Mona Semsarilar

Anionic polyelectrolyte-stabilized nanoparticles via RAFT aqueous dispersion polymerization.

We report the synthesis of anionic sterically stabilized diblock copolymer nanoparticles via polymerization-induced self-assembly using a RAFT aqueous dispersion polymerization formulation. The anionic steric stabilizer is a macromolecular chain-transfer agent (macro-CTA) based on poly(potassium 3-sulfopropyl methacrylate) (PKSPMA), and the hydrophobic core-forming block is based on poly(2-hydroxypropyl methacrylate) (PHPMA). The effect of varying synthesis parameters such as the salt concentration, solids content, relative block composition, and anionic charge density has been studied. In the absence of salt, self-assembly is problematic when using a PKSPMA stabilizer because of lateral repulsion between highly charged anionic chains. However, in the presence of added salt this problem can be overcome by reducing the charge density within the coronal stabilizer layer by either (i) statistically copolymerizing the KSPMA monomer with a nonionic comonomer (2-hydroxyethyl methacrylate, HEMA) or (ii) using a binary mixture of a PKSPMA macro-CTA and a poly(glycerol monomethacrylate) (PGMA) macro-CTA. These diblock copolymer nanoparticles were analyzed by (1)H NMR spectroscopy, gel permeation chromatography (GPC), dynamic light scattering (DLS), transmission electron microscopy (TEM), and aqueous electrophoresis. NMR studies suggest that the HPMA polymerization is complete within 2 h at 70 °C, and DMF GPC analysis confirms that the resulting diblock copolymers have relatively low polydispersities (M(w)/M(n) < 1.30). NMR also suggests a significant degree of hydration for the core-forming PHPMA chains. Depending on the specific reaction conditions, a series of spherical nanoparticles with mean diameters ranging from 50 to 200 nm with tunable anionic surface charge can be prepared. If a binary mixture of anionic and nonionic macro-CTAs is utilized, then it is also possible to access a vesicular morphology.

Efficient synthesis of sterically-stabilized nano-objects via RAFT dispersion polymerization of benzyl methacrylate in alcoholic media.

Synthesis of diblock copolymer nano-objects: alcohol is a good idea! RAFT dispersion polymerization of benzyl methacrylate in alcohol using weak polyelectrolyte-based chain transfer agents allows the facile synthesis of sterically stabilized diblock copolymer nano-objects with very high monomer conversions. Such syntheses are usually problematic when conducted in water due to electrostatic repulsion between highly charged stabilizer chains, which impedes in situ self-assembly. Construction of a detailed phase diagram facilitates reproducible syntheses of well-defined diblock copolymer spheres, worms or vesicles, since it allows mixed phase regions to be avoided. Aqueous electrophoresis studies confirm that these nano-objects can acquire substantial surface charge when transferred to aqueous solution due to ionization (or protonation) of the polyacid (or polybase) stabilizer chains.

Polymerization-Induced Self-Assembly of Galactose-Functionalized Biocompatible Diblock Copolymers for Intracellular Delivery

Recent advances in polymer science are enabling substantial progress in nanobiotechnology, particularly in the design of new tools for enhanced understanding of cell biology and for smart drug delivery formulations. Herein, a range of novel galactosylated diblock copolymer nano-objects is prepared directly in concentrated aqueous solution via reversible addition–fragmentation chain transfer polymerization using polymerization-induced self-assembly. The resulting nanospheres, worm-like micelles, or vesicles interact in vitro with galectins as judged by a turbidity assay. In addition, galactosylated vesicles are highly biocompatible and allow intracellular delivery of an encapsulated molecular cargo.

Poly(methacrylic acid)-based AB and ABC block copolymer nano-objects prepared via RAFT alcoholic dispersion polymerization

A series of well-defined amphiphilic poly(methacrylic acid)–poly(benzyl methacrylate) (PMAA–PBzMA) diblock copolymers are synthesized via polymerization-induced self-assembly using an alcoholic dispersion polymerization formulation. Chain growth is mediated via reversible addition–fragmentation chain transfer polymerization (RAFT) chemistry using a trithiocarbonate-based chain transfer agent (CTA) at 70 °C. The poly(methacrylic acid) block is soluble in ethanol and acts as a steric stabilizer for the growing insoluble PBzMA chains, resulting in the in situ generation of diblock copolymer nano-objects in the form of spheres, worms or vesicles, depending on the precise reaction conditions. Copolymer morphologies can be covalently stabilized via cross-linking to prevent their dissociation when transferred into aqueous solution, which leads to the formation of highly anionic nano-objects due to ionization of the PMAA stabilizer chains. ABC triblock copolymer nanoparticles can also be prepared using this approach, where the third block is based on the semi-fluorinated monomer, 2,2,2-trifluoroethyl methacrylate (TFEMA). GPC studies confirm that chain extension is efficient and high TFEMA conversions can be achieved. Microphase separation between the mutually incompatible PBzMA and semi-fluorinated PTFEMA core-forming blocks occurs, producing a range of remarkably complex semi-fluorinated triblock copolymer morphologies.

One-pot synthesis of an inorganic heterostructure: uniform occlusion of magnetite nanoparticles within calcite single crystals

A facile one-pot method is described for the formation of novel heterostructures in which inorganic nanoparticles are homogeneously distributed throughout an inorganic single crystal matrix. Our strategy uses nanoparticles functionalised with a poly(sodium 4-styrenesulphonate)-poly(methacrylic acid) [PNaStS-PMAA] diblock copolymer as a soluble crystal growth additive. This copolymer plays a number of essential roles. The PMAA anchor block is physically adsorbed onto the inorganic nanoparticles, while the PNaStS block acts as an electrosteric stabiliser and ensures that the nanoparticles retain their colloidal stability in the crystal growth solution. In addition, this strong acid block promotes binding to both the nanoparticles and the host crystal, which controls nanoparticle incorporation within the host crystal lattice. We show that this approach can be used to achieve encapsulation loadings of at least 12 wt% copolymer-coated magnetite particles within calcite single crystals. Transmission electron microscopy shows that these nanoparticles are uniformly distributed throughout the calcite, and that the crystal lattice retains its continuity around the embedded magnetite particles. Characterisation of these calcite/magnetite nanocomposites confirmed their magnetic properties. This new experimental approach is expected to be quite general, such that a small family of block copolymers could be used to drive the incorporation of a wide range of pre-prepared nanoparticles into host crystals, giving intimate mixing of phases with contrasting properties, while limiting nanoparticle aggregation and migration.

Addition of water to an alcoholic RAFT PISA formulation leads to faster kinetics but limits the evolution of copolymer morphology

RAFT dispersion polymerization of benzyl methacrylate (BzMA) has been used previously (E. R. Jones, et al., Macromolecules, 2012, 45, 5091) to prepare poly(2-(dimethylamino)ethyl methacrylate)-poly(benzyl methacrylate) (PDMA–PBzMA) diblock copolymer nanoparticles in ethanol via polymerization-induced self-assembly (PISA). However, the rate of polymerization was relatively slow, with incomplete monomer conversions being obtained when targeting higher mean degrees of polymerization (DP) even after 24 h at 70 °C. Herein we examine the effect of the addition of up to 20% w/w water co-solvent on the kinetics of BzMA polymerization for this PISA formulation. Significantly faster polymerizations were observed: for a target DP of 200, 90% BzMA conversion was achieved within just 6 h in the presence of 20% w/w water, compared to only 35% conversion in anhydrous ethanol under the same conditions. This rate enhancement enables much higher mean DPs to be obtained for the core-forming PBzMA and is attributed to greater partitioning of the BzMA monomer within the particles, which increases the local monomer concentration. However, the presence of water adversely affected the evolution of copolymer morphology from spheres to worms to vesicles when employing a relatively short PDMA chain transfer agent, with only kinetically-trapped spheres being obtained at higher levels of added water. Aqueous electrophoresis studies indicate that the PDMA stabilizer chains acquired partial cationic charge in the presence of water. This leads to more efficient inter-particle repulsion, thus preventing the sphere-sphere fusion events required for an evolution in morphology. In summary, the addition of water to such PISA formulations allows the more efficient synthesis of spherical nanoparticles, but should be used with caution if either diblock copolymer worms or vesicles are desired.

Semi-crystalline diblock copolymer nano-objects prepared via RAFT alcoholic dispersion polymerization of stearyl methacrylate

The RAFT dispersion polymerization of stearyl methacrylate (SMA) is conducted in ethanol at 70 °C using a poly(2-(dimethylamino)ethyl methacrylate) [PDMA] chain transfer agent. The growing PSMA block becomes insoluble in ethanol, which leads to polymerization-induced self-assembly (PISA) and hence produces a range of copolymer morphologies depending on the precise PDMAy–PSMAx formulation. More specifically, pure phases corresponding to either spherical nanoparticles, worm-like nanoparticles or vesicles can be prepared as judged by transmission electron microscopy. However, the worm phase space is relatively narrow, so construction of a detailed phase diagram is required for reproducible syntheses of this morphology. Inter-digitation of the stearyl (C18) side-groups leads to a semi-crystalline PSMA core block and the effect of systematically varying the mean degree of polymerization of both the PDMA and PSMA blocks on the Tm and Tc is investigated using differential scanning calorimetry. Finally, it is demonstrated that these cationic nanoparticles can be employed as colloidal templates for the in situ deposition of silica from aqueous solution.

Synthesis and characterization of poly(amino acid methacrylate)-stabilized diblock copolymer nano-objects

Amino acids constitute one of Natures most important building blocks. Their remarkably diverse properties (hydrophobic/hydrophilic character, charge density, chirality, reversible cross-linking etc.) dictate the structure and function of proteins. The synthesis of artificial peptides and proteins comprising main chain amino acids is of particular importance for nanomedicine. However, synthetic polymers bearing amino acid side-chains are more readily prepared and may offer desirable properties for various biomedical applications. Herein we describe an efficient route for the synthesis of poly(amino acid methacrylate)stabilized diblock copolymer nano-objects. First, either cysteine or glutathione is reacted with a commercially available methacrylate-acrylate adduct to produce the corresponding amino acid-based methacrylic monomer (CysMA or GSHMA). Well-defined water-soluble macromolecular chain transfer agents (PCysMA or PGSHMA macro-CTAs) are then prepared via RAFT polymerization, which are then chain-extended via aqueous RAFT dispersion polymerization of 2-hydroxypropyl methacrylate. In situ polymerization-induced self-assembly (PISA) occurs to produce sterically-stabilized diblock copolymer nano-objects. Although only spherical nanoparticles could be obtained when PGSHMA was used as the sole macro-CTA, either spheres, worms or vesicles can be prepared using either PCysMA macro-CTA alone or binary mixtures of poly(glycerol monomethacrylate) (PGMA) with either PCysMA or PGSHMA macro-CTAs. The worms formed soft free-standing thermo-responsive gels that undergo degelation on cooling as a result of a worm-to-sphere transition. Aqueous electrophoresis studies indicate that all three copolymer morphologies exhibit cationic character below pH 3.5 and anionic character above pH 3.5. This pH sensitivity corresponds to the known behavior of the poly(amino acid methacrylate) steric stabilizer chains.

How Do Spherical Diblock Copolymer Nanoparticles Grow during RAFT Alcoholic Dispersion Polymerization

A poly(2-(dimethylamino)ethyl methacrylate) (PDMA) chain transfer agent (CTA) is used for the reversible addition–fragmentation chain transfer (RAFT) alcoholic dispersion polymerization of benzyl methacrylate (BzMA) in ethanol at 70 °C. THF GPC analysis indicated a well-controlled polymerization with molecular weight increasing linearly with conversion. GPC traces also showed high blocking efficiency with no homopolymer contamination apparent and Mw/Mn values below 1.35 in all cases. 1H NMR studies confirmed greater than 98% BzMA conversion for a target PBzMA degree of polymerization (DP) of up to 600. The PBzMA block becomes insoluble as it grows, leading to the in situ formation of sterically stabilized diblock copolymer nanoparticles via polymerization-induced self-assembly (PISA). Fixing the mean DP of the PDMA stabilizer block at 94 units and systematically varying the DP of the PBzMA block enabled a series of spherical nanoparticles of tunable diameter to be obtained. These nanoparticles were characterized by TEM, DLS, MALLS, and SAXS, with mean diameters ranging from 35 to 100 nm. The latter technique was particularly informative: data fits to a spherical micelle model enabled calculation of the core diameter, surface area occupied per copolymer chain, and the mean aggregation number (Nagg). The scaling exponent derived from a double-logarithmic plot of core diameter vs PBzMA DP suggests that the conformation of the PBzMA chains is intermediate between the collapsed and fully extended state. This is in good agreement with 1H NMR studies, which suggest that only 5−13% of the BzMA residues of the core-forming chains are solvated. The Nagg values calculated from SAXS and MALLS are in good agreement and scale approximately linearly with PBzMA DP. This suggests that spherical micelles grow in size not only as a result of the increase in copolymer molecular weight during the PISA synthesis but also by exchange of individual copolymer chains between micelles and/or by sphere–sphere fusion events.

Comparison of pseudo-living character of RAFT polymerizations conducted under homogeneous and heterogeneous conditions

RAFT dispersion polymerization of 2,2,2-trifluoroethyl methacrylate (TFEMA) is conducted in ethanol at 70 °C using either poly(2-(dimethylamino)ethyl methacrylate) or poly(methacrylic acid) as a macromolecular chain transfer agent. If the diblock copolymer nanoparticles are not too large, the small refractive index difference between the PTFEMA cores and ethanol leads to minimal light scattering. This enables the pseudo-living character of RAFT formulations conducted under solution and dispersion polymerization conditions to be compared by monitoring the loss of RAFT chain-ends via UV-visible absorption spectroscopy. Significantly fewer chain-ends are lost during RAFT dispersion polymerization, suggesting that such heterogeneous formulations have greater pseudo-living character. Moreover, 19F NMR spectroscopy provides the first direct experimental evidence that RAFT dispersion polymerization proceeds via monomer-swollen block copolymer micelles. The relatively low refractive index of PTFEMA complicates GPC analysis, leading to apparent contamination of the diblock copolymer and erroneously high polydispersities. However, this artefact can be corrected by deconvolution of the GPC curves, followed by their reconstruction using appropriate refractive indices.