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Prof. Dr.
Cornelia Palivan
Department of Chemistry
Profiles & Affiliations
Biointerfacing Nanomaterials Research Group

The Palivan Research Group aims to interface synthetic assemblies at various scales with biomolecules and cells to understand their interactions, optimize the spatio-temporal conditions inducing functionality and propose advanced materials for translational applications. The unique advantage of building bio-hybrid systems by a bottom-up strategy is to integrate properties and functionality from both words and even generate new features and achieve multifunctionality. In a bioinspired strategy, our group has made major contributions in three directions of research:

i) active assemblies at the nano- and microscale,

ii) functional multicompartments mimicking organelles and cells,

iii) functional surfaces.

These directions allow modular exchange of the building blocks to achieve complexity and multifunctionality as required for advanced applications in various fields, including medicine, food science, environment science.

Selected Publications
Tarvirdipour, S., Skowicki, M., Maffeis, V., Abdollahi, S. N., Schoenenberger, C.-A., & Palivan, C. G. (2024). Peptide nanocarriers co-delivering an antisense oligonucleotide and photosensitizer elicit synergistic cytotoxicity [Journal-article]. Journal of Colloid and Interface Science. https://doi.org/10.1016/j.jcis.2024.03.021
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Heuberger, Lukas, Messmer, Daniel, dos Santos, Elena C., Scherrer, Dominik, Lörtscher, Emanuel, Schoenenberger, Cora‐Ann, & Palivan, Cornelia G. (2023). Microfluidic Giant Polymer Vesicles Equipped with Biopores for High‐Throughput Screening of Bacteria [Journal-article]. Advanced Science, 11(11). https://doi.org/10.1002/advs.202307103
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Mihali, Voichita, Skowicki, Michal, Messmer, Daniel, & Palivan, Cornelia G. (2023). Clusters of polymersomes and Janus nanoparticles hierarchically self-organized and controlled by DNA hybridization. Nano today, 48, 101741. https://doi.org/10.1016/j.nantod.2022.101741
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Belluati, Andrea, Craciun, Ioana, & Palivan, Cornelia G. (2020). Bioactive Catalytic Nanocompartments Integrated into Cell Physiology and Their Amplification of a Native Signaling Cascade. ACS Nano, 14(9), 12101–12112. https://doi.org/10.1021/acsnano.0c05574
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Einfalt, Tomaz, Witzigmann, Dominik, Edlinger, Christoph, Sieber, Sandro, Goers, Roland, Najer, Adrian, Spulber, Mariana, Onaca-Fischer, Ozana, Huwyler, Jörg, & Palivan, Cornelia G. (2018). Biomimetic artificial organelles with in vitro and in vivo activity triggered by reduction in microenvironment. Nature Communications, 9(1), 1127. https://doi.org/10.1038/s41467-018-03560-x
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Selected Projects & Collaborations
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BIOINSPIRED MULTIFUNCTIONAL BIO-SYNTHETIC SUPRAMOLECULAR ASSEMBLIES
Research Project  | 1 Project Members
Various domains require materials that integrate emerging properties with multifunctionality to efficiently solve complex issues (e.g. early detection and treatment of severe pathologies, sensing and correction of food quality issues, simultaneous determination of the presence of pollutants in water, biofilm formation). Amongst the most promising strategies is the use of bio-inspired bottom-up approaches based on interfacing biomolecules (enzymes, proteins, DNA) with synthetic assemblies (micelles, vesicles, particles). This combination can produce bio-synthetic materials that surpass conventional systems in terms of efficacy and functionality as they profit from the activity and specificity of the biomolecules whilst the synthetic matrix provides the necessary stability and robustness. The objective of this project is to create bio-inspired multifunctional supramolecular assemblies , in which activation and responses are stimuli-triggered. These multifunctional supramolecular assemblies will serve either as multiplexed reaction spaces at the nanoscale with magnetic controlled propulsion or as active surfaces patterned with responsive nano- assemblies. These directions, connected by biomolecules serving as active components, are inspired by aspects of natural organelles and cells, including signalling pathways, responsiveness and triggered production of molecules. Overall, this interdisciplinary project combines physical chemistry, nanoscience, surface science and enzyme biochemistry. The first subproject plan is to create clusters of active Janus-multicompartments by DNA-mediated self-organization of magnetic Janus nanoparticles and catalytic compartments based on polymersomes equipped with active molecules. Two different types of catalytic nanocompartment will be specifically attached to the lobes of Janus nanoparticles and activated by stimuli present in the environment. The intrinsic activity of the encapsulated molecules inside the catalytic nanocompartments will induce multifunctionality into the clusters, whilst the Janus nanoparticles will serve as "shuttles" to support the directional propulsion of the clusters in the presence of a magnetic field. To demonstrate the potential of the system in photodynamic therapy, we have selected enzymes and photosensitizers, respectively, as model compounds inside each type of catalytic nanocompartments. Clusters of active Janus-multicompartments have the advantages of segregation of protected spaces for active molecules and dual functionality with time, and space precision due to the stimuli-responsive manner of their activation and propulsion. The second subproject aims to construct multifunc tional "active surfaces" by specific immobilization of different types of biomolecule-loaded nano-assembly (peptide nanoparticles and polymersomes) on solid supports. These active surfaces will exhibit dual functionality in the presence of stimuli: polymersomes containing enzymes will act as catalytic nanocompartments for sensing pH changes, whilst peptide nanoparticles will release their cargo upon changes in temperature. A controlled surface pattern will be achieved by combining two approaches for immobilization of nano- assemblies on solid supports: DNA-mediated connection for polymersomes and covalent binding for peptide nanoparticles. To illustrate one of the possible applications, we have selected enzymes and flavonoids for sensing and correcting early changes in food quality. Such active surfaces have several advantages including versatility and modularity of specific patterning and multifunctionality associated with simultaneous responses to external stimuli. Knowledge gained from the fundamental study of the molecular factors, interactions and conditions that are essential to build such multifunctional bio-synthetic assemblies will support their development as efficient platform for solving complex issues in various fields, including medicine, food science, environmental sciences, and technology.
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NCCR MSE: Zipping of Synthetic Assemblies Equipped to Produce Multifunctional Clusters for Bio-Applications
Research Project  | 1 Project Members
This project will develop an innovative methodology to create size controlled polymer clusters of compartments that selectively and stably attach to the surface of epithelial cells. Such compartment clusters will be used to attach to scavenger receptors of the cell membranes and support medical applications. By loading specific compartments with different compounds and them zipping them together, the clusters will achieve multifunctionality serving for the development of nanoteranostics and dual-sensing systems. In addition, such segregated confined spaces at the nanoscale can be used to achieve efficient complex cascade reactions in between compartments.
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Active surfaces based on solid supported bilayers of amphiphilic asymetric ABC triblock copolymers for phenols
Research Project  | 2 Project Members
The present project intends to develop a new sensing system based on solid supported bilayers of amphiphilic ABC triblock copolymers for rapid and sensitive detection of phenolic compounds. Due to their differences in properties (hydrophilicity and/or hydrophobicity), ABC copolymers self-assemble and generate different supramolecular systems, such as micelles, vesicles, or various liquid crystalline phases. The project aims to design "active surfaces" of ABC asymmetric triblock copolymers in which active compounds (enzymes, chemical compounds) will be inserted to selectively recognize phenolic compounds. For this purpose, optimal conditions for the transfer of copolymer bilayers on solid support, at the air/water interface will be identified by Langmuir-Blodget (LB) isotherms, and Brewster Angle Microscopy imaging (BAM). Surface properties of uniform thin films of triblock copolymers will be characterized by a combination of ellipsometry, contact angle, FTIR, AFM, and SEM. These thin films will serve as templates for insertion of active (bio)molecules (test 4-aminoantipyrine or chitosan, tyrosinase or laccase, respectively), and production of "active surfaces" for phenols recognition at low concentrations. The functionality of active surfaces will be tested based on an easily detectable reaction/s product (for example a fluorescent product). The project will support the cooperation between the Chemistry Department of the University of Basel, and the Department of Product Design, Mechatronics and Environment of Transilvania University of Brasov, Romania. Obtaining active surfaces based on solid supported bilayers of amphiphilic ABC triblock copolymers represents a first research stage that will further be valorized by a long-term cooperation.