Evidence map›Paper›PMID 22619076›Full record

ArticleJournal of pharmaceutical sciences2012

An intravaginal ring for the simultaneous delivery of multiple drugs.

Marc M Baum, Irina Butkyavichene, Joshua Gilman, Sean Kennedy, Etana Kopin, Amanda M Malone, Cali Nguyen, Thomas J Smith, David R Friend, Meredith R Clark and 1 more

Abstract read
In one paragraph

Article in Journal of pharmaceutical sciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

49 citing papers in PubMed, 96 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Fabrication and characterization of bioprints with Lactobacillus crispatus for vaginal application.Journal of controlled release : official journal of the Controlled Release Society · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. Use of simulated vaginal and menstrual fluids to modelInternational journal of pharmaceutics: X · 2021
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Vaginal rings with exposed cores for sustained delivery of the HIV CCR5 inhibitor 5P12-RANTES.Journal of controlled release : official journal of the Controlled Release Society · 2019
    Article
  18. Review
  19. Article
  20. 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

11 authors at 4 institutions in 1 country.

Marc M BaumDepartment of Chemistry, Oak Crest Institute of Science, Pasadena, California 91107, USA.
Irina Butkyavichene
Joshua Gilman
Sean Kennedy
Etana Kopin
Amanda M Malone
Cali Nguyen
Thomas J Smith
David R Friend
Meredith R Clark
John A Moss
Auritec Pharmaceuticals (United States) · USOak Crest Institute of Science · USEastern Virginia Medical School · USUniversity of Kentucky · US

Funding

Intravaginal ring microbicide formulations comprising multiple anti-HIV agentsR21AI079791 · NIAID · OAK CREST INSTITUTE OF SCIENCE · PI SMITH, THOMAS J. · 2008 to 2009
$419k
Vaginal ring formulation of tenofovir microbicideR21AI076136 · NIAID · OAK CREST INSTITUTE OF SCIENCE · PI SMITH, THOMAS J. · 2009 to 2010
$411k
NIAID NIH HHS 5R21AI076136NIAID NIH HHS 5R21AI079791NIAID NIH HHS R21 AI076136NIAID NIH HHS R21 AI079791
6 · The paper itself

Abstract

Intravaginal delivery of microbicide combinations is a promising approach for the prevention of sexually transmitted infections, but requires a method of providing simultaneous, independent release of multiple agents into the vaginal compartment. A novel intravaginal ring (IVR) platform has been developed for simultaneous delivery of the reverse-transcriptase inhibitor tenofovir (TFV) and the guanosine analogue antiviral acyclovir (ACV) with independent control of release rate for each drug. The IVR is based on a pod design, with up to 10 individual polymer-coated drug cores embedded in the ring releasing through preformed delivery channels. The release rate from each pod is controlled independently of the others by the drug properties, polymer coating, and size and number of delivery channels. Pseudo-zero-order in vitro release of TFV (144 ± 10 µg day) and ACV (120 ± 19 µg day⁻¹) from an IVR containing both drugs was sustained for 28 days. The mechanical properties of the pod IVR were evaluated and compared with the commercially available Estring® (Pfizer, NY, NY). The pod-IVR design enables the vaginal delivery of multiple microbicides with differing physicochemical properties, and is an attractive approach for the sustained intravaginal delivery of relatively hydrophilic drugs that are difficult to deliver using conventional matrix IVR technology.

Indexed as

AcyclovirAdenineAdministration, IntravaginalAnimalsAntiviral AgentsDelayed-Action PreparationsDrug Delivery SystemsEquipment DesignFemaleHIVHIV InfectionsHumansOrganophosphonatesReverse Transcriptase InhibitorsSiliconTenofovirAcyclovirAdenineAntiviral AgentsDelayed-Action PreparationsOrganophosphonatesReverse Transcriptase InhibitorsSiliconTenofovir

Identifiers

PMID22619076
PMCPMC3857731
OpenAlexW2063191170

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.