Highlights
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Ginger-infused sesame oil was developed with enhancement of functional and sensory properties.
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This study investigated the effect of thermal process on flavour of ginger-infused sesame oil.
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Ginger-infused sesame oil was an appropriate bioactive compound carrier.
Keywords: Ginger, Infused sesame oil, Gingerol, Antioxidant capacity
Abstract
Ginger-infused sesame oil enriches the nutrition and provides enhanced flavor for the foods. An original processing procedure and module for evaluation were established in this study, using different raw materials (Guangdong and Chu ginger) and treatments (ginger powder, extract, and both). The quality, functionality, and flavor of the infused oils were evaluated. Ginger-infused sesame oil contained 0.58–3.22 µg/g of 6-gingerol, 0.21–0.88 µg/g of 6-shogaol. The number range of volatile compounds from 48 to 55 identified by gas chromatography-mass spectrometry varies depending on different process procedures. Agglomerative hierarchical clustering analysis revealed the flavor profiles were clustered by different varieties, while gingerol and phytosterol was by different treatments. In conclusion, sesame oil was an appropriate carrier for gingerol and phytosterol, which are characterized by higher antioxidant capacities (p < 0.05). These results show the benefits of developing infused oil products with enhanced functional and sensory properties.
1. Introduction
Over the past few years, the increase of eating disorders has been noted. Frequent consumption of unbalanced meals has led to an increased risk of metabolic disorders, for instance, diabetes, obesity, or dyslipidemia (Albert Perez et al., 2019, Lee et al., 2021). Dietary intervention is crucial for treating such conditions. Functional foods, that have received attraction as a result, provide health-promoting effects that go beyond their nutritional properties. Functional foods can be natural foods or fortified ones, and when ingested to a proper dosage, can achieve health-promoting benefits (Vecchio and Cavallo, 2019, Parks et al., 2020). The growth of functional foods is fueled by industrial innovation, the increasing demands made by health-conscious consumers, and by varying health claims. Products such as fermented diary drinks, plant-based milk, propolis, fish oil, and leutein supplements has received commercial success across the globe (Vecchio & Cavallo, 2019).
The application of natural products as therapeutic agents was common in history. Currently, there is rising interest in the exertion of natural products for treating a variety health conditions such as inflammation. Ginger (Zingiber officinale Rosc.) is a plant used in food, medicine, and cosmetics. Due to the refreshing aroma and spicy, pungent taste, the addition of ginger rhizome enhances the sense of heat and has been widely used as a dietary supplement in traditional medicine (Jang et al., 2004, Koga et al., 2016, Maghraby et al., 2023). Numerous studies have demonstrated ginger (Fam. Zingiberaceae) to be a promising contemporary remedy as it contains gingerol, curcumin, phytosterols, terpenoids, and zerumbone and therefore may prevent cardiovascular diseases and associated pathologies (e.g., diabetes, obesity, and metabolic syndrome) that act as risk factors for cardiovascular diseases (Jang et al., 2004, Yeh et al., 2014, Lal et al., 2021). Sesame (Sesamum indicum L.), a member of the Pedaliaceae family, is one of the earliest oil crops domesticated and consumed by humans. Sesame oil is an aromatic oil produced by cold pressing roasted sesame seeds and is traditionally used as an edible oil. Sesame oil is rich in linoleic and linolenic acids and contains high amounts of biologically active substances such as lignans (338.1–1153.6 mg/100 g), vitamin E (53.4–81.1 mg/100 g), and phytosterols (411.8–488.6 mg/100 g) (Shi et al., 2018, Yin et al., 2021).
Infused oils are convenient food products consumed worldwide, which are used as dressings in various foods, increasing their attractiveness and tastiness. Nowadays, there is high demand for innovative and specialized products of high nutritional quality and with different sensory characteristics (Khatri et al., 2023). Herb-infused oils seem to derive from ancient processing and conservation practices, in which the oils acquired the flavor of the aromatic herbs used and were later used in the preparation of dishes and salads. Infused oils come with advantages, such as versatility, handiness, and rich flavors has turned them into cupboard staples around the world. The aromatic herbs used to infuse the oils not only improve their sensory and nutritional properties but also extend their expiration date and counteract free radicals because of their antioxidant and antimicrobial activities (Díaz-Montaña, Aparicio-Ruiz, & Morales, 2023). In recent research, the addition of essential oils derived from herbs and spices could provide pleasant flavors and improve the oxidative stability in vegetable oils (Abo et al., 2014, Lim et al., 2021).
Ginger-infused sesame oil is often used as a food therapy and medicinal diet therapy in Asia, since ginger has properties described as “interior-warming and cold-dispelling” and sesame oil is said to be “Yin-tonifying (in terms of Qi)” and “replenishing”, combination the benefits are enhanced, making it the ultimate recipe for activating blood circulation in the concept of Traditional Chinese Medicine, which also claims it the best for post-partum women. The objective of this study was to develop a new manufacturing process for ginger-infused sesame oil to promote its functional and flavor properties. Analyses of the quality, functionality, and volatiles of the ginger-infused oil were conducted.
2. Materials and methods
2.1. Materials
The chemicals and solvents used in this research were provided by Merck (Darmstadt, Germany), Sigma-Aldrich (St. Louis, MO, USA), and Chemical Co., Ltd. (Miaoli, Taiwan), including 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (Trolox), 1,1-diphenyl-2-picrylhydrazyl (DPPH), 2,4,6-tripyridyl-S-triazine (TPTZ), 2,2′-azinobis-(3-ethylbenzothiazoline-6-sulfonate) (ABTS), gallic acid, quercetin, Folin–Ciocalteu reagent, 6-gingerol, 6-shogaol, 8-gingerol, 10-gingerol, curcumin, and sesame. All solvents were of HPLC grade.
2.2. Production of ginger-infused sesame oil
Guangdong ginger (Gu) and Chu ginger (Ch) were purchased from three different markets in Nantou County (Taiwan) in September 2020 to achieve three biological replicates. All ginger were mixed then made into powder according to the following description. Sample preparation of this study were listed as following: (1) Ginger powder preparation: The ginger was washed and cut into slices, dried with a hot air at 50 °C for 18 h, ground, and passed through a 40-mesh sieve. (2) Ginger extract preparation: 50 g of ginger powder was mecerated with eight times its volume of ethanol and collected after 3 h, concentrated into a syrup form under a vacuum, then diluted to 10 mL with sesame oil. (3) Ginger-infused sesame oil preparation: (a) Gu/ChEx-So, 10 mL of ginger extract was added to 200 mL of sesame oil in an airtight glass jar; (b) Gu/ChP-So, 200 mL of sesame oil was added into a stainless-steel pot with 50 g of ginger powder, infused for 10 min at 150 °C, and canned in an airtight glass jar; (c) Gu/ChExP-So, 200 mL of sesame oil was added into a stainless-steel pot with 25 g of ginger powder and infused for 10 min at 150 °C. After cooling, 5 mL of ginger extract was added and canned in an airtight glass jar. (4) Sample of control preparation: (d) So, 200 mL of sesame oil (FWUSOW INDUSTRY CO., LTD.) was added into a stainless-steel pot and heated to 150 °C then held in this temperature for 10 min and canned in an airtight glass jar.
2.3. Quality analysis
The peroxide value (POV) of each oil sample was determined as prescribed by the official analytical methods of the Mariotti (2014). The acid value (AV) of the samples was determined by titration with a 0.1 N potassium hydroxide alcoholic solution. The thiobarbituric acid (TBA) content of the samples was measured according to Ghani, Barril, Bedgood, and Prenzler (2017).
The color of each oil sample was measured using a colorimeter (NE-4000, Nippon Denshoku Industries Co. Ltd., Tokyo, Japan). After the instrument was standardized with a white plate (L0 = 97.51, a0 = − 0.16, and b0 = 1.75), the colors of the samples were evaluated at room temperature. The Hunter L, a, and b values correspond to lightness, greenness (−a) or redness (+a), and blueness (−b) or yellowness (+b), respectively. The browning index (BI) was calculated using the following.
Equation:
where x = (a + 1.75L)/(5.645L + a − 3.012b).
2.4. Functional component analysis
This study used standard solutions to investigate the functional components, including 6-gingerol, 6-shogaol, 8-gingerol, 10-gingerol, curcumin, and sesamol. To determine standards quantitatively, we followed the method of Yeh et al. (2014) and used high-performance liquid chromatography (HPLC) with a Hitachi L-2130 pump and L-2400 UV detector from Hitachi, Japan. Sample solutions were filtered through a 0.45 µm filter (3 mm; Millex Filter, Millipore), and 20 µL of the filtrate was analyzed. We built calibration curves of the standards by plotting the peak area vs. each corresponding concentration and used them to quantify the functional components.
The remaining procedures were carried out as previously reported (Yang, Cheng, Ye, Chu, & Chen, 2022), using an Agilent 6890 GC equipped with a DB-1 fused-silica capillary column (60 m × 0.25 mm i.d., 0.25 μm film thickness, Agilent Technologies) coupled to an Agilent 5973 N MSD mass spectrometer (MS). We used Helium as the carrier gas at a 1 mL/min flow rate and maintained the injector temperature at 250 °C. The GC conditions were identical for both GC/MS and GC analysis. GC analyzed the derivatized phytosterol extracts by an injection with 1:30 split ratio at 260 °C. The content of individual sterols was expressed as the percentage of the PS fraction obtained using 5α-Cholestane as an internal standard.
2.5. Antioxidant property assay
DPPH, ABTS, and FRAP tests were carried out to evaluate the antioxidant activity in triplicate (Olszowy & Dawidowicz, 2016). A solution of 1 mL of DPPH methanol was mixed with 0.5 mL of the sample and allowed to stand for 30 min. The mixture was mixed vigorously and incubated for 30 min at ambient temperature without exposure to the light, and the mixture was measured under 517 nm. ABTS radical cation-scavenging activity using method was measured and compared with standard materials' results. ABTS + radicals were produced by reacting the ABTS solution (7 mM, 25 mL) with potassium persulfate (1.4 mM, 0.44 mL), and the mixture was kept in the dark at room temperature for 12–16 h. The sample (1.0 mL) was added to the ABTS + solution (2.5 mL) and mixed vigorously. After reacting at room temperature for 5 min, the absorbance was measured at 734 nm. FRAP using method was measured and compared with standard materials' results. Each oil sample was diluted with an acetone/methanol (2:8) solution to 2 mg/mL and mixed with the FRAP reagent (containing acetate buffer, FeCl3 solution, and TPTZ by the ratio of 10:1:1). With vigorous vortex, the mixture was incubated at ambient temperature for 10 min following with the measurement at 595 nm. The Trolox was selected as the positive control.
2.6. Volatile analysis
To isolate the volatile components of ginger-infused sesame oil, we used simultaneous distillation–extraction (SDE) with a modified Likens-Nickerson apparatus (Lin, Tseng, Li, & Mau, 2008). We added 100 g of ginger-infused sesame oil and 1000 ml of deionized water to the apparatus. Then, we used a solvent mixture of n-pentane and diethyl ether (1:1, v/v) as the extractant. We repeated this process three times and concentrated the filtered extract at 40 °C to 100 ml, which we then stored at −20 °C until analysis using a Vigreux column (i.d. 1.5 × 100 cm; Tung Kwan Glass Co., Hsinchu, Taiwan).
To identify the volatile components of the oil sample, we used the Agilent 6890 GC with the DB-1 column and coupled it to the Agilent 5973 N MSD MS. We identified the constituents by matching their spectra with those recorded in an MS library (Wiley 7 N), and we confirmed them using the Kovats indices or by comparing the GC retention time data with those of authentic standards or published in the literature. The linear RIs were calculated from the retention times of n-alkanes (C5-C25) run under the same chromatographic conditions.
2.7. Statistical analysis
The measurement was obtained in triplicate (n = 3) for each sample and expressed as means ± SD (standard deviation). The data were subjected to a hierarchical cluster analysis (HCA) with squared Euclidean distances. Subsequently, the data were analyzed using principal components analysis (PCA) combined with varimax rotation. The XLSTAT software (version 2010.2.01, Addinsoft Deutschland, Andernach, Germany) was used for the AHC and PCA analyses.
3. Results and discussion
3.1. Quality profile
The thermal processing of ginger-infused sesame oil can impart unique flavors, colors, and textures to foods and increase nutrient digestibility or reduce antinutritional elements (Aydeniz-Guneser, 2021). Heat treatment can also lead to adverse outcomes, such as oil oxidation (Yin et al., 2021). We used the POV, AV, and TBA to evaluate the oxidation state of sesame oil and ginger-infused sesame oil. In this study, the POVs were in the range of 11.96–13.25 meq/kg, the AVs were in the range of 1.74–1.82 mg KOH/g, and the TBAs were in the range of 9.76–10.12 µmole/g (Table 1). The results show that the oil is of sufficient quality and no safety concerns exist.
Table 1.
Oxidation stat, color and browning index values of ginger-infused sesame oil.
| AV* (mg KOH/g) | POV (meq/kg) | TBA (μmole/g) | L | a | b | ΔE** | BI*** | |
|---|---|---|---|---|---|---|---|---|
| So | 1.74 | 11.96 | 10.05 | 23.82* | 0.82 | 1.70 | – | 188.04 |
| GuEx-So | 1.81 | 13.25 | 10.14 | 31.06 | 4.59 | 11.01 | 12.38 | 231.70 |
| GuP-So | 1.78 | 12.16 | 10.12 | 22.91 | 0.18 | 1.40 | 1.15 | 185.07 |
| GuExP-So | 1.78 | 12.11 | 9.98 | 30.09 | 7.14 | 11.29 | 13.09 | 241.32 |
| ChEx-So | 1.76 | 13.12 | 10.07 | 33.79 | 6.03 | 15.51 | 17.81 | 250.66 |
| ChP-So | 1.82 | 12.07 | 9.98 | 22.87 | 0.62 | 1.67 | 0.97 | 187.69 |
| ChExP-So | 1.81 | 12.13 | 9.76 | 31.61 | 6.01 | 12.96 | 14.64 | 243.39 |
Data presented are in triplicate mean.
*AV: acid value; POV: peroxide value; TBA: thiobarbituric acid.
**ΔE:The comprehensive color difference represented.
ΔE = [(ΔL*)2 + (4a*)2 + (4b*)2]1/2.
*** BI: browning index.
The color of ginger-infused sesame oil is highly associated with consumer acceptance of this product. The color difference (ΔE) compares the L, a, and b values of the infused samples to those of plain sesame oil. The ΔE of GuEx-So, GuP-So, GuExP-So, ChEx-So, ChP-So, and ChExP-So were 12.38, 1.15, 13.09, 17.81, 0.97, and 14.64, respectively (Table 2). An important aspect of the quality of ginger-infused sesame oil subjected to heat is its browning index (BI). The BIs of GuEx-So, GuP-So, GuExP-So, ChEx-So, ChP-So, and ChExP-So were 231.70, 185.07, 241.32, 250.66, 187.69, and 243.39, respectively (Table 2). The results show that the addition of ginger extract enhanced the Maillard reaction. The tendency to darken the color of the ginger-infused sesame oil is related to its chemical composition (Ahmad et al., 2021).
Table 2.
Analyzed gingerols and sesamols of ginger-infused sesame oil.
| 6-gingerol (μg/g) |
6-shogaol (μg/g) |
8-gingerol (μg/g) |
10-gingerol (μg/g) |
Curcumin (μg/g) |
Sesamol (μg/g) |
|||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| So | - | - | - | - | - | 0.62 | ± | 0.04 | c | |||||||||||||||
| GuEx-So | 0.99 | ± | 0.08 | a* | 0.22 | ± | 0.01 | a | 0.06 | ± | 0.01 | a | 0.05 | ± | 0.01 | a | 0.31 | ± | 0.03 | b | 0.54 | ± | 0.03 | c |
| GuP-So | 3.22 | ± | 0.18 | d | 0.81 | ± | 0.06 | c | 0.19 | ± | 0.02 | c | 0.11 | ± | 0.02 | b | 1.02 | ± | 0.06 | d | 0.39 | ± | 0.03 | a |
| GuExP-So | 2.51 | ± | 0.21 | c | 0.57 | ± | 0.03 | b | 0.14 | ± | 0.01 | b | 0.08 | ± | 0.02 | b | 0.66 | ± | 0.07 | c | 0.42 | ± | 0.02 | ab |
| ChEx-So | 0.58 | ± | 0.06 | a | 0.21 | ± | 0.01 | a | 0.08 | ± | 0.01 | a | n.d.** | 0.11 | ± | 0.01 | a | 0.45 | ± | 0.04 | b | |||
| ChP-So | 2.11 | ± | 0.18 | c | 0.88 | ± | 0.04 | b | 0.27 | ± | 0.01 | d | n.d. | 0.51 | ± | 0.05 | c | 0.38 | ± | 0.02 | a | |||
| ChExP-So | 1.42 | ± | 0.12 | b | 0.54 | ± | 0.05 | c | 0.21 | ± | 0.01 | c | n.d. | 0.27 | ± | 0.01 | b | 0.42 | ± | 0.03 | ab | |||
* Data presented are in mean ± SD (n = 3) which with different letters are significantly different at p < 0.05.
** n.d.: not detected.
a-d: Date with identical letters in the same column are not significantly different (p < 0.05).
3.2. Functionality profile
Ginger rhizomes with numerous bioactive compounds showed beneficial properties, especially pharmacologically. Among these compounds, gingerol is considered as the most potent and rich component. (Jang et al., 2004, Yeh et al., 2014). The combination of gingerol derivatives, including 6-gingerol, 8-gingerol, and 10-gingerol not only provided therapeutic effects but also its unique flavor and aroma (Yeh et al., 2014, Koga et al., 2016). Previous study showed Gu and Ch contains 6.11 and 5.54 mg/100 g (dry weight) of total gingerol with 6-gingerol and 6-shogaol making up most of the content (Yeh et al., 2014). In this study, the ginger-infused sesame oil contained 0.58–3.22 µg/g of 6-gingerol, 0.21–0.88 µg/g of 6-shogaol, 0.06–0.27 µg/g of 8-gingerol, 0.0.5–0.11 µg/g of 10-gingerol, and 0.11–1.02 µg/g of curcumin (Table 2). The presence of heat or storage for long time, gingerols may transformed into shogaols (Zagórska, Czernicka-Boś, Kukula-Koch, Iłowiecka, & Koch, 2023). Bacterial metabolism also played a vital role, converting 6-Shogaol into 6-paradol, while both showed similar anti-inflammatory and antioxidant properties. Sesame lignans are the main active ingredients in sesame seeds and have strong antioxidant activity (Nayak, Dash, Rayaguru, & Krishnan, 2016).
Lipid soluble bioactive compounds are often limited of their performance in most cooking processes and upon direct consumption. Edible oils have been effective carriers for said compounds. Sesamol was 0.62 µg/g in sesame oil and had a concentration of 0.38–0.54 µg/g in ginger-infused sesame oil (Table 3). Phytosterols also provide health benefits, and they can increase the stability of oils in storage. Δ-5-avenasterol for instance, exhibits anti-polymerization properties, which protects oil compounds from oxidation during heat treatment (Winkler and Warner, 2008, Zhang et al., 2012). Ginger-infused sesame oil contains 163.54–211.67 µg/g of brassicasterol, 32.57–50.03 µg/g of campesterol, 24.03–38.92 µg/g of stigmasterol, and 141.26–205.7 µg/g of β-sitosterol. These results show that ginger can effectively increase the phytosterol content in ginger-infused sesame oil, and the ginger extract is better than the ginger powder for this purpose.
Table 3.
Analyzed phytosterols of ginger-infused sesame oil.
| Brassicasterol (μg/g) |
Campesterol (μg/g) |
Stigmasterol (μg/g) |
β-sitosterol (μg/g) |
|||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| So | 133.65 | ± | 9.68 | a | 25.84 | ± | 1.66 | a | 18.96 | ± | 1.22 | a | 98.69 | ± | 5.63 | a |
| GuEx-So | 211.23 | ± | 14.38 | c | 44.43 | ± | 2.31 | c | 38.92 | ± | 2.91 | d | 205.70 | ± | 13.95 | b |
| GuP-So | 162.51 | ± | 12.86 | b | 32.57 | ± | 2.26 | b | 30.23 | ± | 2.83 | c | 157.48 | ± | 11.66 | c |
| GuExP-So | 179.61 | ± | 14.37 | b | 37.27 | ± | 3.57 | b | 33.52 | ± | 2.64 | cd | 174.81 | ± | 12.95 | d |
| ChEx-So | 211.67 | ± | 15.72 | c | 50.03 | ± | 2.13 | d | 30.09 | ± | 2.19 | c | 188.35 | ± | 13.42 | d |
| ChP-So | 163.54 | ± | 11.41 | b | 34.99 | ± | 2.91 | b | 24.03 | ± | 1.85 | b | 141.26 | ± | 10.63 | b |
| ChExP-So | 177.19 | ± | 13.56 | b | 33.36 | ± | 2.15 | b | 27.91 | ± | 1.93 | b | 145.31 | ± | 12.37 | b |
Data presented are in mean ± SD (n = 3) which with different letters are significantly different at p < 0.05.
a-d: Date with identical letters in the same column are not significantly different (p< 0.05).
Antioxidants hindered the oxidation of oils, including their reaction with free radicals and peroxy or alkoxy radicals, which then led to the propagation step of oxidation (Endo, 2018). The results showed that ginger-infused sesame oil had a better DPPH-scavenging effect, which was 62.57–80.26 % compared to 55.61 % for sesame oil. The ABTS-scavenging effect of ginger-infused sesame oil was 56.64–73.3 % compared to 61.45 % for sesame oil (Table 4). The relevant literature showed that the antioxidant capacity is correlated with the chemical structure of free radicals. Specifically, ABTS presents cationic properties that behave as a proton acceptor or an electron. Hence, ABTS can cope with DPPH which contains an unpaired electron. (Nhu-Trang, Nguyen, Cong-Hau, Anh-Dao, & Behra, 2023). The FRAP of ginger-infused sesame oil was 72.26–88.24 Trolox μg/ml compared to 82.04 Trolox μg/mL for sesame oil (Table 4). The FRAP values quantify the ability of the antioxidant compounds to donate electrons and, thus, reduce the oxidized species. The reducing power of a compound is an indicator of its potential antioxidant activity. Ginger exhibits excellent antioxidant activity and is a source of natural antioxidants that regulate lipid peroxidation and reduce the production of reactive oxygen species (Abdel-Azeem et al., 2013, Nayak et al., 2016, Zagórska et al., 2023).
Table 4.
Antioxidant property of ginger-infused sesame oil.
| DPPH (%) |
ABTS (%) |
FRAP (Trolox μg/g) |
||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| So | 55.61 | ± | 2.36 | a | 61.45 | ± | 3.25 | b | 82.04 | ± | 6.12 | b |
| GuEx-So | 62.57 | ± | 3.74 | b | 56.64 | ± | 2.13 | a | 73.21 | ± | 5.75 | a |
| GuP-So | 72.99 | ± | 2.83 | c | 62.72 | ± | 3.21 | b | 72.26 | ± | 4.51 | a |
| GuExP-So | 74.14 | ± | 3.18 | c | 72.59 | ± | 3.69 | c | 82.90 | ± | 6.32 | ab |
| ChEx-So | 63.79 | ± | 2.96 | b | 57.71 | ± | 2.36 | a | 75.01 | ± | 6.11 | a |
| ChP-So | 77.63 | ± | 3.85 | cd | 68.01 | ± | 2.11 | bc | 80.27 | ± | 5.93 | ab |
| ChExP-So | 80.26 | ± | 4.12 | d | 73.37 | ± | 4.62 | c | 88.24 | ± | 3.68 | b |
Data presented are in mean ± SD (n = 3) which with different letters are significantly different at p < 0.05.
a-d: Date with identical letters in the same column are not significantly different (p < 0.05).
3.3. Flavor profile
Oil infusing is a process of transferring scent, flavor, and functional ingredients into a carrier oil. This process can be done to add flavor to cooking oils. Here, we identified the volatiles of So, GuEx-So, GuP-So, GuExP-So, ChEx-So, ChP-So, and ChExP-So have 31, 55, 53, 49, 48, 57, and 55 compounds, respectively (Table 5). Nitrile compounds contributed to the special aroma of sesame oil (Abdel-Azeem et al., 2013), and various compounds were found, including 2-ethyl-6-methyl-pyrazine, 2,5-dimethyl pyrazine, 2,5-dimethyl-3-ethylpyrazine, 3,5-diethyl-2-methyl pyrazine and methyl pyrazine in this study. Hexanal, nonanal, benzaldehyde, and benzeneacetaldehyde exhibited the highest odor activity value in sesame oil (Jia et al., 2019). Terpene hydrocarbons, including β-sesquiphellandrene, α-curcumin, β-bisabolene, and zingiberene, are the main components that provide a distinct aroma and taste to ginger (Yeh et al., 2014). In this study, ginger-infused sesame oil contained 5.41–23.57 mg/kg of zingiberene, 2.01–8.21 mg/kg of β-sesquiphellandrene, 1.83–5.48 mg/kg of α-curcumin, and 0.94–3.97 mg/kg of β-bisabolene. The experimental results show that bamboo ginger oil exhibits ginger's most notable volatile characteristics, containing both borneol (cooling) and bornyl acetate (piney).
Table 5.
Volatile compounds of ginger-infused sesame oil.
| Compound | M.W | RI | Odor description** |
|---|---|---|---|
| Monoterpene Hydrocarbone | |||
| camphene | 136 | 943 | camphoraceuos, cooling, |
| α-phellandrene | 136 | 994 | citrus, slightly green |
| α-terpinolene | 136 | 1077 | sweet, fresh, citrus |
| Sesquiterpene Hydrocarbone | |||
| δ-elemene | 204 | 1331 | herbal, waxy, fresh |
| (+)-cycloisosativene | 204 | 1363 | – |
| α-copaene | 204 | 1371 | woody, spicy, honey |
| β-elemene | 204 | 1383 | herbal, waxy, fresh |
| α-zingiberene * | 204 | 1396 | spicy, fresh, sharp |
| β-cubebene | 204 | 1421 | herbal, waxy |
| trans-β-farnesene | 204 | 1431 | woody, green, floral |
| δ-selinene | 204 | 1441 | herbal |
| aromadendrene | 204 | 1452 | – |
| α-curcumene * | 202 | 1466 | – |
| germacrene D | 204 | 1470 | – |
| (-)-isoledene | 204 | 1476 | – |
| β-zingiberene | 204 | 1483 | spicy, fresh, sharp |
| γ-cadinene | 204 | 1490 | woody |
| β-bisabolene | 204 | 1496 | balsamic, woody |
| E,E-α-farnesene | 204 | 1498 | woody, green, herbal |
| β-sesquiphellandrene | 204 | 1510 | herbal, fruity, woody |
| trans-γ-bisabolene | 204 | 1518 | woody, citrus, fruity |
| germacrene B | 204 | 1546 | woody, earthy, spicy |
| Oxygenated Sesquiterpene | |||
| butylated hydroxy toluene | 220 | 1488 | camphoreous |
| elemol | 222 | 1532 | green, woody, spicy |
| zingiberenol * | 222 | 1597 | ginger, metallic |
| Alcohol | |||
| pentanol | 88 | 746 | musty, fusel, alcoholic |
| 1-octen-3-ol * | 128 | 964 | earthy, green, oily |
| guaiacol | 124 | 1061 | phenolic, smoky, spicy |
| cumic alcohol | 150 | 1080 | spicy, herbal |
| linalool * | 154 | 1084 | orange, floral |
| borneol | 154 | 1148 | earthy, minty, camphoreous |
| 4-terpineol | 154 | 1160 | musty |
| α-terpineol | 154 | 1171 | pine, terpenic, lilac |
| β-citronellol | 156 | 1208 | rose, oily |
| geraniol * | 154 | 1235 | sweet, floral, fruity |
| Ketones | |||
| 3-octen-2-one | 126 | 1013 | earthy, oily |
| acetophenone | 120 | 1035 | sweet, pungent |
| 2-nonanone | 142 | 1070 | fruity, sweet, waxy |
| camphor | 152 | 1117 | camphoreous |
| 5-nonanone | 142 | 1074 | fruity, sweet, waxy |
| pulegone | 152 | 1158 | peppermint, camphor |
| 2-undecanone | 170 | 1279 | waxy, fruity, fatty |
| Aldehydes | |||
| hexanal | 100 | 800 | fresh, green, fatty |
| heptanal | 114 | 900 | fresh, green, fatty |
| benzaldehyde * | 106 | 930 | almond, fruity |
| benzeneacetaldehyde | 120 | 1006 | honey, sweet, floral |
| 2-octenal | 126 | 1032 | sweet, fatty, |
| nonanal | 142 | 1082 | waxy, aldehydic |
| neral * | 152 | 1122 | sweet, citral |
| citronellal | 154 | 1130 | sweet, floral |
| myrtenal | 150 | 1160 | sweet, spicy, cinnamon |
| geranial | 152 | 1211 | citrus |
| 2,4-decadienal | 152 | 1287 | fatty, chicken, aldehydic |
| Esters | |||
| bornyl acetate | 196 | 1266 | woody, herbal |
| geranyl acetate | 196 | 1357 | waxy, green, floral |
| Hydrocarbon | |||
| toluene | 92 | 751 | sweet |
| butyl benzene | 134 | 1042 | – |
| pentyl benzene | 148 | 1142 | – |
| dodecane | 170 | 1196 | – |
| Nitrile | |||
| methyl pyrazine | 94 | 795 | nutty, cocoa, roasted |
| 2,5-dimethyl pyrazine | 108 | 884 | nutty, musty, earthy |
| 2-ethyl-6-methyl-pyrazine | 122 | 972 | nutty, roasted |
| 2,5-dimethyl-3-ethylpyrazine | 136 | 1056 | nutty, roasted |
| 3,5-diethyl-2-methyl pyrazine | 150 | 1133 | nutty, roasted |
| Miscellaneous compounds | |||
| 2-pentylfuran | 138 | 978 | fruity, green, earthy |
| 2-acetyl-5-methylfuran | 124 | 1003 | sweet, musty, nutty |
| 1,8-cineole | 154 | 1018 | eucalyptus,herbal |
RI: Retention index; cidentified via comparison of the mass spectra with the RI; RI obtained from literature.
*compared with standard compound;**compared with information from The Good Scents Company Information System (https://www. thegoodscentscompany.com); - no odor description to be found.
Heating can cause unpleasant flavors in condiments due to biochemical reactions such as the Maillard reaction, caramelization, and fat oxidation. These reactions can be inconvenient for consumers and are associated with furan production, linked to Maillard reactions and unsaturated fatty acid oxidation (Ludwig et al., 2021, Ni et al., 2022). Additionally, 2,4-Decadienal is a lipid oxidation product that creates a cooked-like aroma (Brewer, 2011). Research has shown that thermal stability of terpenes relate to their structures, and sesquiterpenes exhibit better thermal stability as they increase oxygen-containing moieties through heat-induced oxidation (e.g., zingiberene → zingiberenol and β-elemene → elemol) rather than monoterpenes facing degradation of the terpene skeleton upon the introduction of heat (Yang & Chiang, 2019).
3.4. Chemometricprofile
Several studies have utilized chemometrics to assess the impact of processing on the quality of ginger-infused sesame oil (Yang and Chiang, 2019, Santos et al., 2021, Chiang et al., 2022, Yang et al., 2022, Nhu-Trang et al., 2023). By using multivariate statistical analyses (PCA and AHC), the chemometric profiles of the samples were evaluated. The PCA analysis revealed the relationship between the processing of ginger-infused sesame oil and its functionality (Fig. 1-A). Two principal components accounted for 38.75 % and 33.93 % of the variance, respectively, resulting in a cumulative variance of 72.68 %. The results indicated that the presence of 8-gingerol (R: 0.941), 6-shogaol (R: 0.869), and 6-gingerol (R: 0.723) in ginger-infused sesame oil was effective in clearing DPPH. We then conducted AHC analysis and identified four main clusters: Cluster 1 included GuP-So and ChP-So, Cluster 2 contained GuExP-So and ChExP-So, Cluster 3 comprised GuEx-So and ChEx-So, and Cluster 4 contained only So. We discovered a significant correlation between various treatments and functional performance. The stability and solubility of the functional components in carrier oils played a crucial role in this relationship.
Fig. 1.
PCA and AHC plots of the (a)functionality and (b) flavor of ginger-infused sesame oil.
We also used PCA to analyze the connections between factors, such as ginger-infused sesame oil and flavor. The two principal components displayed a total variance of 76.76 %, with percentage variances of 47.68 % and 28.97 %, as shown in Fig. 1-B. Then, we employed AHC analysis to identify flavor clusters and identified three main clusters: Cluster 1 contained only So, Cluster 2 included GuEx-So, GuP-So, and GuExP-So, while Cluster 3 comprised ChEx-So, ChP-So, and ChExP-So. Our findings indicate that different raw materials significantly influence flavor performance.
Conclusion
By incorporating natural ingredients sourced from food into everyday foods or condiments, we can help tackle nutritional inequalities. One way to do this is by altering the formulation of ginger-infused sesame oil through material selection and different treatment procedures, which can replicate traditional functional foods. Incorporating a combination of ginger powder and the extract is an innovative and promising strategy that enhances the active substance of functional ginger-infused sesame oil. This study offers helpful references and methods for developing functional foods and conditions. However, further research is necessary to explore issues such as consumer acceptance and activity methods of ginger-infused sesame oil, which are critical factors to consider for the future.
CRediT authorship contribution statement
Li-Yun Lin: Writing – review & editing, Writing – original draft, Formal analysis, Data curation, Conceptualization. Chih-Wei Chen: Writing – original draft, Methodology, Formal analysis, Data curation. Hsin-Chun Chen: Formal analysis, Data curation, Conceptualization. Tai-Liang Chen: Project administration, Methodology. Kai-Min Yang: Writing – review & editing, Writing – original draft, Methodology, Formal analysis, Data curation, Conceptualization.
Declaration of competing interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Contributor Information
Li-Yun Lin, Email: lylin@hk.edu.tw.
Chih-Wei Chen, Email: ccwlly@mail.cjcu.edu.tw.
Hsin-Chun Chen, Email: d91628004@ntu.edu.tw.
Kai-Min Yang, Email: ykmin@nqu.edu.tw.
Data availability
The data that has been used is confidential.
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Associated Data
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Data Availability Statement
The data that has been used is confidential.

