Gamma Radiation-Assisted Synthesis of Xanthan Gum/Acrylamide Hydrogels for Drug Delivery

Xanthan gum (XG) and acrylamide (AAm) hydrogels were synthesized using gamma radiation. The novelty lies in the use of a simple methodology to obtain two different architectures, thereby tailoring their physicochemical properties. The first system is a comb-type hydrogel (net-AAm)-g-XG, where the crosslinking of AAm and the XG grafting were carried out in a single step via gamma radiation. The second system consists of an interpenetrating network (IPN) (net-XG)-inter-(net-AAm), where XG was crosslinked with citric acid and then AAm was crosslinked by gamma radiation in the presence of XG gel. Good degrees of grafting (60%) and interpenetration (75%) were obtained at 8 kGy for both systems. Comb-type and IPN hydrogels showed a porous structure, but the pore size was smaller in the interpenetrating network because this architecture has less internal space due to the presence of a second network. Morphological differences affected water absorption and drug loading/release properties. The comb-type showed its maximum swelling (900%) at 24 h, regardless of the grafting amount; while the IPN exhibited a swelling of 400–600% at 3 h, depending on the interpenetration degree. Both systems allowed for ciprofloxacin loading, but release was faster in the IPN (100 min) than in the comb-type hydrogel (300 min).

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Publication Details

Journal
Gels
Published
2026-11-11
DOI
https://doi.org/10.3390/gels12111029
Primary Topic
Hydrogels: synthesis, properties, applications
Type
article
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article

Gamma Radiation-Assisted Synthesis of Xanthan Gum/Acrylamide Hydrogels for Drug Delivery

Guillermina Burillo, Carla Padilla, Alejandra Ortega
Gels
Hydrogels: synthesis, properties, applications
article

Gamma Radiation-Assisted Synthesis of Xanthan Gum/Acrylamide Hydrogels for Drug Delivery

Guillermina Burillo, Carla Padilla, Alejandra Ortega
article en

Abstract

Xanthan gum (XG) and acrylamide (AAm) hydrogels were synthesized using gamma radiation. The novelty lies in the use of a simple methodology to obtain two different architectures, thereby tailoring their physicochemical properties. The first system is a comb-type hydrogel (net-AAm)-g-XG, where the crosslinking of AAm and the XG grafting were carried out in a single step via gamma radiation. The second system consists of an interpenetrating network (IPN) (net-XG)-inter-(net-AAm), where XG was crosslinked with citric acid and then AAm was crosslinked by gamma radiation in the presence of XG gel. Good degrees of grafting (60%) and interpenetration (75%) were obtained at 8 kGy for both systems. Comb-type and IPN hydrogels showed a porous structure, but the pore size was smaller in the interpenetrating network because this architecture has less internal space due to the presence of a second network. Morphological differences affected water absorption and drug loading/release properties. The comb-type showed its maximum swelling (900%) at 24 h, regardless of the grafting amount; while the IPN exhibited a swelling of 400–600% at 3 h, depending on the interpenetration degree. Both systems allowed for ciprofloxacin loading, but release was faster in the IPN (100 min) than in the comb-type hydrogel (300 min).

GelsVol. 12(11)
Universidad Nacional Autónoma de México (MX)
Hydrogels: synthesis, properties, applications
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