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Mollecular engineering is the field where engineering solutions are devised ad hoc using materials from their atoms and molecules rather than from their macroscopic properties. The final properties of a macroscopic unit are thus determined by direct modification of the molecular structure, effectively “bottom-up” designing the material characteristics. In our group, we combine chemistry with physics using biology as inspiration to design hierarchical materials via self-assembly processes. We synthesise copolymers via controlled polymerisation methods tuning each segment mechanical, optical, solubility, degradation properties. 
We thus study the copolymer self-assembly in solution (mostly water). We are particularly interested on how cooperative processes emerging from the interaction between the blocks and the solvent drive the formation of different architectures.





We have collected a broad portfolio of polymerisation protocols to make almost any type of macromolecule as well as characterising their molecular mass and composition. We focus most of our synthetic efforts to make either block amphiphilic copolymers, we have made them combining different chemistries.  We aim to create scalable and straightforward protocols focussing on chemistries that are already clinically used.

See below our current portfolio and the relevant references 

  1. Flores-Merino et al.  Soft Matter 2010

  2. Yilmaz et al. Polymer Chem. 2016

  3. Viswanathan et al JACS 2014

  4. Tian et al Sci Rep 2015

  5. Lomas et al Adv. Mater 2007

  6. Chambon et al. Macromolecules 2012

  7. Blanazs et al. Adv. Funct. Mater., 2009

  8. Fernyhugh et al. Soft Matter., 2008

  9. Gaitzsch et al Angew. Chem. Int. Ed. 2013

  10.  Blanazs et al. JACS. 2011

  11. Battaglia et al. JACS 2005

  12. Fetsch et al Sci Rep. 2016 

  13. Duro Castaño et al In preparation. 2020

  14.  Zhu et al Angew. Chem. Int. Ed. 2019

  15. Battaglia Patent App. WO2019197834A1 2019

  16. Themistou et al  Polymer Chem  2014

  17. Battaglia US Patent App.WO2017158382A1  2019

Polymer Chemistry



Amphiphiles, molecules that contain both hydrophilic and hydrophilic parts, can assemble in water into either spherical or cylindrical micelles or membranes depending on the molecular composition and size. Membranes are a critical component of biological organisation, and natural amphiphiles (phospholipids) set the limits within and between cells. Membranes have to avoid contact between their edges and water, and this drives their deformation to form enclosed structures are known as vesicles typically spherical to minimise surface area.  We have been particularly interested in polymeric amphiphiles comprising hydrophilic and hydrophobic blocks joined together.  The macromolecular nature of the copolymers imposes two unique features to amphiphilic copolymer membranes: (i) hydrophobic entanglement (Battaglia et al JACS 2005) and (ii) hydrophilic brush-like configuration (Smart et al Soft Matter 2009). 

These features make block copolymer vesicles (aka polymersomes)  very different from their low molecular counterparts. Entanglement (for low Tg polymers) means high mechanical deformability and toughness, whilst the brush like configuration enables to surround the polymersome with a dense hydrophilic layer that controls both colloidal stability and interaction with its environment. We have been studying polymersomes formation kinetic for several years and learned how to control both bottom-up or top-down approaches to engineering the polymersome shape topology, making both spherical, tubular and more complex high-genus structures. We have also developed a way to control the polymersome surface topology by combining different polymersome-forming copolymers and, in doing so, tuning the interaction between them. 


We have been studying the formation mechanism of polymersomes for several years and these can be divided into two approaches: from bulk polymers (top-down route) or from unimers, meaning single block copolymer chains (bottom-up route).                                                                                                                                                                                                 

Top-down route

Block copolymers have the tendency to assemble in the solid-state, creating complex mesoscopic structures whose architecture is controlled by the blocks interactions and molar ratios. The transition from such a state to a single vesicle requires both the solvent (i.e. the water) and the single blocks to diffuse one another. However, amphiphilic copolymers, like all amphiphiles, are lyotropic meaning that their mesoscopic organisation changes as a function of the copolymer/water ratio. We mapped out the phase diagrams of vesicles forming copolymers (Battaglia et al Nature Mater 2005 and Battaglia et al Macromolecules 2006). 

Polymersomes formation is strictly controlled by the phase transitions and how copolymers rearrange. We observed that the kinetics of formation begin following a sub-diffusional regime where lyotropic phases rearrange to form lamellar structures that shed into vesicles (Battaglia et al J. Phys Chem B 2006).

This means that if we control the original block copolymer film we can control the final size and destruction of the vesicle (Howse et al Nature Mater 2009).  Also, such properties combined with the intrinsic low diffusivity of polymers allow the emergence of  metastable phases including, lamellarsomes (Battaglia et al Soft Matter 2006), myelin-like structures (Battaglia et al. Angew. Chem. Int. Ed.  2006) and tubular polymersomes (Robertson et al  ACS Nano 2014)

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Bottom-up route

We can dissolve the polymersomes forming block copolymers unimolecularly and change one block solvency to trigger self-assembly. We can achieve this, either by starting with a non-selective solvent and change it gradually for a selective one or using copolymers having one of the blocks with polarity sensitive to pH, temperature or any other controllable variable. Alternatively, we can trigger self-assembly by polymerising from another soluble polymer an insoluble block using the so-called polymerization induced self-assembly (PISA). In all these cases, the polymersome emerges from the collective assembly of the different unimers. We identified two different mechanisms:

(i) the copolymer hydrophobic/hydrophilic ratio or packing factor is changed gradually allowing the formation and evolution of spherical, cylindrical micelles and finally vesicles (Fernyhough et al Soft Matter 2009 and Blanazs et al JACS  2011).

(ii) The copolymer packing factor is changed abruptly and the first nucleation leads to the formation of disk-like micelles which enclose into vesicles. If the unimer pool is maintained, the vesicle continues growing asymmetrically giving rise to high genus vesicles such as toroidal vesicles, double toroid and so on (Pearson et al Macromolecules 2013 Contini et al iScience 2018

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"Topology" derives from the Greek τοποσ, 'topos' (space) and 'logos' (discourse) is the study of geometrical properties and spatial relations unaffected by continuous shape changes. We use here the term surface topology to define the formation of patterns on the polymersomes surface which arise as a consequence of membrane-confined interactions.       If we forced two different membrane-forming copolymers to self-assemble into the same vesicle, the interaction between the two (often repulsive) will lead to the formation of different domains (LoPresti et al ACS Nano 2011).  As shown below, we can use such interactions to control patterning (Ruiz-Perez et al Science Adv.  2016, the polymersome topography (LoPresti et al ACS Nano 2011) and symmetry (Joseph et al Science Adv. 2017)

Copolymer AX


Copolymer BX

Membrane-confined interaction

Triblock AXB

Molecular Mass


Mesoscopic Materials

We combine polymer synthesis with self-assembly to create porous cross-linked materials with porosity, surface chemistry, surface topology, topography, mechanical properties are tuned by supra-molecular interactions. The same block copolymers used for polymersomes can form complex structures, called lyotropic gels with long-ranged orders and architecture controlled by the ratio water/copolymer (Battaglia et al Nature Mater 2005, and Macromolecules 2006, Smart et al Soft Matter 2009)

We also synthesised hydrogels with heterogeneous internal structure, that can be used as a template to either house a second polymer cross-linking creating patterned hydrogels, or to house micelles and vesicle to form soft nanocomposites (Merino et al Soft Matter 2010). We have adapted the synthesis of porous foams prepared by high internal phase emulsion (HIPE)  using amphiphilic copolymers that act as surfactants during the HIPE process (Viswanathan et al JACS. 2012, Macromolecules 2014, Biomaterials 2015 ). Finally, the same principles were applied to electrospun fibres where we demonstrated the effective control of the fibre surface topology (Viswanathan et al Biomacromolecules 2015,. 

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