Evidence map›Paper›PMID 34361131›Full record

ArticleNanomaterials (Basel, Switzerland)2021

Cyanine-5-Driven Behaviours of Hyperbranched Polymers Designed for Therapeutic Delivery Are Cell-Type Specific and Correlated with Polar Lipid Distribution in Membranes.

Joshua D Simpson, Denni L Currin-Ross, Gayathri R Ediriweera, Horst Joachim Schirra, Nicholas L Fletcher, Craig A Bell, Maria C Arno, Kristofer J Thurecht

Abstract read
In one paragraph

Article in Nanomaterials (Basel, Switzerland), 2021. 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
–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

0 citing papers in PubMed.

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

8 authors.

Joshua D SimpsonAustralian Institute for Bioengineering & Nanotechnology, University of Queensland, St. Lucia, QLD 4072, Australia.ORCID 0000-0002-8823-8130
Denni L Currin-RossCentre for Advanced Imaging, University of Queensland, St. Lucia, QLD 4072, Australia.ORCID 0000-0001-5514-2071
Gayathri R EdiriweeraAustralian Institute for Bioengineering & Nanotechnology, University of Queensland, St. Lucia, QLD 4072, Australia.
Horst Joachim SchirraCentre for Advanced Imaging, University of Queensland, St. Lucia, QLD 4072, Australia.ORCID 0000-0002-7541-246X
Nicholas L FletcherAustralian Institute for Bioengineering & Nanotechnology, University of Queensland, St. Lucia, QLD 4072, Australia.ORCID 0000-0002-2993-833X
Craig A BellAustralian Institute for Bioengineering & Nanotechnology, University of Queensland, St. Lucia, QLD 4072, Australia.ORCID 0000-0002-8986-2795
Maria C ArnoSchool of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.ORCID 0000-0003-1734-4777
Kristofer J ThurechtAustralian Institute for Bioengineering & Nanotechnology, University of Queensland, St. Lucia, QLD 4072, Australia.ORCID 0000-0002-4100-3131

Funding

Australian Research Council CE140100036Australian Research Council IC170100035Australian Research Council LP180100486National Health and Medical Research Council APP1148582
6 · The paper itself

Abstract

The ability to predict the behaviour of polymeric nanomedicines can often be obfuscated by subtle modifications to the corona structure, such as incorporation of fluorophores or other entities. However, these interactions provide an intriguing insight into how selection of molecular components in multifunctional nanomedicines contributes to the overall biological fate of such materials. Here, we detail the internalisation behaviours of polymeric nanomedicines across a suite of cell types and extrapolate data for distinguishing the underlying mechanics of cyanine-5-driven interactions as they pertain to uptake and endosomal escape. By correlating the variance of rate kinetics with endosomal escape efficiency and endogenous lipid polarity, we identify that observed cell-type dependencies correspond with an underlying susceptibility to dye-mediated effects and nanomedicine accumulation within polar vesicles. Further, our results infer that the ability to translocate endosomal membranes may be improved in certain cell types, suggesting a potential role for diagnostic moieties in trafficking of drug-loaded nanocarriers.

Indexed as

cellular uptakeendosomal escapefluorescencematerials designnanomedicinepolymerstrafficking

Identifiers

PMID34361131
PMCPMC8308131

What OpenQuestion holds

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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.