Solvent-based Extraction Research Articles

Extraction, separation and kinetics of phenylethanosides from Plantago asiatica L. by an innovative extraction technology—deep eutectic solvent-based ultrasound-assisted extraction

In this paper, the total phenylethanosides (TPS) were extracted efficiently by an innovative extraction technology––deep eutectic solvent-based ultrasound-assisted extraction (DES-UAE) from Plantago asiatica L. Ten diverse types of DESs were synthesized as alternative extraction solutions. The extraction efficiency of DES-3 (constituted by choline chloride and lactic acid) was much higher than those of other DESs. On the basis of single factor tests and Box-Behnken design (BBD), the optimum processing parameters of DES-UAE as follow: DES-3 with molar ratio of 1:3, extraction temperature 51 °C, solid/liquid 22.5 mg/ml, water content 30%, ultrasonic power 65 W, extraction time 23 min. The extraction efficiency of TPS from Plantago asiatica L. was 8.395 mg/ml, which was more superior than those of organic solvents (water, methanol, 50% methanol, ethanol, 50% ethanol). The extraction kinetics experiment results showed that water content had a significant influence upon the extraction efficiency of TPS. At the same time, AB-8 macroporous resin column was used to efficiently isolate TPS from DES extraction with a recovery rate of 88.5%.

Deep Eutectic Solvent-Based Ultrasound-Assisted Strategy for Simultaneous Extraction of Five Macamides from Lepidium meyenii Walp and In Vitro Bioactivities.

This study aimed to develop an integrated approach of deep eutectic solvent-based ultrasound-assisted extraction (DES-UAE) to simultaneously extract five major bioactive macamides from the roots of Lepidium meyenii Walp. Ten different DESs containing choline chloride and selected hydrogen-bond donors were prepared and evaluated based on the extracted macamide content determination using high-performance liquid chromatography (HPLC). Choline chloride/1,6-hexanediol in a 1:2 molar ratio with 20% water exhibited the most promising extraction efficiencies under the optimized parameters verified using single-factor optimization as well as Box-Behnken design. Using the optimized DES-UAE method, the extraction efficiencies of the five macamides were up to 40.3% higher compared to those using the most favorable organic solvent petroleum ether and were also superior to those of the other extraction methods, such as heating and combination of heating and stirring. Furthermore, using the macroporous resin HPD-100, the recoveries of the five target macamides from the DES extraction reached 85.62-92.25%. The 20 μg/mL group of the five macamide extracts showed superior neuroprotective activity against PC12 cell injury than that of the positive drug nimodipine. The macamide extracts also showed higher NO inhibition in LPS-stimulated RAW264.7 cells. Thus, the developed approach was a green and potential alternative that can be used to extract bioactive macamide constituents from L. meyenii in the pharmaceutical and food industries.

Process optimization of deep eutectic solvent-based microwave-assisted extraction of flavonoids from Ziziphi Spinosae Semen using response surface methodology

Total flavonoids were extracted from Ziziphi Spinosae Semen (ZSS) by applying microwave-assisted extraction with low eutectic solvent (DES) as the extractant. This study investigated the effect of 21 different components of DES on the yield of total flavonoids in ZSS. The results revealed that the DES system, which consists of choline chloride and lactic acid with a molar ratio of 2:1, achieved the best flavonoid extraction efficiency. Based on the single-factor test, response surface methodology was used to optimize and determine the optimal process conditions for the extraction of total flavonoids from ZSS with deep eutectic solvent. The maximum flavonoids yields were achieved at 36.24 mg/g within the 50% DES water content, a microwave power of 600 W, a microwave time of 60 s, a liquid-solid ratio of 1:28 mg/mL, an extraction time of 66 min, and an extraction temperature of 93 °C. The macroporous resin was used to recover flavonoids from extracts. The DM130 resin showed higher adsorption/desorption performance. The total flavonoids of ZSS were extracted using the recovered DES with a yield of 32.58 mg/g and a high reusability of 89.9%.

Determination of major and trace elements in plant samples by inductively coupled plasma optical emission spectrometry with deep eutectic solvent extraction based on choline chloride and carboxylic acids.

A rapid, precise, and environmentally friendly approach utilizing an ultrasound assisted deep eutectic solvent-based extraction method was developed for the extraction of Ca, Fe, K, Mg, Mn, Na, P, S and Zn from plant samples. The investigation was conducted on deep eutectic solvents that are based on choline chloride and carboxylic acids. The determination of target analytes in the extracts was carried out using inductively coupled plasma-optical emission spectrometry (ICP-OES). The DESs based on malic acid were found to exhibit the highest extraction recovery values (95-106%). The parameters affecting the extraction of target analytes were optimized using standard reference materials. The target analytes can be effectively extracted from plant samples using 0.5 g of DESs and ultrasonication for 40 minutes. The determination results of the reference samples indicated that the relative error (RE) was below 15.1%, and the relative standard deviation (RSD) was less than 6.3%, demonstrating excellent accuracy and precision. The proposed method was employed to quantify target analytes in actual plant samples. The accuracy of this method was not significantly different from that of the microwave digestion method. The proposed method has been demonstrated to be a valid approach for the determination of target elements in actual plant samples.

Novel process for the upgrading of model torrefaction bio-oils using ammonia

Bio-oils produced from torrefaction or pyrolysis of biomass constitute an under-utilized product that generally requires complicated processing. The high acidity and water content pose storage and transportation issues, and the complex nature of the organic species makes utilization as a chemical feedstock troublesome. Most methodologies to separate and upgrade bio-oils involve multiple distinct steps and solvent-based extractions, complicating the process and adding cost. In this work, we demonstrate a simple one-step solution using ammonia to separate the aqueous and organic phases of a model bio-oil. This process produces an aqueous phase that contains ammonium species that could be utilized as a fertilizer and an organic phase that can be used as an additive for transportation fuels or could be burned to produce electricity.

Multifarious extraction methodologies for ameliorating lipid recovery from algae

Amongst the current alternatives, algae were proven to be a promising source of biofuel, which is renewable and capable of meeting world demand for transportation fuels. However, a suitable lipid extraction method that efficiently releases the lipids from different algal strains remains a bottleneck. The multifarious pretreatment methods are prevalent in this field of lipid extraction, and therefore, this article has critically reviewed the various lipid extraction methods for ameliorating the lipid yield from algae, irrespective of the strains/species. Physical, mechanical, and chemical are the different types of pretreatment methods. In this review, methodologies such as homogenization, sonication, Soxhlet extraction, microwave treatment, and bead-beating, have been studied in detail and are the most commonly used methods for lipid extraction. Specific advanced/emerging processes such as supercritical CO2 extraction, ionic liquid, and CO2 switchable solvent-based algal lipid extraction are yet to be demonstrated at pilot-scale, though promising. The extraction of lipids has to be financially conducive, environmentally sustainable, and industrially applicable for further conversion into biodiesel. Hence, this paper discusses variable pretreatment for lipid extraction and imparts a comparative analysis to elect an efficient, economically sound lipid extraction method for pilot-scale biodiesel production.

An innovative simplified one-pot process for Astaxanthin purification from Paracoccus carotinifaciens

Astaxanthin (ASX) is a carotenoid with several applications in the food and pharmaceutical fields which is recognised as having a higher physiological and commercial value when it is biologically rather than chemically sourced. This work experimentally investigates the bio-fractionation of biomass of the Paracoccus carotinifaciens bacterium by extraction with the switchable hydrophilicity solvent N,N-dimethyl cyclohexylamine (DMCHA) to obtain ASX and related carotenoids in separate form. This is done by means of a sequential process carried out in a single apparatus. DMCHA gave an extraction yield in terms of equivalent ASX extracted per unit mass of processed dry microbial biomass (62.5 %) higher than acetone (48 %) and ethanol (14 %). After the DMCHA was washed from the extract with carbonated water, 88.2 % of the extracted ASX was recovered. The possibility of extracting carotenoids with recycled solvent with a minor (-7.7%) efficiency drop was also demonstrated, as was the lower energy footprint of DMCHA-based than competing volatile solvent-based extraction processes.

Deep eutectic solvent-based ultrasound-assisted extraction of polyphenols from Cosmos sulphureus

In this study, deep eutectic solvents-based ultrasound-assisted extraction (DES-UAE) was done for extraction of polyphenols from Cosmos sulphureus. Among seven kinds of DESs prepared, choline chloride-lactic acid (1:2) was considered as a good candidate for polyphenols extraction due to superior extraction performance. Subsequently, process parameters for DES-UAE were optimized by response surface methodology. The highest total polyphenolic content (TPC) was achieved at 47.5 ℃ temperature, 32.6% water content and 4.0 W/mL ultrasonic energy density. This was 21% higher than that acquired with conventional ethanol-based UAE. Furthermore, Pearson’s correlation coefficient revealed high correlation between TPC and antioxidant activity of extracts (r = 0.85). Moreover, HPLC analysis indicated that the substitution of DES for ethanol in UAE can effectively improve the individual concentrations in extracts of interested polyphenols (chlorogenic acid, caftaric acid, rutin and kaempferol) in the range of from 10.7% to 43.5%. In conclusion, this study implies that DES-UAE is a viable, sustainable, efficient and integrated technique to obtain polyphenols from Cosmos sulphureus. DES-UAE is instrumental for exploring the feasibility of commercial scale extraction of polyphenols.

Acid-assisted oil extraction directly from thraustochytrids fermentation broth and its energy assessment for docosahexaenoic acid-enriched oil production

Thraustochytrids are the most prominent source of polyunsaturated fatty acids, specifically docosahexaenoic acid (DHA). Downstream processing constitutes a significant fraction of total production cost and thus needs judicious optimization. Currently, hazardous solvent-based extraction methods are used to extract oil from the dry or wet thraustochytrids cell mass. The process is also highly energy-intensive due to involvement of dewatering and drying as unit operations. Current work devised an energy-efficient acid-assisted extraction (AAE) methodology to overcome dry and wet biomass-based extraction limitations. AAE recovered 91 % of total oil with 35–40 % PUFA from the direct fermentation broth, eliminating the need for dewatering and drying of fermentation broth/cell biomass. The current work also presents an all-inclusive comparison of the energy assessment of oil extraction from dry and AAE method. AAE produced PUFA enriched oil with a total energy consumption of 210 MJ/kg, which was four times lower than that of conventional dry cell extraction methodology.

Novel Deep Eutectic Solvent-Based Protein Extraction Method for Pottery Residues and Archeological Implications.

Proteomic analysis of absorbed residues is increasingly used to identify the foodstuffs processed in ancient ceramic vessels, but detailed methodological investigations in this field remain rare. Here, we present three interlinked methodological developments with important consequences in paleoproteomics: the comparative absorption and identification of various food proteins, the application of a deep eutectic solvent (DES) for extracting ceramic-bound proteins, and the role of database choice in taxonomic identification. Our experiments with modern and ethnoarcheological ceramics show that DES is generally more effective at extracting ceramic-bound proteins than guanidine hydrochloride (GuHCl), and cereal proteins are absorbed and subsequently extracted and identifiedat least as readily as meat proteins. We also highlight some of the challenges in cross-species proteomics, whereby species that are less well-represented in databases can be attributed an incorrect species-level taxonomic assignment due to interspecies similarities in protein sequence. This is particularly problematic in potentially mixed samples such as cooking-generated organic residues deposited in pottery. Our work demonstrates possible proteomic separation of fishes and birds, the latter of which have so far eluded detection through lipidomic analyses of organic residue deposits in pottery, which has important implications for tracking the exploitation of avian species in various ancient communities around the globe.

Ecofriendly and enhanced biogenic synthesis of silver nanoparticles using deep eutectic solvent-based green tea extracts

In compliance with green chemistry, metallic nanoparticles can be biogenically synthesized using plant extracts. Herein, three different deep eutectic solvents (DESs) were used instead of water to prepare green tea extracts (GTEs). The resultant DES-based GTEs exerted different beneficial effects on the biosynthesis of silver nanoparticles. Compared with the water-based GTE (W-GTE), the DES-based GTEs contained higher levels of catechins (up to 235% more) that are natural reducing and capping agents and showed higher synthesis efficiency. In particular, two DESs, which consist of glycerol and betaine with a common urea molecule and are designated as GU and BU, respectively, could produce silver nanoparticles with superior properties to water. Specifically, GU- and BU-GTE-based silver nanoparticles showed uniformly reduced sizes, 39.12 (±5.33) nm and 43.11 (±6.42) nm, respectively and homogenous face-centered cubic crystallinity. DESs added to W-GTEs lead to synthesis of silver nanoparticles with improved dispersion. The DES-GTE-based silver nanoparticles at 60 μg/mL displayed in vitro anti-cancer activity comparable to doxorubicin at 12.5 μg/mL. These results suggest that the tested DESs could serve as efficient extraction solvents for phytochemicals as well as effective surface modifiers without posing adverse effects for subsequent applications of the synthesized nanoparticles. The favorable effects of GU and BU were found to partially involve ammonia, which was formed during DES preparation at high temperatures (≥80 °C). This study shows that DESs can promote the biogenic synthesis of silver nanoparticles by playing diverse roles depending on the unique properties of the DESs and their constituents.

Extraction of the Anticancer and Antimicrobial Agent, Prodigiosin, from Vibrio gazogenes PB1 and Its Identification by 1D and 2D NMR.

Prodigiosin is a secondary metabolite produced in several species of bacteria. It exhibits antimicrobial and anticancer properties. Methods for the extraction and identification of prodigiosin and their related derivatives from bacterial cultures typically depend on solvent-based extractions followed by NMR spectroscopy. The estuarine bacterium, V. gazogenes PB1, was previously shown to produce prodigiosin. This conclusion, however, was based on analytical data obtained from ultraviolet-visible absorption spectrophotometry and infrared spectroscopy. Complete dependence on these techniques would be considered inadequate for the accurate identification of the various members of the prodiginine family of compounds, which possess very similar chemical structures and near-identical optical properties. In this study, we extracted prodigiosin from a culture of Vibrio gazogenes PB1 cultivated in minimal media, and for the first time, confirmed the synthesis of prodigiosin Vibrio gazogenes PB1 using NMR techniques. The chemical structure was validated by 1H and 13C NMR spectroscopy, and further corroborated by 2D NMR, which included 1H-1H-gDQFCOSY, 1H-13C-gHSQC, and 1H-13C-gHMBC, as well as 1H-1H-homonuclear decoupling experiments. Based on this data, previous NMR spectral assignments of prodigiosin are reaffirmed and in some cases, corrected. The findings will be particularly relevant for experimental work relating to the use of V. gazogenes PB1 as a host for the synthesis of prodigiosin.

Natural Deep Eutectic Solvent-Based Microwave-Assisted Extraction of Total Flavonoid Compounds from Spent Sweet Potato (Ipomoea batatas L.) Leaves: Optimization and Antioxidant and Bacteriostatic Activity.

Natural deep eutectic solvents (NADESs) coupled with microwave-assisted extraction (MAE) were applied to extract total flavonoid compounds from spent sweet potato (Ipomoea batatas L.) leaves. In this study, ten different NADESs were successfully synthesized for the MAE. Based on single-factor experiments, the response surface methodology (RSM) was applied, and the microwave power, extraction temperature, extraction time, and solid–liquid ratio were further evaluated in order to optimize the yields of total flavonoid compounds. Besides, the extracts were recovered by macroporous resin for the biological activity detection of flavonoid compounds. As a result, NADES-2, synthesized by choline chloride and malic acid (molar ratio 1:2), exhibited the highest extraction yield. After that, the NADES-2-based MAE process was optimized and the optimal conditions were as follows: microwave power of 470 W, extraction temperature of 54 °C, extraction time of 21 min, and solid–liquid ratio of 70 mg/mL. The extraction yield (40.21 ± 0.23 mg rutin equivalents/g sweet potato leaves) of the model validation experiment was demonstrated to be in accordance with the predicted value (40.49 mg rutin equivalents/g sweet potato leaves). In addition, flavonoid compounds were efficiently recovered from NADES-extracts with a high recovery yield (>85%) using AB-8 macroporous resin. The bioactivity experiments in vitro confirmed that total flavonoid compounds had good DPPH and O2−· radical-scavenging activity, as well as inhibitory effects on E. coli, S. aureus, E. carotovora, and B. subtilis. In conclusion, this study provides a green and efficient method to extract flavonoid compounds from spent sweet potato leaves, providing technical support for the development and utilization of sweet potato leaves’ waste.

Targeted pectin depletion enhances the potential of high-pressure homogenization to increase the network forming potential of tomato cell wall material

The current study addresses the influence of pectin depletion on the potential of high-pressure homogenization (HPH) to increase the network forming potential of the cell wall material (CWM) from tomato. Therefore, the microstructure, water binding capacity and viscoelastic properties of the alcohol-insoluble residue (AIR) and unextractable fractions (UFs) obtained after different levels and methods of pectin extraction were determined in suspension before and after functionalization by HPH. Before HPH, the AIR and the UFs obtained by solvent-based pectin extraction were all characterized by particles displaying cell-like morphology and the storage modulus (G′) of the respective suspensions was maximal at partial pectin depletion. The network forming potential of the CWM could only be increased by HPH when extensive disruption of the cell wall network was realized instead of mainly breakage. Even when higher pressure levels were applied (up to 80 MPa), preceding weakening of the cell wall network by pectin extraction was a prerequisite to favor efficient disruption of the CWM during HPH above deformation and breakage. Apart from the effect of partial pectin depletion as such on the cell wall strength, the impact of the extraction conditions (e.g., acid conditions at high temperature) weakening the residual cell wall seemed important. This had repercussions on the potential of HPH to functionalize the CWM. While the G’ decreased upon HPH (evaluated at 20 MPa) for non-pectin-depleted or partially pectin-depleted CWM generated by using mild extraction conditions, a clear increase was observed upon HPH of CWM which was partially or extensively pectin-depleted using harsher extraction conditions.

Deep Eutectic Solvent-based Extraction of As, Mn, Pb, Cr, and Ni from Spleen, Kidney, and Brain Samples

Deep Eutectic Solvent-based Extraction of As, Mn, Pb, Cr, and Ni from Spleen, Kidney, and Brain Samples

Temperature-responsive deep eutectic solvent as eco-friendly and recyclable media for the rapid assessment of pyrethroid pesticide residues in surface soil sample

In the modern agricultural model, more and more attention has been paid to green production and sustainable agriculture practices. In this study, a simple and eco-friendly extraction method for the rapid assessment of nine different pyrethroid pesticides in surface soil samples was developed by the temperature-responsive deep eutectic solvent-based ultrasound assisted extraction. Three different temperature-responsive deep eutectic solvent systems of various classes were prepared to extract pyrethroid pesticides from spiked soil samples. The total spiked recovery displayed that temperature-responsive deep eutectic solvent composed of ethanolamine and o-cresol with molar ratio 1:1 was the optimum extraction solvent for temperature-responsive deep eutectic solvent-based ultrasound assisted extraction procedure. Based on Box-Behnken Design, the maximum extraction recovery (%) of total pyrethroid pesticides was 94.23% under the following conditions: extraction temperature of 68 °C, extraction time of 35 min, and solid–liquid ratio of 21 mg/mL. Meaningfully, the extraction recovery of pyrethroid pesticides was still more than 80% after fifth cycles of temperature-responsive deep eutectic solvent, demonstrating that temperature-responsive deep eutectic solvent could be repeatedly used. The detection results of actual soil samples indicated that the pyrethroid pesticide residues (8.42–28.72 μg/kg) in vineyard region were the most serious, which may be due to the high incidence of insect pests and the abuse of pesticides. The temperature-responsive deep eutectic solvent-based ultrasound assisted extraction method with the advantages of fast, trace, and high efficiency could be successfully applied to pyrethroid pesticide residues analysis in surface soil samples.

Ultrasonic-Assisted Extraction of Cannabidiolic Acid from Cannabis Biomass.

Industrial hemp (Cannabis spp.) has many compounds of interest with potential medical benefits. Of these compounds, cannabinoids have come to the center of attention, specifically acidic cannabinoids. The focus is turning toward acidic cannabinoids due to their lack of psychotropic activity. Cannabis plants produce acidic cannabinoids with hemp plants producing low levels of psychotropic cannabinoids. As such, utilization of hemp for acidic cannabinoid extraction would eliminate the need for decarboxylation prior to extraction as a source for the cannabinoids. The use of solvent-based extraction is ideal for obtaining acidic cannabinoids as their solubility in solvents such as supercritical CO2 is limited due to the high pressure and temperature required to reach their solubility constants. An alternative method designed to increase solubility is ultrasonic-assisted extraction. In this protocol, the impact of solvent polarity (acetonitrile 0.46, ethanol 0.65, methanol 0.76, and water 1.00) and concentration (20%, 50%, 70%, 90%, and 100%) on ultrasonic-assisted extraction efficiency has been examined. Results show that water was the least effective and acetonitrile was the most effective solvent examined. Ethanol was further examined since it has the lowest toxicity and is generally regarded as safe (GRAS). Surprisingly, 50% ethanol in water is the most effective ethanol concentration for extracting the highest amount of cannabinoids from hemp. The increase in cannabidiolic acid concentration was 28% when compared to 100% ethanol, and 23% when compared to 100% acetonitrile. While it was determined that 50% ethanol is the most effective concentration for our application, the method has also been demonstrated to be effective with alternative solvents. Consequently, the proposed method is deemed effective and rapid for extracting acidic cannabinoids.

Phytochemical Characterization, Antioxidant and Anti-Proliferative Properties of Rubia cordifolia L. Extracts Prepared with Improved Extraction Conditions.

Rubia cordifolia L. (Rubiaceae) is an important plant in Indian and Chinese medical systems. Extracts prepared from the root, stem and leaf have been used traditionally for the management of various diseases. Some of the known effects are anti-inflammation, neuroprotection, anti-proliferation, immunomodulation and anti-tumor. A comparative account of the extracts derived from different organs that lead to the identification of the most suitable solvent is lacking. We explored the presence of phytochemicals, antioxidant activity and anti-proliferative properties of a variety of solvent-based extracts of root, and methanol extracts of stem and leaf of R. cordifolia L. The antioxidant potential was determined by DPPH, hydrogen peroxide, nitric oxide and total antioxidant assays. The anti-proliferative nature was evaluated by MTT assay on HeLa, ME-180 and HepG2 cells. The composition of the extracts was determined by UPLC-UV-MS. We found that the root extracts had the presence of higher amounts of antioxidants over the stem and leaf extracts. The root extracts prepared in methanol exhibited the highest cytotoxicity in HepG2 cells. The main compounds identified through UPLC-UV-MS of the methanol extract give credibility to the previous results. Our comprehensive study corroborates the preference given to the root over the stem and leaf for extract preparation. In conclusion, we identified the methanol extract of the root to be the most suited to have bioactivity with anti-cancer potential.

A Comparison of Solvent-Based Extraction Methods to Assess the Central Carbon Metabolites in Mouse Bone and Muscle.

The identification of endogenous metabolites has great potential for understanding the underlying tissue processes occurring in either a homeostatic or a diseased state. The application of gas chromatography-mass spectrometry (GC-MS)-based metabolomics on musculoskeletal tissue samples has gained traction. However, limited comparison studies exist evaluating the sensitivity, reproducibility, and robustness of the various existing extraction protocols for musculoskeletal tissues. Here, we evaluated polar metabolite extraction from bone and muscle of mouse origin. The extraction methods compared were (1) modified Bligh–Dyer (mBD), (2) low chloroform (CHCl3)-modified Bligh–Dyer (mBD-low), and (3) modified Matyash (mMat). In particular, the central carbon metabolites (CCM) appear to be relevant for musculoskeletal regeneration, given their role in energy metabolism. However, the sensitivity, reproducibility, and robustness of these methods for detecting targeted polar CCM remains unknown. Overall, the extraction of metabolites using the mBD, mBD-low, and mMat methods appears sufficiently robust and reproducible for bone, with the mBD method slightly bettering the mBD-low and mMat methods. Furthermore, mBD, mBD-low, and mMat were sufficiently sensitive in detecting polar metabolites extracted from mouse muscle; however, they lacked repeatability. This study highlights the need for a re-thinking, towards a tissue-specific optimization of methods for metabolite extractions, ensuring sufficient sensitivity, repeatability, and robustness.

Deep eutectic solvent-based ultrasonic-assisted extraction of phenolic compounds from different potato genotypes: Comparison of free and bound phenolic profiles and antioxidant activity

Potato phenolics exhibit health-promoting effects. Studies on bound phenolics are scarce. Here, significant differences in total phenolic content (TPC), total flavonoid content (TFC) and antioxidant activity in free and bound forms were found among 19 potato genotypes. 7 free and 24 bound phenolics were characterized and quantified using ultrahigh-performance liquid chromatograph-mass spectrometry, among which 22 bound phenolics are reported for the first time in potato. The number and content of identified free and bound phenolics changed considerably among the genotypes. Chlorogenic acid, cryptochlorogenic acid and rutin in free form, and benzoic and caftaric acids in bound form were predominant. Heijingang showed the highest free and total TPC and antioxidant activity, and the largest number of phenolic compounds, whereas S17-1-1 contained the highest free and total TFC and Longshu 7 contained the highest bound phenolic content. Cluster analysis segregated the genotypes into 6 groups. This study provides useful information on benefits of potato in human health.