Evidence map›Paper›PMID 23025592›Full record

ArticleMolecular pharmaceutics2012

Aerosolized antimicrobial agents based on degradable dextran nanoparticles loaded with silver carbene complexes.

Cátia Ornelas-Megiatto, Parth N Shah, Peter R Wich, Jessica L Cohen, Jasur A Tagaev, Justin A Smolen, Brian D Wright, Matthew J Panzner, Wiley J Youngs, Jean M J Fréchet and 1 more

Abstract read
In one paragraph

Article in Molecular pharmaceutics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Polymeric nanoparticles in development for treatment of pulmonary infectious diseases.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2016
    Review
  12. Article
  13. Anti-tumor activity of lipophilic imidazolium salts on select NSCLC cell lines.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2015
    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

11 authors.

Cátia Ornelas-MegiattoCollege of Chemistry, University of California, Berkeley, California 94720-1460, United States.
Parth N Shah
Peter R Wich
Jessica L Cohen
Jasur A Tagaev
Justin A Smolen
Brian D Wright
Matthew J Panzner
Wiley J Youngs
Jean M J Fréchet
Carolyn L Cannon

Funding

Silver carbene complexes as treatment of CF lung diseaseR01AI067856 · NIAID · WASHINGTON UNIVERSITY · PI CANNON, CAROLYN LOUISE · 2006 to 2008
$1.1M
NHLBI NIH HHS HHSN268201000043CNHLBI NIH HHS HHSN268201000046CNIAID NIH HHS R01 AI067856
6 · The paper itself

Abstract

Degradable acetalated dextran (Ac-DEX) nanoparticles were prepared and loaded with a hydrophobic silver carbene complex (SCC) by a single-emulsion process. The resulting particles were characterized for morphology and size distribution using scanning electron microscopy (SEM), transmission electron microscopy (TEM), and dynamic light scattering (DLS). The average particle size and particle size distribution were found to be a function of the ratio of the organic phase to the surfactant containing aqueous phase with a 1:5 volume ratio of Ac-DEX CH(2)Cl(2) (organic):PBS (aqueous) being optimal for the formulation of nanoparticles with an average size of 100 ± 40 nm and a low polydispersity. The SCC loading was found to increase with an increase in the SCC quantity in the initial feed used during particle formulation up to 30% (w/w); however, the encapsulation efficiency was observed to be the best at a feed ratio of 20% (w/w). In vitro efficacy testing of the SCC loaded Ac-DEX nanoparticles demonstrated their activity against both Gram-negative and Gram-positive bacteria; the nanoparticles inhibited the growth of every bacterial species tested. As expected, a higher concentration of drug was required to inhibit bacterial growth when the drug was encapsulated within the nanoparticle formulations compared with the free drug illustrating the desired depot release. Compared with free drug, the Ac-DEX nanoparticles were much more readily suspended in an aqueous phase and subsequently aerosolized, thus providing an effective method of pulmonary drug delivery.

Indexed as

Administration, InhalationDrug CarriersAnti-Infective AgentsDextransMethaneMicrobial Sensitivity TestsMicroscopy, Electron, ScanningMicroscopy, Electron, TransmissionNanoparticlesParticle SizePharmaceutical PreparationsPseudomonas aeruginosaSilverSolubilityStaphylococcus aureusAnti-Infective AgentscarbeneDextransDrug CarriersMethanePharmaceutical PreparationsSilver

Identifiers

PMID23025592
PMCPMC3579655

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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.