Tomasz Horodniczy

Mr. Tomasz Horodniczy


Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

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

Representative Publications

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20 August 2024 in Biomimetics
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Paweł J. PiszkoPaweł J. Piszko
Paweł J. Piszko
APAleksandra Piszko
Aleksandra Piszko
SKSylwia Kiryk
Sylwia Kiryk
JKJan Kiryk
Jan Kiryk
THTomasz Horodniczy
Tomasz Horodniczy
Maciej DobrzyńskiMaciej Dobrzyński
Maciej Dobrzyński
In this systematic review, the authors aimed to investigate the state of knowledge on in vivo evaluations of chitosan and nanometric hydroxyapatite (nanohydroxyapatite, nHAp) scaffolds for bone-tissue regeneration. In March 2024, an electronic search was systematically conducted across the PubMed, Cochrane, and Web of Science databases using the keywords (hydroxyapatite) AND (chitosan) AND (scaffold) AND (biomimetic). Methodologically, the systematic review followed the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) protocol to the letter. Initially, a total of 375 studies were screened, and 164 duplicates were removed. A further 188 articles were excluded because they did not correspond to the predefined topics, and an additional 3 articles were eliminated due to the inability to obtain the full text. The final compilation included 20 studies. All publications indicated a potential beneficial effect of the scaffolds in in vivo bone defect repair. A beneficial effect of hydroxyapatite as a scaffold component was observed in 16 studies, including greater mechanical resistance, cellular differentiation, and enhanced bone damage regeneration. The addition of chitosan and apatite ceramics, which combined the strengths of both materials, had the potential to become a useful bone-tissue engineering material.

13 September 2024 in Applied Sciences
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NSNatalia Struzik
Natalia Struzik
JKJulia Kensy
Julia Kensy
Paweł J. PiszkoPaweł J. Piszko
Paweł J. Piszko
JKJan Kiryk
Jan Kiryk
KWKamila Wiśniewska
Kamila Wiśniewska
Maciej DobrzyńskiMaciej Dobrzyński
Maciej Dobrzyński
Objective: Bone augmentation has become a significant practice in various areas of bone regeneration dentistry. This systematic review analyzes the research focused on evaluating bone substitute materials for the presence of contaminants. Methods: In June 2024, an extensive electronic search was conducted using renowned databases such as PubMed, Web of Science, and Scopus. Specific keywords employed in the search included ((bone AND (substitute) AND (remnants OR (purity)) OR ((graft AND tooth) AND (remnants OR purity)) OR ((graft AND dentin) AND (remnants OR purity)). The search adhered to the PRISMA protocol and the PICO framework. The review concentrated on the origin of bone substitute materials, the processing methods used for these materials, techniques for assessing purity, and types of contamination identified. A total of 594 articles were identified of which 22 met the criteria and were incorporated into the review. Results: Investigations into allogeneic and xenogeneic bone substitute materials have revealed that, despite manufacturers’ assurances of purity, some materials still contain contaminants. Sample analyses demonstrated the presence of donor cellular remains, cellular debris, intertrabecular fat, connective tissue, and collagen. Similarly, synthetically produced bone substitute materials (alloplastic materials) contained various impurities, such as polyvinyl alcohol (PVA), CaO phases, calcium-deficient HAp phases, oily substances containing carbon and silicone, cellulose derivatives, alpha-tricalcium phosphate (α-TCP), and heavy metals. Conclusions: Bone-derived and bone-like graft materials can contain various organic and inorganic impurities.

18 January 2025 in Applied Sciences
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PWPatryk Woś
Patryk Woś
SKSylwia Kiryk
Sylwia Kiryk
TDTomasz Dyl
Tomasz Dyl
JKJan Kiryk
Jan Kiryk
THTomasz Horodniczy
Tomasz Horodniczy
Maciej DobrzyńskiMaciej Dobrzyński
Maciej Dobrzyński
Objective: The aim of this systematic review was to evaluate the effectiveness and safety of various laser wavelengths for debonding orthodontic metal brackets compared to traditional plier-based methods. The primary outcomes assessed were enamel damage, pulp temperature changes, adhesive remnant index (ARI), and shear bond strength (SBS). Materials and Methods: In September 2024, an electronic search was performed across the PubMed, Web of Science (WoS), and Scopus databases, adhering to the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines and the PICO framework. The initial search yielded 453 records. After eliminating 256 duplicates, 197 unique records were left for screening, which ultimately led to the qualification of 8 articles that met the inclusion criteria for both qualitative and quantitative analyses. The risk of bias in the articles was assessed by two independent reviewers. Results: The included studies demonstrated that laser-assisted debonding generally resulted in less adhesive residue on the enamel surface compared to conventional methods, as evidenced by the reductions in ARI scores reported in two studies. Temperature increases during laser use varied depending on the laser type and power settings. The Nd:YAG (neodymium-yttrium, aluminum, garnet) laser was found to cause significant temperature rises, posing a potential risk to pulp tissue, while the Er:YAG (erbium—yttrium, aluminum, garnet) and Er,Cr:YSGG (erbium, chromium—yttrium, scandium, gallium, garnet) lasers produced only negligible increases in pulp temperature. SBS comparisons revealed no significant differences between the laser-assisted and traditional debonding methods. Additionally, diode lasers demonstrated the potential to minimize enamel damage, particularly when operated at lower power settings. Four publications were assessed as high quality (low risk of bias), and another four as moderate quality (average risk of bias). Conclusions: In conclusion, laser-assisted orthodontic metal bracket debonding, when conducted with appropriately calibrated parameters, is a safe method for preserving tooth tissue. However, its advantages appear to be minimal compared to conventional plier-based methods, highlighting the need for further research to justify its broader clinical application.

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WMWojciech Macek
Wojciech Macek
Maciej ChęcińskiMaciej Chęciński
Maciej Chęciński
KGKarolina Grzybowska-Kowalczyk
Karolina Grzybowska-Kowalczyk
MKMaja Kosinska
Maja Kosinska
AHAmelia Hoppe
Amelia Hoppe
Maciej SikoraMaciej Sikora
Maciej Sikora
Background/Objectives: Intra-articular injections are used for temporomandibular disorders (TMDs) resistant to conservative treatment. However, many reviews assess injectable agents combined with arthrocentesis or other co-interventions, limiting interpretation of their standalone effects. This overview aimed to summarize meta-analytic evidence on standalone intra-articular injections for temporomandibular joint disorders. Methods: MEDLINE, BASE, and Europe PMC were searched on 29 March 2026. Systematic reviews with quantitative meta-analyses evaluating standalone intra-articular TMJ injections were included. Data regarding injectable substances, clinical indications, and outcome domains were extracted and synthesized descriptively. Results: Three systematic reviews with meta-analyses were included. The evidence addressed platelet-rich plasma, corticosteroids, sodium hyaluronate, and physiological saline. Reported indications included degenerative joint disease, osteoarthritis, internal derangement, and arthritis. All included agents were reported to be associated with pain reduction. Conclusions: Meta-analytic evidence on standalone intra-articular injections for TMDs remains limited and heterogeneous. Available data suggest potential benefits, mainly for pain reduction, but do not establish clear superiority of any agent. The potential therapeutic activity of physiological saline should be considered when designing future injection trials.

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THTomasz Horodniczy
Tomasz Horodniczy
KKKlaudia Kwiatkowska
Klaudia Kwiatkowska
KCKamila Chęcińska
Kamila Chęcińska
Maciej ChęcińskiMaciej Chęciński
Maciej Chęciński
KGKarolina Grzybowska-Kowalczyk
Karolina Grzybowska-Kowalczyk
Maciej SikoraMaciej Sikora
Maciej Sikora
Background/Objectives: Ultrasound is increasingly used to guide minimally invasive interventions for temporomandibular joint (TMJ) disorders because it enables real-time visualization of the joint, surrounding tissues, and needle position. This scoping review aimed to map and characterize the available evidence on ultrasound-guided minimally invasive interventions for temporomandibular disorders (TMDs). Methods: The review followed PRISMA-ScR guidelines and was registered in the Open Science Framework (osf.io/r42m5). PubMed/MEDLINE, BASE, and Europe PMC were searched up to 4 April 2026. Original clinical and technical studies evaluating ultrasound-guided minimally invasive interventions for TMDs were included. Results: Seventeen studies published between 2012 and 2026 met the eligibility criteria. Ultrasound guidance was used mainly for intra-articular injections, arthrocentesis, and botulinum toxin injections into the lateral pterygoid muscle. Most studies reported reductions in pain and improvements in jaw function. Compared with conventional approaches, several included studies reported more accurate needle placement, fewer insertion attempts, less need for needle repositioning, and shorter procedure times when ultrasound guidance was used. However, these procedural advantages did not consistently translate into superior long-term clinical outcomes. Conclusions: Overall, ultrasound-guided minimally invasive TMJ interventions appear feasible and generally safe, with their main benefit being improved visualization and procedural precision. Further standardized, high-quality studies are needed to clarify their clinical impact.

Verified
Journal Article
Open access
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PSPawel Sikora
Pawel Sikora
Maciej ChęcińskiMaciej Chęciński
Maciej Chęciński
THTomasz Horodniczy
Tomasz Horodniczy
KCKamila Chęcińska
Kamila Chęcińska
NTNatalia Turosz
Natalia Turosz
Maciej SikoraMaciej Sikora
Maciej Sikora
Lubricin, also known as proteoglycan 4 (PRG4), is a key glycoprotein involved in boundary lubrication and maintenance of joint homeostasis in the temporomandibular joint (TMJ). However, the clinical evidence regarding synovial fluid (SF) lubricin levels remains limited and fragmented. This scoping review aimed to map and synthesize the available clinical evidence on lubricin levels in patients with temporomandibular disorders (TMDs) and their relationship to clinical outcomes, particularly pain and mandibular mobility. Searches were conducted in PubMed, Scopus, ACM, BASE, Cochrane, ClinicalTrials.gov, and Google Scholar. After duplicate removal and screening, two studies were included in the final synthesis. Preliminary findings from these studies suggest that (SF) lubricin levels may be lower in more advanced TMJ pathology, particularly in degenerative disease. Earlier stages of internal derangement showed lubricin concentrations closer to those observed in healthy controls, whereas advanced internal derangement and osteoarthritic disease were potentially associated with lower levels. One study also reported an inverse correlation between lubricin concentration and pain intensity, while the other demonstrated impaired boundary lubrication in TMD groups. Overall, the available clinical evidence is very limited and insufficient to establish PRG4 as a validated biomarker but suggests a possible association between reduced SF lubricin levels and more advanced TMJ disease. Further well-designed clinical studies are required to confirm these observations and clarify their diagnostic and therapeutic relevance.