Evidence map›Paper›PMID 36972400›Full record

ArticleACS nano2023

Unraveling an Alternative Mechanism in Polymer Self-Assemblies: An Order-Order Transition with Unusual Molecular Interactions between Hydrophilic and Hydrophobic Polymer Blocks.

Lukas Hahn, Theresa Zorn, Josef Kehrein, Tobias Kielholz, Anna-Lena Ziegler, Stefan Forster, Benedikt Sochor, Ekaterina S Lisitsyna, Nikita A Durandin, Timo Laaksonen and 6 more

Abstract read
In one paragraph

Article in ACS nano, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 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

16 authors.

Lukas HahnInstitute for Functional Materials and Biofabrication, Department of Chemistry and Pharmacy, Julius-Maximilians-University Würzburg, Röntgenring 11, 97070 Würzburg, Germany.
Theresa ZornCenter for Nanosystems Chemistry & Institute of Organic Chemistry, Department of Chemistry and Pharmacy, Julius-Maximilians-University Würzburg, Am Hubland, 97074 Würzburg, Germany.
Josef KehreinInstitute of Pharmacy and Food Chemistry, Department of Chemistry and Pharmacy, Julius-Maximilians-University Würzburg, Am Hubland, 97074 Würzburg, Germany.ORCID 0000-0003-4042-6762
Tobias KielholzInstitute of Pharmaceutical Technology and Buchmann Institute for Molecular Life Sciences, Goethe University Frankfurt, Max-von-Laue-Str. 9, 60438 Frankfurt am Main, Germany.
Anna-Lena ZieglerInstitute for Functional Materials and Biofabrication, Department of Chemistry and Pharmacy, Julius-Maximilians-University Würzburg, Röntgenring 11, 97070 Würzburg, Germany.
Stefan ForsterInstitute for Functional Materials and Biofabrication, Department of Chemistry and Pharmacy, Julius-Maximilians-University Würzburg, Röntgenring 11, 97070 Würzburg, Germany.
Benedikt SochorChair for X-Ray Microscopy, Julius-Maximilians-University Würzburg, Josef-Martin-Weg 63, 97074 Würzburg, Germany.ORCID 0000-0002-5772-8065
Ekaterina S LisitsynaFaculty of Engineering and Natural Science, Tampere University, Korkeakoulunkatu 8, 33720 Tampere, Finland.ORCID 0000-0003-4228-1157
Nikita A DurandinFaculty of Engineering and Natural Science, Tampere University, Korkeakoulunkatu 8, 33720 Tampere, Finland.ORCID 0000-0002-5734-7377
Timo LaaksonenFaculty of Engineering and Natural Science, Tampere University, Korkeakoulunkatu 8, 33720 Tampere, Finland.
Vladimir AseyevSoft Matter Chemistry, Department of Chemistry, Helsinki Institute of Sustainability Science, Faculty of Science, University of Helsinki, 00014 Helsinki, Finland.ORCID 0000-0002-3739-8089
Christoph SotrifferInstitute of Pharmacy and Food Chemistry, Department of Chemistry and Pharmacy, Julius-Maximilians-University Würzburg, Am Hubland, 97074 Würzburg, Germany.ORCID 0000-0003-4713-4068
Kay SaalwächterInstitute of Physics-NMR, Martin-Luther-Universität Halle-Wittenberg, Betty-Heimann-Str. 7, 06120 Halle, Germany.
Maike WindbergsInstitute of Pharmaceutical Technology and Buchmann Institute for Molecular Life Sciences, Goethe University Frankfurt, Max-von-Laue-Str. 9, 60438 Frankfurt am Main, Germany.ORCID 0000-0001-9475-699X
Ann-Christin PöpplerCenter for Nanosystems Chemistry & Institute of Organic Chemistry, Department of Chemistry and Pharmacy, Julius-Maximilians-University Würzburg, Am Hubland, 97074 Würzburg, Germany.
Robert LuxenhoferInstitute for Functional Materials and Biofabrication, Department of Chemistry and Pharmacy, Julius-Maximilians-University Würzburg, Röntgenring 11, 97070 Würzburg, Germany.ORCID 0000-0001-5567-7404

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polymer self-assembly leading to cooling-induced hydrogel formation is relatively rare for synthetic polymers and typically relies on H-bonding between repeat units. Here, we describe a non-H-bonding mechanism for a cooling-induced reversible order-order (sphere-to-worm) transition and related thermogelation of solutions of polymer self-assemblies. A multitude of complementary analytical tools allowed us to reveal that a significant fraction of the hydrophobic and hydrophilic repeat units of the underlying block copolymer is in close proximity in the gel state. This unusual interaction between hydrophilic and hydrophobic blocks reduces the mobility of the hydrophilic block significantly by condensing the hydrophilic block onto the hydrophobic micelle core, thereby affecting the micelle packing parameter. This triggers the order-order transition from well-defined spherical micelles to long worm-like micelles, which ultimately results in the inverse thermogelation. Molecular dynamics modeling indicates that this unexpected condensation of the hydrophilic corona onto the hydrophobic core is due to particular interactions between amide groups in the hydrophilic repeat units and phenyl rings in the hydrophobic ones. Consequently, changes in the structure of the hydrophilic blocks affecting the strength of the interaction could be used to control macromolecular self-assembly, thus allowing for the tuning of gel characteristics such as strength, persistence, and gelation kinetics. We believe that this mechanism might be a relevant interaction pattern for other polymeric materials as well as their interaction in and with biological environments. For example, controlling the gel characteristics could be considered important for applications in drug delivery or biofabrication.

Indexed as

inverse thermogelationmolecular dynamics simulationNMR spectroscopypoly(2-oxazine)poly(2-oxazoline)

Identifiers

PMID36972400
PMCPMC10100562

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Registered trials

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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.