Evidence map›Paper›PMID 40421790›Full record

ReviewDrug development research2025

Functionalized Polydopamine Nanoparticles: A Promising Drug Delivery Platform for the Treatment of Tuberculosis.

Nnamdi Ikemefuna Okafor, Precious Nnaji, Ngozi Francisca Nnolum-Orji, Yahya E Choonara

Abstract readReview
In one paragraph

Review in Drug development research, 2025. 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
–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

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

4 authors.

Nnamdi Ikemefuna OkaforDepartment of Pharmacy and Pharmacology, School of Therapeutics Sciences, Faculty of Health Sciences, Wits Advanced Drug Delivery Platform (WADDP), University of the Witwatersrand, Johannesburg, South Africa.ORCID 0000-0003-3104-9977
Precious NnajiCentre of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom, South Africa.ORCID 0009-0009-9675-4483
Ngozi Francisca Nnolum-OrjiDepartment of Pharmacy and Pharmacology, School of Therapeutics Sciences, Faculty of Health Sciences, Wits Advanced Drug Delivery Platform (WADDP), University of the Witwatersrand, Johannesburg, South Africa.
Yahya E ChoonaraDepartment of Pharmacy and Pharmacology, School of Therapeutics Sciences, Faculty of Health Sciences, Wits Advanced Drug Delivery Platform (WADDP), University of the Witwatersrand, Johannesburg, South Africa.ORCID 0000-0002-3889-1529

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tuberculosis (TB) is considered a major infectious disease by the World Health Organization. The WHO estimates that there are 1.8 million TB deaths, and 10.4 million new cases of the disease reported yearly. While there are conventional therapies for TB, they have drawbacks such as a lengthy pill regimen, rigorous scheduling, and protracted treatment duration, which can result in strains of the disease that are multidrug-resistant (MDR) and extensively drug-resistant (XDR). Future TB control is at risk due to the emergence of MDR strains. This worry has made the hunt for a successful remedy necessary. One biomedical innovation has been the application of nanotechnology, which offers a fresh avenue of treating TB. Such nanotechnology approach includes Polydopamine (PDA) nanoparticles which have demonstrated the ability to reduce these difficulties. In recent times, PDA, which is an intriguing bioinspired polymer, has become a material of choice for designing drug delivery nano-systems. In fact, PDA nanoparticles show several intriguing characteristics, such as easy manufacturing approach, biocompatibility, the ability to scavenge free radicals, and photothermal and photoacoustic features. It is easily functionalized to promote blood circulation, cellular absorption, and drug release, among other functions. As a result, this review has examined the various PDA functionalization techniques aimed at overcoming MDR and enhancing TB treatment.

Indexed as

Antitubercular AgentsDrug Delivery SystemsIndolesNanoparticlesPolymersTuberculosisAnimalsHumansAntitubercular AgentsIndolespolydopaminePolymersdrug deliverydrug resistancefunctionalizationnanoparticlespolydopaminetuberculosis

Identifiers

PMID40421790
PMCPMC12108037

What OpenQuestion holds

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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.