Laban, Bojana B.

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orcid::0000-0002-7758-445X
  • Laban, Bojana B. (5)
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Author's Bibliography

Green synthesis and characterization of nontoxic L-methionine capped silver and gold nanoparticles

Laban, Bojana B.; Ralević, Uroš; Petrović, Sandra; Leskovac, Andreja; Vasić Anićijević, Dragana D.; Marković, Mirjana; Vasić, Vesna M.

(2020)

TY  - JOUR
AU  - Laban, Bojana B.
AU  - Ralević, Uroš
AU  - Petrović, Sandra
AU  - Leskovac, Andreja
AU  - Vasić Anićijević, Dragana D.
AU  - Marković, Mirjana
AU  - Vasić, Vesna M.
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8673
AB  - The simple green method for synthesis of stable L-Methionine (L-Met) capped silver (Ag@LM NPs) and gold (Au@LM NPs) nanoparticles (NPs) without adding any additional reduction agent or stabilizer was developed. Colloidal dispersions were characterized by UV–Vis spectrophotometry. The size and spherical shape of NPs were evaluated by transmission electron microscopy. Their surface covering was confirmed by atomic force microscopy, Fourier transform infrared spectroscopy, dynamic light scattering, and zeta potential measurements. Density functional theory calculations pointed that the preferential adsorption mode of L-Met on both Ag and Au surfaces was a vertical binding geometry via –NH2 group, while horizontal binding mode via [sbnd]S[sbnd] and –NH2 groups is also possible. The genotoxicity (evaluated by the micronucleus assay) of NPs, as well as their effects on some oxidative stress parameters (catalase activity, malondialdehyde level), were assessed in vitro using human peripheral blood cells as a model system. The influence of NPs on the morphology of lymphocyte cells studied using atomic force microscopy revealed that the membrane of cells remained unaffected after the treatment with NPs. When considering the effects of NPs on catalase activity and malondialdehyde level, neither particle type promoted oxidative stress. However, the treatment of lymphocytes with Ag@LM NPs induced a concentration-dependent enhancement of the micronuclei incidence and suppression of the cell proliferation while Au@LM NPs promoted cell proliferation, with no significant effects on micronuclei formation. The Ag@LM NPs were more prone to induce DNA damage than Au@LM NPs, which makes the latter type more suitable for further studies in nano-medicine. © 2019
T2  - Journal of Inorganic Biochemistry
T1  - Green synthesis and characterization of nontoxic L-methionine capped silver and gold nanoparticles
VL  - 204
SP  - 110958
DO  - 10.1016/j.jinorgbio.2019.110958
ER  - 
@article{
author = "Laban, Bojana B. and Ralević, Uroš and Petrović, Sandra and Leskovac, Andreja and Vasić Anićijević, Dragana D. and Marković, Mirjana and Vasić, Vesna M.",
year = "2020",
abstract = "The simple green method for synthesis of stable L-Methionine (L-Met) capped silver (Ag@LM NPs) and gold (Au@LM NPs) nanoparticles (NPs) without adding any additional reduction agent or stabilizer was developed. Colloidal dispersions were characterized by UV–Vis spectrophotometry. The size and spherical shape of NPs were evaluated by transmission electron microscopy. Their surface covering was confirmed by atomic force microscopy, Fourier transform infrared spectroscopy, dynamic light scattering, and zeta potential measurements. Density functional theory calculations pointed that the preferential adsorption mode of L-Met on both Ag and Au surfaces was a vertical binding geometry via –NH2 group, while horizontal binding mode via [sbnd]S[sbnd] and –NH2 groups is also possible. The genotoxicity (evaluated by the micronucleus assay) of NPs, as well as their effects on some oxidative stress parameters (catalase activity, malondialdehyde level), were assessed in vitro using human peripheral blood cells as a model system. The influence of NPs on the morphology of lymphocyte cells studied using atomic force microscopy revealed that the membrane of cells remained unaffected after the treatment with NPs. When considering the effects of NPs on catalase activity and malondialdehyde level, neither particle type promoted oxidative stress. However, the treatment of lymphocytes with Ag@LM NPs induced a concentration-dependent enhancement of the micronuclei incidence and suppression of the cell proliferation while Au@LM NPs promoted cell proliferation, with no significant effects on micronuclei formation. The Ag@LM NPs were more prone to induce DNA damage than Au@LM NPs, which makes the latter type more suitable for further studies in nano-medicine. © 2019",
journal = "Journal of Inorganic Biochemistry",
title = "Green synthesis and characterization of nontoxic L-methionine capped silver and gold nanoparticles",
volume = "204",
pages = "110958",
doi = "10.1016/j.jinorgbio.2019.110958"
}
Laban, B. B., Ralević, U., Petrović, S., Leskovac, A., Vasić Anićijević, D. D., Marković, M.,& Vasić, V. M.. (2020). Green synthesis and characterization of nontoxic L-methionine capped silver and gold nanoparticles. in Journal of Inorganic Biochemistry, 204, 110958.
https://doi.org/10.1016/j.jinorgbio.2019.110958
Laban BB, Ralević U, Petrović S, Leskovac A, Vasić Anićijević DD, Marković M, Vasić VM. Green synthesis and characterization of nontoxic L-methionine capped silver and gold nanoparticles. in Journal of Inorganic Biochemistry. 2020;204:110958.
doi:10.1016/j.jinorgbio.2019.110958 .
Laban, Bojana B., Ralević, Uroš, Petrović, Sandra, Leskovac, Andreja, Vasić Anićijević, Dragana D., Marković, Mirjana, Vasić, Vesna M., "Green synthesis and characterization of nontoxic L-methionine capped silver and gold nanoparticles" in Journal of Inorganic Biochemistry, 204 (2020):110958,
https://doi.org/10.1016/j.jinorgbio.2019.110958 . .
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Nanospectroscopy of thiacyanine dye molecules adsorbed on silver nanoparticle clusters

Ralević, Uroš; Isic, Goran; Vasić Anićijević, Dragana D.; Laban, Bojana B.; Bogdanović, Una; Lazović, Vladimir M.; Vodnik, Vesna; Gajic, Rados

(2018)

TY  - JOUR
AU  - Ralević, Uroš
AU  - Isic, Goran
AU  - Vasić Anićijević, Dragana D.
AU  - Laban, Bojana B.
AU  - Bogdanović, Una
AU  - Lazović, Vladimir M.
AU  - Vodnik, Vesna
AU  - Gajic, Rados
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1890
AB  - The adsorption of thiacyanine dye molecules on citrate-stabilized silver nanoparticle clusters drop-cast onto freshly cleaved mica or highly oriented pyrolytic graphite surfaces is examined using colocalized surface-enhanced Raman spectroscopy and atomic force microscopy. The incidence of dye Raman signatures in photoluminescence hotspots identified around nanoparticle clusters is considered for both citrate- and borate-capped silver nanoparticles and found to be substantially lower in the former case, suggesting that the citrate anions impede the efficient dye adsorption. Rigorous numerical simulations of light scattering on random nanoparticle clusters are used for estimating the electromagnetic enhancement and elucidating the hotspot formation mechanism. The majority of the enhanced Raman signal, estimated to be more than 90%, is found to originate from the nanogaps between adjacent nanoparticles in the cluster, regardless of the cluster size and geometry. (C) 2017 Elsevier B.V. All rights reserved.
T2  - Applied Surface Science
T1  - Nanospectroscopy of thiacyanine dye molecules adsorbed on silver nanoparticle clusters
VL  - 434
SP  - 540
EP  - 548
DO  - 10.1016/j.apsusc.2017.10.148
ER  - 
@article{
author = "Ralević, Uroš and Isic, Goran and Vasić Anićijević, Dragana D. and Laban, Bojana B. and Bogdanović, Una and Lazović, Vladimir M. and Vodnik, Vesna and Gajic, Rados",
year = "2018",
abstract = "The adsorption of thiacyanine dye molecules on citrate-stabilized silver nanoparticle clusters drop-cast onto freshly cleaved mica or highly oriented pyrolytic graphite surfaces is examined using colocalized surface-enhanced Raman spectroscopy and atomic force microscopy. The incidence of dye Raman signatures in photoluminescence hotspots identified around nanoparticle clusters is considered for both citrate- and borate-capped silver nanoparticles and found to be substantially lower in the former case, suggesting that the citrate anions impede the efficient dye adsorption. Rigorous numerical simulations of light scattering on random nanoparticle clusters are used for estimating the electromagnetic enhancement and elucidating the hotspot formation mechanism. The majority of the enhanced Raman signal, estimated to be more than 90%, is found to originate from the nanogaps between adjacent nanoparticles in the cluster, regardless of the cluster size and geometry. (C) 2017 Elsevier B.V. All rights reserved.",
journal = "Applied Surface Science",
title = "Nanospectroscopy of thiacyanine dye molecules adsorbed on silver nanoparticle clusters",
volume = "434",
pages = "540-548",
doi = "10.1016/j.apsusc.2017.10.148"
}
Ralević, U., Isic, G., Vasić Anićijević, D. D., Laban, B. B., Bogdanović, U., Lazović, V. M., Vodnik, V.,& Gajic, R.. (2018). Nanospectroscopy of thiacyanine dye molecules adsorbed on silver nanoparticle clusters. in Applied Surface Science, 434, 540-548.
https://doi.org/10.1016/j.apsusc.2017.10.148
Ralević U, Isic G, Vasić Anićijević DD, Laban BB, Bogdanović U, Lazović VM, Vodnik V, Gajic R. Nanospectroscopy of thiacyanine dye molecules adsorbed on silver nanoparticle clusters. in Applied Surface Science. 2018;434:540-548.
doi:10.1016/j.apsusc.2017.10.148 .
Ralević, Uroš, Isic, Goran, Vasić Anićijević, Dragana D., Laban, Bojana B., Bogdanović, Una, Lazović, Vladimir M., Vodnik, Vesna, Gajic, Rados, "Nanospectroscopy of thiacyanine dye molecules adsorbed on silver nanoparticle clusters" in Applied Surface Science, 434 (2018):540-548,
https://doi.org/10.1016/j.apsusc.2017.10.148 . .
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Mechanism of 3,3 -Disulfopropyl-5,5 -Dichlorothiacyanine Anion Interaction With Citrate-Capped Silver Nanoparticles: Adsorption and J-Aggregation

Laban, Bojana B.; Zeković, Ivana Lj.; Vasić Anićijević, Dragana D.; Marković, Mirjana; Vodnik, Vesna; Luce, Marco; Cricenti, Antonio; Dramićanin, Miroslav; Vasić, Vesna M.

(2016)

TY  - JOUR
AU  - Laban, Bojana B.
AU  - Zeković, Ivana Lj.
AU  - Vasić Anićijević, Dragana D.
AU  - Marković, Mirjana
AU  - Vodnik, Vesna
AU  - Luce, Marco
AU  - Cricenti, Antonio
AU  - Dramićanin, Miroslav
AU  - Vasić, Vesna M.
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1212
AB  - The paper presents the results of the experimental and theoretical study of 3,3-disulfopropyl-5,5-dichlorothiacyanine sodium salt (TC) adsorption and J-aggregation on the surface of citrate-capped silver nano particles (AgNPs) with an average particle size 10 nm. Various nanospectroscopy techniques such as UV-vis, TEM, AFM, DLS, zeta potential, and fluorescence measurements were carried out in order to characterize the hybrid system. Besides this, a set of simple density functional theory calculations (DFT) was performed and this suggested that TC dye, from the thermodynamical point of view, most likely interacted with AgNPs via oxygen atom from SO3- groups. The methods, which considered AgNPs as the macromolecule with several binding sites and TC dye as the ligand, were applied for the analysis of saturation curves constructed from the fluorescence data to obtain the binding constant (K-a = 1.5 x 10(6) M-1) and the average number of TC dye molecules bonded per AgNP (similar to 330). Moreover, TC fluorescence was quenched in the presence of AgNPs on the concentration dependent manner, yielding the linear Stern-Volmer relation accounting for both static and dynamic quenching with the quenching constant K-sv = 2.5 x 10(8) M-1. Kinetic measurements of J-aggregation as the dependence of AgNPs/TC concentration ratio confirmed that the J-aggregation occurred via a two-step process, the first of them being the initial adsorption of dye on AgNPs surface, followed by dye molecules rearrangement and the consecutive growth of TC aggregate layers.
T2  - Journal of Physical Chemistry. C
T1  - Mechanism of 3,3 -Disulfopropyl-5,5 -Dichlorothiacyanine Anion Interaction With Citrate-Capped Silver Nanoparticles: Adsorption and J-Aggregation
VL  - 120
IS  - 32
SP  - 18066
EP  - 18074
DO  - 10.1021/acs.jpcc.6b05124
ER  - 
@article{
author = "Laban, Bojana B. and Zeković, Ivana Lj. and Vasić Anićijević, Dragana D. and Marković, Mirjana and Vodnik, Vesna and Luce, Marco and Cricenti, Antonio and Dramićanin, Miroslav and Vasić, Vesna M.",
year = "2016",
abstract = "The paper presents the results of the experimental and theoretical study of 3,3-disulfopropyl-5,5-dichlorothiacyanine sodium salt (TC) adsorption and J-aggregation on the surface of citrate-capped silver nano particles (AgNPs) with an average particle size 10 nm. Various nanospectroscopy techniques such as UV-vis, TEM, AFM, DLS, zeta potential, and fluorescence measurements were carried out in order to characterize the hybrid system. Besides this, a set of simple density functional theory calculations (DFT) was performed and this suggested that TC dye, from the thermodynamical point of view, most likely interacted with AgNPs via oxygen atom from SO3- groups. The methods, which considered AgNPs as the macromolecule with several binding sites and TC dye as the ligand, were applied for the analysis of saturation curves constructed from the fluorescence data to obtain the binding constant (K-a = 1.5 x 10(6) M-1) and the average number of TC dye molecules bonded per AgNP (similar to 330). Moreover, TC fluorescence was quenched in the presence of AgNPs on the concentration dependent manner, yielding the linear Stern-Volmer relation accounting for both static and dynamic quenching with the quenching constant K-sv = 2.5 x 10(8) M-1. Kinetic measurements of J-aggregation as the dependence of AgNPs/TC concentration ratio confirmed that the J-aggregation occurred via a two-step process, the first of them being the initial adsorption of dye on AgNPs surface, followed by dye molecules rearrangement and the consecutive growth of TC aggregate layers.",
journal = "Journal of Physical Chemistry. C",
title = "Mechanism of 3,3 -Disulfopropyl-5,5 -Dichlorothiacyanine Anion Interaction With Citrate-Capped Silver Nanoparticles: Adsorption and J-Aggregation",
volume = "120",
number = "32",
pages = "18066-18074",
doi = "10.1021/acs.jpcc.6b05124"
}
Laban, B. B., Zeković, I. Lj., Vasić Anićijević, D. D., Marković, M., Vodnik, V., Luce, M., Cricenti, A., Dramićanin, M.,& Vasić, V. M.. (2016). Mechanism of 3,3 -Disulfopropyl-5,5 -Dichlorothiacyanine Anion Interaction With Citrate-Capped Silver Nanoparticles: Adsorption and J-Aggregation. in Journal of Physical Chemistry. C, 120(32), 18066-18074.
https://doi.org/10.1021/acs.jpcc.6b05124
Laban BB, Zeković IL, Vasić Anićijević DD, Marković M, Vodnik V, Luce M, Cricenti A, Dramićanin M, Vasić VM. Mechanism of 3,3 -Disulfopropyl-5,5 -Dichlorothiacyanine Anion Interaction With Citrate-Capped Silver Nanoparticles: Adsorption and J-Aggregation. in Journal of Physical Chemistry. C. 2016;120(32):18066-18074.
doi:10.1021/acs.jpcc.6b05124 .
Laban, Bojana B., Zeković, Ivana Lj., Vasić Anićijević, Dragana D., Marković, Mirjana, Vodnik, Vesna, Luce, Marco, Cricenti, Antonio, Dramićanin, Miroslav, Vasić, Vesna M., "Mechanism of 3,3 -Disulfopropyl-5,5 -Dichlorothiacyanine Anion Interaction With Citrate-Capped Silver Nanoparticles: Adsorption and J-Aggregation" in Journal of Physical Chemistry. C, 120, no. 32 (2016):18066-18074,
https://doi.org/10.1021/acs.jpcc.6b05124 . .
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Mechanism and Kinetics of J-Aggregation of Thiacyanine Dye in the Presence of Silver Nanoparticles

Laban, Bojana B.; Vodnik, Vesna; Dramićanin, Miroslav; Novaković, Mirjana M.; Bibić, Nataša M.; Sovilj, Sofija P.; Vasić, Vesna M.

(2014)

TY  - JOUR
AU  - Laban, Bojana B.
AU  - Vodnik, Vesna
AU  - Dramićanin, Miroslav
AU  - Novaković, Mirjana M.
AU  - Bibić, Nataša M.
AU  - Sovilj, Sofija P.
AU  - Vasić, Vesna M.
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/155
AB  - The aim of the present work was to elucidate the binding mechanism and kinetics of anionic cyanine dye 3,3-disulfopropyl-5,5-dichlorothiacyanine sodium salt (TC) J-aggregation on the surface of silver nanoparticles (AgNPs, particle size similar to 6 nm). The hybrid J-aggregateAgNPs assembly was characterized by TEM analysis, UVvis spectrophotometry, and fluorescence measurements. In the elucidation of TC binding on the surface of AgNPs, they were considered as macromolecules with several binding sites and TC dye was considered as a ligand. Scatchard and Hill analysis revealed that TC binding was a random process rather than cooperative, with similar to 200 bonded TC molecules per AgNP and a binding constant K-a = 4.8 x 10(7) M. The TC-AgNP assembly exerted concentration-dependent fluorescence quenching properties. The linearity of the SternVolmer relation, accounting for both static and dynamic quenching, indicated that only one type of quenching occurred, suggesting that AgNPs quenched the fluorescence of TC with an extraordinarily high SternVolmer constant (KSV) in the range of 10(8) M-1. Additionally, the kinetics of J-aggregation of TC in the presence of AgNPs was studied using a stopped flow technique. Kinetic measurements were performed as a function of the TC and AgNP concentration, yielding sigmoidal kinetic curves. The concentration dependence of the parameters of the kinetic curves indicated that J-aggregate formation on the AgNP surface occurred via a two-step process; the first was adsorption of the initial dye layer, followed by the growth of consecutive layers.
T2  - Journal of Physical Chemistry. C
T1  - Mechanism and Kinetics of J-Aggregation of Thiacyanine Dye in the Presence of Silver Nanoparticles
VL  - 118
IS  - 40
SP  - 23393
EP  - 23401
DO  - 10.1021/jp507086g
ER  - 
@article{
author = "Laban, Bojana B. and Vodnik, Vesna and Dramićanin, Miroslav and Novaković, Mirjana M. and Bibić, Nataša M. and Sovilj, Sofija P. and Vasić, Vesna M.",
year = "2014",
abstract = "The aim of the present work was to elucidate the binding mechanism and kinetics of anionic cyanine dye 3,3-disulfopropyl-5,5-dichlorothiacyanine sodium salt (TC) J-aggregation on the surface of silver nanoparticles (AgNPs, particle size similar to 6 nm). The hybrid J-aggregateAgNPs assembly was characterized by TEM analysis, UVvis spectrophotometry, and fluorescence measurements. In the elucidation of TC binding on the surface of AgNPs, they were considered as macromolecules with several binding sites and TC dye was considered as a ligand. Scatchard and Hill analysis revealed that TC binding was a random process rather than cooperative, with similar to 200 bonded TC molecules per AgNP and a binding constant K-a = 4.8 x 10(7) M. The TC-AgNP assembly exerted concentration-dependent fluorescence quenching properties. The linearity of the SternVolmer relation, accounting for both static and dynamic quenching, indicated that only one type of quenching occurred, suggesting that AgNPs quenched the fluorescence of TC with an extraordinarily high SternVolmer constant (KSV) in the range of 10(8) M-1. Additionally, the kinetics of J-aggregation of TC in the presence of AgNPs was studied using a stopped flow technique. Kinetic measurements were performed as a function of the TC and AgNP concentration, yielding sigmoidal kinetic curves. The concentration dependence of the parameters of the kinetic curves indicated that J-aggregate formation on the AgNP surface occurred via a two-step process; the first was adsorption of the initial dye layer, followed by the growth of consecutive layers.",
journal = "Journal of Physical Chemistry. C",
title = "Mechanism and Kinetics of J-Aggregation of Thiacyanine Dye in the Presence of Silver Nanoparticles",
volume = "118",
number = "40",
pages = "23393-23401",
doi = "10.1021/jp507086g"
}
Laban, B. B., Vodnik, V., Dramićanin, M., Novaković, M. M., Bibić, N. M., Sovilj, S. P.,& Vasić, V. M.. (2014). Mechanism and Kinetics of J-Aggregation of Thiacyanine Dye in the Presence of Silver Nanoparticles. in Journal of Physical Chemistry. C, 118(40), 23393-23401.
https://doi.org/10.1021/jp507086g
Laban BB, Vodnik V, Dramićanin M, Novaković MM, Bibić NM, Sovilj SP, Vasić VM. Mechanism and Kinetics of J-Aggregation of Thiacyanine Dye in the Presence of Silver Nanoparticles. in Journal of Physical Chemistry. C. 2014;118(40):23393-23401.
doi:10.1021/jp507086g .
Laban, Bojana B., Vodnik, Vesna, Dramićanin, Miroslav, Novaković, Mirjana M., Bibić, Nataša M., Sovilj, Sofija P., Vasić, Vesna M., "Mechanism and Kinetics of J-Aggregation of Thiacyanine Dye in the Presence of Silver Nanoparticles" in Journal of Physical Chemistry. C, 118, no. 40 (2014):23393-23401,
https://doi.org/10.1021/jp507086g . .
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Spectroscopic and fluorescence properties of silver-dye composite nanoparticles

Laban, Bojana B.; Vodnik, Vesna; Vujačić, Ana V.; Sovilj, Sofija P.; Jokic, A. B.; Vasić, Vesna M.

(2013)

TY  - JOUR
AU  - Laban, Bojana B.
AU  - Vodnik, Vesna
AU  - Vujačić, Ana V.
AU  - Sovilj, Sofija P.
AU  - Jokic, A. B.
AU  - Vasić, Vesna M.
PY  - 2013
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/5751
AB  - The aim of this work was to investigate the formation of J-aggregates of thiacyanine dye (TC, 5,5-disulfopropyl-3,3-dichlorothiacyanine sodium salt) in the presence of 6 nm spherical silver nanoparticles (Ag NPs) using spectrophotometric and fluorescence methods. The formation of J-aggregates was concentration dependent and characterized by the appearance of the new absorption band with the maximum at 481 nm. Spectrophotometric study of J-aggregate formation and time stability suggested that they were formed on the account of monomer form of TC. Moreover, the stability of J-aggregates increased with the lowering AgNPs concentration. The measurements of fluorescence of the NPs-dye assembly clearly indicated that the fluorescence of TC was quenched by Ag NPs on the concentration dependent manner. The spectrophotometric and fluorescence properties of NPs-dye assembly were found to be quantitatively related to the surface coverage of the dye on the Ag NPs.
T2  - Russian Journal of Physical Chemistry A
T1  - Spectroscopic and fluorescence properties of silver-dye composite nanoparticles
VL  - 87
IS  - 13
SP  - 2219
EP  - 2224
DO  - 10.1134/S0036024413130141
ER  - 
@article{
author = "Laban, Bojana B. and Vodnik, Vesna and Vujačić, Ana V. and Sovilj, Sofija P. and Jokic, A. B. and Vasić, Vesna M.",
year = "2013",
abstract = "The aim of this work was to investigate the formation of J-aggregates of thiacyanine dye (TC, 5,5-disulfopropyl-3,3-dichlorothiacyanine sodium salt) in the presence of 6 nm spherical silver nanoparticles (Ag NPs) using spectrophotometric and fluorescence methods. The formation of J-aggregates was concentration dependent and characterized by the appearance of the new absorption band with the maximum at 481 nm. Spectrophotometric study of J-aggregate formation and time stability suggested that they were formed on the account of monomer form of TC. Moreover, the stability of J-aggregates increased with the lowering AgNPs concentration. The measurements of fluorescence of the NPs-dye assembly clearly indicated that the fluorescence of TC was quenched by Ag NPs on the concentration dependent manner. The spectrophotometric and fluorescence properties of NPs-dye assembly were found to be quantitatively related to the surface coverage of the dye on the Ag NPs.",
journal = "Russian Journal of Physical Chemistry A",
title = "Spectroscopic and fluorescence properties of silver-dye composite nanoparticles",
volume = "87",
number = "13",
pages = "2219-2224",
doi = "10.1134/S0036024413130141"
}
Laban, B. B., Vodnik, V., Vujačić, A. V., Sovilj, S. P., Jokic, A. B.,& Vasić, V. M.. (2013). Spectroscopic and fluorescence properties of silver-dye composite nanoparticles. in Russian Journal of Physical Chemistry A, 87(13), 2219-2224.
https://doi.org/10.1134/S0036024413130141
Laban BB, Vodnik V, Vujačić AV, Sovilj SP, Jokic AB, Vasić VM. Spectroscopic and fluorescence properties of silver-dye composite nanoparticles. in Russian Journal of Physical Chemistry A. 2013;87(13):2219-2224.
doi:10.1134/S0036024413130141 .
Laban, Bojana B., Vodnik, Vesna, Vujačić, Ana V., Sovilj, Sofija P., Jokic, A. B., Vasić, Vesna M., "Spectroscopic and fluorescence properties of silver-dye composite nanoparticles" in Russian Journal of Physical Chemistry A, 87, no. 13 (2013):2219-2224,
https://doi.org/10.1134/S0036024413130141 . .
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