotective compound through pharmacosomal drug delivery system: in vivo bioavailability and cardioprotective activity potential.

Marwa H S Dawoud, Mai A Zaafan, Sarah S Saleh, Islam M Mannaa, Nabila M Sweed

Open access · hybridAbstract read
In one paragraph

Article in Drug delivery and translational research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Chemical profiling ofFrontiers in veterinary science · 2026
    Article
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  7. 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

5 authors at 1 institution in 1 country.

Marwa H S DawoudDepartment of Pharmaceutics, Faculty of Pharmacy, October University for Modern Sciences and Arts, 6th of October City, Egypt. mdawoud@msa.edu.eg.ORCID 0000-0001-8281-4144
Mai A ZaafanDepartment of Pharmacology and Toxicology, Faculty of Pharmacy, October University for Modern Sciences and Arts, 6th of October City, Egypt.
Sarah S SalehDepartment of Analytical Chemistry, Faculty of Pharmacy, October University for Modern Sciences and Arts, 6th of October City, Egypt.
Islam M MannaaDepartment of Pharmaceutics, Faculty of Pharmacy, October University for Modern Sciences and Arts, 6th of October City, Egypt.
Nabila M SweedDepartment of Pharmaceutics, Faculty of Pharmacy, October University for Modern Sciences and Arts, 6th of October City, Egypt.
October University of Modern Sciences and Arts · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vanillic acid (VA) is a phenolic compound with potential antioxidant activity, which improves ischemia-induced myocardial degeneration, by reducing oxidative stress; however, it suffers poor bioavailability owing to its poor solubility. VA-loaded pharmacosomes were optimized using a central composite design, where the effect of phosphatidylcholine:VA molar ratio and the precursor concentration were studied. An optimized formulation (O

Indexed as

Drug Delivery SystemsNanoparticlesAdministration, OralAnimalsAntioxidantsBiological AvailabilityDrug CarriersDrug LiberationParticle SizeRatsSolubilityAntioxidantsDrug CarriersBioavailabilityCardioprotective activityCentral composite designOptimizationRelease rateVanillic acid

Identifiers

PMID37017879
PMCPMC10382421
OpenAlexW4362601848

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.