1088Enhancing delivery efficiency and in vitro bioaccessibility of Cinnamomum zeylanicum extract using liposomal and alginate-based encapsulation

Culas M.S1,2, Kaur L.1,2, Popovich D.G.3, Rashidinejad A.1

1Riddet Institute, Massey University, Private Bag 11 222, Palmerston North, 4442, New Zealand
2School of Food Technology and Natural Sciences, Massey University, Private Bag 11222, Palmerston North 4442, New Zealand
3School of Science Engineering & Technology, 702 Nguyen Van Linh, District 7, RMIT Vietnam, Ho Chi Mingh, Viet Nam

Cinnamomum zeylanicum contains abundant bioactive compounds, particularly cinnamaldehyde and polyphenols, which are associated with significant health benefits such as the regulation of blood glucose levels. Despite their potential, these compounds are highly vulnerable to external factors such as heat and light, leading to reduced stability and bioavailability. Encapsulation offers an effective approach to protect these molecules and regulate their release. The present study offers a comparative evaluation of two encapsulation strategies, including liposomal and alginate-based microencapsulation systems, focusing on their relative protective efficacy and physicochemical stability.

Liposomes were prepared using soy lecithin, while alginate beads were obtained through ionic gelation with calcium chloride. Encapsulation efficiency was evaluated in terms of total phenolic content and cinnamaldehyde concentration. The liposomal system showed efficiencies of 54% for phenolics and 72% for cinnamaldehyde, whereas alginate beads exhibited higher efficiencies of 94% and 84%, respectively. FTIR spectra displayed distinct peak shifts and the appearance of new bands in cinnamon-loaded alginate beads, indicating successful incorporation of the extract and its interaction with the polymer matrix. Differential scanning calorimetry further demonstrated that both encapsulation systems maintained thermal stability up to 120°C.

An in vitro gastro-small intestinal digestion model was employed to evaluate both encapsulation systems with respect to the release behaviour of bioactive compounds. In the gastric phase, the release was relatively low, ranging from 17 to 26% for alginate beads and 24 to 56% for liposomes. In contrast, a substantially higher release was observed in the intestinal phase relative to the gastric phase, with values of up to 85% for alginate and 83% for liposomes, demonstrating effective targeted delivery to the intestinal phase. These results highlight the potential of both alginate- and liposomal-based microencapsulation systems in enhancing the stability and in vitro bioaccessibility of C. zeylanicumbioactives during digestion. Ongoing research in our laboratories is directed toward incorporating the encapsulated extract into functional yoghurt formulations and assessing its potential antidiabetic properties.

Relevant Conference Theme -Innovative hydrocolloid design for delivering optimal nutrition and functional foods

Presentation Type –Poster presentation and poster qualify for consideration for the Elsevier Competition.