TY  - JOUR
AU  - Willaert, Ronnie
AU  - Vanden, Boer, Pieterjan
AU  - Malovichko, Anton
AU  - Alioscha-Perez, Mitchel
AU  - Radotić, Ksenija
AU  - Bartolić, Dragana
AU  - Kalauzi, Aleksandar
AU  - Villalba, Maria Ines
AU  - Sanglard, Dominique
AU  - Dietler, Giovanni
AU  - Sahli, Hichem
AU  - Kasas, Sandor
PY  - 2020
UR  - http://rimsi.imsi.bg.ac.rs/handle/123456789/1335
AB  - Living single yeast cells show a specific cellular motion at the nanometer scale with a magnitude that is proportional to the cellular activity of the cell. We characterized this cellular nanomotion pattern of nonattached single yeast cells using classical optical microscopy. The distribution of the cellular displacements over a short time period is distinct from random motion. The range and shape of such nanomotion displacement distributions change substantially according to the metabolic state of the cell. The analysis of the nanomotion frequency pattern demonstrated that single living yeast cells oscillate at relatively low frequencies of around 2 hertz. The simplicity of the technique should open the way to numerous applications among which antifungal susceptibility tests seem the most straightforward.
PB  - Amer Assoc Advancement Science, Washington
T2  - Science Advances
T1  - Single yeast cell nanomotions correlate with cellular activity
IS  - 26
VL  - 6
DO  - 10.1126/sciadv.aba3139
ER  - 

@article{
author = "Willaert, Ronnie and Vanden, Boer, Pieterjan and Malovichko, Anton and Alioscha-Perez, Mitchel and Radotić, Ksenija and Bartolić, Dragana and Kalauzi, Aleksandar and Villalba, Maria Ines and Sanglard, Dominique and Dietler, Giovanni and Sahli, Hichem and Kasas, Sandor",
year = "2020",
abstract = "Living single yeast cells show a specific cellular motion at the nanometer scale with a magnitude that is proportional to the cellular activity of the cell. We characterized this cellular nanomotion pattern of nonattached single yeast cells using classical optical microscopy. The distribution of the cellular displacements over a short time period is distinct from random motion. The range and shape of such nanomotion displacement distributions change substantially according to the metabolic state of the cell. The analysis of the nanomotion frequency pattern demonstrated that single living yeast cells oscillate at relatively low frequencies of around 2 hertz. The simplicity of the technique should open the way to numerous applications among which antifungal susceptibility tests seem the most straightforward.",
publisher = "Amer Assoc Advancement Science, Washington",
journal = "Science Advances",
title = "Single yeast cell nanomotions correlate with cellular activity",
number = "26",
volume = "6",
doi = "10.1126/sciadv.aba3139"
}

Willaert, R., Vanden, B. P., Malovichko, A., Alioscha-Perez, M., Radotić, K., Bartolić, D., Kalauzi, A., Villalba, M. I., Sanglard, D., Dietler, G., Sahli, H.,& Kasas, S.. (2020). Single yeast cell nanomotions correlate with cellular activity. in Science Advances
Amer Assoc Advancement Science, Washington., 6(26).
https://doi.org/10.1126/sciadv.aba3139

Willaert R, Vanden BP, Malovichko A, Alioscha-Perez M, Radotić K, Bartolić D, Kalauzi A, Villalba MI, Sanglard D, Dietler G, Sahli H, Kasas S. Single yeast cell nanomotions correlate with cellular activity. in Science Advances. 2020;6(26).
doi:10.1126/sciadv.aba3139 .

Willaert, Ronnie, Vanden, Boer, Pieterjan, Malovichko, Anton, Alioscha-Perez, Mitchel, Radotić, Ksenija, Bartolić, Dragana, Kalauzi, Aleksandar, Villalba, Maria Ines, Sanglard, Dominique, Dietler, Giovanni, Sahli, Hichem, Kasas, Sandor, "Single yeast cell nanomotions correlate with cellular activity" in Science Advances, 6, no. 26 (2020),
https://doi.org/10.1126/sciadv.aba3139 . .

TY  - JOUR
AU  - Venturelli, Leonardo
AU  - Kohler, Anne-Celine
AU  - Stupar, Petar
AU  - Villalba, Maria, I
AU  - Kalauzi, Aleksandar
AU  - Radotić, Ksenija
AU  - Bertacchi, Massimiliano
AU  - Dinarelli, Simone
AU  - Girasole, Marco
AU  - Pesic, Milica
AU  - Banković, Jasna
AU  - Vela, Maria E.
AU  - Yantorno, Osvaldo
AU  - Willaert, Ronnie
AU  - Dietler, Giovanni
AU  - Longo, Giovanni
AU  - Kasas, Sandor
PY  - 2020
UR  - http://rimsi.imsi.bg.ac.rs/handle/123456789/1338
AB  - The insurgence of newly arising, rapidly developing health threats, such as drug-resistant bacteria and cancers, is one of the most urgent public-health issues of modern times. This menace calls for the development of sensitive and reliable diagnostic tools to monitor the response of single cells to chemical or pharmaceutical stimuli. Recently, it has been demonstrated that all living organisms oscillate at a nanometric scale and that these oscillations stop as soon as the organisms die. These nanometric scale oscillations can be detected by depositing living cells onto a micro-fabricated cantilever and by monitoring its displacements with an atomic force microscope-based electronics. Such devices, named nanomotion sensors, have been employed to determine the resistance profiles of life-threatening bacteria within minutes, to evaluate, among others, the effect of chemicals on yeast, neurons, and cancer cells. The data obtained so far demonstrate the advantages of nanomotion sensing devices in rapidly characterizing microorganism susceptibility to pharmaceutical agents. Here, we review the key aspects of this technique, presenting its major applications. and detailing its working protocols.
PB  - Wiley, Hoboken
T2  - Journal of Molecular Recognition
T1  - A perspective view on the nanomotion detection of living organisms and its features
IS  - 12
VL  - 33
DO  - 10.1002/jmr.2849
ER  - 

@article{
author = "Venturelli, Leonardo and Kohler, Anne-Celine and Stupar, Petar and Villalba, Maria, I and Kalauzi, Aleksandar and Radotić, Ksenija and Bertacchi, Massimiliano and Dinarelli, Simone and Girasole, Marco and Pesic, Milica and Banković, Jasna and Vela, Maria E. and Yantorno, Osvaldo and Willaert, Ronnie and Dietler, Giovanni and Longo, Giovanni and Kasas, Sandor",
year = "2020",
abstract = "The insurgence of newly arising, rapidly developing health threats, such as drug-resistant bacteria and cancers, is one of the most urgent public-health issues of modern times. This menace calls for the development of sensitive and reliable diagnostic tools to monitor the response of single cells to chemical or pharmaceutical stimuli. Recently, it has been demonstrated that all living organisms oscillate at a nanometric scale and that these oscillations stop as soon as the organisms die. These nanometric scale oscillations can be detected by depositing living cells onto a micro-fabricated cantilever and by monitoring its displacements with an atomic force microscope-based electronics. Such devices, named nanomotion sensors, have been employed to determine the resistance profiles of life-threatening bacteria within minutes, to evaluate, among others, the effect of chemicals on yeast, neurons, and cancer cells. The data obtained so far demonstrate the advantages of nanomotion sensing devices in rapidly characterizing microorganism susceptibility to pharmaceutical agents. Here, we review the key aspects of this technique, presenting its major applications. and detailing its working protocols.",
publisher = "Wiley, Hoboken",
journal = "Journal of Molecular Recognition",
title = "A perspective view on the nanomotion detection of living organisms and its features",
number = "12",
volume = "33",
doi = "10.1002/jmr.2849"
}

Venturelli, L., Kohler, A., Stupar, P., Villalba, M. I., Kalauzi, A., Radotić, K., Bertacchi, M., Dinarelli, S., Girasole, M., Pesic, M., Banković, J., Vela, M. E., Yantorno, O., Willaert, R., Dietler, G., Longo, G.,& Kasas, S.. (2020). A perspective view on the nanomotion detection of living organisms and its features. in Journal of Molecular Recognition
Wiley, Hoboken., 33(12).
https://doi.org/10.1002/jmr.2849

Venturelli L, Kohler A, Stupar P, Villalba MI, Kalauzi A, Radotić K, Bertacchi M, Dinarelli S, Girasole M, Pesic M, Banković J, Vela ME, Yantorno O, Willaert R, Dietler G, Longo G, Kasas S. A perspective view on the nanomotion detection of living organisms and its features. in Journal of Molecular Recognition. 2020;33(12).
doi:10.1002/jmr.2849 .

Venturelli, Leonardo, Kohler, Anne-Celine, Stupar, Petar, Villalba, Maria, I, Kalauzi, Aleksandar, Radotić, Ksenija, Bertacchi, Massimiliano, Dinarelli, Simone, Girasole, Marco, Pesic, Milica, Banković, Jasna, Vela, Maria E., Yantorno, Osvaldo, Willaert, Ronnie, Dietler, Giovanni, Longo, Giovanni, Kasas, Sandor, "A perspective view on the nanomotion detection of living organisms and its features" in Journal of Molecular Recognition, 33, no. 12 (2020),
https://doi.org/10.1002/jmr.2849 . .

TY  - JOUR
AU  - Stupar, Petar
AU  - Chomicki, Wojciech
AU  - Maillard, Caroline
AU  - Mikeladze, David
AU  - Kalauzi, Aleksandar
AU  - Radotić, Ksenija
AU  - Dietler, Giovanni
AU  - Kasas, Sandor
PY  - 2017
UR  - http://rimsi.imsi.bg.ac.rs/handle/123456789/1037
AB  - Our team recently demonstrated that cantilever based devices can detect signature of life in a chemistry independent manner. In this technique, the organism of interest is attached onto a classical AFM cantilever. If alive, it induces nanometre scale oscillations of the cantilever that disappear once the organism is killed. The technique was successfully used on bacteria, yeast, vegetal and mammalian cells. In this work we demonstrate that the method can also be applied to sub-cellular organelles, such as mitochondria. Mitochondria are involved in cellular energy production and are present in most eukaryotic cells. Nowadays, it is believed that mitochondria were originally prokaryotes that colonized eukaryotic cells and that live in an endosymbiotic way ever since. Here we present that mitochondria are also animated by nanometre scale oscillations that depend on their metabolic state and that stop once they are inhibited. This observation opens novel avenues to investigate the numerous mitochondria-related diseases in humans.
PB  - Copernicus Gesellschaft Mbh, Gottingen
T2  - Mechanical Sciences
T1  - Mitochondrial activity detected by cantilever based sensor
EP  - 28
IS  - 1
SP  - 23
VL  - 8
DO  - 10.5194/ms-8-23-2017
ER  - 

@article{
author = "Stupar, Petar and Chomicki, Wojciech and Maillard, Caroline and Mikeladze, David and Kalauzi, Aleksandar and Radotić, Ksenija and Dietler, Giovanni and Kasas, Sandor",
year = "2017",
abstract = "Our team recently demonstrated that cantilever based devices can detect signature of life in a chemistry independent manner. In this technique, the organism of interest is attached onto a classical AFM cantilever. If alive, it induces nanometre scale oscillations of the cantilever that disappear once the organism is killed. The technique was successfully used on bacteria, yeast, vegetal and mammalian cells. In this work we demonstrate that the method can also be applied to sub-cellular organelles, such as mitochondria. Mitochondria are involved in cellular energy production and are present in most eukaryotic cells. Nowadays, it is believed that mitochondria were originally prokaryotes that colonized eukaryotic cells and that live in an endosymbiotic way ever since. Here we present that mitochondria are also animated by nanometre scale oscillations that depend on their metabolic state and that stop once they are inhibited. This observation opens novel avenues to investigate the numerous mitochondria-related diseases in humans.",
publisher = "Copernicus Gesellschaft Mbh, Gottingen",
journal = "Mechanical Sciences",
title = "Mitochondrial activity detected by cantilever based sensor",
pages = "28-23",
number = "1",
volume = "8",
doi = "10.5194/ms-8-23-2017"
}

Stupar, P., Chomicki, W., Maillard, C., Mikeladze, D., Kalauzi, A., Radotić, K., Dietler, G.,& Kasas, S.. (2017). Mitochondrial activity detected by cantilever based sensor. in Mechanical Sciences
Copernicus Gesellschaft Mbh, Gottingen., 8(1), 23-28.
https://doi.org/10.5194/ms-8-23-2017

Stupar P, Chomicki W, Maillard C, Mikeladze D, Kalauzi A, Radotić K, Dietler G, Kasas S. Mitochondrial activity detected by cantilever based sensor. in Mechanical Sciences. 2017;8(1):23-28.
doi:10.5194/ms-8-23-2017 .

Stupar, Petar, Chomicki, Wojciech, Maillard, Caroline, Mikeladze, David, Kalauzi, Aleksandar, Radotić, Ksenija, Dietler, Giovanni, Kasas, Sandor, "Mitochondrial activity detected by cantilever based sensor" in Mechanical Sciences, 8, no. 1 (2017):23-28,
https://doi.org/10.5194/ms-8-23-2017 . .

TY  - JOUR
AU  - Kasas, Sandor
AU  - Radotić, Ksenija
AU  - Longo, Giovanni
AU  - Saha, Bashkar
AU  - Alonso-Sarduy, Livan
AU  - Dietler, Giovanni
AU  - Roduit, Charles
PY  - 2013
UR  - http://rimsi.imsi.bg.ac.rs/handle/123456789/723
AB  - Recently, atomic force microscope (AFM) manufacturers have begun producing instruments specifically designed to image biological specimens. In most instances, they are integrated with an inverted optical microscope, which permits concurrent optical and AFM imaging. An important component of the set-up is the imaging chamber, whose design determines the nature of the experiments that can be conducted. Many different imaging chamber designs are available, usually designed to optimize a single parameter, such as the dimensions of the substrate or the volume of fluid that can be used throughout the experiment. In this report, we present a universal fluid cell, which simultaneously optimizes all of the parameters that are important for the imaging of biological specimens in the AFM. This novel imaging chamber has been successfully tested using mammalian, plant, and microbial cells. Microsc. Res. Tech. 76:357363, 2013.
PB  - Wiley-Blackwell, Hoboken
T2  - Microscopy Research and Technique
T1  - A universal fluid cell for the imaging of biological specimens in the atomic force microscope
EP  - 363
IS  - 4
SP  - 357
VL  - 76
DO  - 10.1002/jemt.22174
ER  - 

@article{
author = "Kasas, Sandor and Radotić, Ksenija and Longo, Giovanni and Saha, Bashkar and Alonso-Sarduy, Livan and Dietler, Giovanni and Roduit, Charles",
year = "2013",
abstract = "Recently, atomic force microscope (AFM) manufacturers have begun producing instruments specifically designed to image biological specimens. In most instances, they are integrated with an inverted optical microscope, which permits concurrent optical and AFM imaging. An important component of the set-up is the imaging chamber, whose design determines the nature of the experiments that can be conducted. Many different imaging chamber designs are available, usually designed to optimize a single parameter, such as the dimensions of the substrate or the volume of fluid that can be used throughout the experiment. In this report, we present a universal fluid cell, which simultaneously optimizes all of the parameters that are important for the imaging of biological specimens in the AFM. This novel imaging chamber has been successfully tested using mammalian, plant, and microbial cells. Microsc. Res. Tech. 76:357363, 2013.",
publisher = "Wiley-Blackwell, Hoboken",
journal = "Microscopy Research and Technique",
title = "A universal fluid cell for the imaging of biological specimens in the atomic force microscope",
pages = "363-357",
number = "4",
volume = "76",
doi = "10.1002/jemt.22174"
}

Kasas, S., Radotić, K., Longo, G., Saha, B., Alonso-Sarduy, L., Dietler, G.,& Roduit, C.. (2013). A universal fluid cell for the imaging of biological specimens in the atomic force microscope. in Microscopy Research and Technique
Wiley-Blackwell, Hoboken., 76(4), 357-363.
https://doi.org/10.1002/jemt.22174

Kasas S, Radotić K, Longo G, Saha B, Alonso-Sarduy L, Dietler G, Roduit C. A universal fluid cell for the imaging of biological specimens in the atomic force microscope. in Microscopy Research and Technique. 2013;76(4):357-363.
doi:10.1002/jemt.22174 .

Kasas, Sandor, Radotić, Ksenija, Longo, Giovanni, Saha, Bashkar, Alonso-Sarduy, Livan, Dietler, Giovanni, Roduit, Charles, "A universal fluid cell for the imaging of biological specimens in the atomic force microscope" in Microscopy Research and Technique, 76, no. 4 (2013):357-363,
https://doi.org/10.1002/jemt.22174 . .

TY  - JOUR
AU  - Radotić, Ksenija
AU  - Roduit, Charles
AU  - Simonović Radosavljević, Jasna
AU  - Hornitschek, Patricia
AU  - Fankhauser, Christian
AU  - Mutavdžić, Dragosav
AU  - Steinbach, Gabor
AU  - Dietler, Giovanni
AU  - Kasas, Sandor
PY  - 2012
UR  - http://rimsi.imsi.bg.ac.rs/handle/123456789/594
AB  - Cell-wall mechanical properties play a key role in the growth and the protection of plants. However, little is known about genuine wall mechanical properties and their growth-related dynamics at subcellular resolution and in living cells. Here, we used atomic force microscopy (AFM) stiffness tomography to explore stiffness distribution in the cell wall of suspension-cultured Arabidopsis thaliana as a model of primary, growing cell wall. For the first time that we know of, this new imaging technique was performed on living single cells of a higher plant, permitting monitoring of the stiffness distribution in cell-wall layers as a function of the depth and its evolution during the different growth phases. The mechanical measurements were correlated with changes in the composition of the cell wall, which were revealed by Fourier-transform infrared (FTIR) spectroscopy. In the beginning and end of cell growth, the average stiffness of the cell wall was low and the wall was mechanically homogenous, whereas in the exponential growth phase, the average wall stiffness increased, with increasing heterogeneity. In this phase, the difference between the superficial and deep wall stiffness was highest. FTIR spectra revealed a relative increase in the polysaccharide/lignin content.
PB  - Cell Press, Cambridge
T2  - Biophysical Journal
T1  - Atomic Force Microscopy Stiffness Tomography on Living Arabidopsis thaliana Cells Reveals the Mechanical Properties of Surface and Deep Cell-Wall Layers during Growth
EP  - 394
IS  - 3
SP  - 386
VL  - 103
DO  - 10.1016/j.bpj.2012.06.046
ER  - 

@article{
author = "Radotić, Ksenija and Roduit, Charles and Simonović Radosavljević, Jasna and Hornitschek, Patricia and Fankhauser, Christian and Mutavdžić, Dragosav and Steinbach, Gabor and Dietler, Giovanni and Kasas, Sandor",
year = "2012",
abstract = "Cell-wall mechanical properties play a key role in the growth and the protection of plants. However, little is known about genuine wall mechanical properties and their growth-related dynamics at subcellular resolution and in living cells. Here, we used atomic force microscopy (AFM) stiffness tomography to explore stiffness distribution in the cell wall of suspension-cultured Arabidopsis thaliana as a model of primary, growing cell wall. For the first time that we know of, this new imaging technique was performed on living single cells of a higher plant, permitting monitoring of the stiffness distribution in cell-wall layers as a function of the depth and its evolution during the different growth phases. The mechanical measurements were correlated with changes in the composition of the cell wall, which were revealed by Fourier-transform infrared (FTIR) spectroscopy. In the beginning and end of cell growth, the average stiffness of the cell wall was low and the wall was mechanically homogenous, whereas in the exponential growth phase, the average wall stiffness increased, with increasing heterogeneity. In this phase, the difference between the superficial and deep wall stiffness was highest. FTIR spectra revealed a relative increase in the polysaccharide/lignin content.",
publisher = "Cell Press, Cambridge",
journal = "Biophysical Journal",
title = "Atomic Force Microscopy Stiffness Tomography on Living Arabidopsis thaliana Cells Reveals the Mechanical Properties of Surface and Deep Cell-Wall Layers during Growth",
pages = "394-386",
number = "3",
volume = "103",
doi = "10.1016/j.bpj.2012.06.046"
}

Radotić, K., Roduit, C., Simonović Radosavljević, J., Hornitschek, P., Fankhauser, C., Mutavdžić, D., Steinbach, G., Dietler, G.,& Kasas, S.. (2012). Atomic Force Microscopy Stiffness Tomography on Living Arabidopsis thaliana Cells Reveals the Mechanical Properties of Surface and Deep Cell-Wall Layers during Growth. in Biophysical Journal
Cell Press, Cambridge., 103(3), 386-394.
https://doi.org/10.1016/j.bpj.2012.06.046

Radotić K, Roduit C, Simonović Radosavljević J, Hornitschek P, Fankhauser C, Mutavdžić D, Steinbach G, Dietler G, Kasas S. Atomic Force Microscopy Stiffness Tomography on Living Arabidopsis thaliana Cells Reveals the Mechanical Properties of Surface and Deep Cell-Wall Layers during Growth. in Biophysical Journal. 2012;103(3):386-394.
doi:10.1016/j.bpj.2012.06.046 .

Radotić, Ksenija, Roduit, Charles, Simonović Radosavljević, Jasna, Hornitschek, Patricia, Fankhauser, Christian, Mutavdžić, Dragosav, Steinbach, Gabor, Dietler, Giovanni, Kasas, Sandor, "Atomic Force Microscopy Stiffness Tomography on Living Arabidopsis thaliana Cells Reveals the Mechanical Properties of Surface and Deep Cell-Wall Layers during Growth" in Biophysical Journal, 103, no. 3 (2012):386-394,
https://doi.org/10.1016/j.bpj.2012.06.046 . .

TY  - JOUR
AU  - Mutavdžić, Dragosav
AU  - Xu, Jianmin
AU  - Thakur, Garima
AU  - Triulzi, Robert
AU  - Kasas, Sandor
AU  - Jeremic, Milorad G
AU  - Leblanc, Roger M.
AU  - Radotić, Ksenija
PY  - 2011
UR  - http://rimsi.imsi.bg.ac.rs/handle/123456789/481
AB  - There has been a lack of quick, simple and reliable methods for determination of nanoparticle size. An investigation of the size of hydrophobic (CdSe) and hydrophilic (CdSe/ZnS) quantum dots was performed by using the maximum position of the corresponding fluorescence spectrum. It has been found that fluorescence spectroscopy is a simple and reliable methodology to estimate the size of both quantum dot types. For a given solution, the homogeneity of the size of quantum dots is correlated to the relationship between the fluorescence maximum position (FMP) and the quantum dot size. This methodology can be extended to the other fluorescent nanoparticles. The employment of evolving factor analysis and multivariate curve resolution-alternating least squares for decomposition of the series of quantum dots fluorescence spectra recorded by a specific measuring procedure reveals the number of quantum dot fractions having different diameters. The size of the quantum dots in a particular group is defined by the FMP of the corresponding component in the decomposed spectrum. These results show that a combination of the fluorescence and appropriate statistical method for decomposition of the emission spectra of nanoparticles may be a quick and trusted method for the screening of the inhomogeneity of their solution.
PB  - Royal Soc Chemistry, Cambridge
T2  - Analyst
T1  - Determination of the size of quantum dots by fluorescence spectroscopy
EP  - 2396
IS  - 11
SP  - 2391
VL  - 136
DO  - 10.1039/c0an00802h
ER  - 

@article{
author = "Mutavdžić, Dragosav and Xu, Jianmin and Thakur, Garima and Triulzi, Robert and Kasas, Sandor and Jeremic, Milorad G and Leblanc, Roger M. and Radotić, Ksenija",
year = "2011",
abstract = "There has been a lack of quick, simple and reliable methods for determination of nanoparticle size. An investigation of the size of hydrophobic (CdSe) and hydrophilic (CdSe/ZnS) quantum dots was performed by using the maximum position of the corresponding fluorescence spectrum. It has been found that fluorescence spectroscopy is a simple and reliable methodology to estimate the size of both quantum dot types. For a given solution, the homogeneity of the size of quantum dots is correlated to the relationship between the fluorescence maximum position (FMP) and the quantum dot size. This methodology can be extended to the other fluorescent nanoparticles. The employment of evolving factor analysis and multivariate curve resolution-alternating least squares for decomposition of the series of quantum dots fluorescence spectra recorded by a specific measuring procedure reveals the number of quantum dot fractions having different diameters. The size of the quantum dots in a particular group is defined by the FMP of the corresponding component in the decomposed spectrum. These results show that a combination of the fluorescence and appropriate statistical method for decomposition of the emission spectra of nanoparticles may be a quick and trusted method for the screening of the inhomogeneity of their solution.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "Analyst",
title = "Determination of the size of quantum dots by fluorescence spectroscopy",
pages = "2396-2391",
number = "11",
volume = "136",
doi = "10.1039/c0an00802h"
}

Mutavdžić, D., Xu, J., Thakur, G., Triulzi, R., Kasas, S., Jeremic, M. G., Leblanc, R. M.,& Radotić, K.. (2011). Determination of the size of quantum dots by fluorescence spectroscopy. in Analyst
Royal Soc Chemistry, Cambridge., 136(11), 2391-2396.
https://doi.org/10.1039/c0an00802h

Mutavdžić D, Xu J, Thakur G, Triulzi R, Kasas S, Jeremic MG, Leblanc RM, Radotić K. Determination of the size of quantum dots by fluorescence spectroscopy. in Analyst. 2011;136(11):2391-2396.
doi:10.1039/c0an00802h .

Mutavdžić, Dragosav, Xu, Jianmin, Thakur, Garima, Triulzi, Robert, Kasas, Sandor, Jeremic, Milorad G, Leblanc, Roger M., Radotić, Ksenija, "Determination of the size of quantum dots by fluorescence spectroscopy" in Analyst, 136, no. 11 (2011):2391-2396,
https://doi.org/10.1039/c0an00802h . .