Evidence map›Paper›PMID 26717238›Full record

ArticleACS applied materials & interfaces2016

Functionalized Mesoporous Silica via an Aminosilane Surfactant Ion Exchange Reaction: Controlled Scaffold Design and Nitric Oxide Release.

Robert J Soto, Lei Yang, Mark H Schoenfisch

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Nitric Oxide: Physiological Functions, Delivery, and Biomedical Applications.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Review
  8. Mechanisms of Foreign Body Response Mitigation by Nitric Oxide Release.International journal of molecular sciences · 2022
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Nitric oxide releasing halloysite nanotubes for biomedical applications.Journal of colloid and interface science · 2021
    Article
  15. Article
  16. Mode of nitric oxide delivery affects antibacterial action.ACS biomaterials science & engineering · 2020
    Article
  17. Article
  18. Article
  19. Article
  20. 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

3 authors.

Robert J SotoDepartment of Chemistry, University of North Carolina at Chapel Hill , CB3290, Chapel Hill, North Carolina 27599, United States.
Lei YangDepartment of Chemistry, University of North Carolina at Chapel Hill , CB3290, Chapel Hill, North Carolina 27599, United States.
Mark H SchoenfischDepartment of Chemistry, University of North Carolina at Chapel Hill , CB3290, Chapel Hill, North Carolina 27599, United States.

Funding

Role of diabetes and nitric oxide release duration on analytical performance of in vivo glucose biosensorsR01DK108318 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SCHOENFISCH, MARK H · 2016 to 2023
$4.5M
NIDDK NIH HHS DK108318NIDDK NIH HHS R01 DK108318
6 · The paper itself

Abstract

Nitric oxide-releasing mesoporous silica nanoparticles (MSNs) were prepared using an aminosilane-template surfactant ion exchange reaction. Initially, bare silica particles were synthesized under basic conditions in the presence of cetyltrimethylammonium bromide (CTAB). These particles were functionalized with nitric oxide (NO) donor precursors (i.e., secondary amines) via the addition of aminosilane directly to the particle sol and a commensurate ion exchange reaction between the cationic aminosilanes and CTAB. N-Diazeniumdiolate NO donors were formed at the secondary amines to yield NO-releasing MSNs. Tuning of the ion exchange-based MSN modification approach allowed for the preparation of monodisperse particles ranging from 30 to 1100 nm. Regardless of size, the MSNs stored appreciable levels of NO (0.4-1.5 μmol mg(-1)) with tunable NO release durations (1-33 h) dependent on the aminosilane modification. Independent control of NO release properties and particle size was achieved, demonstrating the flexibility of this novel MSN synthesis over conventional co-condensation and surface grafting strategies.

Indexed as

AminesIon ExchangeKineticsLuminescent MeasurementsMagnetic Resonance SpectroscopyNanoparticlesNitric OxideNitrogenParticle SizePorositySilanesSilicon DioxideSurface-Active AgentsAminesNitric OxideNitrogenSilanesSilicon DioxideSurface-Active Agentsdrug releasemacromolecular nitric oxide donormesoporous silicaN-diazeniumdiolatenitric oxidesilica nanoparticle

Identifiers

PMID26717238
PMCPMC4734612

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.