Evidence map›Paper›PMID 25479357›Full record

ArticlePloS one2014

Externally controlled triggered-release of drug from PLGA micro and nanoparticles.

Xin Hua, Shengnan Tan, H M H N Bandara, Yujie Fu, Siguo Liu, Hugh D C Smyth

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Drug repurposing for cancer therapy.Signal transduction and targeted therapy · 2024
    Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Novel Therapeutic Strategies Applied toMaterials (Basel, Switzerland) · 2019
    Review
  10. Article
  11. Predicting the tissue depth for remote triggering of drug delivery systems.Journal of controlled release : official journal of the Controlled Release Society · 2018
    Article
  12. Article
  13. Article
  14. Review
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

6 authors.

Xin HuaState Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute of Chinese Academy of Agricultural Science, Harbin 150001, China.
Shengnan TanState Engineering Laboratory of Bio-Resource Eco-Utilization, Northeast Forestry University, Harbin, PR China.
H M H N BandaraCollege of Pharmacy, The University of Texas at Austin, 1 University Station, A1920, Austin, TX 78712, United States of America.
Yujie FuState Engineering Laboratory of Bio-Resource Eco-Utilization, Northeast Forestry University, Harbin, PR China.
Siguo LiuState Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute of Chinese Academy of Agricultural Science, Harbin 150001, China.
Hugh D C SmythCollege of Pharmacy, The University of Texas at Austin, 1 University Station, A1920, Austin, TX 78712, United States of America.

Funding

Multifunctional nanoparticles for enhanced drug delivery to the lungR33HL092812 · NHLBI · UNIVERSITY OF TEXAS AT AUSTIN · PI SMYTH, HUGH DAVID · 2012 to 2013
$1.4M
NHLBI NIH HHS R33 HL092812NHLBI NIH HHS R33HL092812-03
6 · The paper itself

Abstract

Biofilm infections are extremely hard to eradicate and controlled, triggered and controlled drug release properties may prolong drug release time. In this study, the ability to externally control drug release from micro and nanoparticles was investigated. We prepared micro/nanoparticles containing ciprofloxacin (CIP) and magnetic nanoparticles encapsulated in poly (lactic-co-glycolic acid) PLGA. Both micro/nanoparticles were observed to have narrow size distributions. We investigated and compared their passive and externally triggered drug release properties based on their different encapsulation structures for the nano and micro systems. In passive release studies, CIP demonstrated a fast rate of release in first 2 days which then slowed and sustained release for approximately 4 weeks. Significantly, magnetic nanoparticles containing systems all showed ability to have triggered drug release when exposed to an external oscillating magnetic field (OMF). An experiment where the OMF was turned on and off also confirmed the ability to control the drug release in a pulsatile manner. The magnetically triggered release resulted in a 2-fold drug release increase compared with normal passive release. To confirm drug integrity following release, the antibacterial activity of released drug was evaluated in Pseudomonas aeruginosa biofilms in vitro. CIP maintained its antimicrobial activity after encapsulation and triggered release.

Indexed as

BiofilmsCiprofloxacinDelayed-Action PreparationsDrug Delivery SystemsHumansLactic AcidMagnetite NanoparticlesParticle SizePolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerPseudomonas aeruginosaPseudomonas InfectionsCiprofloxacinDelayed-Action PreparationsLactic AcidMagnetite NanoparticlesPolyglycolic AcidPolylactic Acid-Polyglycolic Acid Copolymer

Identifiers

PMID25479357
PMCPMC4257591

What OpenQuestion holds

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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.