Evidence map›Paper›PMID 25231193›Full record

ArticleJournal of pharmaceutical sciences2014

An intravaginal ring for the sustained delivery of antibodies.

Manjula Gunawardana, Marc M Baum, Thomas J Smith, John A Moss

Abstract read
In one paragraph

Article in Journal of pharmaceutical sciences, 2014. 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
3.5field-weighted citation impact, top 8% 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, 36 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Fabrication and characterization of bioprints with Lactobacillus crispatus for vaginal application.Journal of controlled release : official journal of the Controlled Release Society · 2023
    Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. 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
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. A novel intravaginal ring to prevent HIV-1, HSV-2, HPV, and unintended pregnancy.Journal of controlled release : official journal of the Controlled Release Society · 2015
    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

4 authors at 2 institutions in 1 country.

Manjula GunawardanaDepartment of Chemistry, Oak Crest Institute of Science, Pasadena, California; Auritec Pharmaceuticals, Inc., Pasadena, California.
Marc M BaumDepartment of Chemistry, Oak Crest Institute of Science, Pasadena, California.
Thomas J SmithDepartment of Chemistry, Oak Crest Institute of Science, Pasadena, California; Auritec Pharmaceuticals, Inc., Pasadena, California.
John A MossDepartment of Chemistry, Oak Crest Institute of Science, Pasadena, California. Electronic address: j.moss@oak-crest.org.
Auritec Pharmaceuticals (United States) · USOak Crest Institute of Science · US

Funding

Vaginal mAB Delivery SystemsU19AI096398 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ANDERSON, DEBORAH J, MOENCH, THOMAS RAY · 2011 to 2016
$15.0M
NIAID NIH HHS U19 AI096398NIAID NIH HHS U19AI096398
6 · The paper itself

Abstract

Human monoclonal antibodies (mAbs) based on IgG and IgA have shown promise as topical microbicide candidates to protect women from HIV infection. Application of mAbs has been limited, however, by the inability of vaginal gels and conventional intravaginal ring (IVR) designs, the predominant vaginal product formulations, to effectively deliver biomolecules in a coitally independent fashion with retention of bioactivity. We have developed a novel pod-IVR platform that delivers ovine IgG (ov-IgG) as a model for IgG and IgA human mAbs. In vitro release of ov-IgG from the pod-IVRs was sustained for 14 days. Facile control of release rate was achieved by changing the size of delivery channels in the ring structure, and the feasibility of ov-IgG delivery in the range 0.5-30 mg day(-1) from a 10-pod IVR was demonstrated. The activity of ov-IgG in pod-IVR formulations was maintained as confirmed by ELISA binding assay. Pod-IVRs delivering ov-IgG show promise for the effective sustained topical delivery of antibody-based microbicides. This significantly broadens the range of microbicides that can be delivered in a sustained fashion from IVRs and enables a new arsenal of topical biologic microbicide candidates beyond small molecule antiretrovirals.

Indexed as

Drug CarriersAdministration, IntravaginalAnimalsAntibodies, MonoclonalAnti-HIV AgentsChemistry, PharmaceuticalDrug ImplantsDrug StabilityEquipment DesignFeasibility StudiesFemaleHIV InfectionsHumansImmunoglobulin GKineticsModels, ChemicalAntibodies, MonoclonalAnti-HIV AgentsDrug CarriersDrug ImplantsImmunoglobulin GPolyesterspoly(lactide)Siliconescontrolled deliverydrug delivery systemsHIV/AIDSlyophilizationmacromolecular drug deliverymucosal drug deliverypoly(lactic/glycolic) acid (PLGA or PLA)

Identifiers

PMID25231193
PMCPMC4206599
OpenAlexW2090044939

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.