Julia Kulkova

Dr. Julia Kulkova

Senior Researcher Biomedical Engineering Research Group, Biomaterials and Medical Device Research Program, Department of Biomaterials Science and Turku Clinical Biomaterials Centre-TCBC, Institute of Dentistry, University of Turku
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Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2013 in Acta Biomaterialia
Verified
Journal Article
Closed access
Eleonora MarsichEleonora Marsich
Eleonora Marsich
ATAndrea Travan
Andrea Travan
Ivan DonatiIvan Donati
Ivan Donati
GTGianluca Turco
Gianluca Turco
JKJulia Kulkova
Julia Kulkova
SPSergio Paoletti
Sergio Paoletti

8 August 2014 in EJNMMI Research
Verified
Journal Article
Open access
PDF file
HAHelena Ahtinen
Helena Ahtinen
JKJulia Kulkova
Julia Kulkova
LLLaura Lindholm
Laura Lindholm
EEErkki Eerola
Erkki Eerola
AHAntti J Hakanen
Antti J Hakanen
HAHannu Aro
Hannu Aro
Background: Staphylococcus epidermidis (S. epidermidis) has emerged as one of the leading pathogens of biomaterial-related infections. Vascular adhesion protein-1 (VAP-1) is an inflammation-inducible endothelial molecule controlling extravasation of leukocytes. Sialic acid-binding immunoglobulin-like lectin 9 (Siglec-9) is a leukocyte ligand of VAP-1. We hypothesized that 68Ga-labeled 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid-conjugated Siglec-9 motif containing peptide (68Ga-DOTA-Siglec-9) could detect inflammatory response due to S. epidermidis peri-implant infection by positron emission tomography (PET). Methods: Thirty Sprague-Dawley rats were randomized into three groups. A sterile catheter was implanted into the medullary canal of the left tibia. In groups 1 and 2, the implantation was followed by peri-implant injection of S. epidermidis or Staphylococcus aureus (S. aureus) with adjunct injections of aqueous sodium morrhuate. In group 3, sterile saline was injected instead of bacteria and no aqueous sodium morrhuate was used. At 2 weeks after operation, 68Ga-DOTA-Siglec-9 PET coupled with computed tomography (CT) was performed with the measurement of the standardized uptake value (SUV). The presence of the implant-related infection was verified by microbiological analysis, imaging with fluorescence microscope, and histology. The in vivo PET results were verified by ex vivo measurements by gamma counter. Results: In group 3, the tibias with implanted sterile catheters showed an increased local uptake of 68Ga-DOTA-Siglec-9 compared with the intact contralateral bones (SUVratio +29.5%). 68Ga-DOTA-Siglec-9 PET detected inflammation induced by S. epidermidis and S. aureus catheter-related bone infections (SUVratio +58.1% and +41.7%, respectively). The tracer uptake was significantly higher in the S. epidermidis group than in group 3 without bacterial inoculation, but the difference between S. epidermidis and S. aureus groups was not statistically significant. The difference between the S. aureus group and group 3 was neither statistically significant. Conclusion: PET/CT imaging with novel 68Ga-DOTA-Siglec-9 tracer was able to detect inflammatory tissue response induced by catheter implantation and staphylococcal infections.

1 December 2014 in Journal of the Mechanical Behavior of Biomedical Materials
Verified
Journal Article
Closed access
JKJulia Kulkova
Julia Kulkova
NMNiko Moritz
Niko Moritz
ESEsa O. Suokas
Esa O. Suokas
NSNiko Strandberg
Niko Strandberg
KLKari A. Leino
Kari A. Leino
HAHannu Aro
Hannu Aro

1 August 2019 in Journal of the Mechanical Behavior of Biomedical Materials
Verified
Journal Article
Closed access
OLOliver Liesmäki
Oliver Liesmäki
APArtem Plyusnin
Artem Plyusnin
JKJulia Kulkova
Julia Kulkova
LLLippo V.J. Lassila
Lippo V.J. Lassila
PVPekka K. Vallittu
Pekka K. Vallittu
NMNiko Moritz
Niko Moritz

1 February 2020 in Research in Veterinary Science
Verified
Journal Article
Closed access
APArtem Plyusnin
Artem Plyusnin
JKJulia Kulkova
Julia Kulkova
GAGareth Arthurs
Gareth Arthurs
NJNiki Jalava
Niki Jalava
PUPeter Uppstu
Peter Uppstu
NMNiko Moritz
Niko Moritz

25 April 2016 in Medical Engineering & Physics
Verified
Journal Article
Closed access
JKJulia Kulkova
Julia Kulkova
NMNiko Moritz
Niko Moritz
HHHannu Huhtinen
Hannu Huhtinen
RMRiina Mattila
Riina Mattila
Ivan DonatiIvan Donati
Ivan Donati
PVPekka K Vallittu
Pekka K Vallittu
Biostable fiber-reinforced composites (FRC) prepared from bisphenol-A-glycidyldimethacrylate (BisGMA)-based thermosets reinforced with E-glass fibers are promising alternatives to metallic implants due to the excellent fatigue resistance and the mechanical properties matching those of bone. Bioactive glass (BG) granules can be incorporated within the polymer matrix to improve the osteointegration of the FRC implants. However, the creation of a viable surface layer using BG granules is technically challenging. In this study, we investigated the potential of Excimer laser ablation to achieve the selective removal of the matrix to expose the surface of BG granules. A UV-vis spectroscopic study was carried out to investigate the differences in the penetration of light in the thermoset matrix and BG. Thereafter, optimal Excimer laser ablation parameters were established. The formation of a calcium phosphate (CaP) layer on the surface of the laser-ablated specimens was verified in simulated body fluid (SBF). In addition, the proliferation of MG63 cells on the surfaces of the laser-ablated specimens was investigated. For the laser-ablated specimens, the pattern of proliferation of MG63 cells was comparable to that in the positive control group (Ti6Al4V). We concluded that Excimer laser ablation has potential for the creation of a bioactive surface on FRC-implants.