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Journal of Food Quality
Volume 2019, Article ID 2592731, 6 pages
https://doi.org/10.1155/2019/2592731
Research Article

Optimum Extraction Technology for the Seed Oil of Nigella sativa L.

1National R & D Center for Edible Fungus Processing Technology, Henan University, Kaifeng 475004, China
2Joint International Research Laboratory of Food & Medicine Resource Function, Henan University, Kaifeng 475004, China
3Kaifeng Key Laboratory of Functional Components in Health Food, Henan University, Kaifeng 475004, China
4Medicinal and Aromatic Plants Researches Department, Horticulture Research Institute, Agricultural Research Center, Giza 71625, Egypt

Correspondence should be addressed to Wenyi Kang; moc.liamtoh@ynewgnak

Received 11 April 2019; Revised 8 June 2019; Accepted 17 June 2019; Published 2 July 2019

Academic Editor: Anet Režek Jambrak

Copyright © 2019 Changyang Ma et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Seed oil of Nigella sativa L. is a popular edible oil in Egypt. How to improve the extraction efficiency of the oil will expand the use of the resource. In this paper, the four extraction factors, particle size of the seed, liquid-seed ratio, extraction time, and temperature, were optimized by the single-factor and orthogonal experiment to increase the extraction yield and linoleic acid concentration. The results showed that the twice extraction technology could increase the oil rate of 23.55% compared with the once extraction technology. The extraction rate of the once extraction could reach 33.51% under the conditions of liquid-seed ratio: 9 : 1 mL/g, extraction temperature: 35°C, extraction time: 1 h, and particle size: 60 meshes. The optimum twice extraction conditions with the extraction rate of 43.78% were 8 : 1 ml/g, 40°C, 1.5 h, and 60 meshes. Besides, the highest concentration of linoleic acid (58.09 mg/g) was twice extraction condition with 7 : 1 mL/g, 40°C, 2 h, and 60 meshes.

1. Introduction

Nigella sativa L. (Ranunculaceae), a native plant in North Africa, Southern Europe, and Southwest Asia [14], is commonly known as cooking oil used for the curry, cake, Mediterranean cheese, and medicinal purposes in Egypt and Greece for thousand years [5]. According to the previous researches, many biological activities of the seed oil are discovered, such as irritating the digestive system, expelling wind, relieving pain, diuretic effect, sweating, antiworm, anti-inflammatory, treating asthma, tonifying kidney, invigorating brain, strengthening spleen, antioxidant, and so on [610]. Recently, some new functions of the seed oil, antitumor, antidiabetic, anticholesterol, and antiepilepsy are reported [2, 1115]. In the seed, linoleic acid as unsaturated fatty acids is essential to our health [16]. Nowadays, the seeds of N. sativa as the multifunctional food are necessary to determine an efficient extraction method in Egypt, while most researchers are focusing on the component analysis and quality stability [10, 17] instead of evaluating the extraction technology. At present, the extract methods of the edible oil include cold pressing, supercritical CO2 extraction, microwave-assisted extraction, and solvent extraction [10, 17], and solvent extraction is popularly used in many factories with high efficiency, simple operation, and high purity [18, 19].

Therefore, we optimized the factors of extraction technology to increase the yield of oil and the concentration of linoleic acid by single-factor test and orthogonal test.

2. Materials and Method

2.1. Materials

The seeds of N. sativa were collected from Giza, Egypt, in October, 2017 by Dr. Adel Fahmi Ahmed (Medicinal and Aromatic Plants Researches Department, Horticulture Research Institute, Agricultural Research Centre, Giza, Egypt).

n-Hexane was chosen as the extraction solvent in this research [20, 21]. Linoleic acid (purity is 90.9%, batch no. 167466) was purchased from Dr. Ehrenstorfer GmbH.

The method of HPLC (high-performance liquid chromatography) was performed by using the Shimadzu LC-20AT HPLC system with an LC-20AT infusion pump, CTO-10AS column oven, SPD-20A UV detector, LC-Solution chromatographic data analysis system, and Athena C30 chromatographic column.

2.2. Extraction Technology of N. sativa Seed

According to references [2225], the particle size of solid materials, liquid volume for extraction, and extraction temperature and time are all the key factors of oil extract technology. So, these factors were adopted to optimize extract technology of N. sativa seed oil in this research. Meanwhile, twice extraction method, which has been proved to be an efficiency method in the aspects of input and output [26, 27], was carried out in this work. The detailed solvent extraction processes of N. sativa seed are shown in Figure 1.

Figure 1: Flow chart of N. sativa seed oil extraction.

The oil yield can be calculated by using the following formula:

In addition, two steps were conducted for refining the oil extract technology. In the first step, three comparatively ideal levels of the four factors were obtained by a series of single-factor tests. And then, an orthogonal test with four factors and three levels was employed to determine the optimal technology.

2.3. Determination of Linoleic Acid in N. sativa Seed Oil

The standard of linoleic acid was weighed preciously, dissolved in the methanol as mother liquor. After that, the mother liquor was diluted into a series of standard solutions with 3.80, 2.28, 1.52, 0.76, and 0.38 mg/mL, respectively. The standard solutions and samples of extracted oil were all chromatographically analyzed on a PLATINUM C30 column (4.6 mm × 250 mm, 5 μm).

According to the previous research [28], the mobile phase was a mixture of acetonitrile (A)-0.1% phosphoric acid-water (B), which were used in isocratic elution at 90% A and 10% B for 40 min. The flow rate was 1.0 mL/min, and the column temperature was 30°C. The UV detection wavelength was 203 nm with the sample volume of 10 µL. The chromatograms are shown in Figure 2.

Figure 2: HPLC chromatograms of standard substance and N. sativa oil sample. (1) Sample solution; (2) standard solution; (3) solvent; (a) linoleic acid.

In order to test the suitability of the method, repeatability, stability, precision, and recovery tests were examined based on the previous HPLC condition:(i)Six oil samples extracted from the N. sativa seed were analyzed, and the relative standard deviation (RSD) was 1.18% which meant that the method had a good repeatability(ii)One reference solution was tested 6 times in order to test the precision and a desired result (RSD = 0.81%) was achieved(iii)In order to test the stability of the method over time, one oil sample was detected at 0, 4, 8, 12, 16, 20, and 24 h, respectively, and the result showed that the examine result (RSD = 2.68%) would remain stable at least 24 h(iv)Six oil samples with 80% more standard linoleic acid were tested, and the average rate of recovery and RSD were 98.70% and 1.13%, respectively

According to the evaluation of the method, the results indicated that the HPLC condition was qualified for the analysis of linoleic acid in the oil.

The standard curve for analysis of linoleic acid was obtained in the equation, Y = 9366842X − 1156864 (r = 0.9996), where Y is the peak area and X is the concentration of standard with the linear range of 0.38∼3.80 mg.

3. Single-Factor Analysis of the Extraction Technology of N. sativa Seed Oil

3.1. Effect of the Liquid-Seed Ratio on the Extraction Rate

As shown in Figure 3, the oil yield could increase with the increase of solvent volume. When the ratio of liquid and seed was more than 8 : 1 mL/g, the extraction rate of the first extraction step increased slower than before, while the oil yield of the twice extraction started to fluctuate. It is well known that the increase of the solvent could accelerate the diffusion of oil from seed, and it is an effective measure to increase the oil yield in the previous stage. But the growing trend with the increasing solvent would become less and less when the ratio is high enough, especially for the twice extraction technology [27]. So, the ratio range of the liquid and seed was determined as 7 : 1, 8 : 1, and 9 : 1 mL/g.

Figure 3: Effect of liquid-seed ratio on the yield of N. sativa seed oil.
3.2. Effect of the Extraction Temperature on the Extraction Rate

The extraction temperatures were investigated and the results are shown in Figure 4. It presented a downward trend after the first rise from the range of 20 to 40°C. The peak temperature of the first extraction technology was at 30°C while that of the twice extraction was at 35°C. Increasing temperate of the oil would decrease the viscosity and accelerate the molecule movement of oil, but the high temperature would evaporate too much solvent (n-hexane) [22]. That was why the extraction yield changed as shown in Figure 4. According to the trend of the yields of the two extraction processes, 30°C, 35°C, and 40°C were chosen.

Figure 4: Effect of extraction temperature on the yield of N. sativa seed oil.
3.3. Effect of the Extraction Time on the Extraction Rate

The relationship between oil yield and extraction time is shown in Figure 5. When the extraction time was extended, the yield of the oil would increase from 0.5 to 1.5 h and then decline. It might be the time-consuming diffusion process of the oil in solvent. Along with the diffusion process, the solvent would evaporate or most solvent and oil would be trapped in oil residue [18, 29]. So, the yields of the once and twice extraction technologies would decrease at 2 h and 1.5 h extraction, respectively.

Figure 5: Effect of extraction duration on the yield of N. sativa seed oil.
3.4. Effect of the Grinding Degree on the Extraction Rate

In Figure 6, the mesh number of the seed was an important factor which had a remarkable positive relationship with the yield of the extraction oil. Smaller size of particle caused by stronger grinding was good at increasing the surface of the solid material. Besides, the grinding process can destroy the cell structure of the seed and reduce the transportation resistance of oil. [30] The increasing speed of the oil yield for the twice extraction decreased when the mesh number of the seed was over 50. In aspect of the once extraction technology, the increasing speed decreased when the grinding degree of seed reached 40 meshes. So, the mesh number was determined to be around 50 meshes.

Figure 6: Effect of the grinding degree on oil yield of N. sativa seed oil.

4. Results and Discussion

4.1. Design of the Orthogonality Experiment

Based on the result of the single-factor analysis, three levels of the liquid-seed ratio (R), extraction temperature (T), extraction time (t), and grinding degrees (M) were considered in the L9(34) orthogonal test. The concentration of linoleic acid of the twice extraction technology was considered as one critical parameter to evaluate the twice extraction technologies besides the extraction rate of the seed oil. The detailed arrangements of the orthogonal test are listed in Table 1.

Table 1: The factors and levels of orthogonality experiment for the N. sativa seed oil extract technology.
4.2. Effect of the Extraction Time on the Extraction Ratio

In order to compare the different effect of the two extraction technologies on the total yield, statistical analysis of oil production was conducted and the results are shown in Table 2.

Table 2: Significant analysis of the oil yield in the second extraction process.

The test result showed that the second extraction process could increase the extraction rate by 7.86% significantly through the t value test. Although the twice extraction technology would cost twice of the solvent, time, and labor, the second extraction process could improve almost one quarter of the extraction yield (almost 23.46% of the average extraction rate of the 1st extraction step) and decrease the waste of the oil significantly indeed. Therefore, it was largely necessary to implement the twice extraction technology.

4.3. Range Analysis of the Orthogonal Test

The Ki1 and Ki2 were the average extraction rates of the once and twice extraction technology with i level, respectively, and i = 1, 2, or 3. Klinoleic is the average concentration of the linoleic acid in the twice extraction oil, and R1, R2, and Rlinoleic are the corresponding ranges.

In Table 3, the order of factors to affect the extraction efficiency of the first extraction process from strong to weak is grinding degree, extraction temperature, liquid-seed ratio, and extraction time, respectively, while that of the twice extraction technology was grinding degree, extraction temperature, extraction time, and liquid-seed ratio. With the increasing times of the extraction process, the effect of the liquid-seed ratio and extraction time declined obviously, especially the liquid-seed ratio. For the linoleic acid concentration in the oil obtained by the twice extraction technology, grinding degrees was still the most important factor, followed by extraction time, extraction temperature, and liquid-seed ratio.

Table 3: Analytical results of orthogonality experiment.

Through the range analysis of the orthogonality experiment, the corresponding production strategies are listed in Table 4. Though the ideal conditions for the total yield and linoleic acid concentration of the twice extraction technology were different, the extraction condition with the highest yield also extract the largest amount of the linoleic acid.

Table 4: The production strategies of the extraction technology based on the orthogonality experiment.
4.4. Variance Analysis of the Orthogonal Test

In order to confirm the importance of these factors, variance analysis was conducted after the orthogonal test and the results are listed in Table 5.

Table 5: Variance analysis of the orthogonality experiment.

The extreme significance of the total deviation and mean deviation revealed that the four factors considered in this paper could actually affect the oil yield of N. sativa seeds. The grinding degree and extraction temperature were the key factors with the extremely significant effect for the once extraction technology. But for the twice extraction technology, only the grinding degree was the main factor. More time, solvent, and operation during the twice extraction technology obviously declined the effect of extraction temperature and solvent volume.

5. Conclusion

In this paper, the single-factor test and the orthogonal test were used to optimize the oil extraction technology from the seed of N. sativa harvested in Egypt. The ideal level of grinding degree, extraction temperature, liquid-seed ratio, and extraction time for the once and twice extraction technologies were 60 meshes, 35°C, 9 : 1 mL/g, and 1 h and 60 meshes, 40°C, 8 : 1, and 1.5 h, respectively. The extraction rate of the two technologies could achieve 33.51% and 41.37%. Only the grinding degree for the second extraction technology had significant effect on the extraction rate. As for the linoleic acid with the concentration of 58.04 mg/g in the oil from the twice extraction, the optimal extraction condition was 60 meshes, 40°C, 7 : 1 mL/g, and 2 h.

Data Availability

All original data used to support the findings of this study are included within the supplementary information file.

Conflicts of Interest

All authors declare that there are no conflicts of interest regarding this study.

Acknowledgments

This work was supported by the Scientific and Technological Project of Henan Province (192102110214), International Cooperation Project of Kaifeng Science & Technology Bureau (1806004), and Undergraduate Training Program for Innovation and Entrepreneurship in Henan University Minsheng College (MSCXCY2017065).

Supplementary Materials

The data used to support the findings of this study are provided. The first part: the data for the single-factor test. The second part: the data for the orthogonal test. (Supplementary Materials)

References

  1. B. Salih, T. Sipahi, and E. O. Dönmez, “Ancient nigella seeds from Boyalı Höyük in north-central Turkey,” Journal of Ethnopharmacology, vol. 124, no. 3, pp. 416–420, 2009. View at Publisher · View at Google Scholar · View at Scopus
  2. V. Vahitha, K. Perinbam, S. Kadar Basha et al., “Nigella sativa L. and its comprehensive activity against various microbes and cancer: a mini review,” IIOAB Journal, vol. 7, no. 7, pp. 61–67, 2016. View at Google Scholar
  3. A. Khoddami, H. M. Ghazali, A. Yassoralipour, Y. Ramakrishnan, and A. Ganjloo, “Physicochemical characteristics of nigella seed (Nigella sativa L.) oil as affected by different extraction methods,” Journal of the American Oil Chemists’ Society, vol. 88, no. 4, pp. 533–540, 2011. View at Publisher · View at Google Scholar · View at Scopus
  4. J. P. Dzoyem, L. J. McGaw, V. Kuete et al., “Chapter 9-anti-inflammatory and anti-nociceptive activities of African medicinal spices and vegetables,” in Medicinal Spices and Vegetables from Africa, pp. 239–270, Elsevier, Amsterdam, Netherlands, 2017. View at Google Scholar
  5. M. Fawzy, “Nutritional value, functional properties and nutraceutical applications of black cumin (Nigella sativa L.): an overview,” International Journal of Food Science & Technology, vol. 42, no. 10, pp. 1208–1218, 2010. View at Publisher · View at Google Scholar · View at Scopus
  6. B. Amin and H. Hosseinzadeh, “Black cumin (Nigella sativa) and its active constituent, thymoquinone: an overview on the analgesic and anti-inflammatory effects,” Planta Medica, vol. 82, no. 01/02, pp. 8–16, 2016. View at Publisher · View at Google Scholar · View at Scopus
  7. A. M. Kotb, M. Abd-elkareem, N. S. Abou Khalil, and A. E.-D. H. Sayed, “Protective effect of Nigella sativa on 4-nonylphenol-induced nephrotoxicity in Clarias gariepinus (Burchell, 1822),” Science of the Total Environment, vol. 619-620, pp. 692–699, 2018. View at Publisher · View at Google Scholar · View at Scopus
  8. J. H. Hanene, N. Emira, B. Karima et al., “Chemical composition, antibacterial and antifungal properties of Tunisian Nigella sativa fixed oil,” African Journal of Microbiology Research, vol. 6, no. 22, pp. 4675–4679, 2012. View at Publisher · View at Google Scholar
  9. A. F. Ahmed, H. Nan, Z. Xia et al., “Total phenolic and flavoniod content and antioxidant properties of Nigella sativa L. seeds,” Current Topics in Nutraceutical Research, vol. 16, no. 2, pp. 147–154, 2018. View at Google Scholar
  10. L. Kokoska, J. Havlik, I. Valterova, H. Sovova, M. Sajfrtova, and I. Jankovska, “Comparison of chemical composition and antibacterial activity of Nigella sativa seed essential oils obtained by different extraction methods,” Journal of Food Protection, vol. 71, no. 12, pp. 2475–2480, 2008. View at Publisher · View at Google Scholar · View at Scopus
  11. H. Haron, C. Grace-Lynn, and S. Shahar, “Comparison of physicochemical analysis and antioxidant activities of Nigella sativa seeds and oils from Yemen, Iran and Malaysia,” Sains Malaysiana, vol. 43, no. 4, pp. 535–542, 2014. View at Google Scholar
  12. A. Sahebkar, D. Soranna, X. Liu et al., “A systematic review and meta-analysis of randomized controlled trials investigating the effects of supplementation with Nigella sativa (black seed) on blood pressure,” Journal of Hypertension, vol. 34, no. 11, pp. 2127–2135, 2016. View at Publisher · View at Google Scholar · View at Scopus
  13. R. Daryabeygi-khotbehsara, M. Golzarand, M. P. Ghaffari, and K. Djafarian, “Nigella sativa improves glucose homeostasis and serum lipids in type 2 diabetes: a systematic review and meta-analysis,” Complementary Therapies in Medicine, vol. 35, pp. 6–13, 2017. View at Publisher · View at Google Scholar · View at Scopus
  14. G. Kaur, M. Invally, M. K. Khan et al., “A potent nutraceutical combination of Cinnamomum cassia & Nigella sativa for type 1 diabetes mellitus,” Journal of Ayurveda & Integrative Medicine, vol. 9, no. 1, pp. 27–37, 2017. View at Google Scholar
  15. M. K. Shanmugam, F. Arfuso, A. P. Kumar et al., “Modulation of diverse oncogenic transcription factors by thymoquinone, an essential oil compound isolated from the seeds of Nigella sativa L.,” Pharmacological Research, vol. 129, pp. 357–364, 2018. View at Publisher · View at Google Scholar · View at Scopus
  16. B. Nickavar, F. Mojab, K. Javidnia, and M. A. R. Amoli, “Chemical composition of the fixed and volatile oils of Nigella sativa L. from Iran,” Zeitschrift für Naturforschung C, vol. 58, no. 9-10, pp. 629–631, 2003. View at Publisher · View at Google Scholar
  17. M. Kiralan, G. Özkan, A. Bayrak, and M. F. Ramadan, “Physicochemical properties and stability of black cumin (Nigella sativa) seed oil as affected by different extraction methods,” Industrial Crops and Products, vol. 57, pp. 52–58, 2014. View at Publisher · View at Google Scholar · View at Scopus
  18. F. Zhang, G. Luo, R. Xiao et al., “Optimization of extraction process of Gardenia oil by response surface methodology,” China Oils and Fats, vol. 42, no. 12, pp. 10–12, 2017. View at Google Scholar
  19. X. Guo, Y. Peng, C. Hu et al., “Effects of different oil producing processes on characteristics and quality of Xanthoceras sorbifolia bunge oil,” China Oils and Fats, vol. 42, no. 9, pp. 8–13, 2017. View at Google Scholar
  20. W. Gumala, Study on the Extraction Technique of Prunus Mongolica Maxim Seeds Oil, Honder College of Inner Mongolia Normal University, Hohhot, China, 2017.
  21. M. Zhang, Chlorella Vulgaris Photoautotrophic Cultivation, Cell Disruption and Oil Extraction Techniques, Jiangnan University, Wuxi, China, 2013.
  22. J. Li, S. Li, Y. Wu et al., “Optimization of extraction process and analysis of fatty acid composition of okra seed oil,” China Oils and Fats, vol. 38, no. 10, pp. 5–8, 2013. View at Google Scholar
  23. X. Liu, Q. Ma, D. He et al., “Study on ultrasound-assisted solvent extraction of Plukenetia volubilis linneo oil,” Cereals & Oils, vol. 30, no. 1, pp. 74–78, 2017. View at Google Scholar
  24. F. Wang, Y. Liu, and W. Zhang, “Study on extraction and refinement of grape seed oil,” Journal of Harbin University of Commerce (Natural Sciences Edition), vol. 22, no. 2, pp. 50–54, 2006. View at Google Scholar
  25. J. Xing, H. Cao, Y. Chen et al., “Orthogonal design was used to optimize the oil extraction process of bitter almond,” Medical Information, vol. 14, pp. 378-379, 2013. View at Google Scholar
  26. X. Zhao, H. Gao, L. Jia et al., “Solvent extraction and fatty acid composition of Parthenocissus tricuspidate plach seed oil,” China Oils and Fats, vol. 37, no. 2, pp. 80–83, 2012. View at Google Scholar
  27. W. Zeng, Y. Fang, W. Cao et al., “Oil extraction from low temperature dehulled rapeseed cake by isopropyl alcohol and cyclohexane mixture,” Journal of Chinese Cereals and Oils Association, vol. 24, no. 9, pp. 53–56, 2009. View at Google Scholar
  28. Q. Guo, C. Lin, Z. Yin et al., “Chemical constituents of petroleum ether part of endophytic fungus Penicillium oxalicum from Malus halliana,” Journal of Henan University (Medical Science), vol. 36, no. 4, pp. 248–250, 2017. View at Google Scholar
  29. B. Liu, Z. Yin, and X. Zheng, “Study of the ultrasonic-assisted extraction of oil from the Peony seed meal,” Food Research and Development, vol. 37, no. 8, pp. 40–44, 2016. View at Google Scholar
  30. Y. Li, M. Liu, and H. Zhang, “Study on the extraction process of oils from almond skin and physicochemical property of almond skin oil,” Cereals & Oils, vol. 29, no. 4, pp. 24–26, 2016. View at Google Scholar