Kari honlap | Impresszum



Selected publications

 2023 | 2022 20212020 | 2019 | 2018 |  2017 | 2016  | 2015 2014 | 2013


1. Stankovits G, Ábrahám Á, Kiss É, Varga Z, Misra A, Szilágyi A, Gyarmati B.

The interaction between mucin and poly(amino acid)s with controlled cationic group content in bulk phase and in thin layers

International Journal of Biological Macromolecules 2023; 253: 126826


2. Szilágyi BÁ, Gyarmati B, Kiss EL, Budai-Szűcs M, Misra A, Csányi E, László K, Szilágyi A.

In situ gelation of thiolated poly(aspartic acid) derivatives through oxidant-free disulfide formation for ophthalmic drug delivery

Colloids and Surfaces B: Biointerfaces 2023; 225: 113254


1. Mammadova A, Gyarmati B, Sárdi K, Paudics A, Varga Z, Szilágyi A.

Thiolated cationic poly(aspartamides) with side group dependent gelation properties for the delivery of anionic polyelectrolytes

Journal of Materials Chemistry B 2022; 10: 5946-5957

2. Gyarmati B, Stankovits G, Szilágyi BÁ, Galata DL, Gordon P, Szilágyi A.

A robust mucin-containing poly(vinyl alcohol) hydrogel model for the in vitro characterization of mucoadhesion of solid dosage forms

Colloids and Surfaces B: Biointerfaces 2022; 213: 112406





1. Gyarmati B, Mammadova A, Barczikai D, Stankovits G, Misra A, Alavijeh SA, Varga Z, László K, Szilágyi A.

Side group ratio as a novel means to tune the hydrolytic degradation of thiolated and disulfide cross-linked polyaspartamides

Polymer Degradation and Stability 2021; 188: 109577

Mucoadh interact


2. Gyarmati B, Mammadova A, Stankovits G, Barczikai D, Szilágyi A.

Effect of Side Groups on the Hydrolytic Stability of Thiolated and Disulfide Cross-linked Polyaspartamides

Periodica Polytechnica Chemical Engineering 2021; 65:183-191





1. Szilágyi BÁ, Mammadova A, Gyarmati B, Szilágyi A.

Mucoadhesive interactions between synthetic polyaspartamides and porcine gastric mucin on the colloid size scale

Colloids and Surfaces B: Biointerfaces 2020; 194: 111219

Mucoadh interact


2. Németh C, Gyarmati B, Gacs J, Salakhieva DV, Molnár K, Abdullin T, László K, Szilágyi A.

Fast dissolving nanofibrous matrices prepared by electrospinning of polyaspartamides

European Polymer Journal 2020; 130: 109624

Fast dissolving nanofibrous matrices prepared by electrospinning of polyaspartamides




1. Decsi B, Krammer R, Hegedűs K, Ender F, Gyarmati B, Szilágyi A, Tőtős R, Katona G, Paizs C, Balogh GT, Poppe L, Balogh-Weiser D.

Liver-on-a-Chip‒Magnetic Nanoparticle Bound Synthetic Metalloporphyrin-Catalyzed Biomimetic Oxidation of a Drug in a Magnechip Reactor

Micromachines 2019; 10: 668


2. Gyarmati B, Pukánszky B.

Natural polymers, bio-inspired and smart macromolecular materials

European Polymer Journal 2019; 119: 393-399


3. Krisch E, Balogh-Weiser D, Klimko J, Gyarmati B, Laszlo K, Poppe L, Szilagyi A.

Composite beads of silica gel, alginate and poly (aspartic acid) for the immobilization of a lipase enzyme

Express Polymer Letters 2019; 13: 512-523




1. Szilágyi BÁ, Némethy A, Magyar A, Szabó I, Bősze S, Gyarmati B, Szilágyi A.

Amino acid based polymer hydrogel with enzymatically degradable cross-links

Reactive and Functional Polymers 2018; 133: 21-28


2. Krammer O, Gyarmati B, Szilágyi A, Illés B, Bušek D, Dušek K.

The effect of solder paste particle size on the thixotropic behaviour during stencil printing

Journal of Materials Processing Technology 2018; 262:571-576


3. Balogh-Weiser D, Németh C, Ender F, Gyarmati B, Szilágyi A, Poppe L.

Electrospun Nanofibers for Entrapment of Biomolecules

Electrospinning Method Used to Create Functional Nanocomposites Films (2018, IntechOpen, ed. Tomasz Tański)


4. Krisch E, Gyarmati B, Barczikai D, Lapeyre V, Szilágyi BÁ, Ravaine V, Szilágyi A.

Poly(aspartic acid) hydrogels showing reversible volume change upon redox stimulus

European Polymer Journal 2018; 105:459-468


5. Orha L, Tukacs JM, Gyarmati B, Szilágyi A, Kollár L, Mika LT.

Modular synthesis of γ-valerolactone-based ionic liquids and their application as alternative media for copper-catalyzed Ullmann-type coupling reactions

ACS Sustainable Chemistry & Engineering 2018; 6: 5097-5104


6. Budai-Szűcs M, Kiss EL, Szilágyi BÁ, Szilágyi A, Gyarmati B, Berkó S, Kovács A, Horvát G, Aigner Z, Soós J, Csányi E.

Mucoadhesive cyclodextrin-modified thiolated poly(aspartic acid) as a potential ophthalmic drug delivery system

Polymers 2018; 10: 199






1. Gyarmati B, Szilágyi B, Szilágyi A.

Reversible interactions in self-healing and shape memory hydrogels

European Polymer Journal 2017; 93:642-669


2. Németh Cs, Szabó D, Gyarmati B, Gerasimov A, Varfolomeev M, Abdullin T, László K, Szilágyi A. 

Effect of side groups on the properties of cationic polyaspartamides

European Polymer Journal 2017; 93: 805-814


3. Németh Cs, Gyarmati B, Abdullin T, László K, Szilágyi A.

Poly(aspartic acid) with adjustable pH-dependent solubility

Acta Biomaterialia 2017; 49: 486-494


4. Budai-Szűcs M, Horvát G, Gyarmati B, Szilágyi BÁ, Szilágyi A, Berkó S, Ambrus R, Szabó-Révész P, Sandri G, Bonferoni MC, Caramella C, Csányi E.

The effect of the antioxidant on the properties of thiolated poly(aspartic acid) polymers in aqueous ocular formulations

European Journal of Pharmaceutics and Biopharmaceutics 2017; 113: 178-187

5. Krammer O, Gyarmati B, Szilágyi A, Storcz R, Jakab L, Illés B, Géczy A, Dušek K.

Investigating the thixotropic behaviour of Type 4 solder paste during stencil printing

Soldering & Surface Mount Technology 2017; 29: 10-14

6. Salakhieva D, Shevchenko V, Németh C, Gyarmati B, Szilágyi A, Abdullin T.

Structure–biocompatibility and transfection activity relationships of cationic polyaspartamides with (dialkylamino) alkyl and alkyl or hydroxyalkyl side groups

International Journal of Pharmaceutics 2017; 517: 234-246

7. Gyarmati B, Pukánszky B.

Natural polymers and bio-inspired macromolecular materials

European Polymer Journal 2017; 93: 612-617


8. Krisch E, Gyarmati B, Szilágyi A.

Preparation of pH-responsive poly (aspartic acid) nanogels in inverse emulsion

Periodica Polytechnica Chemical Engineering 2017; 61: 19-26 






1. Krisch E, Messager L, Gyarmati B, Ravaine V, Szilágyi A.

Redox- and pH-responsive nanogels based on thiolated poly(aspartic acid) 

Macromolecular Materials and Engineering 2016; 301: 260-266

2. Müller P, Bere J, Fekete E, Móczó J, Nagy B, Kállay M, Gyarmati B, Pukánszky B.

Interactions, structure and properties in PLA/plasticized starch blends

Polymer 2016; 103: 9-18

3. Budai-Szűcs M, Horvát G, Gyarmati B, Szilágyi BÁ, Szilagyi A, Csihi T, Berkó S, Szabó-Révész P, Mori M, Sandri G, Bonferoni MC, Caramella C, Csányi E.

In vitro testing of thiolated poly(aspartic acid) from ophthalmic formulation aspects

Drug Development and Industrial Pharmacy 2016; 42: 1241-1246

4. Budai-Szűcs M, Horvát G, Szilágy BÁ, Gyarmati B, Szilágyi A, Berkó S, Szabó-Révész P, Sandri G, Bonferoni MC, Caramella C, Soós J, Csányi AE.

Cationic Thiolated Poly(aspartamide) Polymer as a Potential Excipient for Artificial Tear Formulations

Journal of Ophthalmology 2016; 2647264 





1. Gyarmati B, Mészár EZ, Kiss L, Deli M, László K, Szilágyi A. 

Supermacroporous chemically cross-linked poly(aspartic acid) hydrogels

Acta Biomaterialia 2015; 22: 32-38.



2. Solti K, Gyarmati B, Szilágyi A.

Szívós polimer hidrogélek

Műanyag- és gumiipari évkönyv 2015;13:100-108.



3. Horvát G, Gyarmati B, Berkó Sz, Szabó-Révész P, Szilágyi BÁ, Szilágyi A, Soós J, Sandri G, Bonferoni MC, Rossi S, Ferrari F, Caramella C, Csányi E, Budai-Szűcs M. 

Thiolated poly(aspartic acid) as potential in situ gelling, ocular mucoadhesive drug delivery system

European Journal of Pharmaceutical Sciences 2015; 67: 1-11


4. Gyarmati B, Hegyesi N, Pukánszky B, Szilágyi A.

A colorimetric method for the determination of degree of chemical cross-linking in aspartic acid based polymer gels

Express Polym. Lett. 2015;9:154-164.


5. Horvát G, Budai-Szűcs M, Berkó S, Révész P, Gyarmati BS,  Szilágyi BÁ, Szilágyi AF, Csányi E.

Egy új típusú polimer, az in situ gélesedő tiolált poliaszparaginsav alkalmazása szemészeti gyógyszerhordozóként

Acta Pharmaceutica Hungarica 2015; 85: 115-122






1. Gyarmati B, Némethy Á, Szilágyi A.

Reversible response of poly(aspartic acid) hydrogels to external redox and pH stimuli

RSC Advances 2014;4:8764-8771

2. Gyarmati B, Krisch E, Szilágyi A.

In situ oxidation-induced gelation of poly(aspartic acid) thiomers

Reactive and Functional Polymers 2014; 84: 29-36

3. Horváth Z, Gyarmati  B, Menyhárd A, Doshev P, Gahleitner M, Varga J, Pukánszky B.

The role of solubility and critical temperatures for the efficiency of sorbitol clarifiers in polypropylene

Drug development and industrial pharmacy 2016; 42: 1241-1246

4. Gyarmati B, Szilágyi A.

Preface for papers presented at AMSALS 2012

Periodica Polytechnica Chemical Engineering 2014;58:47-48 



1. Némethy Á, Solti K, Kiss L, Gyarmati B, Deli MA, Csányi E, Szilágyi A.

pH-and temperature-responsive poly(aspartic acid)-l-poly(N-isopropylacrylamide) conetwork hydrogel

European Polymer Journal 2013; 49: 2392-2403

2. Gyarmati B, Némethy Á, Szilágyi A.

Reversible disulphide formation in polymer networks: A versatile functional group from synthesis to applications

European Polymer Journal 2013; 49: 1268-1286

3. Gyarmati B, Vajna B, Némethy Á, László K, Szilágyi A.

Redox‐and pH‐Responsive Cysteamine‐Modified Poly(aspartic acid) Showing a Reversible Sol–Gel Transition

Macromolecular Bioscience 2013;13: 633-640