| Literature DB >> 34826725 |
Nerea Muñoz-Almagro1, Eduardo Morales-Soriano2, Mar Villamiel3, Luis Condezo-Hoyos4.
Abstract
With the growing of consumer's demand for products ready to eat that can be elaborated with greener technologies without affecting to their organoleptic characteristics, the application of ultrasound combined with microwaves has been widely studied on food preservation treatments (drying, frying), extraction of high-value added compounds and enzymatic hydrolysis of proteins. This review presents a complete picture of current knowledge on the ultrasound combined with microwaves including the mechanisms, influencing factors, advantages and drawbacks, emphasising in several synergistic effects observed in different processes of strong importance in the food industry. Recent research has shown that this hybrid technology could not only minimise the disadvantages of power US for drying and frying but also improve the product quality and the efficiency of both cooking processes by lowering the energy consumption. Regarding extraction, current studies have corroborated that the combined method presents higher yields in less time, in comparison with those in the respective ultrasound and microwave separately. Additionally, recent results have indicated that the bioactive compounds extracted by this combined technology exhibit promising antitumor activities as well as antioxidant and hepatoprotective effects. Remarkably, this hybrid technology has been shown as a good pre-treatment since the structural changes that are produced in the molecules facilitate the subsequent action of enzymes. However, the combination of these techniques still requires a proper design to develop and optimized conditions are required to make a scale process, and it may lead to a major step concerning a sustainable development and utilization of bioactive compounds from natural products in real life.Entities:
Keywords: Food bioactivity; Food quality; Hybrid technology; Microwave; Ultrasound
Mesh:
Year: 2021 PMID: 34826725 PMCID: PMC8626613 DOI: 10.1016/j.ultsonch.2021.105835
Source DB: PubMed Journal: Ultrason Sonochem ISSN: 1350-4177 Impact factor: 7.491
Fig. 1a) Scheme of the hybrid dryer: 1. Fan, 2. Airborne Ultrasound System (AUS), 3. Ultrasound feeder, 4. Electric heater, 5. Air outlet, 6. Ultrasound transducer AUS, 7. Pyrometer, 8. Rotating sample pan, 9. Drive sample pan, 10. Balance, 11. Microwave generator, 12. Control cupboard. b) Photo of the hybrid system. Szadzińska et al. [34].
Fig. 2Convective-microwave drying of strawberries assisted with ultrasound. Szadzinska et al. [38].
Fig. 3Scheme of drum hybrid dryer: 1. Blower, 2. AUS controller, 3. AUS amplifier, 4. Microwave feeders, 5. Heater, 6. Pneumatic valve, 7. Air outlet, 8. Pyrometer, 9. Drum drive, 10. Microwave generators, 11. Balance, 12. Rotatable drum, 13. AUS transducer, 14. Control unit. Musielak et al. [31].
Retention of carotenoids (%) in conventional, ultrasound (US) and microwaves (MW) treated carrot samples. Modified from Kroenke et al. (2018).
| Fresh sample (mg/kg d.m) | CV | CVUS 75 W | CVUS 125 W | CVUS 200 W | CVMW 100 W | CVUS 75 W MW 100 W | CVUS 125 W MW 100 W | CVUS 200 W MW 100 W | |
|---|---|---|---|---|---|---|---|---|---|
| Component | Retention of component (%) | ||||||||
| α-carotene | 144 | 87c | 98 d | 89c | 78b | 54 a | 59 a | 73b | 57 a |
a, b, c, d, e – means in row followed by different letters are significantly different at p < 0.05.
Fig. 4Schematic diagram of ultrasound and microwave-assisted vacuum frying (USMVF) instrument. 1. Oil tank, 2. Microwave source and heating system, 3. Ultrasound source and vacuum pressure balance system, 4. Vacuum chamber, 5. Frying chamber, &. Circulation pump, 7. Electric cabin door system, 8. Bending and centrifugation system, 9. Controller and operation panel. Adapted from Devi et al., [48] and Zhang et al. [97].
Fig. 5Ultrasound in combination with microwave processor (a) commercially available and (b) schematic diagram of ultrasound in combination with microwave bath type system. Adapted from Ojha et al. [98].
Increase of degree of enzymatic hydrolysis of food protein pre-treated by combined ultrasound (US) and microwave (MW).
| Food protein source | US-MW pretreatment | Enzymatic hydrolysis | Increase of degree of hydrolysis (%) | Reference |
|---|---|---|---|---|
| Milk protein concentrates (5% w/w) | US for 10 min (20 kHz, power not reported) and MW for 10 min at 800 W | Digestive enzymes (pepsin at 37° C for 2 h, pH 2.0, and trypsin at 37 °C for 2 h, pH 7.5) | 12.97 ± 1.37 |
Control without pretreatment was used for the comparison; b Number is the US and MW power (Watts) and pretreatment was carried out at 51° C for 8 min.
Fig. 6Ratio of molecular weight (<3 kDa/10 kDa) of sweet potato protein hydrolysates at different times by US-MW-assisted enzymatic hydrolysis. ALC = Alcalase, FLA = Flavourzyme and ALC + FLA = Alcalase + Flavourzyme. Adapted from Habinshuti et al. [75].
Antioxidant activity and ACE inhibition activity of peptides obtained by enzymatic hydrolysis of food proteins pre-treated by combined ultrasound (US) and microwave (MW).
| Food protein source [reference] | US-MW pretreatment | Antioxidant capacity | ACE inhibition activity | ||
|---|---|---|---|---|---|
| DPPH | ABTS | FRAP | |||
| Milk protein concentrates | US for 10 min (20 kHz, power not reported) and MW for 10 min at 800 WUS 40 kHz-50 W and MW power 50 W at 55 °C for 8 minUS100-MW100 | 0.77 (0.62) 3.01 ± 0.04 (3.78 ± 0.04) 5.1 ± 0.3 4.9 ± 0.6 4.5 ± 0.3 2.8 ± 0.1 4.1 ± 0.8 2.3 ± 0.2 4.7 ± 0.8 4.1 ± 0.8 | 1.85 ± 0.03 (2.69 ± 0.04) | 0.32 (0.30) | 6.7 ± 0.7 6.2 ± 0.5 4.9 ± 0.3 5.2 ± 0.6 4.6 ± 0.4 3.5 ± 0.1 7.5 ± 0.5 5.3 ± 0.4 |
| Sweet potato protein | US 40 kHz-MW10-800 at 50 °C for 180 min | OH | ORAC (µg TE/mL) |
IC50 in mg/mL (control);
Control hydrolysates by pepsin = 10.60 ± 0.6 and alcalase = 10.1 ± 0.4;
Control 16.9 ± 0.3;
% of hydroxyl radical scavenging (control) and
Oxyradical Antioxidant Capacity and TE is Trolox Equivalent.
Fig. 7Effects of myofibrillar protein peptide (6 mg/mL) on the activities of catalase (CAT), superoxide dismutase (SOD) and inflammatory biomarkers TNF-α and IL-1β in RAW 264.7 cells stimulated by H2O2. Adapted from Li et al. [74].