Evidence map›Paper›PMID 42357535›Full record

ArticleMolecules (Basel, Switzerland)2026

In Vitro Evaluation of Novel Nano-Sized Colloidal Assemblies Incorporating Hydrophobic Tobramycin Ion Pairs: Enhanced Cellular Uptake with Preserved Antimicrobial Activity Toward Oral Drug Delivery.

Khaled Husam Khaled, Ahmad Saleh Malkawi, Azhar Saleh Malkawi, Razan Haddad, Nasr Alrabadi, Rana Abu-Dahab, Amal Ghaleb Al-Bakri, Airemwen Collins Ovenseri

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Khaled Husam KhaledFaculty of Pharmacy, Cyprus International University, Nicosia 99258, Cyprus.ORCID 0009-0003-5729-3094
Ahmad Saleh MalkawiDepartment of Pharmaceutical Sciences, Faculty of Pharmacy, Jadara University, Irbid 21110, Jordan.ORCID 0009-0008-3997-2874
Azhar Saleh MalkawiDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid 22110, Jordan.
Razan HaddadDepartment of Pharmaceutical Sciences, Faculty of Pharmacy, Jadara University, Irbid 21110, Jordan.ORCID 0000-0001-5437-6394
Nasr AlrabadiDepartment of Pharmacology, Faculty of Medicine, Jordan University of Science and Technology, Irbid 22110, Jordan.ORCID 0000-0002-5541-8362
Rana Abu-DahabDepartment of Biopharmacy and Clinical Pharmacy, The University of Jordan, Amman 11942, Jordan.ORCID 0000-0003-0857-7616
Amal Ghaleb Al-BakriDepartment of Pharmaceutics and Pharmaceutical Technology, School of Pharmacy, The University of Jordan, Amman 11942, Jordan.ORCID 0000-0002-6299-5301
Airemwen Collins OvenseriFaculty of Pharmacy, Cyprus International University, Nicosia 99258, Cyprus.ORCID 0000-0001-8450-0667

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tobramycin is a highly hydrophilic aminoglycoside antibiotic with limited cellular permeability and negligible oral bioavailability, necessitating parenteral administration. This study aimed to develop drug delivery systems based on nano-sized colloidal assemblies (NCAs) incorporating tobramycin ion pairs to enhance its lipophilicity, potential for transition to the oral route, and antimicrobial activities. Tobramycin was ionically paired with oleic acid, lauric acid, and fluorescein and formulated into NCA preconcentrates (F1-F5) using combinations of Tween 80, DMSO, and propylene glycol. The resulting formulations formed stable nanodroplets upon dilution (9.50-16.30 nm) with narrow size distributions (polydispersity index; PDI < 0.3) and moderate negative zeta potentials (-4.99 to -11.13 mV). In vitro release studies indicated sustained drug release for ion-paired systems compared to the rapid release of free tobramycin. Cytotoxicity evaluation in Caco-2 cells demonstrated high biocompatibility at 1:10,000 and 2:10,000 dilutions, while concentration-dependent toxicity at higher doses suggested enhanced intracellular delivery. Cellular uptake studies revealed significantly higher tobramycin internalization (

Indexed as

Anti-Bacterial AgentsAnti-Infective AgentsDrug Delivery SystemsNanoparticlesTobramycinAdministration, OralCaco-2 CellsColloidsDrug LiberationHumansHydrophobic and Hydrophilic InteractionsMicrobial Sensitivity TestsAnti-Bacterial AgentsAnti-Infective AgentsColloidsTobramycinantimicrobial activitiescellular uptakedrug deliverynanocarriersnanoemulsionstobramycin

Identifiers

PMID42357535
PMCPMC13305547

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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.