Evidence map›Paper›PMID 36634053›Full record

ArticlePloS one2023

Distribution and inflammatory cell response to intracranial delivery of radioluminescent Y2(SiO4)O:Ce particles.

Máté Fischer, Amber Zimmerman, Eric Zhang, Joseph Kolis, Ashley Dickey, Mary K Burdette, Praveen Chander, Stephen H Foulger, Jonathan L Brigman, Jason P Weick

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 58% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 2 institutions in 1 country.

Máté FischerDepartment of Neurosciences, University of New Mexico HSC, Albuquerque, New Mexico, United States of America.ORCID 0000-0002-6970-5039
Amber ZimmermanDepartment of Neurosciences, University of New Mexico HSC, Albuquerque, New Mexico, United States of America.
Eric ZhangDepartment of Materials Science and Engineering, Clemson University, Clemson, South Carolina, United States of America.
Joseph KolisDepartment of Materials Science and Engineering, Clemson University, Clemson, South Carolina, United States of America.
Ashley DickeyDepartment of Materials Science and Engineering, Clemson University, Clemson, South Carolina, United States of America.
Mary K BurdetteDepartment of Materials Science and Engineering, Clemson University, Clemson, South Carolina, United States of America.
Praveen ChanderDepartment of Neurosciences, University of New Mexico HSC, Albuquerque, New Mexico, United States of America.
Stephen H FoulgerDepartment of Materials Science and Engineering, Clemson University, Clemson, South Carolina, United States of America.
Jonathan L BrigmanDepartment of Neurosciences, University of New Mexico HSC, Albuquerque, New Mexico, United States of America.
Jason P WeickDepartment of Neurosciences, University of New Mexico HSC, Albuquerque, New Mexico, United States of America.ORCID 0000-0003-3135-9860
Clemson University · USUniversity of New Mexico · US

Funding

University of New Mexico (UNM) Center for Brain Recovery and RepairP20GM109089 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI SHUTTLEWORTH, CLAUDE W · 2015 to 2024
$22.7M
Molecular mechanisms of excitatory postsynaptic diversityR01NS116051 · NINDS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI WEICK, JASON P · 2021 to 2025
$1.8M
Light-based regulation of autophagy processing to target pathological forms of tauR21NS093442 · NINDS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI BHASKAR, KIRAN, WEICK, JASON P · 2016 to 2017
$417k
Functional integration and plasticity of human ESC-derived neuronsR03NS074281 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI WEICK, JASON P · 2011 to 2012
$149k
NIGMS NIH HHS P20 GM109089NINDS NIH HHS R01 NS116051NINDS NIH HHS R03 NS074281
6 · The paper itself

Abstract

Due to increasing advances in their manufacture and functionalization, nanoparticle-based systems have become a popular tool for in vivo drug delivery and biodetection. Recently, scintillating nanoparticles such as yttrium orthosilicate doped with cerium (Y2(SiO4)O:Ce) have come under study for their potential utility in optogenetic applications, as they emit photons upon low levels of stimulation from remote x-ray sources. The utility of such nanoparticles in vivo is hampered by rapid clearance from circulation by the mononuclear phagocytic system, which heavily restricts nanoparticle accumulation at target tissues. Local transcranial injection of nanoparticles may deliver scintillating nanoparticles to highly specific brain regions by circumventing the blood-brain barrier and avoiding phagocytic clearance. Few studies to date have examined the distribution and response to nanoparticles following localized delivery to cerebral cortex, a crucial step in understanding the therapeutic potential of nanoparticle-based biodetection in the brain. Following the synthesis and surface modification of these nanoparticles, two doses (1 and 3 mg/ml) were introduced into mouse secondary motor cortex (M2). This region was chosen as the site for RLP delivery, as it represents a common target for optogenetic manipulations of mouse behavior, and RLPs could eventually serve as an injectable x-ray inducible light delivery system. The spread of particles through the target tissue was assessed 24 hours, 72 hours, and 9 days post-injection. Y2(SiO4)O:Ce nanoparticles were found to be detectable in the brain for up to 9 days, initially diffusing through the tissue until 72 hours before achieving partial clearance by the final endpoint. Small transient increases in the presence of IBA-1+ microglia and GFAP+ astrocytic cell populations were detected near nanoparticle injection sites of both doses tested 24 hours after surgery. Taken together, these data provide evidence that Y2(SiO4)O:Ce nanoparticles coated with BSA can be injected directly into mouse cortex in vivo, where they persist for days and are broadly tolerated, such that they may be potentially utilized for remote x-ray activated stimulation and photon emission for optogenetic experiments in the near future.

Indexed as

BrainNanoparticlesAnimalsBiological TransportBlood-Brain BarrierDrug Delivery SystemsMice

Identifiers

PMID36634053
PMCPMC9836305
OpenAlexW4315753896

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.