abstract
Propolis is a functional food ingredient classified by its physical-chemical characteristics, vegetal source, bee species, and geographical origin. Due to its complex nature and variable composition, the massive use of propolis extracts would require standardization. Several techniques for recovering bioactive compounds from propolis have been reported, varying according to their complexity, degree of automation, and energy dependence. The recovery of propolis target compounds must be carried out using the most appropriate extraction process and the optimized conditions, guaranteeing a better use of the raw material, lower process costs, and good extraction selectivity. This work presents and discusses conventional and alternative techniques developed in the last 20 years. The extraction efficiency, selectivity, the type and amount of solvent, and the conditions to optimize and guarantee safe products (e.g., toxicity and biocompatibility) were reviewed. The current trends were reported, and the technological advances, future perspectives, and applications of the natural bioactive compounds ob-tained from propolis were discussed. A comprehensive determination of the main advantages and disadvantages of the extraction techniques and the impact of operational conditions on the processes' performance was assessed. Based on the available evidence, some future strategies will be scrutinized, not only regarding the future of using propolis and its products but also considering the impact of a propolis-business model crossing the concept of a circular economy and combining it with the idea of resource efficiency.
keywords
ULTRASOUND-ASSISTED EXTRACTION; DEEP EUTECTIC SOLVENTS; SUPERCRITICAL-FLUID EXTRACTION; PRESSURIZED LIQUID EXTRACTION; NEAR-INFRARED SPECTROSCOPY; HIGH HYDROSTATIC-PRESSURE; PHENOLIC-COMPOUNDS; ANTIOXIDANT ACTIVITY; RAW PROPOLIS; ANTIMICROBIAL ACTIVITY
subject category
Engineering
authors
Contieri, LS; Mesquita, LMD; Sanches, VL; Chaves, J; Pizani, RS; da Silva, LC; Vigano, J; Ventura, SPM; Rostagno, MA
our authors
Projects
CICECO - Aveiro Institute of Materials (UIDB/50011/2020)
CICECO - Aveiro Institute of Materials (UIDP/50011/2020)
Associated Laboratory CICECO-Aveiro Institute of Materials (LA/P/0006/2020)
acknowledgements
Acknowledgements The authors acknowledge the funding received from the Funda?a ? o de Amparo a ` Pesquisa do Estado de Sa ? o Paulo (FAPESP) . M.A.R, L. C. da Silva, J. Vigan ? o, L. de Souza Mesquita, M. C. de Souza, R. S. Pizani, and L. S. Contieri are grateful to FAPESP (2018/14582-5; 2019/24537-0; 2020/15774-5; 2020/08421-9; 2018/17089-8; 2019/18772-6; 2020/04067-6; 2020/03623-2) . This study was financed in part by the Coor- dena?a ? o de Aperfei?oamento de Pessoal de N?vel Superior-Brazil (CAPES) -Process 88887.310558/2018-00 and Finance Code 001. M.A. R. thank the Brazilian Science and Research Foundation-CNPq for the productivity grants (302610/2021-9) . This work was developed within the scope of the project CICECO-Aveiro Institute of Materials, UIDB/50011/2020, UIDP/50011/2020 & LA/P/0006/2020, financed by na- tional funds through the FCT/MEC (PIDDAC) .