Fabrication and physicochemical investigation of pH-responsive alginate/ pectin hybrid network hydrogel for improved stability and controlled release of diallyl thiosulfinate

The present investigation explores the formulation and fabrication of alginate-pectin (with varying degree of methoxylation) hybrid network hydrogel beads through ionotropic gelation process as a biocompatible carrier material for encapsulating diallyl thiosulfinate (allicin). The primary aspiration of this research is to overcome allicin's inherent instability which restricts its use in functional food fortification and medicinal products as a bioactive compound with several intriguing health-promoting characteristics. Fabrication of the beads were done through structured parameter optimization. Chemical interaction between allicin and biopolymer matrix was assessed by FTIR-ATR. The ARGE entrapped hydrogel beads had a near spherical shape with sphericity factor similar to 1.0 with an average diameter of similar to 3.5 mm in the hydrated state (density similar to 1.06 g/cm(3)). The beads showed encapsulation efficiency of similar to 70.8 %. The beads efficaciously reduced degradation (<5 %) and stabilized ampule amount of allicin for a prolonged time. Various physicochemical characterizations of the produced beads were done. Further, in vitro release kinetics of allicin from beads were observed in simulated gastrointestinal environment and it showed a sustained release pattern. The release behavior of allicin exhibited a higher release at intestinal pH (similar to 88 %) than stomach pH (similar to 35 %). The formulation expressed commendable antimicrobial activity against gram positive and negative bacteria in both solid and liquid media. Moreover, the encapsulation process retained significant antioxidant potential (>60 %). Anti-inflammatory and hemolysis assay expressed admirable biocompatibility. Hence, the results suggest that the fabricated formulation is suitable for being a drug carrier material for allicin while accentuating its aptitude for upholding hemocompatibility, allicin's concentration, sustained release and bioactivity.