Phytochemicals, Bioactive Properties and Commercial Potential of Calamondin (Citrofortunella microcarpa) Fruits: A Review
Abstract
:1. Introduction
2. General Characteristics of Calamondin Fruit
3. Chemical Composition and Bioactive Compound of Calamondin Fruit
- Food processing, where it can be used as a mask for the bitter taste of alkaloids [14].
- Flavorings for food products with a citrus or lime flavor, such as chewing gum, beverages, etc. [15].
- Pharmaceutical applications, for use as a penetration enhancer for topical creams or lotions [16].
- Perfumery in skin care products, such as lotions, body wash, and soap [17].
- Natural insecticide flavorings [18].
- Organic herbicide products [19].
4. Utilization of Calamondin Fruit
5. Examples of Calamondin Fruit Processing
5.1. Juice and Juice Concentrate
5.2. Pectin
5.3. Tea
5.4. Calamondin Fruit Powder
5.5. Candy Products
5.6. Essential Oils Extraction
- (1)
- A screw press uses mechanical force to extract essential oils from plants by breaking down the bulbous cells that store the oils [63]. Extracting essential oils from calamondin fruit peel using a screw press involves reducing the size of the peel with a rough chopping machine and then compressing it with a cold oil screw press. The output of the screw press is divided into two parts: a solid, or dregs, and a liquid containing essential oils. The essential oil is then separated from the other liquids [65]. Using this method, it is possible to extract one kilogram of lime essential oil from the peel by crushing the lime peel and oil glands and allowing the liquid to flow out of the bottom of the machine [70].
- (2)
- Distillation with water, also known as hydrodistillation, uses the principle of pressure extraction from hot water to extract essential oils from plants by breaking down the bulbous cells that store the oils. The process of extracting essential oils from calamondin fruit peel using hydrodistillation involves reducing the size of the peel with a crushing machine, placing it in a round-bottom flask, filling it with water, and boiling it [63,65]. The hot steam carries the essential oil out and condenses it into a liquid. The hydrodistillation process involves heating the round-bottom flask containing the crushed calamondin fruit peel and water until it boils and becomes steam-containing volatile substances. The steam is then cooled to condense it into a liquid, from which the essential oils are separated. Hydrodistillation is a traditional method used in laboratory-scale extraction of plant essential oils. The hydrodistillation process was carried out by adding 50 g of crushed calamondin fruit peel to a flask, along with 250 milliliters of distilled water (at a ratio of 1 g of solids to 5 milliliters of water). The flask was then heated to boiling under atmospheric pressure to initiate the extraction. During the distillation process, volatile aroma compounds and water mix to form azeotropic mixtures and condense. The mixture is then stratified based on the difference in density. Due to incompatibility, the essential oil fractions are collected and separated from the water after 2 h of distillation [71].
- (3)
- Microwave-assisted distillation uses the principle of electromagnetic extraction and the polar properties of molecules within the sample to extract essential oils. The movement caused by microwaves generates friction and heat, affecting plants’ cellular tissues [64]. To extract essential oils from calamondin fruit peel using this method, the peel is first reduced in size by crushing it. After crushing, the calamondin fruit peel is placed in a round-bottom flask and then in a microwave. The microwaves cause friction between the polar molecules, which generates heat and causes the liquid to boil into steam containing essential oils [68]. The steam is then cooled until it condenses back into a liquid, from which the essential oils are separated. Finally, the essential oils are separated from other liquids using a combination of microwave-assisted distillation. This process was carried out in a laboratory microwave oven at atmospheric pressure. A constant power was set in the microwave, and 500 g of fresh calamondin fruit peels were heated at 500 watts for 15 min. [66]. After that, the essential oil fraction was dried with Na2SO4, gathered in a sealed vial, and kept chilled at 4 °C.
6. Possibility of Adding Commercial Fruit Value
7. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
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Compound | Content | ||||
---|---|---|---|---|---|
Juice | Seed | Peel | Pulp | Fruit Residue | |
Total flavonoids | 0.11 (%) | - | 1.00 (%) | 1.02 (%) | - |
Pectin | - | - | 7.14 (%) | 5.04 (%) | - |
Limonin | - | 0.46 (%) | 0.51 (%) | 0.03 (%) | - |
Reducing sugars | 0.37 (%) | 1.39 (%) | 5.98 (%) | 4.56 (%) | - |
Volatile oils | - | - | 4.25 (%) | - | - |
Aspartic acid | - | - | - | - | 4.42 (g/kg) |
Proline | - | - | - | - | 3.65 (g/kg) |
Cystine | - | - | - | - | 2.10 (g/kg) |
Glutamic acid | - | - | - | - | 1.81 (g/kg) |
Isoleucine | - | - | - | - | 1.00 (g/kg) |
Lysine | - | - | - | - | 0.91 (g/kg) |
Serine | - | - | - | - | 0.78 (g/kg) |
Leucine | - | - | - | - | 0.76(g/kg) |
Arginine | - | - | - | - | 0.72 (g/kg) |
Alanine | - | - | - | - | 0.67 (g/kg) |
Valine | - | - | - | - | 0.67 (g/kg) |
Glycine | - | - | - | - | 0.59 (g/kg) |
Methionine | - | - | - | - | 0.59 (g/kg) |
Phenylalanine | - | - | - | - | 0.57 (g/kg) |
Tyrosine | - | - | - | - | 0.50 (g/kg) |
Histidine | - | - | - | - | 0.20 (g/kg) |
Threonine | - | - | - | - | 0.16 (g/kg) |
Total acid | 6.74 (%) | - | - | - | - |
Volatile oils | - | 30.46 (%) | - | - | - |
Vitamin B2 | - | - | - | - | 44.48 (mg/kg) |
Vitamin B3 | - | - | - | - | 19.31 (mg/kg) |
Vitamin B6 | - | - | - | - | 17.55 (mg/kg) |
Vitamin E | 1.68 (mg/kg) | - | - | - | 15.72 (mg/kg) |
Total Volatile Intensity | Fresh Calamondin Peel (%) | Fresh Calamondin Juice (%) |
---|---|---|
Limonene | 10.53–27.85 | 14.51–14.59 |
(Z)-3-hexenol | 4.85–12.51 | 0.17–1.36 |
Linalool | 9.40–10.29 | - |
1-octanol | 2.55–2.84 | - |
α-terpineol | 4.00–7.80 | 2.29–3.76 |
Isopiperitenone | 1.91 | 0.28–0.76 |
Geraniol | 0.79–1.06 | - |
8-hydroxylinalool | 1.20–2.12 | - |
(Z)-8-hydroxylinalool | - | 0.45–3.58 |
(E)-ρ-mentha-2,8-dien-1-ol | 0.39–1.61 | - |
Hexadecanoic acid | 0.81–1.31 | 3.19–10.88 |
4-hydroxy-benzeneethanol | - | 0.09–7.98 |
Cryptomeridiol | 0.26–069 | 4.95–5.76 |
Stearic acid | 0.19–0.43 | 3.38–3.82 |
α-cadinol | - | 1.23–3.16 |
Limonen-1,2-diol | - | 0.41–2.85 |
Linoleic acid | - | 1.36–2.73 |
Essential Oils | Crude (%) | Refined (%) |
---|---|---|
D-Limonene | 90.40 | 92.87 |
β-Pinene | 3.36 | 3.36 |
α-Pinene | 1.01 | 1.03 |
β-copaene | 0.91 | 0.90 |
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-, [S-(Z)]- | 0.57 | - |
Santolina triene | 0.54 | - |
Carvone | 0.53 | 0.49 |
2,6-Octadien-1-ol, 3,7-dimethyl-, acetate | 0.49 | 0.16 |
Octadecane, 6-methyl- | 0.41 | 0.27 |
α-Terpineol | 0.38 | - |
Bioactive Activities | Calamondin Parts | Component | References |
---|---|---|---|
Antioxidant | Peel | Naringin and Hesperidin | [20] |
Antioxidant | Peel, Pulp | Phenolics and Flavonoids | [21] |
Anti-hepatitis B virus | Peel | Nobiletin, tangeretin and 5-hydroxy-6,7,8,3′,4′-pentamethoxyflavone | [22] |
Antimicrobial | Peel | Flavonoids | [1] |
Antimicrobial | Peel | Essential oil | [23] |
Antimicrobial | Peel | Tannins | [24] |
Anti-inflammatory | Peel | Tannins | [25] |
Tyrosinase inhibitory | Peel | 3′,5′-di-C-β-glucopyranosyl phloretin, Hesperidin and Neohesperidin | [26] |
Anti-hyperglycemia | Peel | Flavonoids | [27] |
Anti-diabetic | Peel | Phenolics | [28] |
Anti-angiogenic | Peel | Phenolics | [29] |
Antimicrobial | Peel, Seeds, Pulp | Flavonoids | [30] |
Antioxidant | Juice | Phenolics | [31] |
Extraction Method | Conditions | Essential Oil Yield | Reference |
---|---|---|---|
Steam-enticing distillation | Raw material/solvent ratio (w/v) of 100/800, extraction time of 70 min. | 2.3913 g/kg | [12] |
Cold pressing | Sugarcane squeezer used to squeeze 1 kg of peel and centrifugation at 6000× g at 4 °C for 40 min. | 0.81 ± 0.25 g/kg | [49] |
Steam distillation (SD) | Peels (150 g) homogenized for 2 min with 600 mL deionized water and placed in a 5 L round-bottom flask. Homogenate steam distilled for 2 h. | 7.11 ± 0.08 g/kg | [49] |
Hot water treatment followed by steam distillation | Peels (150 g) heated in 90 ± 3 °C water for 15 min, homogenized for 2 min with 600 mL deionized water in a 5 L round-bottom flask, followed by SD for 2 h. | 9.13 ± 0.12 g/kg | [49] |
Microwave-assisted hydrodistillation (MAHD) | Extraction with MAHD in optimal conditions for 45 min, 300 W capacity, and 1:3 shells/water ratio. | 2% | [68] |
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Venkatachalam, K.; Charoenphun, N.; Srean, P.; Yuvanatemiya, V.; Pipatpanukul, C.; Pakeechai, K.; Parametthanuwat, T.; Wongsa, J. Phytochemicals, Bioactive Properties and Commercial Potential of Calamondin (Citrofortunella microcarpa) Fruits: A Review. Molecules 2023, 28, 3401. https://doi.org/10.3390/molecules28083401
Venkatachalam K, Charoenphun N, Srean P, Yuvanatemiya V, Pipatpanukul C, Pakeechai K, Parametthanuwat T, Wongsa J. Phytochemicals, Bioactive Properties and Commercial Potential of Calamondin (Citrofortunella microcarpa) Fruits: A Review. Molecules. 2023; 28(8):3401. https://doi.org/10.3390/molecules28083401
Chicago/Turabian StyleVenkatachalam, Karthikeyan, Narin Charoenphun, Pao Srean, Vasin Yuvanatemiya, Chinnawut Pipatpanukul, Kanokporn Pakeechai, Thanya Parametthanuwat, and Jittimon Wongsa. 2023. "Phytochemicals, Bioactive Properties and Commercial Potential of Calamondin (Citrofortunella microcarpa) Fruits: A Review" Molecules 28, no. 8: 3401. https://doi.org/10.3390/molecules28083401
APA StyleVenkatachalam, K., Charoenphun, N., Srean, P., Yuvanatemiya, V., Pipatpanukul, C., Pakeechai, K., Parametthanuwat, T., & Wongsa, J. (2023). Phytochemicals, Bioactive Properties and Commercial Potential of Calamondin (Citrofortunella microcarpa) Fruits: A Review. Molecules, 28(8), 3401. https://doi.org/10.3390/molecules28083401