Table 3.
Technologies | Advantages | Disadvantages | Storage Life | References |
---|---|---|---|---|
Pulsed electric field | Low energy consumption Short processing time Waste-free process |
High initial investment Less efficient for spore inactivation Presence of bubbles effect uniformity Low economic |
Improve tenderization and water holding capacity, less physiological effects due to partial disruption of cellular tissues, increase shelf life of meat | [107] |
Ohmic treatment | Quick process Relatively uniform heating |
High initial cost Relatively electrolytic effect |
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Enzymatic treatment | More recovery yields Low contamination High selectivity rate |
High enzymes cost Prolong processing time Low-efficiency rate |
Increased shelf life through reducing oxidative spoilage, microbial activity, improve textural properties | [131] |
Fluorescence spectroscopy | High data achievement rate Simple and more economic |
Time consumption in sample preparation Not suitable for solid material detection Highly selective method |
Improve protein functionality and conformational changes during protein denaturation | [112] |
Nuclear magnetic resonance | High data evaluation Non-destructive and non-intrusive |
High cost-effective Highly expensive equipment |
Improve sensory properties, chemical composition, nutritional and physicochemical properties | [132] |
Fermentation | More economical Environmentally friendly Useful for bioactive extraction Poor energy consumption |
Slow process Recovery yield and quality effect by microorganism used |
Reduce microbial proliferation, prevent foodborne pathogens, reduce microbial proliferation, therefore, extending shelf life | [133] |
High hydrostatic pressure | Energy efficient High preservative quality Easy to commercialize Wide range of microorganism inactivation |
Cost-effective Less efficient for spore’s inactivation Limited packaging facility |
Prolonged shelf life up to 2 months at 2 oC, reduce microbial load and food spoilage genera, improve quality | [134] |
Fourier transform infrared spectroscopy (FTIR) |
Rapid and reliable Sensitive to conformational changes under various conditions Independent of the physical condition of samples |
Nonlinear problems of the curve High cost Strong IR absorbance of H2O |
Monitored microbial spoilage, texture and colour attributes, authenticate freshness attributes | [114] |
Raman spectroscopy | Required small size sample Less expensive instrumentations Non-destructive |
Higher instrumental costs Stronger biological fluorescence interference Heat effect generated by the laser |
Increase shelf life, improve protein and water contents, reduce microbial load | [135] |
Near-infrared (NIR) spectroscopy | Rapid and non-destructive Non-contact and cost-effective |
Accuracy depends on the reliability of the reference method Does not provide spatial information on the sample Contain unnecessary and redundant information |
Reduce microbial spoilage, predict compositional changes, reduce foodborne pathogens | [136] |
Visible near-infrared (VIS/NIR) spectroscopy | Non-contact Rapid Non-destructive |
Non-independent requires samples with known analyte concentration Specular highlights and uneven illumination under varying sample surface |
Reduce oxidation, optimize product quality, increase shelf life | [137] |
Nuclear magnetic resonance/magnetic resonance imaging (NMR/MRI) spectroscopy | Cost-effective Non-destructive |
Slow process High initial cost Expensive equipment |
Food authentication, detect alteration and unwanted compounds. | [138] |
Ultrafiltration | High energy efficiency Better quality permeates Continuous recovery |
Time-consuming Expensive membranes |
Extend shelf life, reduce disruption of cells, inhibit microbial spoilage | [139] |
Supercritical fluid extraction | Environmentally friendly Rapidly penetrate in sample Mild processing conditions Low processing wastes |
Complex equipment Required a high pressure Use of modifiers |
Minimal disruption of tissue cells, improve quality, reduce bacterial count, improve shelf life | [140] |