Evidence map›Paper›PMID 33122907›Full record

ArticleInternational journal of nanomedicine2020

Comparative Encapsulation Efficiency of Lutein in Micelles Synthesized via Batch and High Throughput Methods.

Lauren E Cosby, Kil Ho Lee, Thomas J Knobloch, Christopher M Weghorst, Jessica O Winter

Open access · goldAbstract readComparative Study
In one paragraph

Article in International journal of nanomedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

2 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
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 1 institution in 1 country.

Lauren E CosbyBiomedical Engineering, The Ohio State University, Columbus, OH 43210, USA.
Kil Ho LeeWilliam G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH 43210, USA.ORCID 0000-0002-8114-0480
Thomas J KnoblochCollege of Public Health, Division of Environmental Health Sciences, The Ohio State University, Columbus, OH 43210, USA.ORCID 0000-0003-3445-2024
Christopher M WeghorstCollege of Public Health, Division of Environmental Health Sciences, The Ohio State University, Columbus, OH 43210, USA.ORCID 0000-0003-2973-3980
Jessica O WinterBiomedical Engineering, The Ohio State University, Columbus, OH 43210, USA.ORCID 0000-0002-5370-0137
The Ohio State University · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
Comprehensive Training in Oral &Craniofacial SciencesT32DE014320 · NIDCR · OHIO STATE UNIVERSITY · PI SHERIDAN, JOHN F · 2001 to 2022
$10.2M
Validation studies for interactive omics: Black raspberry metabolites and the oral microbiome in smokersU01CA188250 · NCI · OHIO STATE UNIVERSITY · PI CLINTON, STEVEN K, KUMAR, PURNIMA · 2014 to 2019
$3.6M
NCI NIH HHS P30 CA016058NCI NIH HHS U01 CA188250NIDCR NIH HHS T32 DE014320
6 · The paper itself

Abstract

purposeBlack raspberries (BRBs) and their anthocyanin-rich hydrophilic fractions (BRB-H) have exhibited significant chemopreventative activity across aerodigestive cancers. Lutein, the primary component of the BRB lipophilic fraction (BRB-L), also demonstrates bioactivity potential, but is less well characterized, in part because of its poor, innate bioavailability. For these lipophilic compounds to be accurately evaluated for anticancer efficacy, it is necessary to increase their functional bioavailability using delivery vehicles. Lutein has been delivered in commercial settings in emulsion form. However, emulsions are unstable, particularly in the gastrointestinal tract, which limit their use as an oral nutraceutical. Here, we evaluated lutein encapsulation and cellular uptake for nanoparticle (NP) delivery vehicles composed of three different materials synthesized via two different approaches.

methodsSpecifically, NPs were synthesized via smaller scale batch interfacial instability (II) sonication and semi-continuous high throughput electrohydrodynamic-mediated mixing nanoprecipitation (EM-NP) methods using polystyrene-polyethylene oxide (PSPEO) or polycaprolactone-polyethylene glycol (PCLPEG) block copolymers and PHOSPHOLIPON 90G

resultsNPs produced via high throughput EM-NP had higher EEs than NPs produced via batch II sonication, and P90G had the greatest EE (55%) and elicited faster cellular uptake in premalignant oral epithelial cells (SCC83) compared to other delivery systems.

conclusionThese qualities suggest P90G could be a beneficial candidate for future lutein in vitro delivery research and clinical translation for oral cancer prevention.

Indexed as

Anticarcinogenic AgentsCell LineDrug Delivery SystemsHumansHydrophobic and Hydrophilic InteractionsLuteinMicellesNanoparticlesNanotechnologyParticle SizePolyestersPolyethylene GlycolsPolymersPrecancerous ConditionsAnticarcinogenic AgentsLuteinMicellespolycaprolactonePolyestersPolyethylene GlycolsPolymersblack raspberriesemulsificationluteinnanoprecipitationoral cancerscalable nanomanufacturing

Identifiers

PMID33122907
PMCPMC7591007
OpenAlexW3094162621

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.