Evidence map›Paper›PMID 35211869›Full record

ArticleDrug delivery and translational research2022

Fused deposition modeling three-dimensional printing of flexible polyurethane intravaginal rings with controlled tunable release profiles for multiple active drugs.

Yufei Chen, Yannick L Traore, Lyndon Walker, Sidi Yang, Emmanuel A Ho

Abstract read
In one paragraph

Article in Drug delivery and translational research, 2022. 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. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Rising role of 3D-printing in delivery of therapeutics for infectious disease.Journal of controlled release : official journal of the Controlled Release Society · 2024
    Review
  10. Formulating biopharmaceuticals using three-dimensional printing.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2024
    Review
  11. Article
  12. Article
  13. Article
  14. 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

5 authors.

Yufei ChenLaboratory for Drug Delivery and Biomaterials, School of Pharmacy, University of Waterloo, 10A Victoria St. S, Ontario, N2G 1C5, Kitchener, Canada.
Yannick L TraoreLaboratory for Drug Delivery and Biomaterials, School of Pharmacy, University of Waterloo, 10A Victoria St. S, Ontario, N2G 1C5, Kitchener, Canada.
Lyndon WalkerCollege of Pharmacy, University of Manitoba, Winnipeg, MB, Canada.
Sidi YangLaboratory for Drug Delivery and Biomaterials, School of Pharmacy, University of Waterloo, 10A Victoria St. S, Ontario, N2G 1C5, Kitchener, Canada.
Emmanuel A HoLaboratory for Drug Delivery and Biomaterials, School of Pharmacy, University of Waterloo, 10A Victoria St. S, Ontario, N2G 1C5, Kitchener, Canada. Emmanuel.ho@uwaterloo.ca.ORCID 0000-0003-4729-9970

Funding

CIHR PJT166153
6 · The paper itself

Abstract

We designed and engineered novel intravaginal ring (IVR) medical devices via fused deposition modeling (FDM) three-dimensional (3D) printing for controlled delivery of hydroxychloroquine, IgG, gp120 fragment (encompassing the CD4 binding site), and coumarin 6 PLGA-PEG nanoparticles (C6NP). The hydrophilic polyurethanes were utilized to 3D-print reservoir-type IVRs containing a tunable release controlling membrane (RCM) with varying thickness and adaptable micro porous structures (by altering the printing patterns and interior fill densities) for controlled sustained drug delivery over 14 days. FDM 3D printing of IVRs were optimized and implemented using a lab-developed Cartesian 3D printer. The structures were investigated by scanning electron microscopy (SEM) imaging and in vitro release was performed using 5 mL of daily-replenished vaginal fluid simulant (pH 4.2). The release kinetics of the IVR segments were tunable with various RCM (outer diameter to inner diameter ratio ranging from 1.12 to 2.61) produced from FDM 3D printing by controlling the printing perimeter to provide daily zero-order release of HCQ ranging from 23.54 ± 3.54 to 261.09 ± 32.49 µg/mL/day. IgG, gp120 fragment, and C6NP release rates demonstrated pattern and in-fill density-dependent characteristics. The current study demonstrated the utility of FDM 3D printing to rapidly fabricate complex micro-structures for tunable and sustained delivery of a variety of compounds including HCQ, IgG, gp120 fragment, and C6NP from IVRs in a controlled manner.

Indexed as

PolyurethanesPrinting, Three-DimensionalDrug Delivery SystemsDrug LiberationFemaleHumansImmunoglobulin GPharmaceutical PreparationsTechnology, PharmaceuticalImmunoglobulin GPharmaceutical PreparationsPolyurethanes3D-printingFused deposition modelingHIVIntravaginal ringNanoparticles

Identifiers

PMID35211869
PMCPMC8870081

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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.