Amphiphilic Polymers: Synthesis, Characterization, Theory and Simulation

A special issue of Polymers (ISSN 2073-4360). This special issue belongs to the section "Polymer Physics and Theory".

Deadline for manuscript submissions: closed (10 December 2022) | Viewed by 5840

Special Issue Editor


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Guest Editor
Department of Mathematics and Physics, University of Lincoln, Lincoln LN6 7TS, UK
Interests: polymers; glass transition; liquids at interfaces; statistical mechanics

Special Issue Information

Dear Colleagues,

Amphiphilic polymers can self-assemble into a wide variety of structures, ranging from simple spherical micelles to complex compound vesicles, which can be used in applications including the encapsulation and delivery of drugs and the construction of artificial cell components. The structures that form depend sensitively on the interaction of several factors, including the architecture of the amphiphilic polymers themselves and the dynamics of the self-assembly process. 

This complexity means that modeling has an important role to play in understanding existing experimental results and guiding future investigations, and this is the motivation for this Special Issue on the theory and simulation of amphiphilic polymers. Submissions are welcome based on any modeling approach, on both the fundamental science and the applications of these molecules, and can be either original research or reviews.

Dr. Martin Greenall
Guest Editor

Manuscript Submission Information

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Keywords

  • amphiphilic polymers
  • self-assembly
  • theory
  • simulation
  • coarse-grained models
  • statistical mechanics

Published Papers (3 papers)

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Research

14 pages, 3017 KiB  
Article
Hedgehog, Chamomile and Multipetal Polymeric Structures on the Nanoparticle Surface: Theoretical Insights
by Aleksandra S. Ushakova and Valentina V. Vasilevskaya
Polymers 2022, 14(20), 4358; https://0-doi-org.brum.beds.ac.uk/10.3390/polym14204358 - 16 Oct 2022
Cited by 2 | Viewed by 1148
Abstract
An analytical theory describing the variety of different morphological structures that spontaneously self-assemble in layers of amphiphilic homopolymers tightly grafted to spherical nanoparticle is proposed. For this purpose, the following structures were identified and outlined: hedgehogs, in which macromolecules are combined into cylindrical [...] Read more.
An analytical theory describing the variety of different morphological structures that spontaneously self-assemble in layers of amphiphilic homopolymers tightly grafted to spherical nanoparticle is proposed. For this purpose, the following structures were identified and outlined: hedgehogs, in which macromolecules are combined into cylindrical aggregates; chamomile, when cylindrical aggregates are connected by their ends into loops; multipetal structure with macromolecules self-assembling into thin lamellae; and unstructured, swollen and uniformly compacted shells. The results are presented in the form of state diagrams and serve as a basis for the directional design of the surface pattern by varying system parameters (particle radius, grafting density and degree of polymerization) and solvent properties (quality and selectivity). Full article
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13 pages, 5867 KiB  
Article
DPD Study on the Interfacial Properties of PEO/PEO-PPO-PEO/PPO Ternary Blends: Effects of Pluronic Structure and Concentration
by Dongmei Liu, Meiyuan Yang, Danping Wang, Xueying Jing, Ye Lin, Lei Feng and Xiaozheng Duan
Polymers 2021, 13(17), 2866; https://0-doi-org.brum.beds.ac.uk/10.3390/polym13172866 - 26 Aug 2021
Cited by 9 | Viewed by 1916
Abstract
Using the method of dissipative particle dynamics (DPD) simulations, we investigated the interfacial properties of PEO/PEO-PPO-PEO/PPO ternary blends composed of the Pluronics L64(EO13PO30EO13), F68(EO76PO29EO76), F88(EO104PO39EO104), [...] Read more.
Using the method of dissipative particle dynamics (DPD) simulations, we investigated the interfacial properties of PEO/PEO-PPO-PEO/PPO ternary blends composed of the Pluronics L64(EO13PO30EO13), F68(EO76PO29EO76), F88(EO104PO39EO104), or F127(EO106PO70EO106) triblock copolymers. Our simulations show that: (i) The interfacial tensions (γ) of the ternary blends obey the relationship γF68 < γL64 < γF88 < γF127, which indicates that triblock copolymer F68 is most effective in reducing the interfacial tension, compared to L64, F88, and F127; (ii) For the blends of PEO/L64/PPO and the F64 copolymer concentration ranging from ccp = 0.2 to 0.4, the interface exhibits a saturation state, which results in the aggregation and micelle formation of F64 copolymers added to the blends, and a lowered efficiency of the L64 copolymers as a compatibilizer, thus, the interfacial tension decreases slightly; (iii) For the blends of PEO/F68/PPO, elevating the Pluronic copolymer concentration can promote Pluronic copolymer enrichment at the interfaces without forming the micelles, which reduces the interfacial tension significantly. The interfacial properties of the blends contained the PEO-PPO-PEO triblock copolymer compatibilizers are, thus, controlled by the triblock copolymer structure and the concentration. This work provides important insights into the use of the PEO-PPO-PEO triblock copolymer as compatibilizers in the PEO and PPO homopolymer blend systems. Full article
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14 pages, 6967 KiB  
Article
Interaction of Diphenhydramine Hydrochloride with Cationic and Anionic Surfactants: Mixed Micellization and Binding Studies
by Naved Azum, Malik Abdul Rub, Sulaiman Yahya Alfaifi and Abdullah M. Asiri
Polymers 2021, 13(8), 1214; https://0-doi-org.brum.beds.ac.uk/10.3390/polym13081214 - 09 Apr 2021
Cited by 16 | Viewed by 2038
Abstract
The focus of the present work is to evaluate the interactions of an anti-allergic drug (diphenhydramine hydrochloride, DPH) with anionic (sodium dodecyl sulfate, SDS) and cationic (cetylpyridinium chloride, CPC) surfactants in the aqueous medium. The mixed micellization behavior and surface properties of drug-surfactant [...] Read more.
The focus of the present work is to evaluate the interactions of an anti-allergic drug (diphenhydramine hydrochloride, DPH) with anionic (sodium dodecyl sulfate, SDS) and cationic (cetylpyridinium chloride, CPC) surfactants in the aqueous medium. The mixed micellization behavior and surface properties of drug-surfactant mixtures have been examined by surface tension measurements. Various theoretical approaches were applied to explore the synergistic or non-ideal behavior of the current mixed systems. Furthermore, the binding studies of drug with surfactants have been elaborated by UV–visible spectroscopy. Benesi–Hildebrand (B-H) theory was used to compute stoichiometric ratio, binding constant, and free energy change for the drug-surfactant mixtures. The outputs are deliberated taking into consideration the use of surfactants as capable drug delivery agents for DPH and hence advance bioavailability. Full article
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