Journal
PREPARATIVE BIOCHEMISTRY & BIOTECHNOLOGY
Volume 51, Issue 7, Pages 686-696Publisher
TAYLOR & FRANCIS INC
DOI: 10.1080/10826068.2020.1852418
Keywords
Microwave assisted extraction; sour cherry peels; anthocyanins; cyanidin-3-glucoside; statistical experimental design; storage stability
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Funding
- Istanbul UniversityCerrahpasa [33900]
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In this study, microwave assisted extraction (MAE) was optimized to recover phenolic compounds rich in anthocyanins from waste sour cherry, with the process parameters optimized using response surface methodology. The optimized conditions resulted in high yields of total phenolic compounds, total anthocyanin, and antioxidant capacity. Stability assays were also conducted to demonstrate the bioactivity profile. All process parameters were found to be significant for the extraction.
Utilization of economical and environmental methods as an alternative process to recover the industrial crops and food products into high-added value compounds is of great significant. In the current study, microwave assisted extraction (MAE) was optimized by response surface methodology (RSM) in order to evaluate the waste of sour cherry as a source of phenolic compounds rich in anthocyanins. The process parameters (microwave power, irradiation time and ethanol solvent concentration) of MAE method were optimized by face centered composite design of RSM. Responses such as total phenolic componds (TPC), total anthocyanin (TA) contents and antioxidant capacity (DPPH) of extracts were measured spectrophotometrically after extractions of samples. The optimized result of MAE was 500 W of microwave power, 90 s of irradation time and 80% ethanol solvent concentration. Antioxidant capacity was tested using by 1,1-diphenyl-2-picryl hydrazyl (DPPH) radical. Chromatographic analysis (HPLC) was also used to measure the concentration of major anthocyanin (cyanidin-3-glucoside) of the samples. Maximum predicted TPC, TA and DPPH yields on optimized conditions were 44.15 mg-GAE/g-FM (mg- gallic acid equivalent per g- fresh matter), 12.47 mg-cyanidin-3-glucoside/g-FM and 69.90 (%, inhibition), respectively. A stability assay under different conditions (light, dark, ambient condition, refrigerator and deep freezer) has been also performed in order to display the stability of bioactivity profile. All of the process parameters were significant at the level of p < 0.0001. [GRAPHICS] .
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