Evidence map›Paper›PMID 29170116›Full record

ArticleInternational journal of pharmaceutics2018

In vivo controlled release of fenretinide from long-acting release depots for chemoprevention of oral squamous cell carcinoma recurrence.

Kari Nieto, Ping Pei, Daren Wang, Susan R Mallery, Steven P Schwendeman

Abstract read
In one paragraph

Article in International journal of pharmaceutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Leukoplakia and Immunology: New Chemoprevention Landscapes?International journal of molecular sciences · 2020
    Review
  6. Article
  7. 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 at 3 institutions in 1 country.

Kari NietoDepartment of Pharmaceutical Sciences, The Biointerfaces Institute, University of Michigan, 2800 Plymouth Rd, Ann Arbor, MI, 48109, United States. Electronic address: kariblai@umich.edu.
Ping PeiDivision of Oral Maxillofacial Pathology & Radiology Ohio State University, 305 W. 12thAve, Columbus, OH, 43210, United States. Electronic address: pei.4@osu.edu.
Daren WangDivision of Oral Maxillofacial Pathology & Radiology Ohio State University, 305 W. 12thAve, Columbus, OH, 43210, United States. Electronic address: wang.7277@osu.edu.
Susan R MalleryDivision of Oral Maxillofacial Pathology & Radiology Ohio State University, 305 W. 12thAve, Columbus, OH, 43210, United States. Electronic address: mallery.1@osu.edu.
Steven P SchwendemanDepartment of Pharmaceutical Sciences, The Biointerfaces Institute, University of Michigan, 2800 Plymouth Rd, Ann Arbor, MI, 48109, United States; Department of Biomedical Engineering, University of Michigan, 2200 Bonisteel Blvd, Ann Arbor, MI, 48109, United States. Electronic address: schwende@umich.edu.
The Ohio State University · USBioSurfaces (United States) · USUniversity of Michigan–Ann Arbor · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Assessment of Chemopreventive Effects of a Mucoadhesive Fenretinide Patch on Premalignant Oral Epithelial LesionsR01CA227273 · NCI · OHIO STATE UNIVERSITY · PI MALLERY, SUSAN R · 2019 to 2024
$2.8M
Secondary Chemoprevention of Oral Cancer by Locally Delivered AgentsR01CA211611 · NCI · OHIO STATE UNIVERSITY · PI MALLERY, SUSAN R · 2017 to 2021
$1.8M
Evaluation of locally-delivered fenretinide and black raspberries for oral cancerR01CA171329 · NCI · OHIO STATE UNIVERSITY · PI MALLERY, SUSAN R · 2012 to 2016
$1.6M
NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA171329NCI NIH HHS R01 CA211611NCI NIH HHS R01 CA227273
6 · The paper itself

Abstract

Local, long-acting release fenretinide (4HPR) millicylindrical implants were prepared and evaluated for their release kinetics in vivo and their ability to suppress oral cancer tumor explant growth. Poly(lactic-co-glycolic acid)(PLGA) implants were prepared as a function of drug loading and the presence of various excipients (pore-formers, solubilizers, crystallization inhibitors) to enhance release of the insoluble 4HPR. Release kinetics and bioerosion of PLGA were monitored both in vitro in a PBS/Tween 80 buffer and in vivo by recovery of the drug remaining at the injection site. 4HPR was released from PLGA implants much slower in vivo than in the drug solubilizing media in vitro, with a 3-week lag phase and continuous release of >2 months, but showed some release enhancement by addition of solubilizers. Water-soluble PVA/sucrose implants for release of 4HPR served to determine if drug dissolution provided suitable controlled release without the PLGA, and this formulation showed continuous drug release over 6 weeks in vivo. Placement of PLGA-4HPR implants adjacent to oral cancer tumor murine xenografts showed inhibition of tumor growth relative to sham implants, indicating the potential for the local 4HPR delivery approach to be useful for oral cancer chemoprevention.

Indexed as

AnimalsAnticarcinogenic AgentsCarcinoma, Squamous CellCell Line, TumorChemopreventionDelayed-Action PreparationsDrug CarriersDrug ImplantsDrug LiberationExcipientsFenretinideHumansLactic AcidMaleMiceMice, NudeAnticarcinogenic AgentsDelayed-Action PreparationsDrug CarriersDrug ImplantsExcipientsFenretinideLactic AcidPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerControlled releaseFenretinideIn vivo releaseLocal deliveryOral cancerPLGA

Identifiers

PMID29170116
PMCPMC6460921
OpenAlexW2768511318

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.