Evidence map›Paper›PMID 37014806›Full record

ArticleMolecular pharmaceutics2023

Single-Administration Long-Acting Microarray Patch with Ultrahigh Loading Capacity and Multiple Releases of Thermally Stable Antibodies.

Khanh T M Tran, Thinh T Le, Vivek Agrahari, M Melissa Peet, Louise A Ouattara, Sharon M Anderson, Trang Huyen Le-Kim, Onkar N Singh, Gustavo F Doncel, Thanh D Nguyen

Open access · greenAbstract read
In one paragraph

Article in Molecular pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Enhancing vaccine stability in transdermal microneedle platforms.Drug delivery and translational research · 2025
    Review
  4. Review
  5. Article
  6. Article
  7. The promise of microneedle technologies for drug delivery.Drug delivery and translational research · 2024
    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

10 authors at 2 institutions in 1 country.

Khanh T M TranDepartment of Biomedical Engineering, University of Connecticut, 181 Auditorium Road, Storrs, Connecticut 06269, United States.
Thinh T LeDepartment of Mechanical Engineering, University of Connecticut, 191 Auditorium Road, Storrs, Connecticut 06269 United States.
Vivek AgrahariCONRAD, Eastern Virginia Medical School, Norfolk, Virginia 23507, United States.
M Melissa PeetCONRAD, Eastern Virginia Medical School, Norfolk, Virginia 23507, United States.
Louise A OuattaraCONRAD, Eastern Virginia Medical School, Norfolk, Virginia 23507, United States.
Sharon M AndersonCONRAD, Eastern Virginia Medical School, Norfolk, Virginia 23507, United States.
Trang Huyen Le-KimDepartment of Mechanical Engineering, University of Connecticut, 191 Auditorium Road, Storrs, Connecticut 06269 United States.
Onkar N SinghCONRAD, Eastern Virginia Medical School, Norfolk, Virginia 23507, United States.
Gustavo F DoncelCONRAD, Eastern Virginia Medical School, Norfolk, Virginia 23507, United States.
Thanh D NguyenDepartment of Biomedical Engineering, University of Connecticut, 181 Auditorium Road, Storrs, Connecticut 06269, United States.ORCID 0000-0003-0813-4807
Eastern Virginia Medical School · USUniversity of Connecticut · US

Funding

PEPFAR
6 · The paper itself

Abstract

Current antibody (Ab) therapies require development of stable formulations and an optimal delivery system. Here, we present a new strategy to create a single-administration long-lasting Ab-delivery microarray (MA) patch, which can carry high doses of thermally stabilized Abs. The MA fabricated by an additive three-dimensional manufacturing technology can be fully embedded into the skin via a single application to deliver doses of Abs at multiple programmable time points, thus sustaining Ab concentrations in systemic circulation. We developed an MA formulation that stabilized and delivered human immunoglobulins (hIg) in a time-controlled manner while maintaining their structure and functionality. As an example, the b12 Ab─a broadly neutralizing Ab against HIV-1─maintained antiviral activity in vitro after MA manufacturing and heat exposure. Pharmacokinetic studies of MA patch-delivered hIg in rats successfully provided a proof of concept for concurrent and time-delayed Ab delivery. These MA patches codeliver different Abs, providing a tool for expanded protection against viral infections or combination HIV therapy and prevention.

Indexed as

AntibodiesHIV InfectionsAnimalsHumansRatsSkinAntibodiesfabricationslong-acting deliverymicroarray patchprotein stabilizationtherapeutic antibodies

Identifiers

PMID37014806
PMCPMC10155177
OpenAlexW4362520989

What OpenQuestion 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 OpenQuestion graph.