Evidence map›Paper›PMID 31323243›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2019

Noninvasive characterization of in situ forming implant diffusivity using diffusion-weighted MRI.

Kelsey A Hopkins, Nicole Vike, Xin Li, Jacqueline Kennedy, Emma Simmons, Joseph Rispoli, Luis Solorio

Abstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

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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

7 authors.

Kelsey A HopkinsWeldon School of Biomedical Engineering, Purdue University, 206 S. Martin Jischke Dr., West Lafayette, IN 47907, USA.
Nicole VikeBasic Medical Sciences, College of Veterinary Medicine, Purdue University, 625 Harrison St., West Lafayette, IN 47907, USA.
Xin LiWeldon School of Biomedical Engineering, Purdue University, 206 S. Martin Jischke Dr., West Lafayette, IN 47907, USA.
Jacqueline KennedyWeldon School of Biomedical Engineering, Purdue University, 206 S. Martin Jischke Dr., West Lafayette, IN 47907, USA.
Emma SimmonsWeldon School of Biomedical Engineering, Purdue University, 206 S. Martin Jischke Dr., West Lafayette, IN 47907, USA.
Joseph RispoliWeldon School of Biomedical Engineering, Purdue University, 206 S. Martin Jischke Dr., West Lafayette, IN 47907, USA; Electrical and Computer Engineering, Purdue University, 465 Northwestern Ave., West Lafayette, IN 47907, USA; Center for Cancer Research, Purdue University, 201 S. University St., West Lafayette, IN 47907, USA. Electronic address: jrispoli@purdue.edu.
Luis SolorioWeldon School of Biomedical Engineering, Purdue University, 206 S. Martin Jischke Dr., West Lafayette, IN 47907, USA; Center for Cancer Research, Purdue University, 201 S. University St., West Lafayette, IN 47907, USA. Electronic address: lsolorio@purdue.edu.

Funding

Transgenic Mouse Core Facility Shared Resource (TMCF-SR)P30CA023168 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI John Tesmer · 1985 to 2026
$43.4M
Engineering the Cancer MicroenvironmentR00CA198929 · NCI · PURDUE UNIVERSITY · PI SOLORIO, LUIS · 2017 to 2019
$697k
Prescription Opioid Formulation to Deter Extraction, Injection, Insufflation, and SmokingR21DA048074 · NIDA · PURDUE UNIVERSITY · PI SOLORIO, LUIS · 2019 to 2020
$420k
Removable second-order trap for common-mode current suppression in multi-nuclear MRI cablingR03EB026231 · NIBIB · PURDUE UNIVERSITY · PI RISPOLI, JOSEPH V · 2018 to 2019
$143k
NCI NIH HHS P30 CA023168NCI NIH HHS R00 CA198929NIBIB NIH HHS R03 EB026231NIDA NIH HHS R21 DA048074
6 · The paper itself

Abstract

In situ forming implants (ISFIs) form a solid drug-eluting depot, releasing drug for an extended period of time after a minimally-invasive injection. Clinical use of ISFIs has been limited because many factors affect drug release kinetics. The aim of this study was to use diffusion-weighted MRI (DWI) to noninvasively quantify spatial-temporal changes in implant diffusivity in situ. ISFIs were formed using poly(lactic-co-glycolic) acid, with a molecular weight of either 15 kDa or 52 kDa, and fluorescein as the mock drug. Drug release, polymer erosion, polymer degradation, and implant diffusivity were analyzed in vitro over 21 days. DWI was also performed in vivo over 5 days. Spatial diffusivity maps of the implant were generated using DWI data. Results showed constant diffusivity at the implant shell ((1.17 ± 0.13) × 10

Indexed as

AnimalsContrast MediaDiffusionDiffusion Magnetic Resonance ImagingDrug Delivery SystemsDrug ImplantsDrug LiberationDrug MonitoringFluoresceinFluorescent DyesMaleMice, Inbred C57BLPolylactic Acid-Polyglycolic Acid CopolymerContrast MediaDrug ImplantsFluoresceinFluorescent DyesPolylactic Acid-Polyglycolic Acid CopolymerControlled releaseDiffusion-weighted imagingDiffusivityDrug deliveryin situ forming implantsMRI

Identifiers

PMID31323243
PMCPMC6815723

What OpenQuestion holds

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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.