Márton Király

Dr. Márton Király

Semmelweis University, Budapest, Hungary
orcid

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

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

Representative Publications

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31 March 2022 in Pharmaceutics
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Journal Article
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MKMárton Király
Márton Király
KSKonrád Sántha
Konrád Sántha
BKBarnabás Kállai-Szabó
Barnabás Kállai-Szabó
KPKriszta Mariann Pencz
Kriszta Mariann Pencz
KLKrisztina Ludányi
Krisztina Ludányi
IAIstván Antal
István Antal
Today, in addition to many different physicochemical and pharmacological properties of the active ingredients and excipients, the developer of a pharmaceutical formulation must take into account several factors during the formulation process in order for the patient to cooperate to use the formulation accurately. One of the innovative solutions in paediatrics may be the use of medicated drinking straws. For our studies, we successfully prepared lactase-containing, rapid disintegration particles by two techniques commonly used in the pharmaceutical industry. The simulation of the usage of the filled straws was presented from a new perspective for the patient by an in vitro method. The effect of the temperature of the liquid used during the administration of the straw and the effect of the frequency during the application on the dissolution rate were investigated. According to our results, in the case of a straw containing rapidly dissolving particles, the temperature of the used liquid and the mode of administration (frequency) play a significant role in the release rate from the composition.

21 July 2022 in Cells
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Journal Article
Open access
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KGKinga Gecse
Kinga Gecse
AÉAndrea Edit Édes
Andrea Edit Édes
TNTamás Nagy
Tamás Nagy
ADAdrienn Katalin Demeter
Adrienn Katalin Demeter
DVDávid Virág
Dávid Virág
Gabriella JuhaszGabriella Juhasz
Gabriella Juhasz
Altered tryptophan (TRP) metabolism may have an important role in migraine susceptibility through its main metabolites, serotonin and kynurenine (KYN). Both affect pain processing and stress response by interfering with neural and brain hypersensitivity and by interacting with chemokines and cytokines that control vascular and inflammatory processes. The involvement of these pathways in migraine has been widely studied, but acute citalopram neuroendocrine challenge on TRP metabolism and cytokine profile has not been investigated yet. In our study, females with episodic migraine without aura and healthy controls were studied before and after acute citalopram or placebo in a double-blind setting. At baseline, increased TRP/large neutral amino acid (LNAA) ratio and decreased RANTES chemokine concentration were detected in migraine patients compared to controls. The challenge induced a significant increase in TRP, KYN, and TRP/LNAA in healthy controls, but not in migraine patients. Furthermore, migraine attack frequency negatively correlated with KYN/TRP ratio and positively correlated with the neuroendocrine-challenge-induced KYN concentration increase. Our results support a decreased breakdown of TRP via KYN pathway and a failure to modulate TRP–KYN pathway during citalopram-induced acute stress together with an increased vascular sensitivity in migraine. These mechanisms may provide useful drug targets for future drug development.

1 June 2021 in Biotechnology Reports
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Journal Article
Open access
MKMárton Király
Márton Király
BKBorbála Dalmadi Kiss
Borbála Dalmadi Kiss
HPHorváth Péter
Horváth Péter
László DrahosLászló Drahos
László Drahos
AMArash Mirzahosseini
Arash Mirzahosseini
KLKrisztina Ludányi
Krisztina Ludányi
• The primary and secondary structure of lactase was not changed by thermal stress. • The glycan structure of lactase showed significant alterations after heat stress. • Changes in the glycosylation structure affected physico-chemical properties of lactase.

26 June 2021 in Biomedicines
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Journal Article
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Zsofia Edit PapayZsofia Edit Papay
Zsofia Edit Papay
SMSabrina Magramane
Sabrina Magramane
MKMárton Király
Márton Király
PSPetra Szalkai
Petra Szalkai
KLKrisztina Ludányi
Krisztina Ludányi
IAIstván Antal
István Antal
Bioconjugation is an emerging field in the food and pharmaceutical industry. Due to its biocompatibility and high ligand binding capacity, albumin is widely used in modern drug delivery systems. However, the protein is sensitive to environmental stresses; albumin conjugates, on the other hand, have improved functional properties. Biopolymers are gaining interest due to their biodegradability and safety, compared to synthetic polymers. In this study, albumin–biopolymer bioconjugates were prepared by nonenzymatic Maillard reaction at 60 °C and 80% relative humidity. This nonenzymatic conjugation takes place between reducing sugars and available amino groups of a protein in certain conditions. The optimal molar ratio and time for the conjugation were studied by several investigation methods, including circular dichroism and fluorescence spectroscopy, sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS–PAGE), and determination of available amino groups with ortho-phthaldialdehyde (OPA) assay. All of the measurements provided evidence for the covalent bonding of albumin and biopolymers, resulting in bioconjugates. Based on the results, a higher molar ratio and longer time are necessary to complete the reaction with the available amino groups. However, the optimal parameters are specific to each given biopolymer. The rheological behavior of the conjugates is characteristic of the initial biopolymer, which can be useful in drug development. Moreover, both the physical characteristics of albumin and the solubility-improving capacity were enhanced. Therefore, the potential use of albumin–biopolymer bioconjugates in the pharmaceutical industry could be considered.

15 November 2021 in Acta Pharmaceutica Hungarica
Verified
Journal Article
Open access
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MKMárton Király
Márton Király
KSKonrád Sántha
Konrád Sántha
BKBarnabás Kállai-Szabó
Barnabás Kállai-Szabó
NKNikolett Kállai-Szabó
Nikolett Kállai-Szabó
IAIstván Antal
István Antal
KLKrisztina Ludányi
Krisztina Ludányi

8 July 2026
Verified
Conference Paper
Closed access
ADAdrienn Katalin Demeter
Adrienn Katalin Demeter
DFDóra Farkas
Dóra Farkas
MKMárton Király
Márton Király
ABAdam Tibor Barna
Adam Tibor Barna
KLKrisztina Ludányi
Krisztina Ludányi
NKNikolett Kállai-Szabó
Nikolett Kállai-Szabó