Synergetic effect of the crosslinker size and polysaccharide type on the acrylamide networks

The microstructures of hydrogels dominate their properties such as swelling, mechanical, etc., and therefore, their applications. Possessing a homogeneous network lead to uniform swelling and mechanical properties throughout the material. Considering the synergistic effect of crosslinker size and po...

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Published inJournal of applied polymer science Vol. 141; no. 35
Main Authors Keten, Selinay, Gönülkirmaz, Ferda, Karacan, Pinar, Ceylan, Deniz, Abdurrahmanoğlu, Suzan
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 15.09.2024
Wiley Subscription Services, Inc
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ISSN0021-8995
1097-4628
DOI10.1002/app.55900

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Abstract The microstructures of hydrogels dominate their properties such as swelling, mechanical, etc., and therefore, their applications. Possessing a homogeneous network lead to uniform swelling and mechanical properties throughout the material. Considering the synergistic effect of crosslinker size and polysaccharide variation, acrylamide hydrogels were synthesized in a single step reaction using tetraethyleneglycol dimethylacrylate (TEGDMA) as a crosslinker in the absence and presence of polysaccharides such as dextran, starch, and sodium alginate. By using the thermal initiator polysaccharides have been used directly without any pre‐functionalization in the single step gelation reaction. All the hydrogel samples were characterized by means of swelling, and mechanical and structural properties. Hydrogels synthesized with TEGDMA as a crosslinker were compared with conventional acrylamide gels prepared using N,N′‐methylenebis(acrylamide) (MBA) and the results emphasized the superior mechanical strength and flexibility of the gels obtained with TEGDMA. Both relatively longer crosslinker and polysaccharide additions have assisted in the formation of a more homogeneous acrylamide network. Polysaccharides which possess plenty of hydroxyl groups have provided a great impact on the swelling properties of the gel samples. Besides the carboxyl groups of alginate backbones have also increased the swelling ratio of the hydrogels additionally. The synergetic effect of the crosslinker and polysaccharide additives on the homogeneity of the acrylamide network and its swelling properties could be suggested for future applications, especially in the area of biomaterials. Enhancement of the acrylamide network by the addition of TEGDMA and Dextran.
AbstractList The microstructures of hydrogels dominate their properties such as swelling, mechanical, etc., and therefore, their applications. Possessing a homogeneous network lead to uniform swelling and mechanical properties throughout the material. Considering the synergistic effect of crosslinker size and polysaccharide variation, acrylamide hydrogels were synthesized in a single step reaction using tetraethyleneglycol dimethylacrylate (TEGDMA) as a crosslinker in the absence and presence of polysaccharides such as dextran, starch, and sodium alginate. By using the thermal initiator polysaccharides have been used directly without any pre‐functionalization in the single step gelation reaction. All the hydrogel samples were characterized by means of swelling, and mechanical and structural properties. Hydrogels synthesized with TEGDMA as a crosslinker were compared with conventional acrylamide gels prepared using N,N′‐methylenebis(acrylamide) (MBA) and the results emphasized the superior mechanical strength and flexibility of the gels obtained with TEGDMA. Both relatively longer crosslinker and polysaccharide additions have assisted in the formation of a more homogeneous acrylamide network. Polysaccharides which possess plenty of hydroxyl groups have provided a great impact on the swelling properties of the gel samples. Besides the carboxyl groups of alginate backbones have also increased the swelling ratio of the hydrogels additionally. The synergetic effect of the crosslinker and polysaccharide additives on the homogeneity of the acrylamide network and its swelling properties could be suggested for future applications, especially in the area of biomaterials. Enhancement of the acrylamide network by the addition of TEGDMA and Dextran.
The microstructures of hydrogels dominate their properties such as swelling, mechanical, etc., and therefore, their applications. Possessing a homogeneous network lead to uniform swelling and mechanical properties throughout the material. Considering the synergistic effect of crosslinker size and polysaccharide variation, acrylamide hydrogels were synthesized in a single step reaction using tetraethyleneglycol dimethylacrylate (TEGDMA) as a crosslinker in the absence and presence of polysaccharides such as dextran, starch, and sodium alginate. By using the thermal initiator polysaccharides have been used directly without any pre‐functionalization in the single step gelation reaction. All the hydrogel samples were characterized by means of swelling, and mechanical and structural properties. Hydrogels synthesized with TEGDMA as a crosslinker were compared with conventional acrylamide gels prepared using N,N′‐methylenebis(acrylamide) (MBA) and the results emphasized the superior mechanical strength and flexibility of the gels obtained with TEGDMA. Both relatively longer crosslinker and polysaccharide additions have assisted in the formation of a more homogeneous acrylamide network. Polysaccharides which possess plenty of hydroxyl groups have provided a great impact on the swelling properties of the gel samples. Besides the carboxyl groups of alginate backbones have also increased the swelling ratio of the hydrogels additionally. The synergetic effect of the crosslinker and polysaccharide additives on the homogeneity of the acrylamide network and its swelling properties could be suggested for future applications, especially in the area of biomaterials.
The microstructures of hydrogels dominate their properties such as swelling, mechanical, etc., and therefore, their applications. Possessing a homogeneous network lead to uniform swelling and mechanical properties throughout the material. Considering the synergistic effect of crosslinker size and polysaccharide variation, acrylamide hydrogels were synthesized in a single step reaction using tetraethyleneglycol dimethylacrylate (TEGDMA) as a crosslinker in the absence and presence of polysaccharides such as dextran, starch, and sodium alginate. By using the thermal initiator polysaccharides have been used directly without any pre‐functionalization in the single step gelation reaction. All the hydrogel samples were characterized by means of swelling, and mechanical and structural properties. Hydrogels synthesized with TEGDMA as a crosslinker were compared with conventional acrylamide gels prepared using N,N′‐ methylenebis(acrylamide) (MBA) and the results emphasized the superior mechanical strength and flexibility of the gels obtained with TEGDMA. Both relatively longer crosslinker and polysaccharide additions have assisted in the formation of a more homogeneous acrylamide network. Polysaccharides which possess plenty of hydroxyl groups have provided a great impact on the swelling properties of the gel samples. Besides the carboxyl groups of alginate backbones have also increased the swelling ratio of the hydrogels additionally. The synergetic effect of the crosslinker and polysaccharide additives on the homogeneity of the acrylamide network and its swelling properties could be suggested for future applications, especially in the area of biomaterials.
Author Karacan, Pinar
Abdurrahmanoğlu, Suzan
Gönülkirmaz, Ferda
Keten, Selinay
Ceylan, Deniz
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Snippet The microstructures of hydrogels dominate their properties such as swelling, mechanical, etc., and therefore, their applications. Possessing a homogeneous...
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SubjectTerms Acrylamide
Biomedical materials
Chemical synthesis
Crosslinking
Dextrans
Homogeneity
hydrogel
Hydrogels
Hydroxyl groups
Mechanical properties
Polysaccharides
Sodium alginate
Swelling ratio
Synergistic effect
tetraethyleneglycol dimethylacrylate
Title Synergetic effect of the crosslinker size and polysaccharide type on the acrylamide networks
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