Evidence map›Paper›PMID 40652023›Full record

ArticleDrug delivery and translational research2026

Microneedle patch-based transnasal delivery of naloxone.

Akeemat Tijani, Carmine Schiavone, Prashant Dogra, Ashana Puri

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
–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.

Akeemat TijaniDepartment of Pharmaceutical Sciences, Bill Gatton College of Pharmacy, East Tennessee State University, Johnson City, TN, 37614, USA.
Carmine SchiavoneDepartment of Chemical, Materials and Industrial Production Engineering, University of Naples Federico II, 80125, Naples, Italy.
Prashant DograMathematics in Medicine Program, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Ashana PuriDepartment of Pharmaceutical Sciences, Bill Gatton College of Pharmacy, East Tennessee State University, Johnson City, TN, 37614, USA. puria1@etsu.edu.ORCID http://orcid.org/0000-0002-6685-5808

Funding

Artificial intelligence-integrated mechanistic modeling for rational design of nanoparticles to improve organ targeting and safetyR01EB035545 · NIBIB · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Prashant Dogra, Achraf Noureddine · 2024 to 2026
$1.3M
East Tennessee State University East Tennessee State UniversityNational Institute of Health NIH R01EB035545NIBIB NIH HHS R01 EB035545
6 · The paper itself

Abstract

This study evaluates dissolving microneedle (MN) patches for naloxone (NAL) delivery via the transnasal route, addressing limitations seen with transdermal application of same and the limitations of conventional NAL intranasal sprays, which often require frequent redosing, particularly for long-acting opioids like fentanyl. MN patches composed of polyvinylpyrrolidone (PVP) and PVP/Chitosan were tested on porcine nasal mucosa. PVP patches achieved significantly higher 1-h cumulative permeation (7295.12 ± 2585.17 µg/cm²) compared to transdermal application (103 ± 15.18 µg/cm², p < 0.05). Over 24 h, cumulative permeation reached 13,113.20 ± 597.39 µg/cm² transnasally versus 4112.89 ± 773.40 µg/cm² transdermally (p < 0.05). Chitosan-PVP MN patches improved bioadhesion and demonstrated high 1-h cumulative permeation (3800.19 ± 940.51 µg/cm²). PVP MN patches with drug-loaded tips (MN/TO, where TO implies "tip only") delivered 933.90 ± 161.60 µg/cm² in 1 h that was also a remarkable increase over transdermal permeation (p < 0.05) but had lower 24 h permeation. Similar observation was seen with the PVP/Chitosan variant with drug loaded in just MN tips indicating that sustained delivery requires drug in both the tips and base. To further refine patch designs, a mathematical modeling framework was employed to simulate drug dissolution, permeation dynamics, and plasma concentration kinetics. Simulations demonstrated that optimized patches could achieve plasma profiles comparable to intranasal and intramuscular administration, while minimizing drug dose and patch size. Increasing drug concentration from 50 to 60 mg/ml decreased permeation, likely due to drug crystallization. Overall, MN patches showed consistent, sustained NAL delivery, providing an alternative option for efficient opioid overdose treatment.

Indexed as

Drug Delivery SystemsNaloxoneNarcotic AntagonistsAdministration, CutaneousAdministration, IntranasalAnimalsChitosanMicroinjectionsNasal MucosaNeedlesPovidoneSwineTransdermal PatchChitosanNaloxoneNarcotic AntagonistsPovidone

Identifiers

PMID40652023
PMCPMC13430813

What OpenQuestion holds

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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.