Evidence map›Paper›PMID 41199000›Full record

ArticleDrug delivery and translational research2026

Design and preparation of novel domperidone loaded polymeric blend electrospun nanofibers for improved oral pharmacodynamic activity.

Kamal Shatla, Eman Sweed, Suleiman Eltokhy, Adel Abdel-Rahman, Abdel Hamid Ismail, Nour Abd El-Sattar, El-Refaie Kenawy, Yusuf Haggag

Abstract read
In one paragraph

Article in Drug delivery and translational research, 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
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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

8 authors.

Kamal ShatlaDepartment of Organic Chemistry, Faculty of Science, Menoufia University, Menoufia, Egypt.
Eman SweedDepartment of Clinical Pharmacology, Faculty of Medicine, Menoufia University, Menoufia, Egypt.
Suleiman EltokhyDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Tanta University, Tanta, 3111, Egypt.
Adel Abdel-RahmanDepartment of Organic Chemistry, Faculty of Science, Menoufia University, Menoufia, Egypt.
Abdel Hamid IsmailDepartment of Organic Chemistry, Faculty of Science, Menoufia University, Menoufia, Egypt.
Nour Abd El-SattarBasic Medical Sciences Department, Faculty of Dentistry, Alryada University for Science & Technology, Sadat City, Egypt.
El-Refaie KenawyDepartment of Chemistry, Polymer Research Group, Faculty of Science, Tanta University, Tanta, Egypt.
Yusuf HaggagDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Tanta University, Tanta, 3111, Egypt. youssif.hagag@pharm.tanta.edu.eg.ORCID 0000-0002-6203-1713

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Domperidone (DOM) is a BCS class II drug which widely used as an oral medication for the control of nausea and vomiting. It showed a very low and variable bioavailability related to its very poor solubility and pre-systemic metabolism. Polymeric nanofibers (PNFs) exhibit unique properties that make them a favorable choice for drug delivery applications. The study aimed to develop an optimum fast-dissolving oral polymeric electrospun nanofiber of DOM using Eudragit L100/Polyvinyl alcohol (EL-100/PVA) polymer blend. The fabrication process was optimized through a set of formulation parameters (composition of the polymer blend, polymer blend concentration, and electrospinning voltage). The DOM-loaded EL-100/PVA NFs were characterized for surface shape, nanosize, % drug loading, DOM in vitro release, drug/polymer interaction, and in vivo prokinetic study. The optimization process showed defect-free DOM-loaded NFs with very low nano diameter, high DOM loading, and superior in vitro dissolution of DOM at intestinal pH (about 90% of the drug released within 5 min). The drug/polymer interaction study demonstrated the conversion of DOM into an amorphous form, which facilitated its dissolution. No physicochemical interaction between DOM and the polymer blend was observed. In vivo prokinetic study signified the orally enhanced prokinetic activity of DOM-loaded NF relative to pure DOM and commercial DOM product. The DOM-loaded EL-100/PVA NFs exhibited a better effect on the gastrointestinal reactivity relative to free DOM and commercial DOM product. The superior in vitro dissolution and in vivo prokinetic activity proved the promising potential of polymeric NFs to improve the oral delivery of DOM. The optimized DOM-loaded EL-100/PVA NFs may allow for dose reduction and low cardiovascular risk compared to conventional DOM tablets.

Indexed as

DomperidoneNanofibersAdministration, OralAnimalsDrug CarriersDrug LiberationMalePolymersPolymethacrylic AcidsPolyvinyl AlcoholRatsSolubilityDomperidoneDrug CarriersPolymersPolymethacrylic AcidsPolyvinyl AlcoholDomperidoneNanofibersOptimizationPolymer blendProkinetic activity

Identifiers

PMID41199000
PMCPMC13183739

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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.