Evidence mapPaperPMID 42393458Full record

ArticleAAPS PharmSciTech2026

Enhanced Stability and Transdermal Delivery of Semaglutide Using an L-Arginine Based Dissolving Microneedle System.

Priyanka Panchal, Snehal Daware, Yi Guo, Ganming Mao, Blase Billack, Pulkit Khatri, Ketan Patel

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Article in AAPS PharmSciTech, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

7 authors.

Priyanka PanchalCollege of Pharmacy and Health Sciences, St. Albert Hall, St. John's University, 8000 Utopia Parkway, Queens, New York, 11439, USA.ORCID http://orcid.org/0000-0001-5168-6901
Snehal DawareCollege of Pharmacy and Health Sciences, St. Albert Hall, St. John's University, 8000 Utopia Parkway, Queens, New York, 11439, USA.ORCID http://orcid.org/0009-0009-5904-8889
Yi GuoCollege of Pharmacy and Health Sciences, St. Albert Hall, St. John's University, 8000 Utopia Parkway, Queens, New York, 11439, USA.ORCID http://orcid.org/0000-0001-8622-2314
Ganming MaoCollege of Pharmacy and Health Sciences, St. Albert Hall, St. John's University, 8000 Utopia Parkway, Queens, New York, 11439, USA.ORCID http://orcid.org/0009-0004-4272-6739
Blase BillackCollege of Pharmacy and Health Sciences, St. Albert Hall, St. John's University, 8000 Utopia Parkway, Queens, New York, 11439, USA.ORCID http://orcid.org/0000-0001-7180-5955
Pulkit KhatriAmbio, Inc., 442 Park West Dr., Grovetown, Georgia, 30813, USA.ORCID http://orcid.org/0000-0002-5498-2439
Ketan PatelCollege of Pharmacy and Health Sciences, St. Albert Hall, St. John's University, 8000 Utopia Parkway, Queens, New York, 11439, USA. patelk2@stjohns.edu.ORCID http://orcid.org/0000-0001-8252-0234

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glucagon-like peptide-1 agonists, especially Semaglutide (SMG), have revolutionized the management of diabetes and obesity, yet its clinical application is hindered by challenges in oral bioavailability and patient adherence to injectable formulations. Transdermal delivery offers a promising alternative, and this study explores dissolving microneedle (DMN) technology for SMG administration. PETOX is a water-soluble polymer utilized for the fabrication of dissolving microneedles and unique stabilization of SMG by incorporating L-arginine. Our study presents the first comprehensive investigation of L-arginine as an excipient in dissolving microneedles to enhance peptide integrity and stability. This study focuses on the development and characterization of DMN arrays formulated with a polymeric blend of hyaluronic acid, PETOX, and L-arginine, designed for the transdermal delivery of SMG. The SMG loaded microneedles (SMG-DMNs) exhibit robust mechanical strength (3.47 N/needle; fracture force), excellent Parafilm M® insertion (> 50% at 450 μm depth), and drug release over 12 h. Extensive SMG-DMNs characterization include ex-vivo porcine skin insertion, scanning electron microscopy, confocal microscopy, and unique agarose-based dissolution model showed effective optimization of polymeric matrix for SMG, ensuring better insertion capabilities. The florescence imaging verified efficient transdermal deposition and penetration of dye suggesting potential transdermal delivery of SMG upon insertion. While the DMN approach addresses key barriers such as low oral bioavailability, injection-related discomfort and patient compliance; challenges persist regarding loss of therapeutic activity and stability of peptide. Nevertheless, DMN technology presents a promising, patient-friendly alternative for peptide therapeutics, with the potential to significantly improve outcomes in T2DM and obesity management.

Indexed as

ArginineGlucagon-Like PeptidesAdministration, CutaneousAnimalsBiological AvailabilityDrug LiberationDrug StabilityExcipientsHyaluronic AcidHypoglycemic AgentsMicroneedle Drug DeliveryNeedlesPolymersSemaglutideSkinSolubilityArginineExcipientsGlucagon-Like PeptidesHyaluronic AcidHypoglycemic AgentsPolymersSemaglutidedissolving microneedleGLP-1obesitysemaglutidetype 2 diabetes mellitus

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What Socratic 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 Socratic graph.