Evidence map›Paper›PMID 40949249›Full record

ArticleACS omega2025

Dissolvable Microneedles Embedded with Chitosan Nanoparticles for Transdermal Delivery of Pramipexole Dihydrochloride in Parkinson's Disease.

Kankanit Phetporkha, Chonticha Saisawang, Nattaphong Rattanavirotkul, Soracha D Thamphiwatana, Doungdaw Chantasart

Abstract read
In one paragraph

Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

Kankanit PhetporkhaDepartment of Biomedical Engineering, Faculty of Engineering, Mahidol University, Nakorn Pathom, 73170, Thailand.ORCID https://orcid.org/0009-0004-6167-7784
Chonticha SaisawangCenter for Advanced Therapeutics, Institute of Molecular Biosciences, Mahidol University, Nakorn Pathom, 73170, Thailand.
Nattaphong RattanavirotkulChakri Naruebodindra Medical Institute, Ramathibodi Medical School, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 111, Bang Pla, Bang Phli, Samut Prakan 10540, Thailand.
Soracha D ThamphiwatanaDepartment of Biomedical Engineering, Faculty of Engineering, Mahidol University, Nakorn Pathom, 73170, Thailand.ORCID https://orcid.org/0000-0003-3664-9488
Doungdaw ChantasartDepartment of Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok 10400, Thailand.ORCID https://orcid.org/0009-0008-2231-0575

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD), a progressive neurodegenerative disorder, presents significant challenges in long-term management due to the limitations of conventional oral dopaminergic therapy. Pramipexole dihydrochloride (Px), though clinically effective, is associated with gastrointestinal side effects and reduced compliance, especially in patients with dysphagia. To address these challenges, we developed a transdermal drug delivery system that integrates Px-loaded chitosan nanoparticles within dissolvable microneedle arrays. This hybrid platform combines the sustained release capability of polymeric nanoparticles with the minimally invasive administration of microneedles. The system is designed to penetrate the stratum corneum, dissolve upon insertion, and release Px nanoparticles for sustained dermal absorption. The microneedle arrays exhibit structural uniformity, mechanical robustness, and efficient skin insertion. The nanoparticles, in turn, enable controlled drug release while maintaining biocompatibility. Biological assessments confirmed the safety of the formulation, showing compatibility with human dermal cells and red blood cells. Moreover, ex vivo permeation studies demonstrated enhanced delivery of Px through human skin compared to free drug formulations. This work offers a promising solution for sustained, noninvasive delivery of dopaminergic therapy, with potential to improve clinical outcomes and quality of life in PD.

Identifiers

PMID40949249
PMCPMC12423965

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.