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Review

Applications of Essential Oils and Plant Extracts in Different Industries

1
Department of Field Crops, Faculty of Agriculture, Ataturk University, 25240 Erzurum, Turkey
2
Department of Genetic and Bioengineering, Yeditepe University, 34755 Istanbul, Turkey
3
Department of Plant Sciences and Biotechnology, Faculty of Life Sciences & Biotechnology, Shahid Beheshti University, Tehran 1983969411, Iran
4
Department of Horticultural Sciences, Faculty of Crop Sciences, Sari Agricultural Sciences and Natural Resources University, Sari 4818168984, Iran
5
Department of Soil Science, Faculty of Agriculture, University of Tabriz, Tabriz 5166616422, Iran
6
Department of Agriculture, University of The Fraser Valley, Abbotsford, BC V2S 7M7, Canada
7
Faculty of Agriculture, Dalhousie University, Truro, NS B2N 5E3, Canada
*
Authors to whom correspondence should be addressed.
Molecules 2022, 27(24), 8999; https://doi.org/10.3390/molecules27248999
Submission received: 26 October 2022 / Revised: 8 December 2022 / Accepted: 14 December 2022 / Published: 16 December 2022

Abstract

:
Essential oils (EOs) and plant extracts are sources of beneficial chemical compounds that have potential applications in medicine, food, cosmetics, and the agriculture industry. Plant medicines were the only option for preventing and treating mankind’s diseases for centuries. Therefore, plant products are fundamental sources for producing natural drugs. The extraction of the EOs is the first important step in preparing these compounds. Modern extraction methods are effective in the efficient development of these compounds. Moreover, the compounds extracted from plants have natural antimicrobial activity against many spoilage and disease-causing bacteria. Also, the use of plant compounds in cosmetics and hygiene products, in addition to their high marketability, has been helpful for many beauty problems. On the other hand, the agricultural industry has recently shifted more from conventional production systems to authenticated organic production systems, as consumers prefer products without any pesticide and herbicide residues, and certified organic products command higher prices. EOs and plant extracts can be utilized as ingredients in plant antipathogens, biopesticides, and bioherbicides for the agricultural sector. Considering the need and the importance of using EOs and plant extracts in pharmaceutical and other industries, this review paper outlines the different aspects of the applications of these compounds in various sectors.

1. Introduction

Essential oils (EOs) are volatile compounds with a slight molecular weight and biological activities synthesized in different plant organs like flowers, buds, leaves, branches, stems, seeds, fruits, woods, roots, etc. [1]. Moreover, EOs contain many active compounds, such as alkaloids, tannins, steroids, glycosides, resins, phenols, volatile oils, and flavonoids [2,3]. Nowadays, EOs are becoming popular natural alternatives to synthetic antioxidants to address consumer concerns about the adverse effects of synthetic antioxidants that have toxic effects on consumers and subsequently lead to various cancers. Therefore, in order to maintain and increase consumers’ health and create food security, new and cheap sources of natural antioxidants are increasingly available [4].
EOs and extracts are of great importance in various industries due to the presence of large amounts of volatile, aromatic, and bioactive compounds [5]. Also, these effective compounds have inherent antioxidant and antimicrobial properties and play an essential role in the pharmaceutical, food, agricultural, cosmetic, and health industries [6]. This review provides an updated perspective on the current uses of EOs and plant extracts, and their components, in food, agriculture, and cosmetic products, focusing on their antibacterial, antifungal, herbicidal, etc., properties.

2. The Main Compounds Constituting Essential Oils and Extracts

EOs are volatile substances and dissolve in alcohol and some organic solvents. Terpenes may be linear or cyclic, and depending on the number and how the carbon atoms are connected, different chemicals such as terpenes (with ten carbon atoms), terpenes (with 15 carbon atoms), and diterpenes (with 20 carbon atoms) are created (Figure 1) [3,7,8]. Some of the most important compounds of EOs include eugenol, carvacrol, cinnamic acid, thymol, cinnamaldehyde, citral, and geraniol [9].
The volatile molecules move across the lipids of the bacterial cell membrane due to their hydrophobic nature, disrupt the cell wall structure, and make them more permeable [11]. This change in membrane permeability leads to the leakage of ions and other cellular materials, and ultimately, to cell death [12]. The antibacterial activities of EOs are strongly related to the type of the main compounds [13]. For example, phenolic compounds such as cinnamaldehyde, citral, carvacrol, eugenol, and thymol have significant and strong activities followed by terpenes, while compounds such as ketones (β-myrcene, α-thujone, or geranyl acetate) have weaker activities, and hydrocarbons are almost inactive [14]. The primary active compounds that effectively stop the growth of microorganisms are carvacrol, eugenol, and thymol. They do this by disrupting the cell membrane, which leads to changes in the flow of electrons, protons’ driving force, active transport, and the coagulation of cell contents. Figure 2 displays the different effects of essential oils on microorganisms [15].
The quality of active ingredients in EOs and plant extracts is directly related to the way and the method of extraction. In general, large amounts of expensive organic solvents, such as alcohol, are used in the industrial extraction of plant extracts and some EOs [16]. EOs and plant extracts are composed of several active ingredients, and their extraction time will differ depending on the active ingredient. For example, a hydrodistillation time study conducted by Semerdjieva et al. [17] showed that the yield and composition of EO in Juniperus virginiana, Juniperus sabina, and Juniperus excelsa vary with the distillation time. Accordingly, in J. virginiana, the highest content of limonene (43%) was obtained during the first 5 min, and the highest content of safrole (37%) was obtained during the window from 10 to 20 min. In J. excelsa, the highest α-pinene (34–36%) was obtained during the first 5 min, limonene (39%) during the first 10 min, and cedrol (50–53%) during the 40 to 240 min range.
Extraction is the preliminary step for separating the desired natural products from the raw materials. Different extraction methods are used based on the ingredients and the compounds in the EOs and the plant extracts [18]. Distillation, sublimation, and solvent extraction are the most common methods used to extract different oils [19].
The conventional and popular methods for extracting active plant substances are water-based classical methods applied to extract EOs, which include steam distillation and hydrodistillation. These techniques extract EO in a balanced quantity without affecting the quality of the EO. Several techniques with unique special mechanisms are created to ensure better extraction efficiency. Ultrasound extraction, microwave extraction, supercritical liquid extraction, and combined extraction with the help of ultrasound waves are advanced extraction techniques [20]. Herbal extracts are divided into the following two groups: liquid extracts and dry extracts.

2.1. Herbal Liquid Extracts

During the liquid extraction process, plant resources such as leaves, roots, or flowers, as well as plant gums, are placed in the vicinity of a specific solvent at a certain temperature, pressure, and heat in the extraction device (extraction reactor), and the majority of the metabolites are taken out. If one wants to use this extract in the food industry, the solvent is separated using an evaporation device. At the end, one will have a total extract containing all of the plant’s active or medicinal substances [21,22]. Some substances in plant extracts are bitter substances, such as flavones, flavonoids, mucilages, saponins, silicic acid, tannins, vitamins, lipids, etc. Flavones and flavonoids exist in free form or in combination with glycosides and chemically belong to phenols. Derivatives of flavones are yellow (‘flavone’ comes from the Latin word ‘flavus’, meaning yellow). Flavones are soluble in the plant cell sap. In general, flavonoids have a softening and moisturizing effect on the skin. Mucilages are carbohydrates with a very complex chemical structure and high molecular weight. These substances are insoluble in alcohol.

2.2. Herbal Dry Extracts

Herbal dry extracts can be obtained in different ways, such as by exposing the liquid cane to the temperature and air of the environment by placing in a spray dryer. When preparing medicinal ointments, tablets, and capsules from herbal or animal sources, dry herbal extracts can be obtained in the same way.

3. Application of Active Herbal Ingredients in the Food Industry

Medicinal plants are extensively utilized as flavoring agents in beverages, foods, and dietary supplements. Typically, we have been using these herbs as seasonings and spices in our foods for years because they give a special flavor to foods. Also, with their antioxidant properties, they can play a pivotal role in improving the health of society. Foods’ safety and organoleptic characteristics are prone to microbial spoilage and oxidation change. These reactions reduce the nutritional value of the products due to the loss of their components and impact their safety and organoleptic characteristics [23]. Due to emerging consumer demands and international markets, food distribution and retail systems have changed the storage and transfer time of products. Therefore, it can be said that increasing the shelf life of perishable foods is one of the biggest challenges of the food packaging industry [24].
In recent years, antimicrobial and antioxidant compounds have been considered as an alternative for food preservation. Bioactive compounds consist of small amounts of additional nutrients and can modulate one or more metabolic processes that can increase health benefits and enhance nutritional value. Furthermore, due to consumer awareness about the problems of synthetic compounds, human health, and their demand for the use of natural compounds like EOs, natural compounds have been recognized as suitable alternatives to improve the shelf life of perishable foods [25].

3.1. The Use of Essential Oils to Preserve Food

EOs have been used for their antimicrobial, antifungal [8], and antioxidant [26,27] properties. These compounds can increase food’s shelf life by producing natural preservatives [28]. The beneficial and harmless aspects of these EOs should be considered to ensure the safety of these compounds for using them in foods [29]. Table 1 shows some important medicinal plants that are used as antibacterials in the food industry.
The antibacterial and antioxidant properties of EOs are due to compounds such as linalool, cinnamaldehyde, thymol, carvacrol, and vanillin, which are acceptable for use in the food industry and increase the shelf life of perishable materials.
All food products are usually affected by microorganisms except for sterilized food products. However, only a tiny portion of these microorganisms have a favorable effect on improving food taste. Most of them reduce the organoleptic quality of the product and cause food spoilage by producing toxins. Accordingly, the microbial safety of food is one of the major concerns of consumers, regulatory organizations, and food industries worldwide. Therefore, several methods of food preservation are used to control or reduce food spoilage. These methods include freezing, restriction of nutrients, acidification, fermentation, pasteurization, and chemical preservatives [40]. Additionally, new technologies such as modified atmosphere packaging, activated films, non-thermal treatments, drying, enhancement of antimicrobial substances, and radiation slow down the growth of microorganisms [41,42]. Such methods are usually associated with reducing the organoleptic features of foods and decreasing consumer acceptability [43].
Most of the antimicrobial substances used are synthetic chemical compounds that slow down the development of microorganisms. These substances include sodium benzoate, potassium sorbate, and nitrites commercially used in fruit juices, dairy products, confectionery, meat, and meat products. Nitrite and nitrate are used in the meat industry to prevent the growth of microorganisms and reduce fat oxidation. Reports have indicated that blue baby syndrome occurs in children due to a large amount of nitrite in their blood [44]. It should be mentioned that many synthetic compounds are also found naturally (benzoic acid in blueberries, sorbic acid in rowanberries, citric acid in lemons, malic acid in apples, tartaric acid in grapes, etc.) [45].
Since ancient times, spices have been used for flavoring and as natural preservatives in foods [46]. Due to the high chemical diversity of natural compounds, plant extracts could control the growth of microbes in food products. In addition, they are used in traditional medicine, functional foods, food supplements, and recombinant protein production. The lack of reproducibility of activity is the main barrier to using EOs in foods. Although EOs contain chemical compounds, they have different qualitative and quantitative fluctuations in their content, which greatly affects their biological effectiveness [47]. The pungent aroma of EOs is the major obstacle that limits their use in foods, which can affect their organoleptic properties and taste [43]. Accordingly, the strong flavor of EOs should be minimized by carefully selecting the EO based on the type of food.
Furthermore, the availability of ingredients and the risk of losing biodiversity are other obstacles to using plant EOs as preservatives [48]. EOs have many bioactive compounds such as terpinol, thujanol, myrtenol, neral, thujone, camphor, and carvone, which indicate significant activities. EOs are generally more active in Gram-positive bacteria due to a peptidoglycan layer on the outer membrane. In Gram-negative bacteria, the outer membrane consists of a double layer of phospholipids which is connected to the inner membrane by lipopolysaccharides. Lipopolysaccharides consist of three basic components—lipid A, a core polysaccharide, and O-side chain—which are responsible for the resistance of Gram-negative bacteria to EOs [14]. In some cases, the combination of two or more compounds produces more activity than when they are used individually, which is called synergistic effects [9]. In general, the value of plants depends on the chemicals present in them, which can affect the microbiological, chemical, and even sensorial quality of foods. These plant chemicals are classified into several categories, including polyphenols, flavonoids, tannins, alkaloids, terpenoids, isothiocyanates, lectins, and polypeptides [49]. The following table (Table 2) indicates a list of plant EOs other than the GRAS group that have antimicrobial activity due to their phytochemical compounds.
Considering the fact that the use of chemical antibiotic compounds has harmful effects on food health and causes problems such as the emergence of antibiotic-resistant bacterial strains, biologically active plant extracts have a great potential to be used as food preservative agents.

3.2. The Use of Plant Extracts to Preserve Meat and Meat Products

One of the main factors that reduces meat quality is lipid oxidation, which is a complex process and can affect the combination and behavior of meat during food processing. Lipid oxidation leads to the formation of several metabolites that strongly affect meat fiber quality [50]. Generally, these complex reactions cause undesirable changes in the sensory and nutritional characteristics of meat and meat products. Therefore, several antioxidant compounds (both natural and synthetic) have been investigated to reduce or prevent these reactions. For this reason, consumers have recently avoided synthetic antioxidants due to their supposed or possible toxicity [51,52].
Table 2. Phytochemical compounds present in some plant EOs.
Table 2. Phytochemical compounds present in some plant EOs.
Plant NameScientific NameThe Tissue UsedPhytochemical CompoundsReference
Viper’s
bugloss
Echium vulgareLeafFlavonoids, catechol,
saponins, steroids
[53]
OnionAllium cepaBulbSaponin, ferulic acid,
beta-sitosterol
[54]
Black cuminNigella sativaSeedglycoside, melanin, saponin[55]
GarlicAllium sativumGarlic clovediallyl disulfide, diallyl
trisulfide, alkenyl cysteine sulfoxide
[56]
TurmericCurcuma longaRhizometrans-β-farnesene, α-
Zingiberene, β-bisabolene
[57]
Plant extracts have greater antioxidant qualities than artificial antioxidants, which can also help the health status of consumers [58]. Due to their activity, natural antioxidants can generally protect biological cells against oxidation processes caused by reactive oxygen species (ROS) [59]. However, the compounds should not harm the features of the products and also be active in low concentrations if they are to have a chance to be used as natural antioxidants in meat and meat-based products [60]. Additionally, they should not be expensive and should be stable during the process. From the perspective of food technology, the real features of natural antioxidants are deeply influenced by their intrinsic nature, production, and storage conditions (for instance, being exposed to oxygen and light, pH, temperature, and storage time), and the compounds should also be non-toxic in doses higher than normal consumption [61]. In recent years, the meat production industry has mainly focused on the development of healthier meat products [62]. This goal was made possible by using two strategies: reducing undesirable substances and increasing the levels of the desired bioactive substances [63].
Polyphenols (such as anthocyanins, tannins, and flavonols) and EOs (mainly composed of terpenes) are bioactive components available in plants that can be used by the meat industry. These combinations can be obtained from different parts of the plant, including its seeds, leaves, and fruits. Black pepper (Piper nigrum L.), for instance, is a hot spice that is used all over the world and is considered one of the most valuable spices due to its pleasant effects (pungent taste) [64]. The principal components of the compounds in black pepper EO are 3-Δ-carene, caryophyllene, α-pinene, β-pinene, and limonene [65]. Oregano (Origanum vulgare L.) is another flavoring plant in various foods around the world [66]. The most important bioactive compounds in oregano are rosmarinic acid, Phenyl β-D-glucopyranoside, catechin, and luteolin-7-o-rutinoside [67]. Green tea (Camellia sinensis) is one of the other valuable plants. It can be consumed as prepared drinks, thick capsules, tablets, and dried leaves for home preparation [64]. Green tea leaves contain bioactive compounds from the family of phenolic compounds, among which epigallocatechin-3-gallate (the main phenolic compound) can be mentioned [68]. Sage (Salvia officinalis L.) can be mentioned as another widely used medicinal plant, which is used in food preparation and in medicine [69]. Some of the major compounds of the common sage plant are α-pinene, β-pinene, limonene, 1,8-cineole, and camphene [70]. Pitanga (Eugenia uniflora L.) is an indigenous plant of South America that is mainly known for its fruits. However, the leaves of this plant have been primarily considered due to the presence of phenolic compounds; for example, quercetin, myricetin, ellagic acid, isorhamnetin, and quinic acid [71]. The guarana plant is also indigenous to Brazil, and the seeds of this plant are used commercially in the food industry to prepare extracts, syrups, and juices [72]. The phenolic compounds present in guarana seeds include anthocyanins (pelargonidin and 4-ethylcatechol), flavones (luteolin and apigenin), phenolic acids (caffeic, dihydrocaffeic, homovanillic acids), and tyrosols (tyrosol, tyrosol acetate and hydroxytyrosol acetate) [73].
The use of natural bioactive compounds to increase shelf life can be mentioned as the uses of plant extracts in meat and related products. This issue is always associated with the effect of these extracts on slowing down oxidative processes, preventing color change, and losing the quality of these products (Table 3). Zhang et al. [74] investigated the effect of EOs extracted from black pepper (0.1 and 0.5%) in the storage of fresh meat (9 days at a temperature of 4 °C). They observed that this EO prevents metmyoglobin formation and reduces the formation of lipid oxidation products after three days of storage. In a study conducted on the use of essences and EOs for the preservation of lamb nuggets (patties), it was found that a combination of EOs and plant oils such as cassia, clove, and thyme resulted in a significant reduction in lipid oxidation during storage (30 days at 4 °C under aerobic condition) [75]. Therefore, using guarana seed extract improves the stability of meat products. Adding guarana seed extract at doses of 250, 500, and 1000 mg/kg leads to the preservation of the color of the hamburger and the reduction of the formation of lipoprotein oxidation products in the beef hamburger [75].
Using extracts rich in bioactive compounds from plant leaves can also improve the preservation of meat products. Ramirez-Rojo et al. [78] investigated the effect of mesquite leaf extract on the sensory aspects of pork meat during the storage process. They reported that the progress of meat lipid-protein oxidation was significantly affected by the strong antioxidant activity of this extract. Furthermore, the evaluation of storage stability indicated that the reduction of redness compared to the control sample (without antioxidants) was until the end of the storage period.
Pythanganism leaves are a source of biologically active compounds used to preserve meat products. Studies have indicated that this extract (250, 500, and 1000 mg/kg) in meat storage (18 days at 2 °C) was accompanied by increased protection against lipoprotein oxidation. Additionally, the color change, which is usually observed during the storage of meat products, is a significant indicator of the potent antioxidant potential of this extract [61]. In another investigation conducted with a focus on improving the stability of the appearance and health of meat products during storage, it was discovered that the antioxidant extract from Moringa oleifera, which is rich in fiber, prevented lipid oxidation during storage (20 days at a temperature of 4 °C).
Studies indicated that using black cumin ethanol extract to prepare salmon-based marinade reduces the amount of yeast and coliform contamination [79]. Furthermore, Lee et al. [80], reported that adding green tea or rosemary (1 or 3%) to rice cake can significantly reduce the population of B. cereus and S. aureus in three days of storage at room temperature (22 °C). Turmeric, which contains a combination of curcuminoids plus EOs, is known as a spice and has a vast range of biological activities [81]. Also, another investigation indicated that the use of turmeric extract (1.5% v/v) alone or in combination with shallot extract (1.5% each, v/v) preserves the quality of packaged trout stored in a refrigerator for more than 20 days [82].

3.3. The Use of Plant Extracts for Food Packaging

Extracts that are rich in bioactive compounds can also be used to improve food packaging features. It should be mentioned that a significant process of active antioxidant packaging for meat replaces artificial additives with natural bioactive compounds [83]. The most typical natural antioxidants employed in these innovative packaging technologies are tocopherols, EOs, and plant extracts such as rosemary, oregano, tea, etc. Accordingly, green tea extract combined in films made from dried protein seeds has been successfully used in the classification of pork, which has reduced lipid oxidation compared to control samples [84]. Studies have shown that a combination of green tea extract in potato starch film significantly improves the mechanical features of meat and reduces the oxidation of packaged fresh beef [85]. In another study, researchers examined the effect of green tea extract on the shelf life of cooked ham (21 days at 2 °C), and reported that the active packaging formulated with green tea extract (1%) was effective in preserving meat color [86]. In another study on lamb ham, it was indicated that the use of oregano extract, without the need for phenol terpene compounds, prevented the oxidation of the bioprotein part compared with the control samples during 120 days of storage at 18 °C [67]. Another study on ham also indicated that the combination of oregano essence and green tea extract (1%) stabilizes the sensory features of cooked ham after 21 days of storage at 2 °C, and results in better surface color change and long-term storage scores [77].

4. Application of Essential Oils and Plant Extracts in the Agriculture Industry

4.1. Application of Essential Oils and Plant Extracts as Insecticides

Plants are a rich source of defensive chemicals. These substances may exhibit insecticidal, repellent, attractant, antinutritional, and growth-regulating effects on insects and usually have minor adverse effects on non-target organisms (parasites and predators) and the environment. Traditionally, synthetic insecticides have been used for many years to control postharvest diseases. Along with the benefits of these insecticides, the expansion of their use has caused consumers to worry about the possible dangers of toxic substances in crop residues. This issue has challenged the usefulness of pesticides and created the need for developing other methods to reduce the usage of chemicals. Controlling and reducing the damage of pathogenic pathogens after harvest using plant products such as plant extracts and essences in recent years could be a suitable alternative to reduce or eliminate the use of chemicals to control postharvest diseases of fruits and vegetables [87]. Currently, there are products based on neem tree extract (neem) and EOs of cloves, rosemary, mint, cinnamon, lemon, thyme, etc., produced commercially for sanitary, agricultural, and greenhouse pest management [88].
Plant extracts as biological stimulants and plant protection products play an essential role for modernizing agriculture [89]. Semerdjieva et al. [90] studied the biological activity of four juniper species EOs as biopesticides and their results demonstrated that all tested EOs have significant insecticidal and repellent activity against two aphid species Sitobion avenae (English seed aphid) and Rhopalosiphum padi (bird oat cherry aphid) at 1%, 2.5% and 5% EO concentrations in solutions. Turmeric (Curcuma longa), in addition to the antibacterial properties mentioned above, produces biological activities such as insect repellant and anti-snake venom activity that can be used as bioinsecticide [91]. Also, various studies have shown that J. virginiana EO have activities against insects and pathogens [17,92,93]. Yohana et al. [94] studied the important anti-mosquito properties of Juniperus virginiana (Cupressaceae) EOs against dominant malaria vectors, and their findings demonstrated that its EO has the potential for the development of new, efficient, safe, and affordable agents for mosquito control. Also, Semerdjieva et al. [95] reported that Satureja pilosa EO has larvicidal and mosquito repellent activities against Aedes aegypti that can be utilized for the development of new mosquito management control products.

4.2. Application of Essential Oils and Plant Extracts as Herbicides

A biological method that uses allelochemicals for controlling weeds is an excellent alternative in organic systems. Most allelochemicals are used as secondary metabolites in plants, like EOs, tannins, alkaloids, and glycosides, as alternative strategies for weed management. For example, the findings of Semerdjieva et al. [96] showed that J. sabina and J. exselsa EOs could manage the control of weed seeds.

4.3. Application of Allelopathy, Essential Oils and Plant Extracts Effects on the Germination of Seeds

The term “allelopathy” in plants is a non-resource-based beneficial or harmful interaction among plants and is more related to allelochemical release [97]. Allelopathy with the help of plant EOs can be practical in modern agriculture. One of its applications in modern agriculture is preventing preharvest sprouting (vivipary) in plants such as wheat and barley [98]. In corn plants, seed germination in the cob head, which can happen due to rain at the time of ripening and before it is harvested due to adverse weather conditions, causes a significant decrease in yield and quality. Of course, preharvest germination depends on many other factors, such as seed maturity stage, dormancy, the cultivar’s genetic resistance, the amount and duration of rainfall, and environmental temperature [99].
Zheljazkov et al. [30] studied the allelopathic effects of EOs from some different plant species, especially hyssop (Hyssopus officinalis), lavender (Lavandula angustifolia), English thyme (Thymus vulgaris), costmary (Chrysanthemum balsamita), lovage (Levisticum officinale), and cumin (Cuminum cyminum), on the seed germination and seedling growth of wheat (Triticum aestivum) and barley (Hordeum vulgare), and their results can be used in the development of commercial products for controlling the preharvest sprouting of wheat and barley. Their results showed that there are different percentages of EOs in different plants. Cuminum cyminum containing 49.6% cumin aldehyde, 10.4% para-cymene, 11.6% α-terpinen-7-al, and 9.1% β-pinene completely inhibited the germination of barley and wheat with the application of 10, 30, and 90 µL, respectively. EOs of C. balsamita (43.7% camphor, 32.4% trans-thujone, and 11.6% camphene) and H. officinalis (39.8% cis-pinocamphone, 9.8% trans-pinocamphone, 11.4% β-pinene, and 7.5% β-phellandrene (in amounts of 30 and 90 μL) completely inhibited barley and wheat roots per seed, root length, seedling height and germination (%), respectively. The percentage of wheat seed germination was completely inhibited by using L. angustifolia and T. vulgaris EOs at concentrations of 30 and 90 µL, respectively. Several studies have shown that cumin, hyssop, castor oil, and lavender EOs have the potential for controlling aphids such as Rhopalosiphum padi [100]. In a study by Mancini et al. [101], it was observed that EOs of cumin reduce germination percentage from 100 to 1000 mg L−1, which led the researchers to conclude that cumin EOs is an allelopathic agent for weed control and should be a promising agent for organic cultivation. Lavandula angustifolia EOs was also shown to prevent the emergence of seedlings of the weed species Amaranthus retroflexus and Portulaca oleracea without much negative effect on tomato [102].

4.4. Application of Essential Oils and Plant Extracts as Antibacterial and Antifungal Agents

Bacteria are one of the leading causes of plant diseases and cause damage to many agricultural products. These plant pathogens can reduce vegetables’ shelf life and cause significant economic losses for farmers and producers of vegetable products. In recent years, the indiscriminate use of chemical bactericides and antibiotics to control plant diseases has caused resistance in pathogenic bacteria. For this reason, finding compounds of natural origin has been considered an effective and safe approach to restrain the growth of bacteria and improve the shelf life of foods. Due to the presence of antimicrobial compounds, plant extracts have a high potential to be used as natural preservatives and can be used to control decay and raise the shelf life of plant products. Therefore, considering the effectiveness of medicinal plants in eliminating disease agents and diseases, these plants can also play a remarkable role in eliminating monocytes and insects that cause agricultural damage.
Semerdjieva et al. [103], when studying juniper tree species (J. oxycedrus L.), showed that EOs extracted by water distillation through standard Clevenger apparatus (Clevenger) and semi-commercial steam distillation (SCom) have balanced activity against selected pathogens (Botrytis cinerea, Fusarium spp., Rhizoctonia solani, Colletotrichum spp., and Cylindrocarpon pauciseptatum). Table 4 shows a list of plants and combinations of effective substances with antipathogen properties.

5. Application of Essential Oils and Plant Extracts in the Cosmetics Industry

The use of EOs and herbal extracts as cosmetics has attracted peoples’ attention for a long time, and active substances obtained from plants were used as perfumes or cosmetics. Historical findings obtained from the countries of origin of these plants, such as India, China, Egypt, and Iran, confirm the long-time usage of medicinal plants as cosmetic products.
It is estimated that more than 80% of the world’s population uses conventional medicine (plant extracts or their active compounds) to meet their health needs [111]. For example, in ancient Egypt, the oil of medicinal plants was extracted by steaming, while the Romans and Greeks used the distillation method for extraction. Also, with the advent of Islamic civilization, the use of medicinal plants accelerated with innovative approaches, and the methods of extracting oil, EO, and their substance took a practical step in the path of evolution. In addition, the EO obtained from species like Cedrus libani, Ocimum kilimandscharicum, Artemisia annua, Acacia vestita, Piper angustifolium, Sassafras albidum, and Rosmarinus officinalis contains camphor, which has been identified as an aromatic substance for centuries, and in ancient Japan and China. In other Asian and European countries, it has been used medicinally as well as in culinary and cosmetic applications [112,113].
Currently, consumers’ tendency to purchase herbal cosmetics, which is both environmentally friendly and renewable, has increased [114]. In recent years, “natural cosmetics” recorded a large quota of cosmetics (about $40 billion by 2021, which is about 10% of the global cosmetics market) [115]. Due to their anti-inflammatory, antimicrobial, and antioxidant properties, plant EOs, either as active ingredients or as preservatives, are used in various cosmetic products such as moisturizers, lotions, and cleansers in skin care. Cosmetics, conditioners, masks, or anti-dandruff products are used in hair care products, lipsticks or perfumes in perfumery [115].
By adding rosemary and chamomile EOs to shampoo, EOs can quickly penetrate the scalp, feed the hair follicles, moisturize the hair, strengthen the hair, and eliminate the adverse molecules that block the pores of the skin [116]. EOs have a major impact on stimulating hair growth and preventing hair loss [117]. It was reported that topical mint oil extracted from Mentha piperita with a relatively low dose (3% weight on weight) is typically used to stimulate hair growth [118]. One of the most common applications of EOs in skin care is to prevent acne from appearing, using the ability of EOs to inhibit Propionibacterium acnes, which Citronella’s EO has the ability to do [119]. EOs can be used in sunscreen creams because they can absorb most ultraviolet rays (in the wavelength range of 290 to 400 nm), prevent aging, sunburn, wrinkles, and other skin damage [120]. A cream formulation that contains EOs of Calendula officinalis was studied in laboratory conditions, and the results confirmed that the prepared formula had good properties for protecting the skin from exposure to sunlight [121].
Preservatives are added to cosmetic products to prevent microbial spoilage and thus increase the shelf life of the products. It is also necessary to protect the consumer against potential infections. Although chemical preservatives prevent microbial growth, their safety is questioned by consumers. Therefore, there is a considerable interest in producing preservative-free or self-preservative cosmetics [122]. Therefore, the use of essences and extracts derived from plants in the production of cosmetics as multipurpose antimicrobial compounds, both as an alternative or natural preservatives and with anti-pathogenic properties, can help to improve the quality of these products. Some species from Nepta, for example Nepeta cataria var (Citriodora), Nepeta cataria, and Nepeta grandiflora, are used in herbal cosmetics. In these three species, the major compounds were nepetalactone and geraniol in N. cataria; citronellol and geraniol in N. Citriodora; and o-cymene, c-terpinene, carvacrol and p-cymene in N. Grandiflora [123]. Table 5 shows a list of plants and combinations of effective substances with antipathogen properties for use in the cosmetic and health industries.

6. Conclusions and Future Perspectives

EOs and extracts contain important secondary metabolites produced from many plant species and can be used as rich sources for the preparation of herbal medicines or as preservatives and antioxidants in pharmaceutical, food, agricultural, and cosmetic products. Also, due to the presence of various active ingredients, they have antibacterial, antifungal, antiviral, insecticidal, and allelopathic properties, and these properties can be used to improve the quality of the products, to increase the shelf life of the products, and to protect plants from pests and plant diseases. However, since the safety of chemical preservatives in the food, cosmetics, and agricultural industries has been questioned, more studies are necessary to evaluate EOs and plant extracts as alternatives for use in various industries. Furthermore, due to the presence of different bioactive compounds in EOs and extracts, it is necessary to check the compounds in them. Efforts need to be directed towards the use of automation and high throughput screening to search for novel bioactivities of EOs. Also, the huge amount of information generated by in vitro assays must be confirmed by vivo assays and large-scale clinical investigations.

Author Contributions

P.B., R.S., S.K. and M.K.: conceptualization, visualization, review, supervision, analysis, writing—original draft, review and editing; B.A.L., J.H. and T.A.: literature search, collection of data, review and editing. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Jain, P.L.; Patel, S.R.; Desai, M.A. Patchouli oil: An overview on extraction method, composition and biological activities. J. Essent. Oil Res. 2022, 34, 1–11. [Google Scholar] [CrossRef]
  2. Amirifar, A.; Hemati, A.; Asgari Lajayer, B.; Pandey, J.; Astatkie, T. Impact of various environmental factors on the biosynthesis of alkaloids in medicinal plants. In Environmental Challenges and Medicinal Plants; Aftab, T., Ed.; Springer: Cham, Switzerland, 2022; pp. 229–248. [Google Scholar] [CrossRef]
  3. Asgari Lajayer, B.; Ghorbanpour, M.; Nikabadi, S. Heavy metals in contaminated environment: Destiny of secondary metabolite biosynthesis, oxidative status and phytoextraction in medicinal plants. Ecotoxicol. Environ. Saf. 2017, 145, 377–390. [Google Scholar] [CrossRef] [PubMed]
  4. Khodaei, N.; Nguyen, M.M.; Mdimagh, A.; Bayen, S.; Karboune, S. Compositional diversity and antioxidant properties of essential oils: Predictive models. LWT 2021, 138, 110684. [Google Scholar] [CrossRef]
  5. Samadi, S.; Asgari Lajayer, B.; Moghiseh, E.; Rodríguez-Couto, S. Effect of carbon nanomaterials on cell toxicity, biomass production, nutritional and active compound accumulation in plants. Environ. Technol. Innov. 2021, 21, 101323. [Google Scholar] [CrossRef]
  6. Aćimović, M.; Šovljanski, O.; Šeregelj, V.; Pezo, L.; Zheljazkov, V.D.; Ljujić, J.; Tomić, A.; Ćetković, G.; Čanadanović-Brunet, J.; Miljković, A. Chemical composition, antioxidant, and antimicrobial activity of Dracocephalum moldavica L. essential oil and hydrolate. Plants 2022, 11, 941. [Google Scholar] [CrossRef] [PubMed]
  7. Franz, C.; Novak, J. Sources of essential oils. In Handbook of Essential Oils; CRC Press: Boca Raton, FL, USA, 2020; pp. 41–83. [Google Scholar]
  8. Bajpai, V.K.; Baek, K.-H.; Kang, S.C. Control of Salmonella in foods by using essential oils: A review. Food Res. Int. 2012, 45, 722–734. [Google Scholar] [CrossRef]
  9. Burt, S. Essential oils: Their antibacterial properties and potential applications in foods—A review. Int. J. Food Microbiol. 2004, 94, 223–253. [Google Scholar] [CrossRef]
  10. Sidhu, Y. In vitro micropropagation of medicinal plants by tissue culture. Plymouth Stud. Sci. 2010, 4, 432–449. [Google Scholar]
  11. Cosentino, S.; Tuberoso, C.I.G.; Pisano, B.; Satta, M.; Mascia, V.; Arzedi, E.; Palmas, F. In-vitro antimicrobial activity and chemical composition of Sardinian thymus essential oils. Lett. Appl. Microbiol. 1999, 29, 130–135. [Google Scholar] [CrossRef]
  12. Dorman, H.D.; Deans, S.G. Antimicrobial agents from plants: Antibacterial activity of plant volatile oils. J. Appl. Microbiol. 2000, 88, 308–316. [Google Scholar] [CrossRef]
  13. Aroiee, H.; Babaei, M.; Ajdanian, L.; Javdani, M.; Azizi, M.; Asgari Lajayer, B.; Dell, B. Effect of Essential Oil of Seven Medicinal Plants on Longevity, Non-germination, and Qualitative and Quantitative Traits of Solanum tuberosum cv. Agria. J. Food Process. Preserv. 2022, 46, e16754. [Google Scholar] [CrossRef]
  14. Bhavaniramya, S.; Vishnupriya, S.; Al-Aboody, M.S.; Vijayakumar, R.; Baskaran, D. Role of essential oils in food safety: Antimicrobial and antioxidant applications. Grain Oil Sci. Technol. 2019, 2, 49–55. [Google Scholar] [CrossRef]
  15. Braga, P.C.; Dal Sasso, M.; Culici, M.; Galastri, L.; Marceca, M.T.; Guffanti, E.E. Antioxidant potential of thymol determined by chemiluminescence inhibition in human neutrophils and cell-free systems. Pharmacology 2006, 76, 61–68. [Google Scholar] [CrossRef] [PubMed]
  16. Chemat, F.; Vian, M.A.; Cravotto, G. Green extraction of natural products: Concept and principles. Int. J. Mol. Sci. 2012, 13, 8615–8627. [Google Scholar] [CrossRef] [Green Version]
  17. Semerdjieva, I.B.; Shiwakoti, S.; Cantrell, C.L.; Zheljazkov, V.D.; Astatkie, T.; Schlegel, V.; Radoukova, T. Hydrodistillation extraction kinetics regression models for essential oil yield and composition in Juniperus virginiana, J. excelsa, and J. sabina. Molecules 2019, 24, 986. [Google Scholar] [CrossRef] [Green Version]
  18. Rassem, H.H.; Nour, A.H.; Yunus, R.M. Techniques for extraction of essential oils from plants: A review. Aust. J. Basic Appl. Sci. 2016, 10, 117–127. [Google Scholar]
  19. Su, Z.Q.; Wu, X.L.; Bao, M.J.; Li, C.W.; Kong, S.Z.; Su, Z.R.; Lai, X.P.; Li, Y.C.; Chen, J.N. Isolation of (-)-patchouli alcohol from patchouli oil by fractional distillation and crystallization. Trop. J. Pharm. Res. 2014, 13, 359–363. [Google Scholar] [CrossRef] [Green Version]
  20. Rai, A.; Bhargava, R.; Mohanty, B. Simulation of supercritical fluid extraction of essential oil from natural products. J. Appl. Res. Med. Aromat. Plants 2017, 5, 1–9. [Google Scholar] [CrossRef]
  21. Prabhu, K.; Bhute, A.S. Plant based natural dyes and mordants: A Review. J. Nat. Prod. Plant Resour. 2012, 2, 649–664. [Google Scholar]
  22. Kordjazi, A.; Feizy, J. A review of novel methods of extracting plant extracts. NAISL 2019, 2, 13–23. [Google Scholar]
  23. Long, C.; Wu, S.-B.; Cho, W. Chemical basis of traditional medicines and new potential applications. Evid. Based Complement. Alternat. Med. 2014, 2014, 723502. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Vermeiren, L.; Devlieghere, F.; van Beest, M.; de Kruijf, N.; Debevere, J. Developments in the active packaging of foods. Trends Food Sci. Technol. 1999, 10, 77–86. [Google Scholar] [CrossRef]
  25. Sacchetti, G.; Maietti, S.; Muzzoli, M.; Scaglianti, M.; Manfredini, S.; Radice, M.; Bruni, R. Comparative evaluation of 11 essential oils of different origin as functional antioxidants, antiradicals and antimicrobials in foods. Food Chem. 2005, 91, 621–632. [Google Scholar] [CrossRef]
  26. Teixeira, B.; Marques, A.; Ramos, C.; Batista, I.; Serrano, C.; Matos, O.; Neng, N.R.; Nogueira, J.M.; Saraiva, J.A.; Nunes, M.L. European pennyroyal (Mentha pulegium) from Portugal: Chemical composition of essential oil and antioxidant and antimicrobial properties of extracts and essential oil. Ind. Crops Prod. 2012, 36, 81–87. [Google Scholar] [CrossRef]
  27. Roby, M.H.H.; Sarhan, M.A.; Selim, K.A.-H.; Khalel, K.I. Evaluation of antioxidant activity, total phenols and phenolic compounds in thyme (Thymus vulgaris L.), sage (Salvia officinalis L.), and marjoram (Origanum majorana L.) extracts. Ind. Crops Prod. 2013, 43, 827–831. [Google Scholar] [CrossRef]
  28. Holley, R.A.; Patel, D. Improvement in shelf-life and safety of perishable foods by plant essential oils and smoke antimicrobials. Food Microbiol. 2005, 22, 273–292. [Google Scholar] [CrossRef]
  29. Bakkali, F.; Averbeck, S.; Averbeck, D.; Idaomar, M. Biological effects of essential oils–a review. Food Chem. Toxicol. 2008, 46, 446–475. [Google Scholar] [CrossRef]
  30. Zheljazkov, V.D.; Jeliazkova, E.A.; Astatkie, T. Allelopathic Effects of Essential Oils on Seed Germination of Barley and Wheat. Plants 2021, 10, 2728. [Google Scholar] [CrossRef]
  31. Carraminana, J.; Rota, C.; Burillo, J.; Herrera, A. Antibacterial efficiency of Spanish Satureja montana essential oil against Listeria monocytogenes among natural flora in minced pork. J. Food Protect. 2008, 71, 502–508. [Google Scholar] [CrossRef]
  32. Oral, N.; Guelmez, M.; Vatansever, L.; ABAMÜSLüM, G. Application of antimicrobial ice for extending shelf life of fish. J. Food Protect. 2008, 71, 218–222. [Google Scholar] [CrossRef]
  33. Vazirian, M.; Kashani, S.T.; Ardekani, M.R.S.; Khanavi, M.; Jamalifar, H.; Fazeli, M.R.; Toosi, A.N. Antimicrobial activity of lemongrass (Cymbopogon citratus (DC) Stapf.) essential oil against food-borne pathogens added to cream-filled cakes and pastries. J. Essent. Oil Res. 2012, 24, 579–582. [Google Scholar] [CrossRef]
  34. Keskin, D.; Güvensen, N. Investigation of antimicrobial properties and chemical composition of different extracts of Sweet gum leaves (Liquidambar orientalis). Int. J. Agric. Environ. Food Sci. 2022, 6, 13–18. [Google Scholar] [CrossRef]
  35. Jafari-Sales, A.; Hossein-Nezhad, P.; Bolouri, P. Identification of chemical composition of essential oil and evaluation of antimicrobial effects of ethanolic extract of Mentha pulegium on Staphylococcus aureus and Escherichia coli. Health Biotechnol. Biopharma 2019, 3, 29–38. [Google Scholar]
  36. Khalil, R.; Li, Z.-G. Antimicrobial activity of essential oil of Salvia officinalis L. collected in Syria. Afr. J. Biotechnol. 2011, 10, 8397–8402. [Google Scholar]
  37. Zheljazkov, V.D.; Semerdjieva, I.; Yankova-Tsvetkova, E.; Astatkie, T.; Stanev, S.; Dincheva, I.; Kačániová, M. Chemical Profile and Antimicrobial Activity of the Essential Oils of Helichrysum arenarium (L.) Moench. and Helichrysum italicum (Roth.) G. Don. Plants 2022, 11, 951. [Google Scholar] [CrossRef]
  38. Kebede, B.H.; Forsido, S.F.; Tola, Y.B.; Astatkie, T. Free radical scavenging capacity, antibacterial activity and essential oil composition of turmeric (Curcuma domestica) varieties grown in Ethiopia. Heliyon 2021, 7, e06239. [Google Scholar] [CrossRef]
  39. Semerdjieva, I.B.; Radoukova, T.; Cantrell, C.L.; Astatkie, T.; Kacaniova, M.; Borisova, D.; Zheljazkov, V.D. Essential oil composition of Pinus heldreichii Christ., P. peuce Griseb., and P. mugo Turra as a function of hydrodistillation time and evaluation of its antimicrobial activity. Ind. Crops Prod. 2022, 187, 115484. [Google Scholar] [CrossRef]
  40. Davidson, P.M. Chemical preservatives and natural antimicrobial compounds. In Food Microbiology: Fundamentals and Frontiers; Doyle, M.P., Beuchat, L.R., Montville, T.J., Eds.; ASM Press: Washington, DC, USA, 1997; pp. 520–556. [Google Scholar]
  41. Da Silva Dannenberg, G.; Funck, G.D.; Mattei, F.J.; da Silva, W.P.; Fiorentini, Â.M. Antimicrobial and antioxidant activity of essential oil from pink pepper tree (Schinus terebinthifolius Raddi) in vitro and in cheese experimentally contaminated with Listeria monocytogenes. Innov. Food Sci. Emerg. Technol. 2016, 36, 120–127. [Google Scholar] [CrossRef]
  42. Xie, Q.; Liu, G.; Zhang, Y.; Yu, J.; Wang, Y.; Ma, X. Active edible films with plant extracts: A updated review of their types, preparations, reinforcing properties, and applications in muscle foods packaging and preservation. Crit. Rev. Food Sci. Nutr. 2022, 1–23. [Google Scholar] [CrossRef]
  43. Negi, P.S. Plant extracts for the control of bacterial growth: Efficacy, stability and safety issues for food application. Int. J. Food Microbiol. 2012, 156, 7–17. [Google Scholar] [CrossRef]
  44. Gassara, F.; Kouassi, A.P.; Brar, S.K.; Belkacemi, K. Green alternatives to nitrates and nitrites in meat-based products—A review. Crit. Rev. Food Sci. Nutr. 2016, 56, 2133–2148. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Tiwari, B.K.; Valdramidis, V.P.; O’Donnell, C.P.; Muthukumarappan, K.; Bourke, P.; Cullen, P. Application of natural antimicrobials for food preservation. J. Agric. Food Chem. 2009, 57, 5987–6000. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Ota, A.; Ulrih, N.P. An overview of herbal products and secondary metabolites used for management of type two diabetes. Front. Pharmacol. 2017, 8, 436. [Google Scholar] [CrossRef] [Green Version]
  47. Perricone, M.; Arace, E.; Corbo, M.R.; Sinigaglia, M.; Bevilacqua, A. Bioactivity of essential oils: A review on their interaction with food components. Front. Microbiol. 2015, 6, 76. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  48. Prakash, B.; Kedia, A.; Mishra, P.K.; Dubey, N. Plant essential oils as food preservatives to control moulds, mycotoxin contamination and oxidative deterioration of agri-food commodities–Potentials and challenges. Food Control 2015, 47, 381–391. [Google Scholar] [CrossRef]
  49. Edeoga, H.O.; Okwu, D.; Mbaebie, B. Phytochemical constituents of some Nigerian medicinal plants. Afr. J. Biotechnol. 2005, 4, 685–688. [Google Scholar] [CrossRef] [Green Version]
  50. Domínguez, R.; Pateiro, M.; Gagaoua, M.; Barba, F.J.; Zhang, W.; Lorenzo, J.M. A comprehensive review on lipid oxidation in meat and meat products. Antioxidants 2019, 8, 429. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  51. Falowo, A.B.; Mukumbo, F.E.; Idamokoro, E.M.; Lorenzo, J.M.; Afolayan, A.J.; Muchenje, V. Multi-functional application of Moringa oleifera Lam. in nutrition and animal food products: A review. Food Res. Int. 2018, 106, 317–334. [Google Scholar] [CrossRef]
  52. Oswell, N.J.; Thippareddi, H.; Pegg, R.B. Practical use of natural antioxidants in meat products in the US: A review. Meat Sci. 2018, 145, 469–479. [Google Scholar] [CrossRef]
  53. Praveena, B.; Pradeep, S.N. Antioxidant and antibacterial activities in the leaf extracts of Indian borage (Plectranthus amboinicus). Food Nutr. Sci. 2012, 3, 146–152. [Google Scholar]
  54. Tang, X.; Cronin, D.A. The effects of brined onion extracts on lipid oxidation and sensory quality in refrigerated cooked turkey breast rolls during storage. Food Chem. 2007, 100, 712–718. [Google Scholar] [CrossRef]
  55. Tiruppur Venkatachallam, S.K.; Pattekhan, H.; Divakar, S.; Kadimi, U.S. Chemical composition of Nigella sativa L. seed extracts obtained by supercritical carbon dioxide. J. Food Sci. Technol. 2010, 47, 598–605. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  56. Horníčková, J.; Velíšek, J.; Ovesna, J.; Stavělíková, H. Distribution of S-alk (en) yl-L-cysteine sulfoxides in garlic (Allium sativum L.). Czech J. Food Sci. 2009, 27, S232–S235. [Google Scholar] [CrossRef] [Green Version]
  57. Negi, P.; Jayaprakasha, G.; Jagan Mohan Rao, L.; Sakariah, K. Antibacterial activity of turmeric oil: A byproduct from curcumin manufacture. J. Agric. Food Chem. 1999, 47, 4297–4300. [Google Scholar] [CrossRef] [PubMed]
  58. Jayawardana, B.C.; Warnasooriya, V.B.; Thotawattage, G.; Dharmasena, V.; Liyanage, R. Black and green tea (Camellia sinensis L.) extracts as natural antioxidants in uncured pork sausages. J. Food Process. Preserv. 2019, 43, e13870. [Google Scholar] [CrossRef]
  59. Lin, M.; Zhang, J.; Chen, X. Bioactive flavonoids in Moringa oleifera and their health-promoting properties. J. Funct. Foods 2018, 47, 469–479. [Google Scholar] [CrossRef]
  60. Alirezalu, K.; Hesari, J.; Nemati, Z.; Munekata, P.E.; Barba, F.J.; Lorenzo, J.M. Combined effect of natural antioxidants and antimicrobial compounds during refrigerated storage of nitrite-free frankfurter-type sausage. Food Res. Int. 2019, 120, 839–850. [Google Scholar] [CrossRef]
  61. Lorenzo, J.M.; Pateiro, M.; Domínguez, R.; Barba, F.J.; Putnik, P.; Kovačević, D.B.; Shpigelman, A.; Granato, D.; Franco, D. Berries extracts as natural antioxidants in meat products: A review. Food Res. Int. 2018, 106, 1095–1104. [Google Scholar] [CrossRef]
  62. Heck, R.T.; Saldaña, E.; Lorenzo, J.M.; Correa, L.P.; Fagundes, M.B.; Cichoski, A.J.; de Menezes, C.R.; Wagner, R.; Campagnol, P.C.B. Hydrogelled emulsion from chia and linseed oils: A promising strategy to produce low-fat burgers with a healthier lipid profile. Meat Sci. 2019, 156, 174–182. [Google Scholar] [CrossRef]
  63. Domínguez, R.; Gullón, P.; Pateiro, M.; Munekata, P.; Zhang, W.; Lorenzo, J. Tomato as Potential Source of Natural Additives for Meat Industry. A Review. Antioxidants 2020, 9, 73. [Google Scholar] [CrossRef] [Green Version]
  64. Hu, L.; Yin, C.; Ma, S.; Liu, Z. Assessing the authenticity of black pepper using diffuse reflectance mid-infrared Fourier transform spectroscopy coupled with chemometrics. Comput. Electr. Agric. 2018, 154, 491–500. [Google Scholar] [CrossRef]
  65. Wang, Y.; Li, R.; Jiang, Z.-T.; Tan, J.; Tang, S.-H.; Li, T.-T.; Liang, L.-L.; He, H.-J.; Liu, Y.-M.; Li, J.-T. Green and solvent-free simultaneous ultrasonic-microwave assisted extraction of essential oil from white and black peppers. Ind. Crops Prod. 2018, 114, 164–172. [Google Scholar] [CrossRef]
  66. Drabova, L.; Alvarez-Rivera, G.; Suchanova, M.; Schusterova, D.; Pulkrabova, J.; Tomaniova, M.; Kocourek, V.; Chevallier, O.; Elliott, C.; Hajslova, J. Food fraud in oregano: Pesticide residues as adulteration markers. Food Chem. 2019, 276, 726–734. [Google Scholar] [CrossRef] [PubMed]
  67. Fernandes, R.; Trindade, M.; Tonin, F.; Pugine, S.; Lima, C.; Lorenzo, J.; De Melo, M. Evaluation of oxidative stability of lamb burger with Origanum vulgare extract. Food Chem. 2017, 233, 101–109. [Google Scholar] [CrossRef] [PubMed]
  68. Barbalho, S.M.; Bosso, H.; Salzedas-Pescinini, L.M.; de Alvares Goulart, R. Green tea: A possibility in the therapeutic approach of inflammatory bowel diseases?: Green tea and inflammatory bowel diseases. Complement. Ther. Med. 2019, 43, 148–153. [Google Scholar] [CrossRef]
  69. Ghorbani, A.; Esmaeilizadeh, M. Pharmacological properties of Salvia officinalis and its components. J. Tradit. Complement. Med. 2017, 7, 433–440. [Google Scholar] [CrossRef]
  70. Vosoughi, N.; Gomarian, M.; Pirbalouti, A.G.; Khaghani, S.; Malekpoor, F. Essential oil composition and total phenolic, flavonoid contents, and antioxidant activity of sage (Salvia officinalis L.) extract under chitosan application and irrigation frequencies. Ind. Crops Prod. 2018, 117, 366–374. [Google Scholar] [CrossRef]
  71. de Souza, C.E.S.; da Silva, A.R.P.; Rocha, J.E.; Gomez, M.C.V.; Rolóm, M.; Coronel, C.; da Costa, J.G.M.; Netto, M.L.; Rolim, L.A.; Coutinho, H.D.M. LC–MS characterization, anti-kinetoplastide and cytotoxic activities of natural products from Eugenia jambolana Lam. and Eugenia uniflora. Asian Pac. J. Trop. Biomed. 2017, 7, 836–841. [Google Scholar] [CrossRef]
  72. Marques, L.L.M.; Ferreira, E.D.F.; de Paula, M.N.; Klein, T.; de Mello, J.C.P. Paullinia cupana: A multipurpose plant—A review. Rev. Bras. Farmacogn. 2019, 29, 77–110. [Google Scholar] [CrossRef]
  73. Pateiro, M.; Barba, F.J.; Domínguez, R.; Sant’Ana, A.S.; Khaneghah, A.M.; Gavahian, M.; Gómez, B.; Lorenzo, J.M. Essential oils as natural additives to prevent oxidation reactions in meat and meat products: A review. Food Res. Int. 2018, 113, 156–166. [Google Scholar] [CrossRef]
  74. Zhang, J.; Wang, Y.; Pan, D.-D.; Cao, J.-X.; Shao, X.-F.; Chen, Y.-J.; Sun, Y.-Y.; Ou, C.-R. Effect of black pepper essential oil on the quality of fresh pork during storage. Meat Sci. 2016, 117, 130–136. [Google Scholar] [CrossRef] [PubMed]
  75. de Carvalho, F.A.L.; Lorenzo, J.M.; Pateiro, M.; Bermúdez, R.; Purriños, L.; Trindade, M.A. Effect of guarana (Paullinia cupana) seed and pitanga (Eugenia uniflora L.) leaf extracts on lamb burgers with fat replacement by chia oil emulsion during shelf life storage at 2 °C. Food Res. Int. 2019, 125, 108554. [Google Scholar] [CrossRef] [PubMed]
  76. Domínguez, R.; Barba, F.J.; Gómez, B.; Putnik, P.; Kovačević, D.B.; Pateiro, M.; Santos, E.M.; Lorenzo, J.M. Active packaging films with natural antioxidants to be used in meat industry: A review. Food Res. Int. 2018, 113, 93–101. [Google Scholar] [CrossRef]
  77. Šojić, B.; Pavlić, B.; Zeković, Z.; Tomović, V.; Ikonić, P.; Kocić-Tanackov, S.; Džinić, N. The effect of essential oil and extract from sage (Salvia officinalis L.) herbal dust (food industry by-product) on the oxidative and microbiological stability of fresh pork sausages. LWT 2018, 89, 749–755. [Google Scholar] [CrossRef]
  78. Ramírez-Rojo, M.I.; Vargas-Sánchez, R.D.; Torres-Martínez, B.d.M.; Torrescano-Urrutia, G.R.; Lorenzo, J.M.; Sánchez-Escalante, A. Inclusion of ethanol extract of mesquite leaves to enhance the oxidative stability of pork patties. Foods 2019, 8, 631. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  79. Elgayyar, M.; Draughton, F. Use of extracts of Nigella sativa to inhibit spoilage and pathogenic microorganisms in rainbow trout. In Proceedings of the Annual Meeting of International Association of Milk, Food and Environmental Sanitarians, Detroit, MI, USA, 1–4 August 1999. [Google Scholar]
  80. Lee, S.-Y.; Gwon, S.-Y.; Kim, S.-J.; Moon, B.K. Inhibitory effect of commercial green tea and rosemary leaf powders on the growth of foodborne pathogens in laboratory media and oriental-style rice cakes. J. Food Protect. 2009, 72, 1107–1111. [Google Scholar] [CrossRef] [PubMed]
  81. Meng, F.; Zhou, Y.; Ren, D.; Wang, R. Turmeric: A review of its chemical composition, quality control, bioactivity, and pharmaceutical application. In Natural and Artificial Flavoring Agents and Food Dyes; Grumezescu, A.M., Holban, A.M., Eds.; Elsevier Inc.: London, UK, 2018; pp. 299–350. [Google Scholar]
  82. Pezeshk, S.; Rezaei, M.; Hosseini, H. Effects of turmeric, shallot extracts, and their combination on quality characteristics of vacuum-packaged rainbow trout stored at 4 ± 1 °C. J. Food Sci. 2011, 76, M387–M391. [Google Scholar] [CrossRef]
  83. Madane, P.; Das, A.K.; Pateiro, M.; Nanda, P.K.; Bandyopadhyay, S.; Jagtap, P.; Barba, F.J.; Shewalkar, A.; Maity, B.; Lorenzo, J.M. Drumstick (Moringa oleifera) flower as an antioxidant dietary fibre in chicken meat nuggets. Foods 2019, 8, 307. [Google Scholar] [CrossRef] [Green Version]
  84. Zanetti, M.; Carniel, T.K.; Dalcanton, F.; dos Anjos, R.S.; Riella, H.G.; de Araújo, P.H.; de Oliveira, D.; Fiori, M.A. Use of encapsulated natural compounds as antimicrobial additives in food packaging: A brief review. Trends Food Sci. Technol. 2018, 81, 51–60. [Google Scholar] [CrossRef]
  85. Bora, A.F.M.; Ma, S.; Li, X.; Liu, L. Application of microencapsulation for the safe delivery of green tea polyphenols in food systems: Review and recent advances. Food Res. Int. 2018, 105, 241–249. [Google Scholar] [CrossRef]
  86. Pateiro, M.; Domínguez, R.; Bermúdez, R.; Munekata, P.E.; Zhang, W.; Gagaoua, M.; Lorenzo, J.M. Antioxidant active packaging systems to extend the shelf life of sliced cooked ham. Curr. Res. Food Sci. 2019, 1, 24–30. [Google Scholar] [CrossRef] [PubMed]
  87. Antunes, M.D.C.; Cavaco, A.M. The use of essential oils for postharvest decay control. A review. Flavour Fragr. J. 2010, 25, 351–366. [Google Scholar] [CrossRef]
  88. Isman, M.B.; Singh, B. Botanical Insecticides, Deterrents, Repellents and Oils; CABI: Oxfordsh, UK, 2010; pp. 433–445. [Google Scholar]
  89. Godlewska, K.; Ronga, D.; Michalak, I. Plant extracts-importance in sustainable agriculture. Ital. J. Agron. 2021, 16, 1851. [Google Scholar] [CrossRef]
  90. Semerdjieva, I.; Zheljazkov, V.D.; Radoukova, T.; Dincheva, I.; Piperkova, N.; Maneva, V.; Astatkie, T.; Kačániová, M. Biological Activity of Essential Oils of Four Juniper Species and Their Potential as Biopesticides. Molecules 2021, 26, 6358. [Google Scholar] [CrossRef]
  91. Dosoky, N.S.; Setzer, W.N. Chemical composition and biological activities of essential oils of Curcuma species. Nutrients 2018, 10, 1196. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  92. Eller, F.; Clausen, C.A.; Green, F.; Taylor, S. Critical fluid extraction of Juniperus virginiana L. and bioactivity of extracts against subterranean termites and wood-rot fungi. Ind. Crops Prod. 2010, 32, 481–485. [Google Scholar] [CrossRef]
  93. Eller, F.; Vander Meer, R.; Behle, R.; Flor-Weiler, L.; Palmquist, D.E. Bioactivity of cedarwood oil and cedrol against arthropod pests. Environ. Entomol. 2014, 43, 762–766. [Google Scholar] [CrossRef]
  94. Yohana, R.; Chisulumi, P.S.; Kidima, W.; Tahghighi, A.; Maleki-Ravasan, N.; Kweka, E.J. Anti-mosquito properties of Pelargonium roseum (Geraniaceae) and Juniperus virginiana (Cupressaceae) essential oils against dominant malaria vectors in Africa. Malar. J. 2022, 21, 219. [Google Scholar] [CrossRef]
  95. Semerdjieva, I.B.; Zheljazkov, V.; Cantrell, C.L.; Astatkie, T.; Ali, A. Essential oil yield and composition of the Balkan endemic Satureja pilosa Velen.(Lamiaceae). Molecules 2020, 25, 827. [Google Scholar] [CrossRef] [Green Version]
  96. Semerdjieva, I.; Atanasova, D.; Maneva, V.; Zheljazkov, V.; Radoukova, T.; Astatkie, T.; Dincheva, I. Allelopathic effects of Juniper essential oils on seed germination and seedling growth of some weed seeds. Ind. Crops Prod. 2022, 180, 114768. [Google Scholar] [CrossRef]
  97. Hierro, J.L.; Callaway, R.M. The ecological importance of allelopathy. Annu. Rev. Ecol. Evol. Syst. 2021, 52, 25–45. [Google Scholar] [CrossRef]
  98. Nonogaki, M.; Nonogaki, H. Prevention of preharvest sprouting through hormone engineering and germination recovery by chemical biology. Front. Plant Sci. 2017, 8, 90. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  99. Mares, D.J.; Mrva, K. Wheat grain preharvest sprouting and late maturity alpha-amylase. Planta 2014, 240, 1167–1178. [Google Scholar] [CrossRef] [PubMed]
  100. Yousefzadi, M.; Ebrahimi, S.N.; Sonboli, A.; Miraghasi, F.; Ghiasi, S.; Arman, M.; Mosaffa, N. Cytotoxicity, antimicrobial activity and composition of essential oil from Tanacetum balsamita L. subsp. balsamita. Nat. Prod. Commun. 2009, 4, 119–122. [Google Scholar] [CrossRef] [Green Version]
  101. Mancini, E.; Senatore, F.; Del Monte, D.; De Martino, L.; Grulova, D.; Scognamiglio, M.; Snoussi, M.; De Feo, V. Studies on chemical composition, antimicrobial and antioxidant activities of five Thymus vulgaris L. essential oils. Molecules 2015, 20, 12016–12028. [Google Scholar] [CrossRef] [Green Version]
  102. Felsociova, S.; Kacaniova, M.; Horská, E.; Vukovic, N.; Hleba, L.; Petrová, J.; Rovná, K.; Stricik, M.; Hajduová, Z. Antifungal activity of essential oils against selected terverticillate penicillia. Ann. Agric. Environ. Med. 2015, 22, 38–42. [Google Scholar] [CrossRef]
  103. Semerdjieva, I.B.; Zheljazkov, V.D.; Dincheva, I.; Astatkie, T.; Kačániová, M. Chemotypes of Juniperus oxycedrus in Bulgaria and the antimicrobial activity of galbuli essential oils. Ind. Crops Prod. 2020, 158, 113005. [Google Scholar] [CrossRef]
  104. Stangarlin, J.; Kuhn, O.; Assi, L.; Schwan-Estrada, K. Control of plant diseases using extracts from medicinal plants and fungi. Sci. Microb. Pathog. Commun. Curr. Res. Technol. Adv. 2011, 2, 1033–1042. [Google Scholar]
  105. Rodrigues, E.; Schwan-Estrada, K.R.F.; Fiori-Tutida, A.C.G.; Stangarlin, J.R.; Cruz, M.E.S. Fungitoxicidade, atividade elicitora de fitoalexinas e proteção de alface em sistema de cultivo orgânico contra Sclerotinia sclerotiorum pelo extrato de gengibre. Summa Phytopathol. 2007, 33, 124–128. [Google Scholar] [CrossRef]
  106. Franzener, G.; Martinez-Franzener, A.; Stangarlin, J.; Furlanetto, C.; Schwan-Estrada, K. Protection of tomato plants by Tagetes patula aqueous extract against Meloidogyne incognita. Nematol. Bras. 2007, 31, 27–36. [Google Scholar]
  107. Bolandnazar, A.; Ghadamyari, M.; Memarzadeh, M.; Sandi, J. Effect of some micro and nanoemulsified essential oils and plant extract on sweet potato whitefly, Bemisia tabaci (Gennadius), under laboratory condition. Plant Pest Res. 2017, 7, 23–37. [Google Scholar]
  108. Zaker, M.; Mosallanejad, H. Antifungal activity of some plant extracts on Alternaria alternata, the causal agent of alternaria leaf spot of potato. Pak. J. Biol. Sci. 2010, 13, 1023–1029. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  109. Behdani, M.; Pooyan, M.; Abbasi, S. Evaluation of antifungal activity of some medicinal plants essential oils against Botrytis cinerea, causal agent of postharvest apple rot, in vitro. Int. J. Agric. Crop Sci. 2012, 4, 1012–1016. [Google Scholar]
  110. Zheljazkov, V.D.; Kacaniova, M.; Dincheva, I.; Radoukova, T.; Semerdjieva, I.B.; Astatkie, T.; Schlegel, V. Essential oil composition, antioxidant and antimicrobial activity of the galbuli of six juniper species. Ind. Crops Prod. 2018, 124, 449–458. [Google Scholar] [CrossRef]
  111. Foroughi, A. A review on medicinal plants; An emphasis on antimicrobial effects. Vet. Res. Biol. Prod. 2022, 35, 2–17. [Google Scholar]
  112. Chen, W.; Vermaak, I.; Viljoen, A. Camphor—A fumigant during the black death and a coveted fragrant wood in ancient Egypt and Babylon—A review. Molecules 2013, 18, 5434–5454. [Google Scholar] [CrossRef] [Green Version]
  113. Zheljazkov, V.D.; Cantrell, C.L.; Jeliazkova, E.A.; Astatkie, T.; Schlegel, V. Essential Oil Yield, Composition, and Bioactivity of Sagebrush Species in the Bighorn Mountains. Plants 2022, 11, 1228. [Google Scholar] [CrossRef]
  114. Mahesh, S.K.; Fathima, J.; Veena, V.G. Cosmetic potential of natural products: Industrial applications. In Natural Bio-Active Compounds; Springer: Singapore, 2019; pp. 215–250. [Google Scholar]
  115. Guzmán, E.; Lucia, A. Essential oils and their individual components in cosmetic products. Cosmetics 2021, 8, 114. [Google Scholar] [CrossRef]
  116. Abelan, U.S.; de Oliveira, A.C.; Cacoci, É.S.P.; Martins, T.E.A.; Giacon, V.M.; Velasco, M.V.R.; Lima, C.R.R.d.C. Potential use of essential oils in cosmetic and dermatological hair products: A review. J. Cosmet. Dermatol. 2022, 21, 1407–1418. [Google Scholar] [CrossRef]
  117. Benson, H.A.; Roberts, M.S.; Leite-Silva, V.R.; Walters, K. Cosmetic Formulation: Principles and Practice; CRC Press: Boca Raton, FL, USA, 2019. [Google Scholar]
  118. Oh, J.Y.; Park, M.A.; Kim, Y.C. Peppermint oil promotes hair growth without toxic signs. Toxicol. Res. 2014, 30, 297–304. [Google Scholar] [CrossRef] [Green Version]
  119. Lertsatitthanakorn, P.; Taweechaisupapong, S.; Aromdee, C.; Khunkitti, W. In vitro bioactivities of essential oils used for acne control. Int. J. Aromather. 2006, 16, 43–49. [Google Scholar] [CrossRef]
  120. Lohani, A.; Mishra, A.K.; Verma, A. Cosmeceutical potential of geranium and calendula essential oil: Determination of antioxidant activity and in vitro sun protection factor. J. Cosmet. Dermatol. 2019, 18, 550–557. [Google Scholar] [CrossRef] [PubMed]
  121. Mishra, A.; Mishra, A.; Chattopadhyay, P. Assessment of in vitro sun protection factor of Calendula officinalis L.(asteraceae) essential oil formulation. J. Young Pharm. 2012, 4, 17–21. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  122. Varvaresou, A.; Papageorgiou, S.; Tsirivas, E.; Protopapa, E.; Kintziou, H.; Kefala, V.; Demetzos, C. Self-preserving cosmetics. Int. J. Cosmet. Sci. 2009, 31, 163–175. [Google Scholar] [CrossRef] [PubMed]
  123. Mohamed, H.F.; Mahmoud, A.A.; Alatawi, A.; Hegazy, M.H.; Astatkie, T.; Ahl, S.-A.; Hussein, A. Growth and essential oil responses of Nepeta species to potassium humate and harvest time. Acta Physiol. Plant. 2018, 40, 204. [Google Scholar] [CrossRef]
  124. Herman, A.; Herman, A.P.; Domagalska, B.W.; Młynarczyk, A. Essential oils and herbal extracts as antimicrobial agents in cosmetic emulsion. Indian J. Microbiol. 2013, 53, 232–237. [Google Scholar] [CrossRef] [Green Version]
  125. Shamlou, M.; Yavarmanesh, M. Evaluation of the antibacterial effects of aqueous and ethanolic extracts of Aloe Vera on pathogenic bacteria (Staphylococcus aureus, Escherichia coli, Listeria monocytogenes). FSCT 2015, 13, 149–159. [Google Scholar]
  126. Zheljazkov, V.D.; Sikora, V.; Dincheva, I.; Kačániová, M.; Astatkie, T.; Semerdjieva, I.B.; Latkovic, D. Industrial, CBD, and wild hemp: How different are their essential oil profile and antimicrobial activity? Molecules 2020, 25, 4631. [Google Scholar] [CrossRef]
  127. Zheljazkov, V.D.; Sikora, V.; Semerdjieva, I.B.; Kačániová, M.; Astatkie, T.; Dincheva, I. Grinding and fractionation during distillation alter hemp essential oil profile and its antimicrobial activity. Molecules 2020, 25, 3943. [Google Scholar] [CrossRef]
  128. Majd, A.; Mehrabian, S.; Jafari, Z. The study of Antimicrobial effects of urtica dioica’s extract. Iran. J. Med. Arom. Plan. 2003, 19, 286–312. [Google Scholar]
  129. Jafari-Sales, A.; Bolouri, P. Evaluation of the antimicrobial effects of Glycyrrhiza glabra l. on some gram positive and gram negative pathogenic bacteria in laboratory conditions. Jorjani Biomed. J. 2018, 6, 78–84. [Google Scholar] [CrossRef]
Figure 1. Classification of the active ingredients of medicinal plants (modified from Sidhu [10]).
Figure 1. Classification of the active ingredients of medicinal plants (modified from Sidhu [10]).
Molecules 27 08999 g001
Figure 2. Various types of the mechanisms of the activities of EOs on microorganisms.
Figure 2. Various types of the mechanisms of the activities of EOs on microorganisms.
Molecules 27 08999 g002
Table 1. EOs and plant extracts with antimicrobial properties that are used in the food industry.
Table 1. EOs and plant extracts with antimicrobial properties that are used in the food industry.
The Scientific Name Effective Compounds in%MicroorganismsReference
Lavandula angustifolia47% linalool acetate, 28.4% linaloolAeromonas caviae
Pseudomonas aeruginosa
Salmonella enterica
[30]
Origanumvulgare38.2% para-cymene, 25.6% thymol, and 13.6% γ-terpinene)Clostridium botulinum spores[30]
Salviarosmarinuslimonene (6.23),
camphene (6.0), and
linalool (5.7)
Listeria monocytogenes[31]
Thymusserpyllumcarvacrol (0.2–0.6)Salmonella enteritidis
Salmonella typhimurium, Escherichia coli serovar
Yersinia enterocolitica serotype
[32]
Cymbopogoncitratusgeranial (33.3), limonene (5.8), and geranyl
acetate
Staphylococcus aureus, Escherichia coli, Candida albicans, Bacillus cereus and Salmonella
typhimurium
[33]
Eucalyptuscamaldulensiscineole (eucalyptol)
(80–90)
Listeria monocytogenes, Staphylococcus aureus,
Bacillus cereus, Salmonella typhimurium, and Esherichia coli
[34]
MenthapulegiumMentha, 1,8-cineoleStaphylococcus aureus and Escherichia coli[35]
Salviaofficinalisα, β-tuyon, 1,8-sineol, kamforStaphylococcus aureus and Streptococcus, Candida
albicans
[36]
Helichrysumitalicum1,8-cineole, α-copaene, (E)-β-ionone, γ-
cadinene, selina-3,7(11)-diene, epi-α-cadinol,
α-cadinol, octadecane, isophytol and tricosane
Staphylococcus aureus, Bacillus subtilis, Aspergillus brasiliensis,[37]
Curcuma longaα-Turmerone (35.16),
ar-Turmerone (25.47), and Curlone (18.19)
S. aureus[38]
Juniperusoxycedrusα-pinene, limonene, α-curcumene, γ-cadinene, δ-cadinene, manoyl
oxidearyophyllene, α-caryophyllene,
caryophyllene oxide
Yersinia enterocolitica, Staphylococcus aureus subsp. aureus, Enterococcus faecalis, Streptococcusp neumoniae, Candida kruseii, and C. tropicalis.[39]
Table 3. List of uses of plant extracts as natural antioxidants in meat and meat products.
Table 3. List of uses of plant extracts as natural antioxidants in meat and meat products.
Herbal Essential OilTarget ProductAmount ConsumedTime and
Conditions of
Storage
ResultReference
Black pepperFresh meat0.1–0.5%9 days at 4 °C B and C[61]
Guarana seedLamb burger250 mg/kg18 days at 2 °CB and C[76]
Mesquite leafMinced meat0.1–0.05%10 days at 4 °C A and C[73]
Moringa Chicken nuggets1–2%20 days at 4 °CA, C and D[75]
Green teaChopped cooked ham1%21 days at 2 °CC[77]
OreganoLamb burger13.32, 17.79, 24.01
mL/kg
120 days at 18 °CA and C[67]
Chopped cooked ham1% D[77]
A = lipid oxidation reduction; B = lipoprotein oxidation reduction; C = reduction of color oxidation; D = decrease sensory degradation.
Table 4. Some medicinal plants with anti-pathogenic properties that are used in the agricultural industry.
Table 4. Some medicinal plants with anti-pathogenic properties that are used in the agricultural industry.
Scientific Name of the PlantCompounds Pathogen NameReference
Artemisia persicaArtemisininCochliobolussativus[104]
Zingiber officinaleGingerburn and oleoresinSclerotinia sclerotiorum[105]
Tagetes patulaQuercetagetin; quercetin;
patuletin; quercetin-3-glucoside
Meloidogyne incognita[106]
Thymus vulgarisThymol and carvacrolBemisia tabaci[107]
Erwinia Amylovora
Lavandula angustifolialinalol, linalil Alternaria alternate[108]
Pimpinella anisumAnetol Aspergillus flavus, Phoma sorghina, Alternaria alternata, Botrytis cinerea[109]
Nigella sativaCarvon
Juniper galbulidβ-Elemene, γ-Elemene,
and τ-Muurolol
lostridium perfringens, Juniperuscommunis against Candida clabrata, and Juniperus oxycedrus against
Staphylococcus aureus
[110]
Table 5. Some medicinal plants used in the cosmetic industry.
Table 5. Some medicinal plants used in the cosmetic industry.
Scientific Name of the PlantCompounds in%FunctionReference
Matricaria chamomillaCamazolin, alpha bisabololAs natural cosmetic preservatives in cream[124]
Calendula officinalisFlavonol glycoside and beta-carotene (30–40)
Lavandulla officinallislinalol (35–55),
linalyl
Aloe veraAntrakinonlarAs natural cosmetic preservatives in cream[125]
Cannabis sativaCannabidiolSkin anti infections[126,127]
Urtica dioicaPolyphenolAs strong cleaning in shampoos[128]
Glycyrrhiza glabraGlycyrrhizinAnti-inflammatory of skin in cream[129]
Juniper galbuliβ-Elemene, γ-
Elemene,
τ-Muurolol
Anti-inflammatory of skin in cream[110]
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Bolouri, P.; Salami, R.; Kouhi, S.; Kordi, M.; Asgari Lajayer, B.; Hadian, J.; Astatkie, T. Applications of Essential Oils and Plant Extracts in Different Industries. Molecules 2022, 27, 8999. https://doi.org/10.3390/molecules27248999

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Bolouri P, Salami R, Kouhi S, Kordi M, Asgari Lajayer B, Hadian J, Astatkie T. Applications of Essential Oils and Plant Extracts in Different Industries. Molecules. 2022; 27(24):8999. https://doi.org/10.3390/molecules27248999

Chicago/Turabian Style

Bolouri, Parisa, Robab Salami, Shaghayegh Kouhi, Masoumeh Kordi, Behnam Asgari Lajayer, Javad Hadian, and Tess Astatkie. 2022. "Applications of Essential Oils and Plant Extracts in Different Industries" Molecules 27, no. 24: 8999. https://doi.org/10.3390/molecules27248999

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