Evidence map›Paper›PMID 32090217›Full record

ArticleNanoscale2020

Employing bicontinuous-to-micellar transitions in nanostructure morphology for on-demand photo-oxidation responsive cytosolic delivery and off-on cytotoxicity.

Sharan Bobbala, Sean D Allen, Sijia Yi, Michael Vincent, Molly Frey, Nicholas B Karabin, Evan A Scott

Abstract read
In one paragraph

Article in Nanoscale, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 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.

Sharan BobbalaDepartment of Biomedical Engineering, Northwestern University, Evanston, Illinois 60208, USA. evan.scott@northwestern.edu.
Sean D AllenInterdepartmental Biological Sciences Program, Northwestern University, Evanston, Illinois 60208, USA.
Sijia YiChemistry of Life Processes Institute, Northwestern University, Evanston, Illinois 60208, USA.
Michael VincentDepartment of Biomedical Engineering, Northwestern University, Evanston, Illinois 60208, USA. evan.scott@northwestern.edu.
Molly FreyInterdepartmental Biological Sciences Program, Northwestern University, Evanston, Illinois 60208, USA.
Nicholas B KarabinDepartment of Biomedical Engineering, Northwestern University, Evanston, Illinois 60208, USA. evan.scott@northwestern.edu.
Evan A ScottDepartment of Biomedical Engineering, Northwestern University, Evanston, Illinois 60208, USA. evan.scott@northwestern.edu and Interdepartmental Biological Sciences Program, Northwestern University, Evanston, Illinois 60208, USA and Chemistry of Life Processes Institute, Northwestern University, Evanston, Illinois 60208, USA and Simpson Querrey Institute, Northwestern University, Chicago, Illinois 60611, USA.ORCID http://orcid.org/0000-0002-8945-2892

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LEONIDAS C. PLATANIAS · 1993 to 2026
$153.9M
Chemistry of Life Processes Predoctoral Training ProgramT32GM105538 · NIGMS · NORTHWESTERN UNIVERSITY · PI KELLEHER, NEIL L · 2013 to 2022
$2.7M
Development of combination immunotherapies for atherosclerotic inflammationDP2HL132390 · NHLBI · NORTHWESTERN UNIVERSITY · PI SCOTT, EVAN ALEXANDER · 2015 to 2015
$2.3M
Leveraging immunostimulatory pathways that enhance BCG vaccination for the rational design of synthetic neonatal vaccine formulationsR21AI137932 · NIAID · NORTHWESTERN UNIVERSITY · PI DOWLING, DAVID JAMES, SCOTT, EVAN ALEXANDER · 2019 to 2020
$468k
NCI NIH HHS P30 CA060553NHLBI NIH HHS DP2 HL132390NIAID NIH HHS R21 AI137932NIGMS NIH HHS T32 GM105538
6 · The paper itself

Abstract

Bicontinuous nanospheres (BCNs) are underutilized self-assembled nanostructures capable of simultaneous delivery of both hydrophilic and hydrophobic payloads. Here, we demonstrate that BCNs assembled from poly(ethylene glycol)-block-poly(propylene sulfide) (PEG-b-PPS), an oxidation-sensitive copolymer, are stably retained within cell lysosomes following endocytosis, resisting degradation and payload release for days until externally triggered. The oxygen scavenging properties and enhanced stability of the bicontinuous PEG-b-PPS nanoarchitecture significantly protected cells from typically cytotoxic application of pro-apoptotic photo-oxidizer pheophorbide A and chemotherapeutic camptothecin. The photo-oxidation triggered transition from a bicontinuous to micellar morphology overcame this stability, allowing on-demand cytosolic delivery of camptothecin for enhanced control over off-on cytotoxicity. These results indicate that inducible transitions in the nanostructure morphology can influence intracellular stability and toxicity of self-assembled nanotherapeutics.

Indexed as

LightMicellesAnimalsAntineoplastic Agents, PhytogenicCamptothecinCell SurvivalChlorophyllCytosolDrug CarriersEndocytosisLysosomesMiceNanostructuresOxidation-ReductionPolyethylene GlycolsRAW 264.7 CellsAntineoplastic Agents, PhytogenicCamptothecinChlorophyllDrug CarriersMicellespheophorbide aPolyethylene Glycolspoly(ethylene glycol)-stabilized poly(propylene sulfide)Singlet OxygenSulfides

Identifiers

PMID32090217
PMCPMC7197099

What OpenQuestion holds

Textmetadata
LicenceTDM
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.