TY - JOUR T1 - The Composite Microbeads of Alginate, Carrageenan, Gelatin, and Poly-(Lactic-co-Glycolic Acid): Swelling, Cefaclor Loading and Release TT - Aljinat, Karragenan, Jelatin ve Poli-(Laktik-ko-Glikolik Asit) Kompozit Mikroboncukları: Şişme, Sefaklor Yükleme ve Salınımı AU - Semerci Arıkan, Buse AU - Baybaş, Demet PY - 2025 DA - August Y2 - 2025 DO - 10.35414/akufemubid.1560061 JF - Afyon Kocatepe Üniversitesi Fen Ve Mühendislik Bilimleri Dergisi PB - Afyon Kocatepe University WT - DergiPark SN - 2149-3367 SP - 738 EP - 756 VL - 25 IS - 4 LA - en AB - Composite microbeads were synthesized as a combination of two, three, or four of the following components: alginate(A), carrageenan(C), gelatin(G), and/or poly (lactic-co-glycolic acid)(P). Herein, Cefaclor(Cef) was investigated as a model drug to study the usability of the beads in drug delivery. The composite microspheres with medication and drug-free were synthesized under different conditions. Fourier Transform Infrared (FTIR) spectra of these composites were compared. The effects of synthesis conditions such as component amounts, cross-linker ion amounts on swelling, entrapment efficiency, and release kinetics of materials were examined. The maximum swelling comparison of the hydrogel composites is A(981%)>AP(747%)>ACGP(641%)>ACG(618%)>ACP(464%)>AC(442%)>AGP(295%)>AG(157%). Adding PLGA to the alginate sphere reduces the swelling contrast adding PLGA to the composite beads containing other components increases the swelling %. As the amount of PLGA added to the ACP spheres increases, the swelling decreases. The maximum entrapment efficiency of cefaclor in micro-composites is ACP(93%)>AC(76%)>AP(66%)>ACG=AGP(46%)>AG(40%)>ACGP(39%)>A(36%). All release experiments were carried out in simulated gastric fluid without enzyme at body temperature, with new solutions in a shaking medium. The release of cefaclor from the composite beads did not generally show a burst effect. The selected data fit the first-order release kinetics and the Korsmeyer Peppas and Higuchi drug release models. KW - cefaklor release KW - alginate KW - carrageenan KW - gelatin KW - poly(lactic-co-glycolic acid) N2 - Kompozit mikroboncuklar, aşağıdaki bileşenlerden ikisinin, üçünün veya dördünün bir kombinasyonu olarak sentezlendi: aljinat (A), karragenan (C), jelatin (G) ve/veya poli (laktik-ko-glikolik asit) (P). Burada, ilaç salınımında boncukların kullanılabilirliğini incelemek için model ilaç olarak Sefaklor (Cef) araştırıldı. İlaçlı ve ilaçsız kompozit mikroküreler farklı koşullar altında sentezlendi. Bu kompozitlerin Fourier Dönüşümlü Kızılötesi (FTIR) spektrumları karşılaştırıldı. Bileşen miktarları, çapraz bağlayıcı iyon miktarları gibi sentez koşullarının şişme, tutulma verimliliği ve malzemelerin salım kinetiği üzerindeki etkileri incelendi. Hidrojel kompozitlerinin maksimum şişme karşılaştırması A(981%)>AP(747%)>ACGP(641%)>ACG(618%)>ACP(464%)>AC(442%)>AGP(295%)>AG(157%) şeklindedir. Aljinat küresine PLGA eklenmesi şişme kontrastını azaltırken, diğer bileşenleri içeren kompozit boncuklara PLGA eklenmesi şişme %'sini artırır. ACP kürelerine eklenen PLGA miktarı arttıkça şişme azalır. Sefaklorun mikro kompozitlerdeki maksimum tutulma etkinliği ACP(93%)>AC(76%)>AP(66%)>ACG=AGP(46%)>AG(40%)>ACGP(39%)>A(36%)'dır. Tüm salım deneyleri, çalkalama ortamında yeni çözeltilerle, vücut sıcaklığında enzimsiz simüle edilmiş mide sıvısında gerçekleştirildi. Sefaklorun kompozit boncuklardan salımında genellikle bir patlama etkisi görülmedi. Seçilen veriler birinci dereceden salım kinetiğine ve Korsmeyer Peppas ve Higuchi ilaç salım modellerine uymaktadır. CR - Arsalan, A., Ahmad, I., Ali, S., A. 2017. in. Berthardt, L,V, (ed). Advances in Medicine and Biolog: Nova Science Publishers Inc., 123. pp 1-52. 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