Evidence map›Paper›PMID 28802690›Full record

ArticleBiomaterials2017

Nanoparticle-releasing nanofiber composites for enhanced in vivo vaginal retention.

Emily A Krogstad, Renuka Ramanathan, Christina Nhan, John C Kraft, Anna K Blakney, Shijie Cao, Rodney J Y Ho, Kim A Woodrow

Abstract read
In one paragraph

Article in Biomaterials, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

21 citing papers in PubMed, 66 citations in OpenAlex.

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  17. Sustained-release Griffithsin nanoparticle-fiber composites against HIV-1 and HSV-2 infections.Journal of controlled release : official journal of the Controlled Release Society · 2020
    Article
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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

8 authors at 1 institution in 1 country.

Emily A KrogstadDepartment of Bioengineering, University of Washington, Seattle, WA 98195, United States.
Renuka RamanathanDepartment of Bioengineering, University of Washington, Seattle, WA 98195, United States.
Christina NhanDepartment of Bioengineering, University of Washington, Seattle, WA 98195, United States.
John C KraftDepartment of Pharmaceutics, University of Washington, Seattle, WA 98195, United States.
Anna K BlakneyDepartment of Bioengineering, University of Washington, Seattle, WA 98195, United States.
Shijie CaoDepartment of Bioengineering, University of Washington, Seattle, WA 98195, United States.
Rodney J Y HoDepartment of Bioengineering, University of Washington, Seattle, WA 98195, United States; Department of Pharmaceutics, University of Washington, Seattle, WA 98195, United States.
Kim A WoodrowDepartment of Bioengineering, University of Washington, Seattle, WA 98195, United States. Electronic address: woodrow@uw.edu.
University of Washington · US

Funding

Transform Dissemination and Implementation Science in CTSA ProgramsUL1TR002319 · NCATS · UNIVERSITY OF WASHINGTON · PI John K. Amory · 2017 to 2026
$100.0M
INSTITUTE FOR TRANSLATIONAL HEALTH SCIENCE (UL1): BPCAUL1RR025014 · NCRR · UNIVERSITY OF WASHINGTON · PI DISIS, MARY L. · 2007 to 2011
$51.5M
VENEREAL DISEASET32AI007140 · NIAID · UNIVERSITY OF WASHINGTON · PI Julia Cook Dombrowski · 1985 to 2026
$19.4M
Targeted Long-acting Combination Antiretroviral Therapy (TLC-ART)UM1AI120176 · NIAID · UNIVERSITY OF WASHINGTON · PI COLLIER, ANN CORNWALL, HO, RODNEY J.Y. · 2015 to 2019
$15.0M
Pharmacological Sciences SupplementT32GM007750 · NIGMS · UNIVERSITY OF WASHINGTON · PI ATKINS, WILLIAM M · 1985 to 2023
$12.6M
pH Responsive anti-HIV NanoparticlesR01AI077390 · NIAID · UNIVERSITY OF WASHINGTON · PI HO, RODNEY J.Y. · 2009 to 2013
$3.9M
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
Nanoparticle microbicides for delivery of combination antiretroviral drugsR33AI094412 · NIAID · UNIVERSITY OF WASHINGTON · PI WOODROW, KIM A. · 2013 to 2015
$1.6M
Nanoparticle microbicides for delivery of combination antiretroviral drugsR21AI094412 · NIAID · UNIVERSITY OF WASHINGTON · PI WOODROW, KIM A. · 2011 to 2012
$394k
NCATS NIH HHS UL1 TR002319NCRR NIH HHS UL1 RR025014NIAID NIH HHS R01 AI077390NIAID NIH HHS R01 AI112002NIAID NIH HHS R21 AI094412NIAID NIH HHS R33 AI094412NIAID NIH HHS T32 AI007140NIAID NIH HHS UM1 AI120176NIGMS NIH HHS T32 GM007750
6 · The paper itself

Abstract

Current approaches for topical vaginal administration of nanoparticles result in poor retention and extensive leakage. To overcome these challenges, we developed a nanoparticle-releasing nanofiber delivery platform and evaluated its ability to improve nanoparticle retention in a murine model. We individually tailored two components of this drug delivery system for optimal interaction with mucus, designing (1) mucoadhesive fibers for better retention in the vaginal tract, and (2) PEGylated nanoparticles that diffuse quickly through mucus. We hypothesized that this novel dual-functioning (mucoadhesive/mucus-penetrating) composite material would provide enhanced retention of nanoparticles in the vaginal mucosa. Equivalent doses of fluorescent nanoparticles were vaginally administered to mice in either water (aqueous suspension) or fiber composites, and fluorescent content was quantified in cervicovaginal mucus and vaginal tissue at time points from 24 h to 7d. We also fabricated composite fibers containing etravirine-loaded nanoparticles and evaluated the pharmacokinetics over 7d. We found that our composite materials provided approximately 30-fold greater retention of nanoparticles in the reproductive tract at 24 h compared to aqueous suspensions. Compared to nanoparticles in aqueous suspension, the nanoparticles in fiber composites exhibited sustained and higher etravirine concentrations after 24 h and up to 7d, demonstrating the capabilities of this new delivery platform to sustain nanoparticle release out to 3d and drug retention out to one week after a single administration. This is the first report of nanoparticle-releasing fibers for vaginal drug delivery, as well as the first study of a single delivery system that combines two components uniquely engineered for complementary interactions with mucus.

Indexed as

Administration, IntravaginalAnimalsDelayed-Action PreparationsDrug Delivery SystemsFemaleFluorescent DyesMiceMice, Inbred C57BLMucous MembraneNanofibersNanoparticlesNitrilesPyridazinesPyrimidinesReverse Transcriptase InhibitorsVaginaDelayed-Action PreparationsetravirineFluorescent DyesNitrilesPyridazinesPyrimidinesReverse Transcriptase InhibitorsElectrospinningMicrobicidesNanofibersNanoparticlesPharmacokineticsVaginal drug delivery

Identifiers

PMID28802690
PMCPMC5599218
OpenAlexW2741299362

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.