Evidence map›Paper›PMID 41659329›Full record

ArticleRSC advances2026

Nitric oxide-releasing hyaluronic acid as an antibacterial and immunomodulatory acne therapeutic.

Samantha L Picciotti, Torrance M Jenkins, Tsian D Ramrattan, Mark H Schoenfisch

Abstract read
In one paragraph

Article in RSC advances, 2026. 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. Review
  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

4 authors.

Samantha L PicciottiDepartment of Chemistry, University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599 USA schoenfisch@unc.edu.
Torrance M JenkinsDepartment of Chemistry, University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599 USA schoenfisch@unc.edu.
Tsian D RamrattanDepartment of Chemistry, University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599 USA schoenfisch@unc.edu.
Mark H SchoenfischDepartment of Chemistry, University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599 USA schoenfisch@unc.edu.ORCID https://orcid.org/0000-0002-2212-0658

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acne vulgaris (acne) is a common skin disorder associated with significant psychosocial impact. Current clinical therapies include topical and systemic antibiotics, benzoyl peroxide, and retinoids. While moderately effective, these clinical therapies fail to target all four major pathogenic causes of acne and are associated with painful side effects. Nitric oxide (NO), an endogenous signaling molecule, represents a promising alternative to conventional acne treatments due to its innate antibacterial and immunomodulatory functions. As NO is highly reactive, macromolecular NO donors are required for its controlled, solution-phase delivery. Prior work has utilized silica nanoparticle scaffolds to store and deliver NO, with the silica scaffold being considered inert. Herein, NO-releasing hyaluronic acid (HA), an endogenously produced biopolymer, was modified with NO donors to enable a dual-action therapeutic capable of addressing the pathogenic factors responsible for acne development. The molecular weight of these HA derivatives proved important with respect to bactericidal activity against

Identifiers

PMID41659329
PMCPMC12879550

What OpenQuestion holds

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LicenceCC BY-NC
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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.