Evidence map›Paper›PMID 26286184›Full record

ArticlePharmaceutical research2016

Tunable Release of Multiclass Anti-HIV Drugs that are Water-Soluble and Loaded at High Drug Content in Polyester Blended Electrospun Fibers.

Daniel Carson, Yonghou Jiang, Kim A Woodrow

Open access · greenAbstract read
In one paragraph

Article in Pharmaceutical research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.9field-weighted citation impact, top 7% of its field
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

40 citing papers in PubMed, 85 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Drug Eluting Embolization Particles for Permanent Contraception.ACS biomaterials science & engineering · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. Nanotechnology-based antiviral therapeutics.Drug delivery and translational research · 2021
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Electrospun Nanofibers for Cancer Therapy.Advances in experimental medicine and biology · 2021
    Review
  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 at 1 institution in 1 country.

Daniel CarsonDepartment of Bioengineering, University of Washington, Foege N410D, 3720 15th Ave NE, Seattle, Washington, 98195-5061, USA.
Yonghou JiangDepartment of Bioengineering, University of Washington, Foege N410D, 3720 15th Ave NE, Seattle, Washington, 98195-5061, USA.
Kim A WoodrowDepartment of Bioengineering, University of Washington, Foege N410D, 3720 15th Ave NE, Seattle, Washington, 98195-5061, USA. woodrow@uw.edu.
University of Washington · US

Funding

Combination HIV prevention in drug-eluting fibers: designing for efficacy and useR01AI112002 · NIAID · UNIVERSITY OF WASHINGTON · PI WOODROW, KIM A. · 2014 to 2017
$2.3M
A NanoGuard Vaginal Matrix as a Dual-Protection Contraceptive MicrobicideR21AI098648 · NIAID · UNIVERSITY OF WASHINGTON · PI WOODROW, KIM A. · 2012 to 2013
$396k
NIAID NIH HHS AI098648NIAID NIH HHS AI112002NIAID NIH HHS R01 AI112002NIAID NIH HHS R21 AI098648
6 · The paper itself

Abstract

objectivesSustained release of small molecule hydrophilic drugs at high doses remains difficult to achieve from electrospun fibers and limits their use in clinical applications. Here we investigate tunable release of several water-soluble anti-HIV drugs from electrospun fibers fabricated with blends of two biodegradable polyesters.

methodsDrug-loaded fibers were fabricated by electrospinning ratios of PCL and PLGA. Fiber morphology was imaged by SEM, and DSC was used to measure thermal properties. HPLC was used to measure drug loading and release from fibers. Cytotoxicity and antiviral activity of drug-loaded fibers were measured in an in vitro cell culture assay.

resultsWe show programmable release of hydrophilic antiretroviral drugs loaded up to 40 wt%. Incremental tuning of highly-loaded drug fibers within 24 h or >30 days was achieved by controlling the ratio of PCL and PLGA. Fiber compositions containing higher PCL content yielded greater burst release whereas fibers with higher PLGA content resulted in greater sustained release kinetics. We also demonstrated that our drug-loaded fibers are safe and can sustain inhibition of HIV in vitro.

conclusionsThese data suggest that we were able to overcome current limitations associated with sustained release of small molecule hydrophilic drugs at clinically relevant doses. We expect that our system represents an effective strategy to sustain delivery of water-soluble molecules that will benefit a variety of biomedical applications.

Indexed as

Anti-HIV AgentsAntiretroviral Therapy, Highly ActiveBiodegradable PlasticsCell SurvivalDrug Delivery SystemsHeLa CellsHIV-1HumansKineticsLactic AcidNanofibersPolyestersPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerSolubilityTenofovirAnti-HIV AgentsBiodegradable PlasticsLactic AcidpolycaprolactonePolyestersPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerTenofovirWaterelectrospinninghigh loadingHIVprogrammable releasetenofovir

Identifiers

PMID26286184
PMCPMC5217171
OpenAlexW1145855424

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.