Evidence map›Paper›PMID 25580246›Full record

ArticleJournal of materials chemistry. B2014

Photo-triggerable Hydrogel-Nanoparticle Hybrid Scaffolds for Remotely Controlled Drug Delivery.

Shreyas Shah, Pijus K Sasmal, Ki-Bum Lee

Abstract read
In one paragraph

Article in Journal of materials chemistry. B, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Recent Developments in Nanoparticle-Hydrogel Hybrid Materials for Controlled Release.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  2. Review
  3. Article
  4. Visible and NIR light photoactivatableRSC medicinal chemistry · 2023
    Article
  5. Article
  6. Review
  7. Review
  8. Enhancing regenerative approaches with nanoparticles.Journal of the Royal Society, Interface · 2017
    Review
  9. Article
  10. 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

3 authors.

Shreyas ShahDepartment of Chemistry & Chemical Biology, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, U.S.A.
Pijus K SasmalDepartment of Chemistry & Chemical Biology, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, U.S.A.
Ki-Bum LeeDepartment of Chemistry & Chemical Biology, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, U.S.A.

Funding

Combinatorial approaches for studying multiple cues regulating human pluripotentDP2OD006462 · OD · RUTGERS, THE STATE UNIV OF N.J. · PI LEE, KIBUM · 2009 to 2009
$2.3M
Novel magnetic core/shell nanoparticle-based stem cell therapy to direct neural sR21NS085569 · NINDS · RUTGERS, THE STATE UNIV OF N.J. · PI LEE, KIBUM · 2013 to 2014
$421k
NIH HHS DP2 OD006462NINDS NIH HHS R21 NS085569
6 · The paper itself

Abstract

Remotely-triggerable drug delivery systems enable the user to adjust dosing regimens on-demand based on a patient's physiological response and clinical needs. However, currently reported systems are limited by the non-specific leakage of drugs in the absence of triggering and the lack of repeatability over multiple cycles of release. To this end, we have designed a unique hydrogel-nanoparticle hybrid scaffold that provides a chemically-defined, remotely-triggerable and on-demand release of small molecule drugs. Our hybrid platform consists of three distinct components: 1) a photo-triggerable chemical compound, which serves to release a covalently-bound drug upon photo-irradiation, 2) a nanoparticle, which serves to covalently bind the photo-triggerable compound, and 3) a polymeric hydrogel, which serves to hold the drug-conjugated nanoparticle. Upon photo-irradiation, the activation of the photo-triggerable compound is designed to initiate a series of intramolecular chemical rearrangements, which would cleave the covalently-bound drug and release it from the hydrogel. The combination of these distinct components in a single scaffold proved to be an effective drug delivery system, as demonstrated by the delivery of a model drug to a malignant cancer line. Our hybrid scaffold can be easily tuned for practically any biological application of interest, thus offering immense potential for clinical therapies.

Identifiers

PMID25580246
PMCPMC4285771

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.