Mehmet Ali Karaca, Ali Reza Kamali, Bita Erin Kamali, Bilge Temiz, Furkan Özben, Duygu Ege, Hale Saybaşılı
{"title":"Gallic Acid Loaded Alginate-Gelatin Beads for Potential Bone Tissue Engineering Applications","authors":"Mehmet Ali Karaca, Ali Reza Kamali, Bita Erin Kamali, Bilge Temiz, Furkan Özben, Duygu Ege, Hale Saybaşılı","doi":"10.1002/bip.70033","DOIUrl":null,"url":null,"abstract":"<p>In this study, alginate/gelatin (AL/GEL) spherical beads are prepared and encapsulated with 1 wt % of needle-shaped gallic acid (GA) crystals to develop a drug delivery system. The % encapsulation efficiency of GA into AL/GEL beads, its release rate, and the stability of the beads are evaluated, followed by cytocompatibility studies. The interactions between GA, AL, and GEL are examined by using FTIR. Morphological observations reveal that increasing the GEL concentration above 0.4 wt.% possibly hinders the binding of calcium ions with the carboxylate groups of AL, resulting in the formation of beads with larger diameters. In contrast, the bead diameter decreases with the incorporation of GA due to hydrogen bonding. EDX analysis of GA-loaded AL/GEL beads indicated that GA binds to the GEL-rich region. Furthermore, EDX analysis of mineralized beads demonstrated that GA enhanced calcium deposition near the alginate-rich region. In vitro studies demonstrate that AL/GEL beads loaded with ≤ 0.5 (wt.) % GA are cytocompatible and MC3T3-E1 murine pre-osteoblast cells proliferated over a 5-day period. Overall, the prepared beads show potential as a drug delivery system for bone regeneration applications.</p>","PeriodicalId":8866,"journal":{"name":"Biopolymers","volume":"116 4","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2025-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/bip.70033","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biopolymers","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/bip.70033","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
In this study, alginate/gelatin (AL/GEL) spherical beads are prepared and encapsulated with 1 wt % of needle-shaped gallic acid (GA) crystals to develop a drug delivery system. The % encapsulation efficiency of GA into AL/GEL beads, its release rate, and the stability of the beads are evaluated, followed by cytocompatibility studies. The interactions between GA, AL, and GEL are examined by using FTIR. Morphological observations reveal that increasing the GEL concentration above 0.4 wt.% possibly hinders the binding of calcium ions with the carboxylate groups of AL, resulting in the formation of beads with larger diameters. In contrast, the bead diameter decreases with the incorporation of GA due to hydrogen bonding. EDX analysis of GA-loaded AL/GEL beads indicated that GA binds to the GEL-rich region. Furthermore, EDX analysis of mineralized beads demonstrated that GA enhanced calcium deposition near the alginate-rich region. In vitro studies demonstrate that AL/GEL beads loaded with ≤ 0.5 (wt.) % GA are cytocompatible and MC3T3-E1 murine pre-osteoblast cells proliferated over a 5-day period. Overall, the prepared beads show potential as a drug delivery system for bone regeneration applications.
期刊介绍:
Founded in 1963, Biopolymers publishes strictly peer-reviewed papers examining naturally occurring and synthetic biological macromolecules. By including experimental and theoretical studies on the fundamental behaviour as well as applications of biopolymers, the journal serves the interdisciplinary biochemical, biophysical, biomaterials and biomedical research communities.