Evidence map›Paper›PMID 30627887›Full record

ArticleAAPS PharmSciTech2019

Development of Theranostic Perfluorocarbon Nanoemulsions as a Model Non-Opioid Pain Nanomedicine Using a Quality by Design (QbD) Approach.

Michele Herneisey, Lu Liu, Eric Lambert, Nicholas Schmitz, Shannon Loftus, Jelena M Janjic

Abstract read
In one paragraph

Article in AAPS PharmSciTech, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 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

6 authors.

Michele HerneiseyGraduate School of Pharmaceutical Sciences, School of Pharmacy, Duquesne University, Pittsburgh, Pennsylvania, 15282, USA.
Lu LiuGraduate School of Pharmaceutical Sciences, School of Pharmacy, Duquesne University, Pittsburgh, Pennsylvania, 15282, USA.
Eric LambertGraduate School of Pharmaceutical Sciences, School of Pharmacy, Duquesne University, Pittsburgh, Pennsylvania, 15282, USA.
Nicholas SchmitzGraduate School of Pharmaceutical Sciences, School of Pharmacy, Duquesne University, Pittsburgh, Pennsylvania, 15282, USA.
Shannon LoftusDepartment of Biology, The University of Scranton, Scranton, Pennsylvania, 18510, USA.
Jelena M JanjicGraduate School of Pharmaceutical Sciences, School of Pharmacy, Duquesne University, Pittsburgh, Pennsylvania, 15282, USA. janjicj@duq.edu.

Funding

Multimodal (PET/MR/NIR) imaging supported drug delivery in inflammatory diseasesR21EB023104 · NIBIB · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ANDERSON, CAROLYN J., JANJIC, JELENA M · 2016 to 2017
$409k
Theranostic Pain Nanomedicines: imaging inflammation, reducing pain and need for opioidsR21DA039621 · NIDA · DUQUESNE UNIVERSITY · PI JANJIC, JELENA M · 2015 to 2016
$328k
Dual Mode Nanoemulsions for 19F MRI and Fluorescence DetectionR41EB009618 · NIBIB · CELSENSE, INC. · PI JANJIC, JELENA M · 2009 to 2009
$132k
NIBIB NIH HHS R21 EB023104NIBIB NIH HHS R41 EB009618NIDA NIH HHS R21 DA039621
6 · The paper itself

Abstract

Pain nanomedicine is an emerging field in response to current needs of addressing the opioid crisis in the USA and around the world. Our group has focused on the development of macrophage-targeted perfluorocarbon nanoemulsions as inflammatory pain nanomedicines over the past several years. We present here, for the first time, a quality by design approach used to design pain nanomedicine. Specifically, we used failure mode, effects, and criticality analysis (FMECA) which identified the process and composition parameters that were most likely to impact nanoemulsion critical quality attributes (CQAs). From here, we applied a unique combination approach that compared multiple linear regression, boosted decision tree regression, and partial least squares regression methods in combination with correlation plots. The presented combination approach allowed for in-depth analyses of which formulation steps in the nanoemulsification processes control nanoemulsion droplet diameter, stability, and drug loading. We identified that increase in solubilizer (transcutol) content increased drug loading and decreased nanoemulsion stability. This was mitigated by inclusion of perfluorocarbon oil in the internal phase. We observed negative correlation (R

Indexed as

Analgesics, Non-NarcoticCelecoxibDrug DevelopmentEmulsionsFluorocarbonsNanoparticlesSonicationTheranostic NanomedicineAnalgesics, Non-NarcoticCelecoxibEmulsionsFluorocarbonsmultiple linear regressionpain nanomedicineQuality by designrisk assessmenttheranostic perfluorocarbon nanoemulsion

Identifiers

PMID30627887
PMCPMC10290815

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.