Evidence map›Paper›PMID 24673568›Full record

ArticleThe Journal of pharmacy and pharmacology2015

Laser-engineered dissolving microneedle arrays for protein delivery: potential for enhanced intradermal vaccination.

Maelíosa T C McCrudden, Barbara M Torrisi, Sharifah Al-Zahrani, Cian M McCrudden, Marija Zaric, Christopher J Scott, Adrien Kissenpfennig, Helen O McCarthy, Ryan F Donnelly

Open access · greenAbstract read
In one paragraph

Article in The Journal of pharmacy and pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 19% of its field
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

20 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Dermal Microvascular Units in Domestic Pigs (Frontiers in veterinary science · 2022
    Article
  8. Review
  9. Review
  10. Review
  11. Dissolving undercut microneedle arrays for multicomponent cutaneous vaccination.Journal of controlled release : official journal of the Controlled Release Society · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Transdermal delivery of gentamicin using dissolving microneedle arrays for potential treatment of neonatal sepsis.Journal of controlled release : official journal of the Controlled Release Society · 2017
    Article
  17. Review
  18. Article
  19. Article
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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 at 2 institutions in 2 countries.

Maelíosa T C McCruddenSchool of Pharmacy, Medical Biology Centre, Queen's University Belfast, Belfast, UK.
Barbara M Torrisi
Sharifah Al-Zahrani
Cian M McCrudden
Marija Zaric
Christopher J Scott
Adrien Kissenpfennig
Helen O McCarthy
Ryan F Donnelly
Queen's University Belfast · GBInstitute of Infection and Immunity · CA

Funding

Biotechnology and Biological Sciences Research Council BB/E020534/1Biotechnology and Biological Sciences Research Council BB/FOF/287Biotechnology and Biological Sciences Research Council BB/K020234/1Wellcome TrustWellcome Trust WT094085MA
6 · The paper itself

Abstract

objectivesWe aimed to highlight the utility of novel dissolving microneedle (MN)-based delivery systems for enhanced transdermal protein delivery. Vaccination remains the most accepted and effective approach in offering protection from infectious diseases. In recent years, much interest has focused on the possibility of using minimally invasive MN technologies to replace conventional hypodermic vaccine injections.

methodsThe focus of this study was exploitation of dissolving MN array devices fabricated from 20% w/w poly(methyl vinyl ether/maleic acid) using a micromoulding technique, for the facilitated delivery of a model antigen, ovalbumin (OVA). KEY

findingsA series of in-vitro and in-vivo experiments were designed to demonstrate that MN arrays loaded with OVA penetrated the stratum corneum and delivered their payload systemically. The latter was evidenced by the activation of both humoral and cellular inflammatory responses in mice, indicated by the production of immunoglobulins (IgG, IgG1, IgG2a) and inflammatory cytokines, specifically interferon-gamma and interleukin-4. Importantly, the structural integrity of the OVA following incorporation into the MN arrays was maintained.

conclusionWhile enhanced manufacturing strategies are required to improve delivery efficiency and reduce waste, dissolving MN are a promising candidate for 'reduced-risk' vaccination and protein delivery strategies.

Indexed as

Drug Delivery SystemsMicroinjectionsSkin AbsorptionAdministration, CutaneousAnimalsAntigensInterferon-gammaInterleukin-4LasersMaleatesMethyl EthersMiceNeedlesOvalbuminPolyvinylsSkinAntigensIL4 protein, humanInterferon-gammaInterleukin-4Maleatesmaleic acidMethyl EthersOvalbuminpoly(vinyl methyl ether)PolyvinylsVaccineslaser-engineeringmicroneedlesprotein deliveryvaccination

Identifiers

PMID24673568
PMCPMC7938851
OpenAlexW1572242534

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.