skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

Attention:

The NSF Public Access Repository (PAR) system and access will be unavailable from 10:00 PM to 12:00 PM ET on Tuesday, March 25 due to maintenance. We apologize for the inconvenience.


Title: UV-induced vesicle to micelle transition: a mechanistic study
The morphology of self-assembled block copolymer aggregates is highly dependent on the relative volume fraction of the hydrophobic block. Thus, a dramatic change in the volume fraction of the hydrophobic block can elicit on-demand morphological transitions. Herein, a novel hydrophobic monomer containing a photolabile nitrobenzyl (Nb) protecting group was synthesized and incorporated into a block copolymer with poly(ethylene glycol) methacrylate. This motif allows for the hydrophobic volume fraction of the amphiphilic block copolymer to be dramatically reduced in situ to induce a morphological transition upon irradiation with UV light. Two amphiphilic block copolymers, Nb 94 and Nb 176, with hydrophobic weight fractions of 80% and 86%, respectively, were synthesized and their self-assembly in water studied. Nb 94 assembled into vesicles with R h = 235 nm and underwent a morphological transition after 21 minutes of UV irradiation to spherical micelles with R h = 27 nm, determined by dynamic light scattering and confirmed by transmission electron microscopy. At intermediate irradiation times (14–20 min), Nb 94 vesicles swelled to a larger size, but underwent a morphological transition over the course of hours or days, depending on the exact irradiation time. Nb 176 assembled into large compound vesicles with a hydrodynamic radius ( R h ) of 973 nm, as determined by dynamic light scattering (DLS), which decreased to ca. 700 nm after 300 minutes of UV irradiation with no apparent morphological transition. This study elucidates the mechanism and kinetics of the morphological transitions of block copolymer assemblies induced by a change in the hydrophobic volume fraction of the polymer.  more » « less
Award ID(s):
1904631
PAR ID:
10157079
Author(s) / Creator(s):
; ; ; ; ; ;
Date Published:
Journal Name:
Polymer Chemistry
Volume:
10
Issue:
44
ISSN:
1759-9954
Page Range / eLocation ID:
6037 to 6046
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. null (Ed.)
    Recent developments in the field of polymer vesicles, i.e. polymersomes, have demonstrated that disrupting the equilibrium conditions of the milieu could lead to shape transformation into stable non-spherical morphologies, bringing on-demand shape control to reality and bearing great promise for cell mimicry and a variety of biomedical applications. Here, we studied the self-assembly behavior of glassy amphiphilic triblock copolymers, poly(ethylene glycol)- block -polystyrene- stat -poly(coumarin methacrylate)- block -poly(ethylene glycol) (PEG- b -P(S- stat -CMA)- b -PEG), and their response to various stimuli. By changing the respective molecular weights of both the hydrophobic P(S- stat -CMA) and the hydrophilic PEG blocks, we varied the hydrophobic volume fraction thereby accessing a range of morphologies from spherical and worm-like micelles, as well as polymersomes. For the latter, we observed that slow osmotic pressure changes induced by dialysis led to a decrease in size while rapid osmotic pressure changes by addition of a PEG fusogen led to morphological transformations into rod-like and tubular polymersomes. We also found out that chemically crosslinking the vesicles before inducing osmotic pressure changes led to the vesicles exhibiting hypotonic shock, atypical for glassy polymersomes. We believe that this approach combining the robustness of triblock copolymers and light-based transformations will help expand the toolbox to design ever more complex biomimetic constructs. 
    more » « less
  2. The positional effect of stimuli-responsive units in tri-component copolymer vesicles is studied to explore variations in the host–guest properties of the assembly. We study this by placing pH-responsive diisopropylaminoethyl moieties in three distinct locations of a block copolymer assembly. In two of the three variations, these functionalities were randomly distributed in the hydrophobic or the hydrophilic domains of an amphiphilic diblock copolymer. In a third variation, this responsive functionality was incorporated as the middle block in a triblock copolymer. The results reveal that the solvent exposure of the responsive units holds the key for controlling the rate of molecular release from these polymer vesicles. The study also shows that equilibrium changes in the morphology of an assembly are not good indicators of the responsive host–guest properties of a polymer assembly. 
    more » « less
  3. ABSTRACT Carbohydrates are the fundamental building blocks of many natural polymers, their wide bioavailability, high chemical functionality, and stereochemical diversity make them attractive starting materials for the development of new synthetic polymers. In this work, one such carbohydrate,d‐glucopyranoside, was utilized to produce a hydrophobic five‐membered cyclic carbonate monomer to afford sugar‐based amphiphilic copolymers and block copolymers via organocatalyzed ring‐opening polymerizations with 4‐methylbenzyl alcohol and methoxy poly(ethylene glycol) as initiator and macroinitiator, respectively. To modulate the amphiphilicities of these polymers acidic benzylidene cleavage reactions were performed to deprotect the sugar repeat units and present hydrophilic hydroxyl side chain groups. Assembly of the polymers under aqueous conditions revealed interesting morphological differences, based on the polymer molar mass and repeat unit composition. The initial polymers, prior to the removal of the benzylidenes, underwent a morphological change from micelles to vesicles as the sugar block length was increased, causing a decrease in the hydrophilic–hydrophobic ratio. Deprotection of the sugar block increased the hydrophilicity and gave micellar morphologies. This tunable polymeric platform holds promise for the production of advanced materials for implementation in a diverse range of applications. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem.2019,57, 432–440 
    more » « less
  4. In this work, the deformation mechanisms underlying the room temperature deformation of the pseudomorphic body centered cubic (BCC) Mg phase in Mg/Nb nanolayered composites are studied. Nanolayered composites comprised of 50% volume fraction of Mg and Nb were synthesized using physical vapor deposition with the individual layer thicknesses h of 5, 6.7, and 50 nm. At the lower layer thicknesses of h = 5 and 6.7 nm, Mg has undergone a phase transition from HCP to BCC such that it formed a coherent interface with the adjoining Nb phase. Micropillar compression testing normal and parallel to the interface plane shows that the BCC Mg nanolayered composite is much stronger and can sustain higher strains to failure than the HCP Mg nanolayered composite. A crystal plasticity model incorporating confined layer slip is presented and applied to link the observed anisotropy and hardening in the deformation response to the underlying slip mechanisms. 
    more » « less
  5. Abstract Thermogels that exhibit a sol‐gel transition at body temperature represent a promising class of injectable biomaterials for biomedical applications. Thermogels reported thus far are generally composed of amphiphilic block copolymer micelles with an isotropic thermosensitive surface that induces intermicellar aggregation upon heating. Despite the promise, these hydrogels exhibit low mechanical strengths due to their uncontrollable aggregation resulting in void formation. To gain better control over intermicellar assembly, herein a novel thermogel design concept is presented based on patchy polymeric micelles bearing multiple thermosensitive surface domains. These domains serve as “patches” to bridge the micelles to form a percolated network structure. Patchy micelles are prepared from a binary mixture of amphiphilic block copolymers: Poly(N‐acryloylmorpholine)‐b‐poly(N‐benzylacrylamide) (PAM‐PBzAM) and poly (N‐isopropyl acrylamide)‐b‐poly(N‐benzylacrylamide) (PNIPAM‐PBzAM), where PBzAM, PAM and PNIPAM are the hydrophobic, hydrophilic and thermosensitive blocks, respectively. At 25 °C, the polymers self‐assembled into mixed shell micelles having a phase‐separated shell with PAM‐ and PNIPAM‐rich domains. At 37 °C, the PNIPAM domains undergo a hydrophilic‐to‐hydrophobic transition to induce intermicellar assembly into entangled worm‐like structures resulting in hydrogel formation. Patchy micelles form a homogeneous network structure without voids. The micelle design significantly affects the inter‐micellar assembly, the thermogelling behavior, and the mechanical properties of the hydrogels. 
    more » « less