People

Assistant Professor

 Ing. Viola Tokárová, Ph.D.

Viola

Assistant Professor

work phone+420220444013

VŠCHT Praha – building B, T04

 

 

Education

  • 2010 – 2014   Ph.D. at ICT Prague; Chemical and Process Engineering
  • 2008 – 2010   MSc. at ICT Prague; Chemical Engineering, Bioengineering and Process Simulations

International experience

  • 2015 – 2017 Postdoctoral Fellowship, McGill University, Bioengineering Department
  • 2012 – 2015 Rutgers University in New Jersey, USA in co-operation with Dr. R. Ramachandran (project AMVIS)
  • 2011 – 2012 Graz University of Technology, Austria in co-operation with prof. G. Gübitz (project AKTION)

 

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  • microfluidics
  • biosimulations and biocomputations
  • inorganic nanoparticles
  • surface modification
  • thermo-responsive polymer microparticles
  • adhesion studies of polymer microparticles
  • antigen-antibody interaction
  • specific adhesion of nano- and mickroparticles to biological substrates
  • ZETA 2018-2019 – Development of biomimetic particles for antibacterial applications
  • GAČR 2017-2019 – Synthesis of biomimetic nanoparticulate materials using a microfluidic platform and investigation of their interaction with cells
  • AKTION 2011-2012 – Development of chitosan based biomedical polymers with antibacterial properties

Hanson, K. L., Fulga, F., Dobroiu, S., Solana, G., Kašpar, O., Tokárová, V., Nicolau, D. V., “Polymer surface properties control the function of heavy meromyosin in dynamic nanodevices”, Biosensors and Bioelectronics (2016) More

The actin-myosin system, responsible for muscle contraction, is also the force-generating element in dynamic nanodevices operating with surface-immobilized motor proteins. These devices require materials that are amenable to micro- and nano-fabrication, but also preserve the bioactivity of molecular motors. The complexity of the protein-surface systems is greatly amplified by those of the polymer-fluid interface; and of the structure and function of molecular motors, making the study of these interactions critical to the success of molecular motor-based nanodevices. We measured the density of the adsorbed motor protein (heavy meromyosin, HMM) using quartz crystal microbalance; and motor bioactivity with ATPase assay, on a set of model surfaces, i.e., nitrocellulose, polystyrene, poly(methyl methacrylate), and poly(butyl methacrylate), poly(tert-butyl methacrylate). A higher hydrophobicity of the adsorbing material translates in a higher total number of HMM molecules per unit area, but also in a lower uptake of water, and a lower ratio of active per total HMM molecules per unit area. We also measured the motility characteristics of actin filaments on the model surfaces, i.e., velocity, smoothness and deflection of movement, determined via in vitro motility assays. The filament velocities were found to be controlled by the relative number of active HMM per total motors, rather than their absolute surface density. The study allowed the formulation of the general engineering principles for the selection of polymeric materials for the manufacturing of dynamic nanodevices using protein molecular motors.

Kašpar, O., Zhang, H., Tokárová, V., Boysen, R. I.,  Suñé, G. R.,  Borrise, X., Murano, F.P., Hearn, M. T. W., Nicolau, D.V., “Confinement of water droplets on rectangular micro/nano-arrayed surfaces”, Lab Chip, 16, 2487-2493 (2016) More

Micro-patterned surfaces with alternate hydrophilic and hydrophobic rectangular areas effectively confine water droplets down to attolitre volumes. The contact angle, volume, and geometry of the confined droplets as a function of the geometry and physico-chemical properties of the confining surfaces have been determined by phenomenological simulations, validated by atomic force microscopy measurements. The combination between experiments and simulations can be used for the purposeful design of arrays with surface-addressable hydrophobicity employed in digital microfluidics and high-throughput screening nanoarrays.

Filipponi, L., Livingston, P., Kašpar, O., Tokárová, V., Nicolau, D.V., “Protein patterning by microcontact printing using pyramidal PDMS stamps”, Biomedical Microdevices 18, 1-7 (2016) More

Micro-contact printing, μCP, is a well-established soft-lithography technique for printing biomolecules. μCP uses stamps made of Poly(dimethylsiloxane), PDMS, made by replicating a microstructured silicon master fabricated by semiconductor manufacturing processes. One of the problems of the μCP is the difficult control of the printing process, which, because of the high compressibility of PDMS, is very sensitive to minute changes in the applied pressure. This over-sensitive response leads to frequent and/or uncontrollable collapse of the stamps with high aspect ratios, thus decreasing the printing accuracy and reproducibility. Here we present a straightforward methodology of designing and fabricating PDMS structures with an architecture which uses the collapse of the stamp to reduce, rather than enlarge the variability of the printing. The PDMS stamp, organized as an array of pyramidal micro-posts, whose ceiling collapses when pressed on a flat surface, replicates the structure of the silicon master fabricated by anisotropic wet etching. Upon application of pressure, depending on the size of, and the pitch between, the PDMS pyramids, an air gap is formed surrounding either the entire array, or individual posts. The printing technology, which also exhibits a remarkably low background noise for fluorescence detection, may find applications when the clear demarcation of the shapes of protein patterns and the distance between them are critical, such as microarrays and studies of cell patterning.

Oka S., Emady H., Kašpar O., Tokárová V., Muzzio F.J., Štěpánek F., Ramachandran R., “The effects of improper mixing and preferential wetting of active and excipient ingredients on content uniformity in high shear wet granulation”, Powder Technol. 278, 266-277 (2015) More

 This work focuses on the content non-homogeneity in granules across size classes in a high shear wet granulation process as a result of powder segregation during dry mixing coupled with preferential wettability of one of the ingredients with the binder fluid.

A two component API-excipient system comprised of acetaminophen (APAP) and microcrystalline cellulose PH-101 (MCC) is investigated in a high shear granulation environment for content uniformity of the granules with respect to APAP. It was found that the fine granules were super potent while the coarse granules were starved of the APAP. This was attributed to a dual cause of powder segregation during dry mixing and superior wettability of the MCC compared to APAP. Post the dry mixing stage, the top layer of the powder bed is found to be sub-potent due to percolation of the smaller APAP particles to the bottom of the bed as they find spaces between the larger MCC particles. Thus, a drop of the binder fluid which falls on the bed is likely to be surrounded by MCC particles, which give them a higher chance of being incorporated in the nucleus. Moreover, MCC being the superior wetting of the two ingredients, also preferentially attaches itself to the growing granules. The granules are thus starved of the APAP leading to disparity in content across size classes.

Lastly, the effect of content non-uniformity was categorically quantified on the rate of active release. It was observed that content non-uniformity results in a lack of predictability and consequently control, on the rate of release of the active ingredient from the granules. This work highlights the need for qualitative understanding and quantitative analysis of factors that contribute to the occurrence of granule content non-uniformity, if one is to enable inherently robust pharmaceutical product design.

Sarvašová N., Ulbrich P., Tokárová V., Zadražil A., Štěpánek F., “Artificial swarming: towards radiofrequency control of reversible micro-particle aggregation and deposition”, Powder Technol. 278, 17-25 (2015) More

The ability to undergo a transition between dispersed or single-cellular state and aggregated or multi-cellular state provides distinct evolutionary advantages to many natural organisms. Due to a change of hydrodynamic diameter over several orders of magnitude and associated change of fluid–particle interaction (settling velocity) or intra-particle transport phenomena (heat transfer and/or diffusion) that typically scales with the square of the particle size, radically different behaviour can be achieved in terms of transport in a fluid environment, sourcing nutrition, escaping predators or maintaining homeostasis. In this work we report on the implementation of an artificial system that is able to undergo a reversible transition between dispersed and aggregated state, using the principles of “remote control” by radiofrequency (RF) signals. The individual artificial cells are represented by hollow-core SiO2/Fe3O4/PNIPAM microparticles with a stimuli-responsive porous shell that possess the following functionalities: (i) RF-induced local particle heating, due to the presence of superparamegnetic nanoparticles in the structure; (ii) temperature switchable storage/release functionality due to a combination of hollow-core porous silica skeleton with a PNIPAM layer; and (iii) temperature switchable aggregation, due to the hydrophilic/hydrophobic transition of the PNIPAM layer. The combination of RF-switchable aggregation and temperature-responsive release kinetics of a lipophilic substance makes it possible to trigger particle aggregation and deposition remotely, and thus control the release kinetics of encapsulated payload in both time and space.

Oka S., Kašpar O., Tokárová V., Sowrirajan K., Wu H., Khan H., Muzzio F., Štěpánek F., Ramachandran R., “A quantitative study of the effect of process parameters on key granule characteristics in a high shear wet granulation process”, Adv. Powder Technol. 26, 315-322 (2015) More

The objective of the current work was to investigate the effect of liquid to solid ratio (L/S), impeller speed and the wet massing time on the critical quality attributes of granules in a high shear wet granulation process for a two component (API and excipient) system. The parameters were evaluated for their effect on granule properties using a design of experiment based approach. Granules were characterized for their particle size distribution, content uniformity, morphology and porosity. The liquid to solid (L/S) ratio was found to have a dominant effect on the median particle size and exhibited a clear trend. The system was found to be extremely well mixed for all conditions thus implying robust composition uniformity within and between batches, independent of process parameters. The release kinetics of granules within the batch were found to be identical, independent of particle size. The granules were found to be fairly spherical as observed through a scanning electron microscope with no distinct agglomeration. The images indicate granulation by layering and consolidation. All three process parameters were found to have an effect on granule porosity, with the wet massing time having the most pronounced effect. A judicious selection of the afore mentioned process parameters will enable a balance between granule growth and porosity to be achieved without compromising on the mixing efficiency of the process thereby allowing one to build quality into the final product.

Kašpar O., Tokárová V., Oka S., Sowrirajan K., Ramachandran R., Štěpánek F., “Combined UV/Vis and micro-tomography investigation of acetaminophen dissolution from granules”, Int. J. Pharm. 458, 272-281 (2013) More

The X-ray micro-tomography (micro-CT) technique has been used to visualize the microstructure of granules produced by high shear wet granulation and the dynamic evolution of porosity during granule dissolution. Using acetaminophen (paracetamol) as the active pharmaceutical ingredient (API) and microcrystalline cellulose (Avicel PH-200) as an excipient, the porosity of the granules was systematically influenced by the granulation process parameters (binder/solids ratio, impeller speed and wet massing time). An increase of granule porosity from 7% to 10% and 18% lead to a decrease of the dissolution time t90 from 435 min to 98 min and 37 min, respectively. The combination of time-resolved micro-CT imaging with UV/vis detection of the quantity dissolved made it possible to evaluate the effective diffusion coefficient of the API through the granule structure, and thus establish a quantitative structure–property relationship for dissolution. A power-law dependence of the effective diffusivity on porosity (Archie’s law) was found to hold.

Tokárová V., Pittermannová A., Král V., Řezáčová P., Štěpánek F., “Feasibility and constraints of particle targeting using antigen-antibody interaction”, Nanoscale 5, 11490-11498 (2013) More

This work is concerned with the surface modification of fluorescent silica nanoparticles by a monoclonal antibody (M75) and the specific bioadhesion of such particles to surfaces containing the PG domain of carbonic anhydrase IX (CA IX), which is a trans-membrane protein specifically expressed on the surfaces of several tumor cell lines. The adhesion strength of antibody-bearing silica nanoparticles to antigen-bearing surfaces was investigated under laminar flow conditions in a microfluidic cell and compared to the adhesion of unmodified silica nanoparticles and nanoparticles coupled with an unspecific antibody. Adhesion to cancer cells using flow cytometry was also investigated and in all cases the adhesion strength of M75-modified nanoparticles was significantly stronger than for the unmodified or unspecific nanoparticles, up to several orders of magnitude in some cases. The specific modification of nano- and microparticles by an antibody-like protein therefore appears to be a feasible approach for the targeting of tumor cells. [aio_button align=”right” animation=”none” color=”gray” size=”small” icon=”education” text=”PDF” relationship=”dofollow” url=”http://pubs.rsc.org/en/content/articlepdf/2013/nr/c3nr04340a”]

Kašpar O., Tokárová V., Nyanhongo G. S., Gübitz G., Štěpánek F., “Effect of cross-linking method on the activity of spray-dried chitosan microparticles with immobilized laccase”, Food Bioprod. Proces. 91, 525-533 (2013) More

The effect of processing method on the properties of cross-linked chitosan microparticles and on the enzymatic activity of laccase immobilized in the particles has been investigated. Chitosan has been cross-linked by tri-polyphosphate (TPP) using two methods – the so called ex situ cross-linking whereby the solutions of chitosan, TPP and the enzyme have been pre-mixed and spray-dried by a standard two-fluid kinetic nozzle, and a novel in situ cross-linking method, whereby the solutions have been contacted at the tip of a three-fluid nozzle and cross-linking occurred within a drying droplet. The influence of the cross-linking method on the particle size and morphology, surface charge, and swelling ratio has been determined. The enzymatic activity of laccase toward the oxidation of a chromophore substrate (ABTS) has been systematically investigated and found to be superior in particles produced by the in situ cross-linking method.

Tokárová V., Kašpar O., Knejzlík Z., Ulbrich P., Štěpánek F., “Development of spray-dried chitosan microcarriers for nanoparticle delivery”, Powder Technol. 235, 797-805 (2013) More

The design of chitosan microspheres for the encapsulation and release of nanoparticles has been considered. The composite microcarriers have been produced by spray drying and the effect of factors including the chitosan cross-linking ratio (using tri-polyphosphate as the cross-linking agent), nanoparticle loading in the polymer matrix and the internal structure of the microspheres (uniform dispersion of nanoparticles vs. core-shell structure) on the in vitro release kinetics have been systematically investigated. The antibacterial performance of the composite microspheres containing Ag nanoparticles has been evaluated against three different strains of bacteria in a suspension culture. The bioadhesive character of the chitosan carrier particles has lead to the formation of stable aggregates with the bacteria, which enhanced the antibacterial efficacy of the released nanoparticles through the contact mechanism.

Zadražil A., Tokárová V., Štěpánek F., “Remotely triggered release from composite hydrogel sponges”, Soft Matter 8, 1811-1816 (2012) More

A thermoresponsive poly(N-isopropylacrylamide) (PNIPAM) hydrogel crosslinked withmethylene bisacrylamide (MBA), with the ability to undergo a volume change of approximately 50%, was used to fabricate a hydrogel “sponge” with oil microdrops encapsulated within its structure by the polymerization of an O/W emulsion. By adding 1.5 wt.% of iron oxide nanoparticles to the hydrogel structure it is possible to trigger the hydrogel volume change remotely by exposing the composite to an alternating magnetic field in the radiofrequency range, which heats up the nanoparticles. The increase of the hydrogel temperature leads to its shrinking and subsequently the encapsulated oil droplets are squeezed out. It was shown that the oil is released gradually during cyclic volume change (repeated heating and cooling) and the amount of oil content released during the first 8–15 shrinking cycles was in the range 1–3% v/v per cycle. The total amount of the released oil phase was in the range 18–24% v/v and it was found to be affected by the size of the encapsulated microdroplets, with the larger ones being squeezed out preferentially.

Tokárová V., Pittermannová A., Čech J., Ulbrich P., Štěpánek F., “Thermo-responsive adhesion properties of composite hydrogel microcapsules”, Soft Matter 8, 1087-1095 (2012) More

The present work describes the synthesis and characterisation of thermo-responsive microcapsules consisting of poly-N-isopropylacrylamide (PNIPAM) hydrogel, hydrophilic citrate-stabilized super-paramagnetic iron oxide nanoparticles (SPIONs) that perform the function of a local heat source and hydrophobic nanoparticles (either SiO2 or oleic acid-coated SPIONs) that stabilize the microcapsule surface. The microcapsules have been synthesized by the inverse Pickering emulsion polymerisation method. The effect of iron oxide concentration in the hydrogel on the shape, size, shrinkage ratio and heating rate of the microcapsules has been systematically investigated. The adhesion properties of the composite microcapsules towards a range of substrates have been characterised in a microfluidic flow cell and it was found that the temperature-induced change of the microcapsule size is an effective way of controlling adhesion. The induction heating of the embedded SPIONs makes it possible to control adhesion remotely in environments where macroscopic heating is not possible.

Ing. Ondřej Kašpar, Ph.D.

Ondra

Assistant Professor

work phone+420220444013

VŠCHT Praha – building B, T04

 

 

Education

  • 2010 – 2014   Ph.D. at ICT Prague; Chemical and Process Engineering
  • 2008 – 2010   MSc. at ICT Prague; Chemical Engineering, Bioengineering and Process Simulations

International experience

  • 2015 – 2017 Postdoctoral Fellowship, McGill University, Bioengineering Department
  • 2012 – 2015 Rutgers University in New Jersey, USA in co-operation with Dr. R. Ramachandran (project AMVIS)
  • 2011 – 2012 Graz University of Technology, Austria in co-operation with prof. G. Gübitz (project AKTION)

 

e-mail_icon     linkedin     
  • microfluidic systems
  • CFD simulation of two-phase flow
  • simulation of wetting phenomena (Surface Evolver)
  • CAD design and 3D modeling
  • image analysis and post-processing
  • natural antibacterial systems
  • spray drying and encapsulation
  • μ-CT and structural analysis
  • ZETA 2018-2019 – Development of biomimetic particles for antibacterial applications
  • GAČR 2017-2019 – Synthesis of biomimetic nanoparticulate materials using a microfluidic platform and investigation of their interaction with cells
  • AKTION 2011-2012 – Development of chitosan based biomedical polymers with antibacterial properties

van Delft, F. C., Ipolitti, G., Nicolau, D. V., Perumal, A. S., Kašpar, O., Kheireddine, S., & Wachsmann-Hogiu, S. (2018). Something has to give: scaling combinatorial computing by biological agents exploring physical networks encoding NP-complete problems. Interface Focus8(6) (2018)More

On-chip network-based computation, using biological agents, is a new hardware-embedded approach which attempts to find solutions to combinatorial problems, in principle, in a shorter time than the fast, but sequential electronic computers. This analytical review starts by describing the underlying mathematical principles, presents several types of combinatorial (including NP-complete) problems and shows current implementations of proof of principle developments. Taking the subset sum problem as example for in-depth analysis, the review presents various options of computing agents, and compares several possible operation ‘run modes’ of network-based computer systems. Given the brute force approach of network-based systems for solving a problem of input size C, 2C solutions must be visited. As this exponentially increasing workload needs to be distributed in space, time, and per computing agent, this review identifies the scaling-related key technological challenges in terms of chip fabrication, readout reliability and energy efficiency. The estimated computing time of massively parallel or combinatorially operating biological agents is then compared to that of electronic computers. Among future developments which could considerably improve network-based computing, labelling agents ‘on the fly’ and the readout of their travel history at network exits could offer promising avenues for finding hardware-embedded solutions to combinatorial problems.

Zůza, D., Šoltys, M., Mužík, J., Lizoňová, D., Lhotka, M., Ulbrich, P., Kašpar, O., Štěpánek, F., “Silica particles with three levels of porosity for efficient melt amorphisation of drugs”, Micropor. Mesopor. Mater. 274, 61-69 (2019)More

Silica particles with a unique multi-level pore structure have been prepared in order to enable efficient melt-in amorphisation of pharmaceutical substances. The dissolution rate of drugs with a low aqueous solubility can be enhanced by their conversion from a crystalline to an amorphous form. In order to avoid spontaneous re-crystallisation over time, the amorphous form must be stabilised, in this case by melt-in sorption into a porous carrier. To stabilise the amorphous state, pore diameters not exceeding approximately ten times the equivalent molecular diameter are required. However, since the permeability of porous media scales with the square of the mean pore diameter, carrier particles with pores in the nanometer range suffer from slow melt-in rates. Therefore, silica particles with a novel multi-level porous structure have been proposed in this work. The particles combine a central hollow cavity, a network of conducting macro-pores for enhanced transport rate, and a mesoporous matrix for efficient stabilisation of the amorphous state. The particles were prepared by the hydrolysis of TEOS using a soft-templating method with octylamine. We show that by systematically modulating the hydrolysis rate by the presence of ethanol (a reaction by-product), particles with the desired pore structure, particle size and morphology can be formed. Furthermore, we demonstrate their superior transport properties during melt sorption, high drug loading capacity and the ability to stabilise the amorphous state of a drug.

Šoltys, M., Balouch, M., Kašpar, O., Lhotka, M., Ulbrich, P., Zadražil, A., Kovačík, P., Štĕpánek, F., “Evaluation of scale-up strategies for the batch synthesis of dense and hollow mesoporous silica microspheres”, Chemical Engineering Journal, 334, 1135-1147 (2018) More

Despite the wide application interest in mesoporous silica micro- and nano-particles and a number of synthesis routes reported in the literature, the question of chemical engineering scale-up of the synthetic routes has rarely been addressed. The present work reports the results of an experimental and computational study of batch scale-up by a factor of 40× in the specific case of two types of dense and hollow mesoporous silica microparticles produced by the hydrolysis of tetraethoxysilane (TEOS) using a CTAB surfactant template. Volume and concentration based scale-up approaches have been investigated and systematically compared using a similarity index that included parameters related to the particle size distribution (d10, d50, d90) and pore structure (mean pore diameter, specific surface area, total pore volume, sorption hysteresis loop). The particle size distribution was found to be dependent mainly on the hydrodynamic conditions, expressed by the homogenization time, while the pore structure and the overall yield of the process were found to depend mainly on the CTAB/TEOS ratio. Overall, successful scale-up criteria in both volume and concentration based approaches have been identified.

Hanson, K. L., Fulga, F., Dobroiu, S., Solana, G., Kašpar, O., Tokárová, V., Nicolau, D. V., “Polymer surface properties control the function of heavy meromyosin in dynamic nanodevices”, Biosensors and Bioelectronics (2016) More

The actin-myosin system, responsible for muscle contraction, is also the force-generating element in dynamic nanodevices operating with surface-immobilized motor proteins. These devices require materials that are amenable to micro- and nano-fabrication, but also preserve the bioactivity of molecular motors. The complexity of the protein-surface systems is greatly amplified by those of the polymer-fluid interface; and of the structure and function of molecular motors, making the study of these interactions critical to the success of molecular motor-based nanodevices. We measured the density of the adsorbed motor protein (heavy meromyosin, HMM) using quartz crystal microbalance; and motor bioactivity with ATPase assay, on a set of model surfaces, i.e., nitrocellulose, polystyrene, poly(methyl methacrylate), and poly(butyl methacrylate), poly(tert-butyl methacrylate). A higher hydrophobicity of the adsorbing material translates in a higher total number of HMM molecules per unit area, but also in a lower uptake of water, and a lower ratio of active per total HMM molecules per unit area. We also measured the motility characteristics of actin filaments on the model surfaces, i.e., velocity, smoothness and deflection of movement, determined via in vitro motility assays. The filament velocities were found to be controlled by the relative number of active HMM per total motors, rather than their absolute surface density. The study allowed the formulation of the general engineering principles for the selection of polymeric materials for the manufacturing of dynamic nanodevices using protein molecular motors.

Kašpar, O., Zhang, H., Tokárová, V., Boysen, R. I.,  Suñé, G. R.,  Borrise, X., Murano, F.P., Hearn, M. T. W., Nicolau, D.V., “Confinement of water droplets on rectangular micro/nano-arrayed surfaces”, Lab Chip, 16, 2487-2493 (2016) More

Micro-patterned surfaces with alternate hydrophilic and hydrophobic rectangular areas effectively confine water droplets down to attolitre volumes. The contact angle, volume, and geometry of the confined droplets as a function of the geometry and physico-chemical properties of the confining surfaces have been determined by phenomenological simulations, validated by atomic force microscopy measurements. The combination between experiments and simulations can be used for the purposeful design of arrays with surface-addressable hydrophobicity employed in digital microfluidics and high-throughput screening nanoarrays.

Filipponi, L., Livingston, P., Kašpar, O., Tokárová, V., Nicolau, D.V., “Protein patterning by microcontact printing using pyramidal PDMS stamps”, Biomedical Microdevices 18, 1-7 (2016) More

Micro-contact printing, μCP, is a well-established soft-lithography technique for printing biomolecules. μCP uses stamps made of Poly(dimethylsiloxane), PDMS, made by replicating a microstructured silicon master fabricated by semiconductor manufacturing processes. One of the problems of the μCP is the difficult control of the printing process, which, because of the high compressibility of PDMS, is very sensitive to minute changes in the applied pressure. This over-sensitive response leads to frequent and/or uncontrollable collapse of the stamps with high aspect ratios, thus decreasing the printing accuracy and reproducibility. Here we present a straightforward methodology of designing and fabricating PDMS structures with an architecture which uses the collapse of the stamp to reduce, rather than enlarge the variability of the printing. The PDMS stamp, organized as an array of pyramidal micro-posts, whose ceiling collapses when pressed on a flat surface, replicates the structure of the silicon master fabricated by anisotropic wet etching. Upon application of pressure, depending on the size of, and the pitch between, the PDMS pyramids, an air gap is formed surrounding either the entire array, or individual posts. The printing technology, which also exhibits a remarkably low background noise for fluorescence detection, may find applications when the clear demarcation of the shapes of protein patterns and the distance between them are critical, such as microarrays and studies of cell patterning. [aio_button align=”left” animation=”none” color=”gray” size=”small” icon=”education” text=”PDF” relationship=”dofollow” url=”http://download.springer.com/static/pdf/951/art%253A10.1007%252Fs10544-016-0036-4.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs10544-016-0036-4&token2=exp=1453747686~acl=%2Fstatic%2Fpdf%2F951%2Fart%25253A10.1007%25252Fs10544-016-0036-4.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs10544-016-0036-4*~hmac=d7042a3164df12df168de6f89cfa91c00d503f27afefd76a6235d9c6a198b883″]

Oka S., Emady H., Kašpar O., Tokárová V., Muzzio F.J., Štěpánek F., Ramachandran R., “The effects of improper mixing and preferential wetting of active and excipient ingredients on content uniformity in high shear wet granulation”, Powder Technol. 278, 266-277 (2015) More

 This work focuses on the content non-homogeneity in granules across size classes in a high shear wet granulation process as a result of powder segregation during dry mixing coupled with preferential wettability of one of the ingredients with the binder fluid.

A two component API-excipient system comprised of acetaminophen (APAP) and microcrystalline cellulose PH-101 (MCC) is investigated in a high shear granulation environment for content uniformity of the granules with respect to APAP. It was found that the fine granules were super potent while the coarse granules were starved of the APAP. This was attributed to a dual cause of powder segregation during dry mixing and superior wettability of the MCC compared to APAP. Post the dry mixing stage, the top layer of the powder bed is found to be sub-potent due to percolation of the smaller APAP particles to the bottom of the bed as they find spaces between the larger MCC particles. Thus, a drop of the binder fluid which falls on the bed is likely to be surrounded by MCC particles, which give them a higher chance of being incorporated in the nucleus. Moreover, MCC being the superior wetting of the two ingredients, also preferentially attaches itself to the growing granules. The granules are thus starved of the APAP leading to disparity in content across size classes.

Lastly, the effect of content non-uniformity was categorically quantified on the rate of active release. It was observed that content non-uniformity results in a lack of predictability and consequently control, on the rate of release of the active ingredient from the granules. This work highlights the need for qualitative understanding and quantitative analysis of factors that contribute to the occurrence of granule content non-uniformity, if one is to enable inherently robust pharmaceutical product design.

Oka S., Kašpar O., Tokárová V., Sowrirajan K., Wu H., Khan H., Muzzio F., Štěpánek F., Ramachandran R., “A quantitative study of the effect of process parameters on key granule characteristics in a high shear wet granulation process”, Adv. Powder Technol. 26, 315-322 (2015) More

The objective of the current work was to investigate the effect of liquid to solid ratio (L/S), impeller speed and the wet massing time on the critical quality attributes of granules in a high shear wet granulation process for a two component (API and excipient) system. The parameters were evaluated for their effect on granule properties using a design of experiment based approach. Granules were characterized for their particle size distribution, content uniformity, morphology and porosity. The liquid to solid (L/S) ratio was found to have a dominant effect on the median particle size and exhibited a clear trend. The system was found to be extremely well mixed for all conditions thus implying robust composition uniformity within and between batches, independent of process parameters. The release kinetics of granules within the batch were found to be identical, independent of particle size. The granules were found to be fairly spherical as observed through a scanning electron microscope with no distinct agglomeration. The images indicate granulation by layering and consolidation. All three process parameters were found to have an effect on granule porosity, with the wet massing time having the most pronounced effect. A judicious selection of the afore mentioned process parameters will enable a balance between granule growth and porosity to be achieved without compromising on the mixing efficiency of the process thereby allowing one to build quality into the final product.

Kašpar O., Tokárová V., Oka S., Sowrirajan K., Ramachandran R., Štěpánek F., “Combined UV/Vis and micro-tomography investigation of acetaminophen dissolution from granules”, Int. J. Pharm. 458, 272-281 (2013) More

The X-ray micro-tomography (micro-CT) technique has been used to visualize the microstructure of granules produced by high shear wet granulation and the dynamic evolution of porosity during granule dissolution. Using acetaminophen (paracetamol) as the active pharmaceutical ingredient (API) and microcrystalline cellulose (Avicel PH-200) as an excipient, the porosity of the granules was systematically influenced by the granulation process parameters (binder/solids ratio, impeller speed and wet massing time). An increase of granule porosity from 7% to 10% and 18% lead to a decrease of the dissolution time t90 from 435 min to 98 min and 37 min, respectively. The combination of time-resolved micro-CT imaging with UV/vis detection of the quantity dissolved made it possible to evaluate the effective diffusion coefficient of the API through the granule structure, and thus establish a quantitative structure–property relationship for dissolution. A power-law dependence of the effective diffusivity on porosity (Archie’s law) was found to hold.

Kašpar O., Tokárová V., Nyanhongo G. S., Gübitz G., Štěpánek F., “Effect of cross-linking method on the activity of spray-dried chitosan microparticles with immobilized laccase”, Food Bioprod. Proces. 91, 525-533 (2013) More

The effect of processing method on the properties of cross-linked chitosan microparticles and on the enzymatic activity of laccase immobilized in the particles has been investigated. Chitosan has been cross-linked by tri-polyphosphate (TPP) using two methods – the so called ex situ cross-linking whereby the solutions of chitosan, TPP and the enzyme have been pre-mixed and spray-dried by a standard two-fluid kinetic nozzle, and a novel in situ cross-linking method, whereby the solutions have been contacted at the tip of a three-fluid nozzle and cross-linking occurred within a drying droplet. The influence of the cross-linking method on the particle size and morphology, surface charge, and swelling ratio has been determined. The enzymatic activity of laccase toward the oxidation of a chromophore substrate (ABTS) has been systematically investigated and found to be superior in particles produced by the in situ cross-linking method.

Tokárová V., Kašpar O., Knejzlík Z., Ulbrich P., Štěpánek F., “Development of spray-dried chitosan microcarriers for nanoparticle delivery”, Powder Technol. 235, 797-805 (2013) More

The design of chitosan microspheres for the encapsulation and release of nanoparticles has been considered. The composite microcarriers have been produced by spray drying and the effect of factors including the chitosan cross-linking ratio (using tri-polyphosphate as the cross-linking agent), nanoparticle loading in the polymer matrix and the internal structure of the microspheres (uniform dispersion of nanoparticles vs. core-shell structure) on the in vitro release kinetics have been systematically investigated. The antibacterial performance of the composite microspheres containing Ag nanoparticles has been evaluated against three different strains of bacteria in a suspension culture. The bioadhesive character of the chitosan carrier particles has lead to the formation of stable aggregates with the bacteria, which enhanced the antibacterial efficacy of the released nanoparticles through the contact mechanism.

Kašpar O., Jakubec M., Štěpánek F., “Characterization of spray dried chitosan-TPP microparticles formed by two- and three-fluid nozzles”, Powder Technol. 240, 31-40 (2013) More

Chitosan microparticles cross-linked by tri-polyphosphate (TPP) anions have been prepared by spray drying. Two different cross-linking methods have been employed — ex-situ cross-linking whereby aqueous solution of cross-linked chitosan nanoparticles has been spray-dried by a two-fluid nozzle, and a novel in-situ cross-linking method, whereby solutions of chitosan and TPP have been fed to a three-fluid nozzle and cross-linking occurred within individual droplets. The size and morphology of the resulting microparticles have been characterised and their dependence on the cross-linking ratio and the initial chitosan concentration determined. Particles produced by the three-fluid nozzle were found to have favourable properties in terms of stability in aqueous media and they allow the use of higher chitosan concentrations, which makes them suitable for microencapsulation applications.

Post-Doc Researchers

Ing. Edyta Wawrzyńska, Ph.D.

Edyta

Postdoc

work phone+420220442033

VŠCHT Praha – building B, Z B2-248

 

 

Education

  • 2011 – 2015     The International Ph.D. Program, Faculty of Chemistry, Warsaw University of Technology, Poland
  • 2006 – 2011     Master of Science in Engineering, Chair of Chemistry and Technology of Polymers, The Faculty of Chemistry, Warsaw University of Technology, Poland

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  • 2016 – 2018    Scientific internships, The Polymer Institute, Slovak Academy of Sciences, Slovakia
  • 2016 – 2018    Postdoctoral researcher, Institute of Macromolecular Chemistry, Czech Academy of Sciences, Czech Republic
  • 2014 – 2015    Scientific internship, Institute of Physical Chemistry, Faculty of Chemistry, University of Vienna, Austria
  • 2012 – 2013    Scientific internship, Institute of Physical Chemistry, Faculty of Chemistry, University of Vienna, Austria
  • 2019 – present
    NewSurf: New method of surface fabrication for non-enzymatic cell harvesting for pharmacological or medical use
  • 2016 – 2018
    MH CR (No. 16-28254A), Controlled vascularization of micro-porous scaffold for subsequent cellular transplantation
  • 2011 – 2015
    MPD Project 2010: Towards Advanced Functional Materials and Novel Devices – Joint University of Warsaw and Warsaw University of Technology International Ph.D. Program;
    Project: Advanced polymeric materials – From calculation to application
  • 2010 – 2011
    MARGEN E.U. project concerning the development of new generation biodegradable packaging materials
  • 2010 – 2011
    BIOPOL project concerning the development of a technology of biodegradable polyesters with the use of renewable raw materials
  • Polymer and material science
  • Thermoresponsive polymers
  • Cell harvesting
  • Biodegradable polymers
  • Polymer scaffolds
  • Protein release
  • LbL coatings
  • Hyperbranched polymers
  • Drug delivery

E. Wawrzyńska, and D. Kubies. “Alginate matrices for protein delivery-a short review.” Physiological research 67 (2018).More

Growth factors are powerful molecules that regulate cellular growth, proliferation, healing, and cellular differentiation. A delivery matrix that incorporates growth factors with high loading efficiencies, controls their release, and maintains bioactivity would be a powerful tool for regenerative medicine. Alginate has several unique properties that make it an excellent platform for the delivery of proteins. Mild gelling conditions can minimize the risk of protein denaturation; moreover, alginate can serve as protection from degradation until protein release. Various modifications have been proposed to tune alginate binding and release proteins, simultaneously adjusting alginate degradability, mechanical stiffness, swelling, gelation properties and cell affinity. The primary objective of this article is to review the literature related to recent advances in the application of alginate matrices in protein delivery in regenerative medicine. A special emphasis is put on the relevance of delivery of growth factors and chemokine.

A. Kundys, A. Plichta, Z. Florjanczyk, A. Zychewicz, P. Lisowska, P. Parzuchowski, E. Wawrzyńska, Multi-arm star polymers of lactide obtained in melt in the presence of hyperbranched oligoglycerols, Polymer International, 2016 (65), 927 – 937. More

Multi‐arm star poly(l‐lactide) (PLLA) was synthesized in bulk, via ring‐opening polymerization of l‐lactide initiated by: trimethylolpropane, pentaerythritol, dipentaerythritol, myo‐inositol and hyperbranched polyglycerols. The synthesis was carried out on a laboratory scale and also in a model research installation equipped with a 2 L polymerization reactor. Matrix‐assisted laser desorption ionization time‐of‐flight analysis of the products synthesized in the presence of simple polyols and tin 2‐ethylhexanoate revealed that the reactions were not entirely selective and the final products were a mixture of multi‐arm star, linear and cyclic PLLA. The reactions co‐initiated by polyglycerols (PGs) led to polymer mixtures with molar masses in the range 13.5–102 kg mol−1 and intrinsic viscosity significantly lower than that of linear PLLA with the same molar mass. In order to obtain more hydrophobic PG initiator, a suitable method of modification of PG structure was developed. The PG and modified PG branching agents were used to prepare multi‐arm star PLLA in the model semi‐technical installation. Molar masses of the resulting polymers were in the range 169–249 kg mol−1 and exhibited much lower intrinsic viscosity than the linear homologue. The rheological properties of synthesized materials with commercial PLLA blends as well as thermal and mechanical properties were analysed.

P. Parzuchowski, J. Gregorowicz, E. P. Wawrzyńska, D. Wiącek, G. Rokicki, The Phase Behavior in Supercritical Carbon Dioxide of Hyperbranched Copolymers with Architectural Variations, The Journal of Supercritical Fluids, 2016 (107), 657 – 668. More

Hyperbranched polymers (HBPs) have been known and extensively investigated for over two decades. However, there are still areas that need to be explored. Recently, much effort has been placed in developing drug delivery systems based on macromolecules of three-dimensional structure. This paper describes the synthesis of random hyperbranched copolyesters of 2,2-bis(hydroxymethyl)propionic acid (bis-MPA) and ε-caprolactone (ε-CL) and their phase behavior in supercritical carbon dioxide (scCO2) after modification with fluorinated anhydrides or chlorotrimethylsilane. The structure of the copolyesters was investigated by means of 1H and 13C NMR, FTIR spectroscopies, and MALDI-TOF spectrometry. The influence of the content of chain extender units of 6-hydroxyhexanoic acid (formed from ε-CL) and terminal group functionalities on the solubility of hyperbranched polymers was investigated. The phase behavior of the polymers in supercritical carbon dioxide was explored as a function of concentration and temperature. It was shown that introduction of small amounts (5–10%) of chain extender units into the dense structure of branched poly(bis-MPA) facilitates solubility of a polymer in scCO2. Viscosity and contact angle measurements were performed for the synthesized polymers. 

E. Wawrzyńska, A. Sikorski, G. Zifferer, Monte Carlo Simulation Studies of Regular and Irregular Dendritic Polymers, Macromolecular Theory and Simulations, 2015 (5), 477- 489. More

A dynamic Monte Carlo method was employed to study regular as well as irregular dendrimers with up to G = 8 generations with functionality F = 3 under athermal conditions. The size of dendrimers showed the same scaling law with respect to chain‐length n as linear chains, keeping G at a constant value. If n was varied via G at fixed spacer‐length m its scaling behavior was similar to that of collapsed globules, at least for large values of G. Asphericity strongly decreased with an increase of G. The composition of irregular dendrimers remained unchanged with respect to F and G but the spacer‐lengths were distributed according to several models. Quite generally, distributions became broader, size larger and shape less symmetric compared to the regular case. These effects increased with an increase of dispersity of the branches.

P. G. Parzuchowski, J. Gregorowicz, Z. Fraś, E. P. Wawrzyńska, E. Brudzyńska, G.Rokicki, Hyperbranched poly(ether-siloxane) amphiphiles of surprisingly high solubility in supercritical carbon dioxide, The Journal of Supercritical Fluids, 2014 (95), 222 – 227.More

In this work, we present a simple method for preparation of an inexpensive CO2-philic amphiphiles for solubilization and related applications. The poly(ether-siloxane)s we have synthesized showed very good solubility in supercritical carbon dioxide, despite the fact they contained hydrophilic polyether structures. So far, incorporation of any type of substituents to the poly(dimethylsiloxane) (PDMS) chains resulted in decrease of the solubility in scCO2. We showed that, it is possible to obtain copolymers containing both hydrophilic (polyether) and hydrophobic (polysiloxane) parts which have better solubility in scCO2 than respective homopolymers. The proposed synthetic route should allow the design of a wide range of related CO2-philic hyperbranched materials.

E. Wawrzyńska, S. Eisenhaber, P. Parzuchowski, A. Sikorski, G. Zifferer, Monte Carlo Simulation Studies of the Size and Shape of Regular Three Generation Dendrimers, Macromolecular Theory and Simulations, 2014, 23, 288 – 299.More

By the use of a dynamic Monte Carlo method, three‐generation dendrimers of type F1F2F2 with functionalities F1 = 3 to 6 and F2 = 2 to F1–1 are simulated and investigated as functions of spacer lengths, with a total chain length up to 200 000 segments. Highly diluted athermal and theta solutions are studied as well as properties of non‐reversal random walk dendrimers for comparison. For athermal conditions mean square dimensions obey the same scaling law regarding the total number of bonds as linear chains, irrespective of functionality and complexity. Likewise the theta parameter is the same for all systems investigated. Dimensions of theta systems are slightly expanded as compared to non‐reversal random walk data, the effect increasing with increasing F1 and F2 while shape data near to theta conditions fairly well coincide with those of non‐reversal random walks.

P. Polanowski, E. Wawrzyńska, A. Sikorski, Percolation in two-dimensional copolymer systems, Macromolecular Theory and Simulations, 2013, 22, 238 – 245.More

The aim of the study is the investigation of the percolation phenomena in some model copolymer systems. Diblock, triblock, random copolymers, and a blend of homopolymers are studied. For this purpose, we developed an idealized model of polymeric systems. The positions of polymer segments are restricted to vertices of a simple cubic lattice. The chains are at good solvent conditions – the excluded volume is the only interaction between the segments of the chain. The properties of the model chains are determined by means of Monte Carlo simulations with a sampling algorithm based on chain’s local changes of conformation. The differences and similarities in the percolation behavior are shown and discussed. The percolation threshold is found to be very weakly dependent on the chain length, however, it appears that the main factor that influenced the percolation threshold is the screening effect of other parts of chains.

J. Gregorowicz, E. Wawrzyńska, P.G. Przuchowski, Z. Fraś, G. Rokicki, K. Wojciechowski, S. A. Wieczorek, A. Wiśniewska, A. Plichta, K. Dąbrowski, Synthesis, Characterization, and Solubility in Supercritical Carbon Dioxide of Hyperbranched Copolyesters, Macromolecules, 2013, 46 (18), 7180 – 7195.More

Hyperbranched polymers (HBPs) have been known and extensively investigated for over two decades. However, there are still areas that need to be explored. Recently, much effort has been placed in developing drug delivery systems based on macromolecules of three-dimensional structure. This paper describes the synthesis of random hyperbranched copolyesters of 2,2-bis(hydroxymethyl)propionic acid (bis-MPA) and ε-caprolactone (ε-CL) and their phase behavior in supercritical carbon dioxide (scCO2) after modification with fluorinated anhydrides or chlorotrimethylsilane. The structure of the copolyesters was investigated by means of 1H and 13C NMR, FTIR spectroscopies, and MALDI-TOF spectrometry. The influence of the content of chain extender units of 6-hydroxyhexanoic acid (formed from ε-CL) and terminal group functionalities on the solubility of hyperbranched polymers was investigated. The phase behavior of the polymers in supercritical carbon dioxide was explored as a function of concentration and temperature. It was shown that introduction of small amounts (5–10%) of chain extender units into the dense structure of branched poly(bis-MPA) facilitates solubility of a polymer in scCO2. Viscosity and contact angle measurements were performed for the synthesized polymers.

M. Tryznowski, K. Tomczyk, Z. Fraś, J. Gregorowicz, G. Rokicki, E. Wawrzyńska, P. Parzuchowski, Aliphatic Hyperbranched Polycarbonates: Synthesis, Characterization, and Solubility in Supercritical Carbon Dioxide, Macromolecules, 2012, 45 (17), 6819 – 6829.More

Recently much effort has been devoted to developing drug delivery systems based on macromolecules of three-dimensional structure. In addition to dendrimers which are widely studied, hyperbranched polymers are gaining more and more attention. Among numerous polymeric materials used in drug delivery systems, aliphatic polycarbonates are one of the most interesting ones due to biocompatibility, nontoxic degradation products, and the absence of autocatalytic effect during the degradation process. However, they show poor solubility in supercritical carbon dioxide. This paper describes the synthesis of 5-(4-hydroxybutyl)-1,3-dioxan-2-one and its application for preparation of hyperbranched aliphatic polycarbonates. Linear analogues of the poly(5-(4-hydroxybutyl)-1,3-dioxan-2-one) were prepared, too, and the structures were compared by means of 13C NMR. Ring-opening polymerization of 5-(4-hydroxybutyl)-1,3-dioxan-2-one led to polymers containing solely primary hydroxyl groups which were subsequently reacted with trifluoroacetic anhydride. The phase behavior of fluorinated polymer in supercritical carbon dioxide was explored as a function of concentration and temperature. Modified hyperbranched polycarbonate showed reasonably good solubility in carbon dioxide. It was shown that hyperbranched structure of a polymer facilitate solubility even though the carbonate structural units do not promote solubility in scCO2.

Ph.D. students

Ing. Lucie Mašková

Lucie

Ph.D. student

work phone+420220442033

VŠCHT Praha – building B, Z B2-248

 

 

Education

  • 2019 – present Ph.D. at UCT Prague; Chemical Engineering
    “Study of transport phenomena and enzymatic kinetics of artificial garlic cell produced by spray drying”
  • 2017 – 2019   MSc. at UCT Prague; Chemical Engineering and Bioengineering
  • 2014 – 2017   BSc. at UCT Prague; Drug Synthesis and Production

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  • spray-drying
  • encapsulation
  • powder characterization

Ing. Matěj Černý (supervisor Mgr. Anna Fučíková, Ph.D. – Charles University)

Matej

Ph.D. student

work phone+420220442033

VŠCHT Praha – building B, Z B2-248

 

 

Education

  • 2019 – present Ph.D.  at Charles University
  • 2017 – 2019   MSc. at UCT Prague; Chemical Engineering and Bioengineering
  • 2014 – 2017   BSc. at UCT Prague; Nano and Microtechnology in Chemical Engineering

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  • nanotechnology
  • microfluidics

Master students

Bc. David Zůza

David

Master student

work phone+420220443048

VŠCHT Praha – building B, B 308

 

 

Education

  • 2018 – present MSc. at UCT Prague; Chemical Engineering and Bioengineering
  • 2015 – 2018   BSc. at UCT Prague; Analytical and Physical chemistry

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  • silica particles
  • microfluidics
  • 3D printing
  • D. Zůza, M. Šoltys, F. Štěpánek: Study of continuous microfluidic preparation of mesoporous silica microparticles, SSCHE 2017, 22.-26.5.2016, Demänovská dolina, Slovakia (fulltext, poster)
  • PR Manager (4Students.cz) – since April 2017
  • Memeber of Student asociation 4Students.cz – since September 2015
  • Memeber of Student asociation VŠCHT na Majales – since January 2016

Zůza, D.; Šoltys, M.; Mužík, J.; Lizoňová, D.; Lhotka, M.; Ulbrich, P.; Kašpar, O.; Štěpánek, F., Silica particles with three levels of porosity for efficient melt amorphisation of drugs. Microporous and Mesoporous Materials 2018 More

Silica particles with a unique multi-level pore structure have been prepared in order to enable efficient melt-in amorphisation of pharmaceutical substances. The dissolution rate of drugs with a low aqueous solubility can be enhanced by their conversion from a crystalline to an amorphous form. In order to avoid spontaneous re-crystallisation over time, the amorphous form must be stabilised, in this case by melt-in sorption into a porous carrier. To stabilise the amorphous state, pore diameters not exceeding approximately ten times the equivalent molecular diameter are required. However, since the permeability of porous media scales with the square of the mean pore diameter, carrier particles with pores in the nanometer range suffer from slow melt-in rates. Therefore, silica particles with a novel multi-level porous structure have been proposed in this work. The particles combine a central hollow cavity, a network of conducting macro-pores for enhanced transport rate, and a mesoporous matrix for efficient stabilisation of the amorphous state. The particles were prepared by the hydrolysis of TEOS using a soft-templating method with octylamine. We show that by systematically modulating the hydrolysis rate by the presence of ethanol (a reaction by-product), particles with the desired pore structure, particle size and morphology can be formed. Furthermore, we demonstrate their superior transport properties during melt sorption, high drug loading capacity and the ability to stabilise the amorphous state of a drug.

Bc. Kateryna Korniienko

Katka

Master student

work phone+420220443048

VŠCHT Praha – building B, B 308

 

 

Education

  • 2019 – present MSc. at UCT Prague; Chemical Engineering and Bioengineering
  • 2016 – 2019  BSc. at UCT Prague; Nano and Microtechnology in Chemical Engineering

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  • nanotechnology
  • encapsulation
  • biosimulation

Bc. Jan Šugar

Honza

Master student

work phone+420220443048

VŠCHT Praha – building B, B 308

 

 

Education

  • 2019 – present MSc. at UCT Prague; Chemical Engineering and Bioengineering
  • 2016 – 2019   BSc. at UCT Prague; Chemistry

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  • Pursuing my Master Degree in Chemical Engineering and Bioingeneering at UCT Prague, I would like to gain some real-life experience by immersing myself to industrial scientific R&D.
  • 04/2018 – 07/2019
    Biochemistry Lab Intern – IOCB Prague
    Bachelor Thesis – Production, purification and characterisation of an internal globular domain from the human membrane protein iRhom

 

  • 02/2014 – 05/2016
    Spectroscopy and Physical Organic Chemistry Lab Intern – IOCB Prague 
  • EF Education First – English Language Course, Oxford (07/2018 – 08/2018)
    Final Certificate of Achievement awarded C2 Proficiency Level
  • Driving licence (category B) (08/2015 – Present)

Šugar, Jan, and Petr Bouř. Quantitative analysis of sugar composition in honey using 532‐nm excitation Raman and Raman optical activity spectra.” Journal of Raman Spectroscopy 47.11 (2016): 1298-1303.More

Raman spectroscopy based on the 1064‐nm laser excitation was suggested as a handy non‐invasive technique allowing to quickly determine sugar content in honey and similar food products. In the present study, the green 532‐nm laser radiation is explored instead as it provides higher‐quality spectra in a shorter time. The sample fluorescence was quenched by purification with activated carbon. For control mixture decomposition of Raman spectra to standard subspectra led to a typical error of the sugar content of 3%. Raman optical activity (ROA) spectra that could be measured at the shorter excitation wavelength as well provided a lower accuracy (~8%) than the Raman spectra because of instrumental sensitivity and noise limitations. The results show that Raman spectroscopy provides elegant and reliable means for fast analyses of sugar‐based food products. Copyright © 2016 John Wiley & Sons, Ltd.

Bachelor students

Lucie Večerková

Katka

Bachelor student

work phone+420220443048

VŠCHT Praha – building B, B 308

 

 

Education

  • 2018 – present  BSc. at UCT Prague; Chemistry

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Visiting students

Andrea Rukavina

 

My name is Andrea Rukavina and I am currently finishing the 1st year of the master degree in Biotechnology at University of Ljubljana, Slovenia. In 2015 I was accepted for Erasmus+ student exchange at University of Chemistry and Technology in Prague. Due to beautiful experiences and gained knowledge, I decided to come back for an internship and join the Laboratory of Biomimetic Engineering where I can put my knowledge into practice. Moreover, there are several projects ongoing and I chose the one that suits my research interests – encapsulation of enzymes and the evaluation of antimicrobial activity of naturally sourced compounds. I am looking forward to progressing and further work with the team.

 

EDUCATION

2013-2016: Academic Study Programme (BSc) in Food Science and Nutrition, Biotechnical Faculty, University of Ljubljana, Slovenia

2017-present: Master Study Programme (MSc) in Biotechnology, Biotechnical Faculty, University of Ljubljana, Slovenia

INTERNATIONAL EXPERIENCES

2015: Erasmus+ student exchange at University of Chemistry and Technology in Prague, Department of Chemical Engineering

2017: Erasmus+ student internship at Laboratory of Biomimetic Engineering, University of Chemistry and Technology in Prague, Department of Chemical Engineering


Ingrid Lyonnet

Master student

work phone: +33 6 06 91 41 39

VŠCHT Praha – building B

 

EDUCATION

2014-2016: Classes Préparatoires aux Grandes Ecoles (CPGE), Lycée Claude-Fauriel, Engineering Universities specializing in Maths, Physics and Chemistry, Saint-Etienne, France

2016-present: Ecole Nationale Supérieure des Industries Chimiques (ENSIC), Chemical and Process Engineering University, Nancy, France

Research interests

  • encapsulation
  • microfluidics
  • spray drying
  • testing of antibacterial activity

Project

Artificial garlic cell” – synthesis and characterization of structured microparticles and testing their antimicrobial effect


Catarina Mendes

My name is Catarina Mendes, I’m a 22 years old Portuguese student, member of the Board of European Students of Technology (Lisbon’s Local Group). Currently, I’m in the first semester of the master degree in Chemical Engineering at UCT Prague, as an Erasmus student.

EDUCATION

2014-present: Integrated master’s degree at IST Lisbon, Universidade de Lisboa, Chemical Engineering

 

Project

Synthesis and Characterization of Nanoparticles


Maria Terrucha

My name is Maria Terrucha. I’m a Portuguese student from IST Lisbon in my first year of a master degree in Chemical Engineering. Currently, I’m at UCT Prague doing Erasmus+ Exchange Project. My experimental background includes different approaches, gained through several years where I had the opportunity to do Laboratories of Chemistry, Organic Chemistry, Chemistry-Physics, Biochemistry and Molecular Biology, Chemical Analysis, Processes of Chemical and Biological Engineering, Sciences of Chemical Engineering, and most recently, Laboratory of Chemical Engineering. This year I joined the Laboratory of Biomimetic Engineering, to be part of the project that fits my research interests – “Artificial garlic cell”.

EDUCATION

2014-present: Integrated master’s degree at IST Lisbon, Universidade de Lisboa, Chemical Engineering

Project

Artificial garlic cell


Christian Orozco

My name is Christian Orozco, and I am a 21 years old Ecuadorian student. I started master degree in Chemical Engineering at Instituto Superior Técnico, in Lisbon. Currently, I am doing an Erasmus+ exchange project in Prague. Before my arrival, I was accepted to be part of the team of the Laboratory of Biomimetics Engineering. Since the first day, I felt that I could count on all the members of the team and that everyone could contribute something to my apprenticeship. It’s an amazing experience that I won’t forget easily 🙂

 

EDUCATION

2015-present: Integrated master’s degree at IST Lisbon, Universidade de Lisboa, Chemical Engineering

Project

Microfluidic fabrication of composite hydrogel microparticles in the size range of blood cells

Alumni

Bc. Sara Selenica

Sara

 

Ing. Aliye Hazal Koyuncu

Hazal

 

Ing. Jakub Svoboda

Jakub