| Literature DB >> 35539187 |
Xiao-Lan Yu1, Yong He1.
Abstract
Tea saponins, found in Camellia plants, are natural non-ionic surfactants that offer obvious beneficial effects in soil remediation. Most tea saponins are extracted from the Camellia oleifera seed meal, with the leaves and flowers of Camellia sinensis as potential sources. Water extraction and ultrasound-assisted water extraction combined with acetone precipitation are recommended for the industrial extraction and purification of tea saponins, considering multiple factors. The detailed physical, chemical and biochemical properties of tea saponins need to be clarified, especially whether tea saponins with slightly different structures from distinct sources have different soil remediation properties. Applied in leaching remediation, phytoremediation and microbial remediation, tea saponins desorb heavy metals from contaminated soil as well as enhancing their bioavailability. Tea saponins improve the accumulation of pollutants by hyperaccumulators as well as the degradation of organic pollutants by microorganisms. Currently the mechanisms of tea saponins are not clear, although they are proven to be effective natural surfactants for the remediation of contaminated soils. This review enriches our understanding of tea saponins from various aspects and encourages further studies of industrial extraction and purification, and the field remediation mechanisms of tea saponins, making better use of Camellia plants and contributing to environmental protection. This journal is © The Royal Society of Chemistry.Entities:
Year: 2018 PMID: 35539187 PMCID: PMC9082184 DOI: 10.1039/c8ra02859a
Source DB: PubMed Journal: RSC Adv ISSN: 2046-2069 Impact factor: 4.036
Sources of tea saponins
| Species | Plant organ | References |
|---|---|---|
|
| Leaf, stem |
|
|
| Seed |
|
|
| Seed |
|
|
| Root, flower, seed, leaf |
|
|
| Seed |
|
Methods for extracting tea saponins
| Extraction method | Extracting agent [volume fraction] | Yield (%) | References | |
|---|---|---|---|---|
| Water extraction | Water | 8.04–8.5 |
| |
| Ultrasound-assisted water extraction | 21.32 |
| ||
| Alcohol extraction | Methanol | [70%] | 14.45 |
|
| Ethanol | [63–100%] | 7.28–28.81 |
| |
| [70%] + 0.1% NH4·H2O | 22.41 |
| ||
| [75%] + 3% NaOH | 21.35 |
| ||
|
| [90%] | 15.31 |
| |
| Microwave-assisted alcohol extraction | Ethanol | [50–65%] | 12.16–18.56 |
|
| Ultrasound-assisted alcohol extraction | Ethanol | [70–80%] | 18.54–28.38 |
|
| [75%] + 0.1% NH4·H2O | 19.50 |
| ||
| Microwave ultrasound-assisted extraction | Ethanol | [72%] | 13.5 |
|
| Microwave light wave-assisted extraction | Ethanol | [80%] | 8.68 |
|
| Aqueous enzymatic | Cellulase | 6.8–20.23 |
| |
| Neutral protease | 6 |
| ||
| Supercritical fluid CO2 extraction | Ethanol | [65%] | 15.23 |
|
| Homogenate extraction | Ethanol | [78%] | 21.09 |
|
Variables optimized in the extraction of tea saponins
| Method | Variable | Method | Variable |
|---|---|---|---|
| Common extraction | Particle size | Microwave-assisted extraction | Microwave power |
| Liquid–solid ratio | Microwave treatment time | ||
| Extraction time | Ultrasound-assisted extraction | Ultrasonic power | |
| Extraction temperature | Ultrasonic frequency | ||
| Number of extractions | Ultrasonic treatment time | ||
| Alcohol extraction | Alcohol type | Light-wave-assisted extraction | Light-wave treatment time |
| Alcohol volume fraction | Supercritical fluid CO2 extraction | Pressure | |
| Aqueous enzymatic extraction | Fungus type | Medium | |
| Fungus concentration | CO2 flow rate |
Methods for the refined purification of tea saponins
| Refined method | Precipitating agent | Purity (%) | References |
|---|---|---|---|
| Two-phase system extraction | 20% (NH4)2SO4 + 23% | 78.12 |
|
| Reversed-phase column chromatography | Methanol | 95 |
|
| Ethanol | 99.12 |
| |
| Macroporous resin | AB-8 | >80–96.13% |
|
| XR910X | 94.26 |
| |
| D101 | 60.14 |
| |
| Molecularly imprinted polymers | Acrylamide–β-cyclodextrin | 89 |
|
| Flocculation + ultrafiltration | Chitosan | 85 |
|
| Ultrafiltration | 91 |
| |
| Precipitation | Acetone | 72.06 to >93 |
|
| Cholesterol | >98.5 |
| |
| Ether | 97.9 |
| |
| Recrystallization | Ethanol–hydrochloric acid | 81.8 |
|
Methods for identifying and quantifying tea saponins
| Identification | Quantification |
|---|---|
| High performance liquid chromatography (HPLC) | Gravimetric method |
| Reversed-phase high performance liquid chromatography (RP-HPLC) | Spectrophotometry |
| Mass spectrometry (MS) | Thin layer chromatography |
| Nuclear magnetic resonance (13C or 1H NMR) | High performance liquid chromatography (HPLC) |
Applications of tea saponins in leaching remediation for removing heavy metals
| Heavy metal (form) | Tea saponin concentration | Removal ratio (%) | References | |
|---|---|---|---|---|
| Pb, Cd, Zn, Cu | 7% | 6.74, 42.38, 13.07, 8.75 |
| |
| Pb, Cd, Cr, Mn | 20% | 60.5, 72.6, 10.9, 38.8 |
| |
| Pb | (Exchangeable) | 6% | 69.8 |
|
| (Carbonate fraction) | 54.8 | |||
| (Fe–Mn oxides) | 30.4 | |||
| (Organic fraction) | 40.9 | |||
| (Residual fraction) | 7.1 | |||
| Pb, Zn, Cu | 22% | ∼35, ∼38, ∼28 |
| |
| Pb, Cd, Zn, Cu | 7% | 43.71, 96.36, 71.73, 20.56 |
| |
| Pb, Cd | 7% | 50.0, 62.6 |
| |
| Pb, Zn, Cu | 4% | 9.72, 22.81, 11.32 |
| |
| Pb, Ni | 5.0 g L−1 | 83.5, 87.1 |
| |
| Cd, Ni | 7.5 g L−1 | 94.1, 89.4 |
| |
The order of removal ratios corresponds to the order of heavy metals listed in the first column.
These three removal ratios were obtained from figures and are not accurate.
Applications of tea saponins in leaching remediation for removing organic pollutants
| Organic pollutants (form) | Tea saponin concentration | Removal ratio (%) | Comments | References | |
|---|---|---|---|---|---|
| PBDEs | 5.0 g L−1 | 94.6 | Two successive soil washing cycles + 5.0 ml L−1 peanut oil |
| |
| PCBs | 97.1 | ||||
| PAHs | 95.1 | ||||
| PAHs | (3) | 7.5 g L−1 | 98.2 | Two successive soil washing cycles + 15.0 ml L−1 soybean oil |
|
| (4) | 96.4 | ||||
| (5) | 92.3 | ||||
| PAHs | (3) | 2% | 84.3 | +50 mM KNO3 |
|
| (4) | 92.3 | ||||
| (5) | 85.6 | ||||
Applications of tea saponins in phytoremediation
| Pollutant | Accumulator | Tea saponin concentration | Increase in ratio (%) | References |
|---|---|---|---|---|
| Cd |
| 40 mg L−1 | Above: 8; under: 11 |
|
| Cd |
| 3 g kg−1 |
| |
| Cd |
| 0.3% | Leaf: 30.1; stem: 156.8; root: 96.9 |
|
| Pyrene |
| 40 mg L−1 | Above: 135; under: 40 |
|
| PCBs |
| 0.1% | PCB 14 : 172 |
|
| PCB 18 : 168 | ||||
| PCB 77 : 94 | ||||
| PCB 156 : 140 |
‘Above’ means parts of the plant above the ground and ‘under’ means parts of the plant under the ground.
These data were measured at the root of the plant.
Applications of tea saponins in microbial remediation
| Pollutant | Bacteria | Tea saponin concentration | Biodegradation efficiency | References |
|---|---|---|---|---|
| PCBs | WTS | 1000 mg L−1 | PCB 77 : 4.3 times |
|
| PCB 118 : 4.8 times | ||||
| PCB 138 : 2.8 times | ||||
| YTS | PCB 77 : 7.1 times | |||
| PCB 118 : 9.1 times | ||||
| PCB 138 : 8.9 times | ||||
| BDE209 |
| 1 g L−1 (5 days) | 55% |
|
| Triphenyl tin |
| 60 mg L−1 (7 days) | 1 mg L−1 to 283 μg L−1 |
|
| Diphenyl tin | 1 mg L−1 to 270 μg L−1 | |||
| Monophenyl tin | 1 mg L−1 to 235 μg L−1 |
WTS and YTS were separated from soil and temporally named by the authors of ref. 113.