Evidence map›Paper›PMID 31394320›Full record

ArticleJournal of colloid and interface science2019

Extended release of dexamethasone from oleogel based rods.

Russell Macoon, Timothy Guerriero, Anuj Chauhan

Open access · greenAbstract read
In one paragraph

Article in Journal of colloid and interface science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Recent Advances in Kaolinite Nanoclay as Drug Carrier for Bioapplications: A Review.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Review
  5. Development of fiber opticADMET & DMPK · 2022
    Article
  6. Article
  7. Ophthalmic delivery of hydrophilic drugs through drug-loaded oleogels.European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences · 2021
    Article
  8. Article
  9. In vitro release of hydrophobic drugs by oleogel rods with biocompatible gelators.European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences · 2020
    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 2 institutions in 1 country.

Russell MacoonDepartment of Chemical Engineering, University of Florida, Gainesville, FL 32611, United States. Electronic address: rmacoon@ufl.edu.
Timothy GuerrieroDepartment of Chemical Engineering, University of Florida, Gainesville, FL 32611, United States. Electronic address: timg386@ufl.edu.
Anuj ChauhanDepartment of Chemical Engineering, Colorado School of Mines, Golden, CO 80401, United States. Electronic address: chauhan@mines.edu.
University of Florida · USColorado School of Mines · US

Funding

RESEARCH TRAINING IN VISION SCIENCET32EY007132 · NEI · UNIVERSITY OF FLORIDA · PI W CLAY SMITH · 1991 to 2026
$3.8M
NEI NIH HHS T32 EY007132
6 · The paper itself

Abstract

hypothesisTopical and systemic methods are not able to deliver ophthalmic drugs for treatment of retinal diseases. Consequently, invasive monthly intravitreal injections through the eyeball are required to deliver retinal drugs. A reduction in the frequency of the injection through extended release of the drugs could have significant clinical benefits. EXPERIMENTS: Oleogels containing ethyl cellulose as the gelator at 10% (wt%) in soybean oil were loaded with dexamethasone above the solubility limit and expunged from a syringe to create cylindrical rods for extended drug delivery. The devices were imaged to explore particle distribution and drug release was measured under sink conditions in buffer. A model was developed and fitted to data to determine effective drug diffusivity.

findingsDexamethasone is released slowly due to the presence of the drug particles that serve as drug depots. The release increases from 600 to 3000 h as the drug loading is increased from 3% to 28%. The release profiles can be modeled by considering drug dissolution and diffusion, as well as the tortuosity of the matrix due to the presence of the voids formed after the drug particles have dissolved. The proposed approach is promising as the release profiles of the drug are comparable to commercial devices.

Indexed as

CelluloseDexamethasoneOrganic ChemicalsParticle SizeSolubilitySurface PropertiesCelluloseDexamethasoneethyl celluloseoleogelsOrganic ChemicalsDexamethasoneDrug deliveryModelingOleogelPosterior segment

Identifiers

PMID31394320
PMCPMC6764860
OpenAlexW2966589155

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.