Evidence map›Paper›PMID 39653959›Full record

ArticleDrug delivery and translational research2025

Fabrication and mechanical/biological evaluations of dissolving bird-bill microneedle arrays.

Natsumi Amano, Yuusei Takaki, Harunori Takei, Masaaki Matsuo, Masaya Hara, Yasunori Tashiro, Takahiro Oniki, Takahiro Ito, Tomohiro Hikima

Abstract read
In one paragraph

Article in Drug delivery and translational research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Microneedle-Assisted Cell Delivery and Therapy.Research (Washington, D.C.) · 2026
    Review
  3. 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

9 authors.

Natsumi AmanoDepartment of Bioscience and Bioinformatics, Kyushu Institute of Technology, 680-4 Kawazu, Iizuka, Fukuoka, 820-8502, Japan.
Yuusei TakakiDepartment of Systems Design and Informatics, Kyushu Institute of Technology, 680-4 Kawazu, Iizuka, Fukuoka, 820-8502, Japan.
Harunori TakeiDepartment of Systems Design and Informatics, Kyushu Institute of Technology, 680-4 Kawazu, Iizuka, Fukuoka, 820-8502, Japan.
Masaaki MatsuoMishima Kosan Co., Ltd., 2-1-15 Edamitsu, Yahatahigashi, Kitakyushu, 805-0002, Japan.
Masaya HaraMishima Kosan Co., Ltd., 2-1-15 Edamitsu, Yahatahigashi, Kitakyushu, 805-0002, Japan.
Yasunori TashiroMishima Kosan Co., Ltd., 2-1-15 Edamitsu, Yahatahigashi, Kitakyushu, 805-0002, Japan.
Takahiro OnikiMishima Kosan Co., Ltd., 2-1-15 Edamitsu, Yahatahigashi, Kitakyushu, 805-0002, Japan.
Takahiro ItoDepartment of Systems Design and Informatics, Kyushu Institute of Technology, 680-4 Kawazu, Iizuka, Fukuoka, 820-8502, Japan.
Tomohiro HikimaDepartment of Bioscience and Bioinformatics, Kyushu Institute of Technology, 680-4 Kawazu, Iizuka, Fukuoka, 820-8502, Japan. hikima@bio.kyutech.ac.jp.ORCID 0000-0001-7169-9996

Funding

Japan Society for the Promotion of Science 22K12846
6 · The paper itself

Abstract

Coated microneedles (MNs) have several disadvantages, including limited drug doses, decreased skin puncture ability due to drug coating, and a risk of clogging and infection due to repeated application. We aimed to fabricate a dissolving bird-bill MN (dBB MN) with a vertical groove between two thin plate-shaped needles and needle pedestal. Moreover, we evaluated its ability to transdermally deliver a large-molecular-weight insulin into the systemic circulation. Hydrogels with various concentrations of polyvinylpyrrolidone (PVP) or sodium hyaluronate (HA) were prepared, and dBB MN arrays were fabricated by micromolding under negative pressure for potential mass production. The needle height of the dBB MN was at the maximum when the hydrogel was 25 w/w% PVP, with a viscosity of 8-9 Pa∙s. Furthermore, the buckling force of dBB MNs made from 25 w/w% PVP was 130.6 ± 51.0 mN, which increased to 195.6 ± 65.3 mN when insulin was added at 1 w/w%. The skin insertion ability of dBB MN was investigated using swain skin, with micro-holes were confirmed on the skin surface. dBB MN showed biphasic dissolution in the skin; the plate-shaped needles were immediately dissolved within 10 min, while the needle pedestal was slowly dissolved over 180 min. The blood glucose concentration in diabetic rats decreased slowly and significantly after a 3-h application of the insulin-loaded dBB MN array. Therefore, the dBB MN array demonstrated sufficient ability to puncture skin and transdermally deliver a large-molecular-weight drug into the systemic circulation. These findings suggest that the dBB MN array holds promise as a minimal invasive drug delivery platform, with potential applications in improving patient adherence and expanding access to essential therapies, particularly in resource-limited settings.

Indexed as

Drug Delivery SystemsHypoglycemic AgentsInsulinNeedlesAdministration, CutaneousAnimalsBlood GlucoseDiabetes Mellitus, ExperimentalHyaluronic AcidHydrogelsMaleMicroinjectionsPovidoneRatsRats, Sprague-DawleySkinBlood GlucoseHyaluronic AcidHydrogelsHypoglycemic AgentsInsulinPovidoneBiocompatible polymerBird-bill microneedleDissolving microneedle arrayPolyvinylpyrrolidoneTransdermal drug delivery

Identifiers

PMID39653959
PMCPMC12137373

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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.