HPLC-MSn identification and quantification of phenolic compounds in hazelnut kernels,oil and bagasse pellets

The paper reports the phenolic content of kernels, bagasse pellets (residue of oil pressing) and oils from five different cultivars and a mix of cultivars. Phenolic compounds were identified by high-performance liquid chromatography coupled with mass spectrometry. Two compounds, glansreginin A and glansreginin B, were detected for the first time in hazelnuts. The main polyphenolic subclass comprised of mono- and oligomeric flavan 3-ols, which accounted between 34.2 and 58.3% in hazelnut kernels and between 36.7 and 48.6% in pellets of the total phenolics detected. In hazelnut oils four compounds have been detected, their content levels ranged from 0.97 to 0.01 μg g^− 1. Total phenolic content ranged from 491.2 to 1700.4 mg GAE kg^− 1 in kernels, from 848.4 to 1148.5 mg GAE kg^− 1 in pellets and only from 0.14 to 0.25 mg GAE g^− 1 in oils. The percentage of radical scavenging activity ranged from 60.0 to 96.4% for kernels, 63.0 to 73.2% for pellets and from 17.7 to 29.9% for oil. The study provides clear evidence on high phenolic contents and similarly high antioxidant potential of hazelnut kernels and bagasse pellets. The latter could be used as ingredients in cooking and baking or even for production of plant-based pharmaceuticals.     

Optimization of supercritical fluid extraction of bioactive compounds from grape (Vitis labrusca B.) peel by using response surface methodology

Supercritical fluid extraction (SFE) was applied for the extraction of valuable compounds from grape (Vitis labrusca B.) peel. Extraction was carried out according to an orthogonal array design (OAD) and independent variables selected were temperature, pressure and modifier concentration. SFE process was optimized by using response surface methodology (RSM) for the extract yield, total phenols, antioxidants and total anthocyanins from grape peel. Effects of extraction temperature and pressure were found to be significant on all responses. Optimal SFE conditions were identified as 45–46 °C temperature, 160–165 kg cm^? 2 pressure and 6–7% ethanol as modifier for maximum extract yield (12.31%), total phenols (2.156 mg GAE/100 mL), antioxidants (1.628 mg/mL) and total anthocyanins (1.176 mg/mL). Experimental values for response variables at these optimal conditions match well with the predicted values. Grape peel extracts obtained by SFE showed more than 93% DPPH radical scavenging activities.Industrial relevanceThis study describes the response surface optimization of supercritical fluid extraction (SFE) process for the enhanced recovery of total phenols, antioxidant and anthocyanins from grape peel. SFE uses CO₂ as supercritical fluid which is environment friendly solvent; allows extraction at lower temperature and the extracts obtained possess higher quality and safety. Industrially, it may be used as a promising technique for the extraction of bioactive compounds from plant materials.     

Combined densification and pulsed electric field treatment for selective polyphenols recovery from fermented grape pomace

The aim of this study is to assess a new process for the valorization of fermented grape pomace using pulsed electric fields (PEF). The combination of densification and PEF treatment was applied on grape pomace of low relative humidity, without any addition of conductive liquid. The kinetics of extraction and the composition of polyphenols were evaluated throughout the subsequent hydro-alcoholic extraction at different temperatures.Optimal parameters of PEF treatment (field strength E = 1.2 kV·cm^− 1; energy input W = 18 kJ·kg^− 1; density ρ = 1.0 g·cm^− 3) increased the content of total polyphenols regardless of the temperature of extraction. The ratio of total anthocyanins to total flavan-3-ols at 20 °C was equal to 7.1 and 9.0 for control and PEF treated modalities, respectively. These results demonstrate the selective nature of PEF treatment in anthocyanin extraction, and thus reveal new possibilities to produce extracts with different biochemical compositions.Industrial relevanceThis study examines the feasibility of densification combined with PEF pre-treatment of relatively low humidity grape pomace for the enhancement of bioactive compounds extraction. The concentration of total phenolic compounds obtained after PEF treatment showed that the use of this technique is relevant for an industrial use, since solvent amount and extraction time can be reduced. Moreover, the selective nature of PEF opens the opportunity to produce extracts of different biochemical compositions. This process is an alternative to conventional pre-treatments of raw material (e.g. dehydration and grinding), which have impacts on product quality and are more energy consuming.     

Optimization of solid–liquid extraction of phytochemicals from Garcinia indica Choisy by response surface methodology

A central composite rotatable design was employed to study the effect of ultrasound assisted extraction conditions namely sonication amplitude (10–90%), sonication cycle (0.1–1.0 s^?1), solid–liquid ratio (2–10) and extraction time (5–35 min) on the total anthocyanin extraction from Garcinia indica Choisy. Overall extractions of total anthocyanin, acidity and antioxidant activity were considered as response variables. The significant (p < 0.05) response surface models with high coefficients of determination values (R²) ranging from 0.91 to 0.93 were fitted for the experimental data, which indicated that the polynomial response models fitted well for describing the extraction efficiencies of anthocyanin, acidity and antioxidant activity. Based on the design, the optimal conditions for obtaining higher extraction were extraction time 35 min, cycle ranging from 0.44 to 0.48 s^?1, percentage amplitude ranging from 10 to 14%, and solid–liquid ratio 10. The graphical optimization of superimposed contour plots fulfilled the conditions to obtain total anthocyanin (Y₁) ≥ 135 mg/100 g DW, total titratable acidity (Y₂) ≤ 25 g/100 g DW and antioxidant activity (Y₃) ≥ 14.5 M Trolox/100 g DW. The study demonstrated that response surface methodology can be utilized for deriving the optimum conditions for extraction of anthocyanin from G. indica Choisy.     

Optimization of the subcritical water extraction of phenolic antioxidants from Crocus sativus petals of saffron industry residues: Box-Behnken design and principal component analysis

Subcritical water extraction was investigated as a green technology for the extraction of phenolic compounds from Crocus sativus petals. A Box-Behnken design was utilized to determine the optimal extraction conditions. Extraction temperature (120–160 °C), extraction time (20–60 min) and water to solid (W/S) ratio (20–40 mL/g) were considered as the variables for the extraction of phenolic compounds. A second order polynomial model was fitted to each response and the regression coefficients were determined using least square methodology. There was a good correspondence between the experimental data and their predicted counterparts. The optimum conditions of extraction were estimated to be W/S ratio of 36 mL/g, temperature of 159 °C and time of 54 min. Extraction using these optimized conditions achieved the best TPC (1616 mg/100 g), TFC (239 mg/100 g), %DPPH_sc (86.05%) and FRAP value (5.1 mM). Principal components analysis (PCA) allowed a better understanding of interactions between properties of extracted phenolic antioxidants.Industrial relevanceApplication of subcritical water was shown to be a practical technique to extract the phenolic compounds of saffron petals as an underutilized bulk agro-waste. The higher phenolic antioxidants obtained in extractions carried out by this technique is of major interest from an industrial point of view, since solvent amounts were reduced and extraction times shortened. Thus, the application of this emerging technology for extraction uses and low-cost raw materials is an economical alternative to conventional extraction methods according to industry demands and a sustainable development.     

Supercritical CO2 extraction of allicin from garlic flakes: Screening and kinetic studies

The nutraceutical industry is currently interested in obtaining garlic extracts using mild extraction processes to recover high levels of labile allicin. This work studied oleoresin yield and extraction selectivity for allicin in the supercritical CO₂ extraction of freeze-dried aqueous garlic homogenate as a function of sample conditioning and process conditions. Agglomeration phenomena, which is responsible for substrate lumps in packed beds and flow channeling in the bed during extraction, was avoided by lowering sample moisture below 31 g kg^? 1 water/substrate, and/or process temperature below 65 °C. Oleoresin yield increased slightly with extraction pressure (15–45 MPa) and dramatically with process temperature (35–65 °C), but the concentration of allicin in the extract decreased as the temperature increased. Thus, an optimal combination of intermediate temperature and pressure was selected that allowed reasonably large yields (≥ 19 g kg^? 1 oleoresin/substrate) and extraction selectivities (≥ 75 mg kg^? 1 allicin/oleoresin). Based on experimental results, a 4 h extraction process at 55 °C and 30 MPa using 55 kg kg^? 1 CO₂/substrate was recommended. Cumulative extraction plots for oleoresin and allicin were successfully adjusted using a linear driving force mass transfer model.     

Phenolic composition,antioxidant and antimicrobial activities of free and bound phenolic extracts of Moringa oleifera seed flour

Phenolic compounds, antioxidant and antibacterial activities of defatted Moringa oleifera seed flour (DMF) were investigated. The total phenolic and flavonoid contents were measured using colorimetric methods. Free phenolic acid and flavonoid profiles were analyzed by high performance liquid chromatography, while antioxidant capacities were evaluated using scavenging assays of 1,1-diphenyl-2-picrylhydrazyl radical (DPPH), ferric reducing antioxidant power and total antioxidant capacity. The results showed that extractability of phenolic compounds was significantly higher (p < 0.05) in bound phenolic extract (4173.00 ± 32.22 mg gallic acid equivalents (GAE)/100 g) than in free phenolic extract (780.00 ± 14.2 mg GAE/100 g) and it showed higher antioxidant and antimicrobial activities. The IC₅₀ value for DPPH radical scavenging activity was 0.9 ± 0.05 and 14.9 ± 0.07 mg/mL for bound phenolic and free phenolic extracts, respectively. Bound phenolic extract was more effective (minimum inhibitory concentration (MIC), 0.06–0.157%) than free phenolic extract (MIC, 0.117–0.191%) against tested bacteria. Ten phenolic compounds (gallic acid, p-coumaric acid, ferulic acid, caffeic acid, protocatechuic acid, cinnamic acid, catechin, epicatechin, vanillin and quercetin) were identified and quantified in both extracts. These natural plant phenolics from Moringa seeds could be a good source of antioxidants and antibacterials for food and pharmaceutical industries.     

Global grape aroma potential and its individual analysis by SBSE–GC–MS

Among the aroma compounds present within grapes, a significant part is assumed to come from specific odourless precursors found mainly as glycosidic compounds which are known as bound fraction. In this paper, the individual composition of non-aromatic red grape bound fraction has been assayed for first time by SBSE–GC–MS and compared with the global total aroma potential measured spectrophotometrically at the wineries, in which the anthocyanins interferences have been removed. Glycosidic aroma compounds have been extracted by macerating grapes with different extractants (EtOH_aq or SO₂) at different times and subjected to acidic hydrolysis at 70 °C for 2 h. The best extraction condition, expressed as the higher aroma compounds concentration (terpenes + C₁₃ norisoprenoids + 2-phenylethanol + C₆ compounds), was the ethanolic aqueous extraction carried out for 2 h, reducing considerably the extraction times proposed in the literature. The method was successfully used to discriminate non-aromatic red grape varieties, (Petit-Verdot, Merlot and Monastrell) being limonene, linalool, 2-hexen-1-ol, TDN and 2-phenylethanol the aromas that contributed most to the differentiation. An aromatic white table grape such as Early sugar was also assayed to check its higher volatile composition in comparison with the other red varieties. The percentage of favourable aromas (terpenes + C₁₃ norisoprensoids + bencene derivates) is always higher than the unfavourable ones (C6) for all tested varieties, especially Early Sugar. It has also been observe that the spectrophotometric measurements are overestimated when compared with SBSE–GC–MS, probably due to the free sugar content and other glycosidic compounds.     

Glycine max (L.) Merr., Vigna radiata L. and Medicago sativa L. sprouts: A natural source of bioactive compounds

The consumption of sprouts, common in Asia, has been growing in western countries, once they are a natural healthy food and considered as a valuable dietary supplement. Comparing with their mature counterparts, sprouts are usually richer in health-promoting phytochemicals. So, the nutritional composition and the biological potential of widely consumed sprouts of three species – Glycine max (L.) Merr., Vigna radiata L. and Medicago sativa L. – were compared for the first time. Phenolic compounds and phytosterols were analyzed by HPLC–DAD and organic acids by HPLC–UV. The volatile profile was determined by HS-SPME/GC–IT/MS. Fourteen phenolic compounds (including four isoflavones), three sterols one triterpene, sixteen fatty acids, seven organic acids and thirty volatile compounds were determined. The antioxidant activity was assessed against DPPH^?, superoxide and nitric oxide radicals. G. max sprouts were the most active against DPPH^? (IC₅₀ = 1.337 mg/mL), while those of M. sativa were the most effective against superoxide and nitric oxide radicals (IC₅₀ = 67 μg/mL and IC₅₀ = 426 μg/mL, respectively). Data provide evidence of great similarities between G. max and M. sativa sprouts, both being rich in phenolic compounds, fatty acids and volatiles, and exhibiting better antioxidant activity. On the other hand, V. radiata showed higher amounts of sterols, triterpenes and organic acids. In this study it was found that the sprouts are a good source of bioactive compounds in our diet with health-promoting antioxidants.     

Citharexylum solanaceum fruit extracts: Profiles of phenolic compounds and carotenoids and their relation with ROS and RNS scavenging capacities

Citharexylum solanaceum is a native fruit from Brazil, which both bioactive compounds and antioxidant potential were not yet investigated. Thus, the freeze-dried extracts of seed and pulp + skin of C. solanaceum fruits were obtained after solid-liquid extraction with ethanol and their bioactive compounds composition, namely phenolic compounds and carotenoids, were determined. The antioxidant capacity of both extracts against physiologically relevant reactive oxygen species (ROS) and reactive nitrogen species (RNS) was further investigated. Both C. solanaceum extracts showed high contents of phenolic compounds; however, pulp + skin extract presented 2.4-times more phenolic compounds (33.54 mg/g) than the seed extract (14.09 mg/g). Verbascoside (phenylpropanoid) was the major compound identified in both extracts (11–25 mg/g). Regarding the carotenoid composition, all-trans-lutein (14–42 μg/g) and all-trans-β-carotene (13–44 μg/g) were the major compounds in both extracts. The high content of phenolic compounds and carotenoids in pulp + skin extract might explain its higher scavenging capacity against all the ROS/RNS as compared to seed extract. In general, both extracts showed better scavenging capacity for the RNS than for the ROS. Our results indicate that C. solanaceum fruits can be explored as an important natural source of antioxidant compounds.     

Ultrasound-assisted enzyme catalyzed hydrolysis of olive waste and recovery of antioxidant phenolic compounds

The ultrasound-assisted enzyme hydrolysis (UAEH) procedure for extraction of phenolics from olive waste (OW) was established. The optimized conditions obtained with response surface methodology (RSM) were pH 5.75, treatment 40 min and temperature 55 °C, the yield obtained reached to 4.0%. The extraction kinetics model was fitted well to the ln (C_t/C₀) = kt, and the rate constants (k) increased with the increased in the extraction temperature. Moreover, the values of k were higher and the activation energy was lower than ultrasound treatment alone. The thermodynamic parameters indicated the extraction process was easier under the UAEH. Compared with the petroleum ether and n-butyl alcohol, ethyl acetate extract fraction had high phenolic content (64.4 mg/g), especially hydroxytyrosol and tyrosol (17.2 mg/g and 14.1 mg/g), and exhibited excellent antioxidant activities in DPPH·, ABTS⁺·and FRAP assay. These finding revealed that OW could be used for a enrich source of natural phenolic compounds for development of food industry.Industrial relevanceOlive waste (OW) has been widely paid attention as sources of high-added value compounds, such as phenolic which can be obtained by the several methods. And phenolic extract as a food additive can not only improve the sensory quality of food, but also can enhance antioxidant capacity in fatty food matrices. Moreover, the use of this extract has better economic benefits than synthetic additives usually used in food industry. In this study, a novel green, simple and efficient technology was employed to extract the phenolic compounds, which was suitable for large-scale industrial use. The results indicated that ultrasound-assisted enzyme hydrolysis (UAEH) has significant potential in the extraction process of phenolics from OW exhibiting higher phenolic yield in shorter extraction times.     

Thermodynamic analysis of the sorption isotherms of pure and blended carbohydrate polymers

The adsorption isotherms of gum Arabic (GA), mesquite gum (MG), and maltodextrin DE 10 (MD), and a blend of the three gums (17%GA–66%MG–17%MD) were determined at 25, 35, and 40 °C. All isotherms were fitted using the GAB model and the thermodynamic properties (enthalpies and entropies, differential and integral) were estimated by the Clausius–Clapeyron method. The minimum integral entropy was considered as the point of maximum stability where strong bonds between the adsorbate and adsorbent occurred, and water is less available and likely to participate in spoilage reactions. The point of maximum stability was found between 12.24 and 14.68 kg H₂O/100 kg d.s. (corresponding to water activity, a_w, of 0.32–0.57) for GA, 12.12–14.27 kg H₂O/100 kg d.s. (a_w = 0.33–0.55) for MG, and 11.37–13.84 kg H₂O/100 kg d.s. (a_w = 0.28–0.55) for the biopolymer blend, in the temperature range studied.     

Green tea preparation and its influence on the content of bioactive compounds

The effect of different extraction conditions and storage time of prepared infusions on the content of bioactive compounds of green teas and their antioxidant capacity were investigated. The content of total phenols, total flavonoids and total non-flavonoids in green teas was determined spectrophotometrically, while 7 flavan-3-ols, 6 phenolic acids and 3 methylxanthines were identified and quantified by using high performance liquid chromatography (HPLC–PDA). Among the tested green teas bagged green tea Twinings of London was recognized as the richest source of phenolic compounds (3585 mg/L GAE of total phenols). The most abundant phenolic constituents of green tea were flavan-3-ols, of which EGCG was prevailing in all teas (94.54–357.07 mg/L). The highest content of caffeine, as the most abundant methylxanthine, was determined in powdered green tea. The findings of this investigation suggest that extraction efficiency of studied bioactive compounds from green tea depends on the extraction conditions and that maximum extraction efficiency is achieved during aqueous extraction at 80 °C, for 5′ (powder), 15′ (bagged) and 30′ (loose leaf). In order to determine the antioxidant capacity of teas the DPPH, ABTS and FRAP assays were applied. Regardless of the extraction conditions all green teas exhibited significant antioxidant capacity in vitro, which was in correlation with their phenolic content, confirming that green tea is one of the best dietary sources of antioxidants.     

Simultaneous determination of anthocyanins,coumarins and phenolic acids in fruits,kernels and liqueur of Prunus mahaleb L

In the fresh tissues of Prunus mahaleb L., three classes of phenolics were characterised: phenolic acid derivatives (main compound being o-coumaric acid glucoside), quercetin glycosides, and anthocyanins (cyanidin 3,5-diglucoside, cyanidin 3-sambubioside, cyanidin 3-xylosyl-rutinoside and cyanidin 3-rutinoside). Coumarin was also identified. The kernels showed a high content of coumarin (0.87 mg g^?1) which is the main class of metabolites in this sample, but present in pitted berries as well (0.63 mg g^?1). Flavonoids are mainly concentrated in the skin and pulp (0.55 mg g^?1). In ‘Mirinello di Torremaggiore’ liqueur, produced from P. mahaleb L. in accordance with traditional procedures, anthocyanins make up 16.5%, phenolic acids 43.3%, coumarin 36.2% and flavonoids 4% of total compounds. Anthocyanins are the main class in solid residues from liqueur production (70%). These findings point out that solid residues of P. mahaleb can be considered an interesting and innovative source of appreciable amounts of cyanidin glycosides (3.3 mg g^?1).     

Use of Supercritical Assisted Atomization to produce nanoparticles from olive pomace extract

Olive pomace is one of the most interesting wastes containing bioactive compounds; the extraction of polyphenols can represent an innovative solution for the reduction of the environmental hazard of this solid and the simultaneous recovery of high-added value compounds. In this study, Supercritical Assisted Atomization (SAA) was employed for the encapsulation in maltodextrin of phenolic compounds extracted from olive pomace. The effect of the ratio of maltodextrin content to total solid content of the extract and drying temperature on physical characteristics, total phenolic content and antioxidant properties of the powdered product were studied. The results confirmed the efficiency of the SAA process to encapsulate phenolic compounds from olive pomace extract. Particles with average diameter of 712 nm with high total polyphenol content (105.0 ± 0.1 mg_{Caffeic Acid Equivalent/}g_{Dry Powder}) and antiradical power (98.8 ± 3.0 mg_DPPH/mL_extract) were obtained. These particles rich in bioactive compounds can be used as functional component in formulations of new food, cosmetic or pharmaceutical products.Industrial relevanceOlive pomace is considered to be a low-cost and renewable source of high-added value compounds, such as polyphenols which can be valorized by several methodologies. In this work, we assessed the efficiency of Supercritical Assisted Atomization (SAA) in order to encapsulate phenolic compounds extracted from olive pomace. The particles obtained by SAA have spherical morphology with average diameter of 712 nm. The polyphenol-rich nanoparticles produced using this technique can be potentially used in the formulation of novel food or nutraceutical products.     

Ionic liquid-based ultrasound-assisted surfactant-emulsified microextraction for simultaneous determination of three important flavoring compounds in plant extracts and urine samples

For the first time, a novel, efficient and environmentally friendly method termed ionic liquid-based ultrasound-assisted surfactant-emulsified microextraction (IL-UA-SE-ME) was developed and compared with normal-, reversed-, surfactant assisted-dispersive liquid–liquid microextraction and ultrasound-assisted surfactant-based emulsification microextraction methods for the analysis of three bioactive and flavoring compounds (para-anisaldehyde, trans-anethole and its isomer estragole) in some fresh plants (fennel and basil), their extracts and urine samples. The results showed that IL-UA-SE-ME is a much more effective method and under the optimum conditions (including extraction solvent: 90 μL of [C₆MIM][PF₆]; disperser: 5 mg of N-dodecylbenzenesulfonic acid sodium salt; sample pH: 3; sonication time: 5 min; and centrifuging time: 5 min), limits of detection, limits of quantification, linear ranges, recoveries, and enrichment factors were in the range of 16–22 ng mL^− 1, 49–67 ng mL^− 1, 0.04–90 μg mL^− 1, 94.3%–101.1%, and 118–127, respectively.     

Pressurized low polarity water extraction of lignans from whole flaxseed

The application of pressurized low polarity water (PLPW) extraction to the production of flaxseed lignans-rich products has been studied, and the key geometric and process conditions, including temperature, flow rate, and total volume have been determined and optimized. Maximum amounts of lignans and other flaxseed bioactive, including proteins were extracted at 160 °C and 5.2 MPa. However, on a dry weight basis the most concentrated extracts in terms of lignans and other phenolic compounds were obtained at 140 °C and 5.2 MPa. A flow rate of 0.5 mL/min was optimal for the extraction of lignans from flaxseed (Linum usitatissimum L.) and a total volume of 30–40 mL/g of seed was required to maximize the recovery. Higher flow rates increased the rate of the extraction but required larger water volumes. Bed depth to ID ratios of 5–18 resulted in faster extraction and maximum recovery (90–95%) at water to seed ratios of 30–50 mL/g. Larger depth to ID ratios (15–18) would allow the use of lower solvent to solid ratios (14–20 mL/g) and would still result in yields of 84–90%.     

Sequential high pressure extractions applied to recover piceatannol and scirpusin B from passion fruit bagasse

Passion fruit seeds are currently discarded on the pulp processing but are known for their high piceatannol and scirpusin B contents. Using pressurized liquid extraction (PLE), these highly valuable phenolic compounds were efficiently extracted from defatted passion fruit bagasse (DPFB). PLE was performed using mixtures of ethanol and water (50 to 100% ethanol, w/w) as solvent, temperatures from 50 to 70 °C and pressure at 10 MPa. The extraction methods were compared in terms of the global yield, total phenolic content (TPC), piceatannol content and the antioxidant capacity of the extracts. The DPFB extracts were also compared with those from non-defatted passion fruit bagasse (nDPFB). Identification and quantification of piceatannol were performed using UHPLC–MS/MS. The results showed that high TPC and piceatannol content were achieved for the extracts obtained from DPFB through PLE at 70 °C and using 50 and 75% ethanol as the solvent. The best PLE conditions for TPC (70 °C, 75% ethanol) resulted in 55.237 mg GAE/g dried and defatted bagasse, whereas PLE at 70 °C and 50% ethanol achieved 18.590 mg of piceatannol/g dried and defatted bagasse, and such yields were significantly higher than those obtained using conventional extraction techniques. The antioxidant capacity assays showed high correlation with the TPC (r > 0.886) and piceatannol (r > 0.772). The passion fruit bagasse has therefore proved to be a rich source of piceatannol and PLE showed high efficiency to recover phenolic compounds from defatted passion fruit bagasse.     

Supercritical CO2 extraction of nimbin from neem seeds––a modelling study

The extraction of nimbin from neem seeds using supercritical carbon dioxide is investigated in this paper. A model that accounts for intraparticle diffusion (D_e) and external mass transfer of nimbin (k_f) is presented for the supercritical extraction process. Mass transfer is based on local equilibrium adsorption between solute (nimbin) and solid (neem solid). The external mass transfer coefficient was determined by fitting the theoretical extraction curve to experimental data. The following range of conditions: 0.24–1.24 cm³/min of CO₂, 10–26 MPa, 308–333 K, 1.0–2.5 g of neem kernel powder and 0.0575–0.185 cm of particle size of neem kernel powder, were considered. In addition, a new correlation for Sherwood number (Sh) was developed in terms of the dimensionless groups; Reynolds number (Re) and Schmidt number (Sc) from optimisation results. This correlation was compared to previous correlations and was found to give superior results when compared to experimental data.