Evidence map›Paper›PMID 28536462›Full record

ArticleScientific reports2017

Surface PEGylation of Mesoporous Silica Nanorods (MSNR): Effect on loading, release, and delivery of mitoxantrone in hypoxic cancer cells.

Amit Wani, Galbokka H Layan Savithra, Ayat Abyad, Shrey Kanvinde, Jing Li, Stephanie Brock, David Oupický

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 49 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Amit WaniDepartment of Pharmaceutical Sciences, Wayne State University, Detroit, MI, 48201, USA.
Galbokka H Layan SavithraDepartment of Chemistry, Wayne State University, Detroit, MI, 48202, USA.
Ayat AbyadDepartment of Chemistry, Wayne State University, Detroit, MI, 48202, USA.
Shrey KanvindeDepartment of Pharmaceutical Sciences, Center for Drug Delivery and Nanomedicine, University of Nebraska Medical Center, Omaha, NE, 68198, United States.
Jing LiDepartment of Pharmaceutical Sciences, Center for Drug Delivery and Nanomedicine, University of Nebraska Medical Center, Omaha, NE, 68198, United States.
Stephanie BrockDepartment of Chemistry, Wayne State University, Detroit, MI, 48202, USA.
David OupickýDepartment of Pharmaceutical Sciences, Wayne State University, Detroit, MI, 48201, USA. david.oupicky@unmc.edu.
Wayne State University · USUniversity of Nebraska Medical Center · US

Funding

Multilayered redox-responsive nanoparticles for delivery of drug-siRNA combinatioR01EB015216 · NIBIB · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI OUPICKY, DAVID · 2014 to 2017
$1.3M
NIBIB NIH HHS R01 EB015216
6 · The paper itself

Abstract

Mesoporous silica nanomaterials show great potential to deliver chemotherapeutics for cancer treatment. The key challenges in the development of injectable mesoporous silica formulations are colloidal instability, hemolysis and inefficient drug loading and release. In this study, we evaluated the effect of PEGylation of mesoporous silica nanorods (MSNR) on hemolysis, colloidal stability, mitoxantrone (MTX) loading, in vitro MTX release, and cellular MTX delivery under hypoxic conditions. We found that PEGylation prevented dose-dependent hemolysis in the concentrations studied (0-10 mg/ml) and improved colloidal stability of MSNR. A negative effect of PEGylation on MTX loading was observed but PEGylated MSNR (PMSNR) demonstrated increased MTX release compared to non-PEGylated particles. Under hypoxic conditions, a decrease in the IC50 of MTX and MTX-loaded MSNR was observed when compared to normoxic conditions. These results showed that MSNR could deliver the chemotherapeutic agent, MTX to tumor cells and induce effective cell killing. However, the effect of PEGylation needs to be carefully studied due to the observed adverse effect on drug loading.

Indexed as

AnimalsAntineoplastic AgentsCell HypoxiaCell Line, TumorCell SurvivalDrug Delivery SystemsDrug LiberationHemolysisHumansMitoxantroneNanotubesNeoplasmsPolyethylene GlycolsPorositySheepSilicon DioxideAntineoplastic AgentsMitoxantronePolyethylene GlycolsSilicon Dioxide

Identifiers

PMID28536462
PMCPMC5442097
OpenAlexW2615884758

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.