Nutraceuticals from natural sources have shown potential new leads in functional food products. Despite a broad range of health-promoting effects, these compounds are easily oxidized and unstable, making their utilization as nutraceutical ingredients limited. In this study, the encapsulated stingless bees' propolis in liposome was prepared using soy phosphatidylcholine and cholesterol by thin-film hydration technique. Three different formulations of phosphatidylcholine composition and cholesterol prepared by weight ratio was conducted to extract high propolis encapsulation. Physicochemical changes in the result of the encapsulation process are briefly discussed using scanning electron microscopy and Fourier Transform Infrared Spectroscopy. A dynamic light-scattering instrument was used to measure the hydrodynamic diameter, polydispersity index, and zeta potential. The increment of the liposomal size was observed when the concentration of extract loaded increased. In comparing three formulations, F2 (8:1 w/w) presented the best formulation as it yielded small nanoparticles of 275.9 nm with high encapsulation efficiency (66.9%). F1 (6:1 w/w) formed large particles of liposomes with 422.8 nm, while F3 (10:1 w/w) showed low encapsulation efficiency with (by) 38.7%. The liposome encapsulation will provide an effective nanocarrier system to protect and deliver the flavonoids extracted from stingless bees' propolis.
The inherent source of gelatin used for commercial hard capsules causes a surging demand for vegetarian capsules. In this work, carrageenan is utilized in preparing hard capsules to meet consumer preferences. Hydroxypropyl methylcellulose (HPMC) was incorporated as a reinforcing agent to improve the low mechanical properties of hard capsules made of carrageenan. The HPMC concentration was manipulated from 0.2 to 1.0 w/v% in the carrageenan matrix. The increasing concentration of HPMC exerts significant effects on the tensile strength and elongation at break, with an improvement of 59.1% and 46.9%, respectively, at the optimized HPMC concentration of 0.8 w/v%. The loop strength of the capsule is also increased by 56.4% with decreasing moisture content. The downfield movement from around 3.20 ppm of the carrageenan proton to 3.33 ppm in the proton nuclear magnetic resonanance ( 1H‐NMR) spectrum suggests the formation of intermolecular hydrogen bonding between carrageenan and HPMC, which correlates to the results of Fourier‐transform infrared spectroscopy (FTIR) and zeta potential. The glass transition temperature of the film was increased from 37.8 to 65.3°C, showing an upgrade in thermal stability. The film possesses a major mass loss with an activation energy of 64.7 kJ/mol with an increment of 43.4% compared to the control carrageenan. These findings support the conclusion that HPMC enhanced the mechanical properties and thermal stability of the carrageenan film, and the comprehensive analysis of the molecular interaction and decomposition kinetics subsequently may expand the application fields of the carrageenan‐HPMC hard capsule as an alternative to gelatin in the future.
Vegetarian hard capsule has attracted surging demand as an alternative to gelatin; however, only few have been commercialized. Carrageenan extracted from seaweed has the potential to be utilized as a hard capsule material. Improving the mechanical and thermal properties of carrageenan biocomposite is therefore of great importance for future use in the drug delivery system. Hence, carboxymethyl sago starch (CMSS) was incorporated to strengthen the carrageenan biocomposite in a concentration range from 0 to 1.0% w/v. The intermolecular hydrogen bonding formed between carrageenan and CMSS was revealed via density functional theory (DFT) calculations and substantiated by 1 H NMR and FTIR spectra. The result showed that the hydrogen bond is established between hydroxyl (carrageenan)−carbonyl (CMSS) groups at a distance of 1.87 Å. The bond formation subsequently increased the tensile strength of the biocomposite film and the loop strength of the hard capsule by 20.6 and 7.7%, respectively. The glass transition temperature of the film was increased from 37.8 to 47.8 °C, increasing the thermal stability. The activation energy upon decomposition of the film is 74.4 kJ•mol −1 , representing a 26.2% increase over the control carrageenan. These findings demonstrate that incorporation of CMSS increases the properties of carrageenan biocomposite and provides a promising alternative to animal-based hard capsules.
This research was intended to synthesize liposome as a nanocarrier to encapsulate quercetin, which is prone to degradation and susceptible to low bioavailability upon oral administration. The liposomes were synthesized by thin-film hydration method and followed by probe sonication for downsizing. Soy phosphatidylcholine (SPC) and cholesterol (CHOL) were employed as the composition of the phospholipid bilayer. Results indicated a dependence of sonication amplitude and time in the formation of free liposomes (FL). The average size of quercetin-loaded liposomes (QL) prepared was 346.4 nm with a narrow polydispersity index (0.22) and a high magnitude of zeta potential (-49.6 mV). These characterizations depict that a homogenous nanovesicle suspension with high stability was successfully synthesized. Quercetin was incorporated into the liposomes with a high encapsulation efficiency of 90.7% and loading capacity of 9.3%. This viable nanocarrier perhaps will provide ingenious protection for a wider spectrum of active agents in food and biopharmaceutical products.
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