Applications of Selected Nanoencapsulated Indigenous Essential Oils in Medicine, Food, and Agriculture: A Review
Abstract
1. Introduction
2. Materials and Methods
2.1. Literature Search Strategy
2.2. Selection Criteria
2.3. Data Extraction and Critical Analysis
2.4. Limitations
3. Indigenous Essential Oils of South Africa
| Extraction Method | Principle of Operation | Temperatures | Extraction Time | Yield | Selectivity for Bioactive Compounds | Industrial Scalability | Advantages | Disadvantages | References |
|---|---|---|---|---|---|---|---|---|---|
| Hydrodistillation | Plant material is heated in water to release volatile oils through vaporization and condensation. | 100 °C | 2–6 h | Moderate | Moderate | High | Simple setup; low operational cost; widely standardized for research | Prolonged extraction, heat-sensitive compounds will be subjected to thermal degradation | [46,47] |
| Cold pressing | Plant material is mechanically pressed without applying heat to release oils. | Ambient | Minutes to 1 h | Moderate | Low–Moderate | High (for citrus industry) | Preserves natural aroma profile; no thermal degradation | Oil may hold non-volatile residues, restricted mainly to citrus peels | [51] |
| Steam Distillation | Volatile compounds are vaporized by steam that passes through and then condensed. | 100–120 °C | 1–4 h | Moderate–High | Moderate | Very high | Widely used industrial method; produces relatively pure essential oils | Not suited for compounds with low heat tolerance, excessive power usage | [47,49] |
| Microwave-Assisted Extraction (MAE) | Rapid heat is caused by microwave radiation, resulting in bursting of plant cells and release of essential oils. | 50–120 °C | 10–30 min | High | High | Moderate | Rapid extraction; energy efficient; improved yield | Thermal degradation when temp is uncontrolled, equipment cost | [52] |
| Ultrasound-Assisted Extraction (UAE) | Ultrasonic waves cause cavitation, which disrupts the plant cell walls and improves solvent penetration. | 25–60 °C | 15–60 min | Moderate–High | High | Moderate | Reduced extraction time; improved mass transfer | Not easily scalable, solvent is required | [53,54] |
| Supercritical CO2 Extraction (SFE) | Bioactive and aromatic compounds are isolated by high-pressure carbon dioxide. | 35–60 °C | 30–120 min | High | Very high | Moderate | High purity extracts; no solvent residue; tunable selectivity | Equipment is very expensive, high operational pressure | [55,56] |
| Enzyme-Assisted Extraction (EAE) | The degradation of the cell wall by enzymes releases EOs found in plant tissues. | 30–50 °C | 1–24 h | High | High | Low-moderate | Environmentally friendly; improves release of intracellular compounds | High-priced enzymes, enzyme stability issues | [57,58] |
| Plant Species | Common Name | Family | Plant Part | Major Chemical Constituents | Traditional Uses | Biological Activities | Geographical Distribution | Conservation Status | References |
|---|---|---|---|---|---|---|---|---|---|
| Agathosma betulina (P.J.Bergius) Pillans | Buchu | Rutaceae | Leaves | sabinene, p-cymene, β-pinene, α-pinene, α-thujene, myrcene, limonene, linalool, and terpinen-4-ol. Sabinene | Antibiotic protectant, stomach, cleaning of wounds, kidney, and urinary tract diseases | Antimicrobial, anti-inflammatory | Western Cape | Declining | [47,61] |
| Artemisia afra | African wormwood | Asteraceae | Leaves | Rutin, acacetin, thujone, Artemisia ketone, 1.8-cineole, camphor | Coughs, colds, and malaria | Antimicrobial, anti-inflammatory, and antiparasitic | Gauteng, Limpopo, Eastern Cape, KwaZulu-Natal, and Western Cape | Least concern | [62,63] |
| Cymbopogon citratus | Lemon grass | Poaceae | Leaves and flowers | artemisia ketone, linalool, northujane, verbenone, naphthalene, d-cadinene, hedycaryol, and α- eudesmol | anti-rodent, vermifuge, emetic, anti- infective, and anti-plasmodic; treating morning sickness | Anti-inflammatory | Eastern Cape, Gauteng, KwaZulu-Natal, Limpopo, Mpumalanga, North West, Western Cape | Least concern | [64,65] |
| Helichrysum odoratissimum | imphepho (Xhosa and Zulu), kooigoed (Afrikaans), and phefo, towane (Sotho) | Asteraceae | Aerial parts of the plant | β-pinene, limonene, 1,8-cineole, α-humulene and β-caryophyllene | Treat coughs, colds, and fever. Spiritually, it is burned for cleansing and connecting with ancestors. | Antiseptic and anti-inflammatory | Limpopo, Mpumalanga, KwaZulu-Natal, Eastern Cape, Western Cape. | Least Concern | [66,67] |
| Leonotis leonurus | Wild dagga | Lamiaceae | Leaves | limonene, β-ocimene, γ-terpinene, β-caryophyllene, α-humulene, and germacrene D. | Headache, dysmenorrhea, stomach ache, epilepsy, rheumatic pain, spasms, nervous agitation, improvement of memory, hysteria, and depression | Antioxidant, antimicrobial, anticonvulsant, antidiabetic, and anti-inflammatory. | Eastern Cape, KwaZulu-Natal, Limpopo, Mpumalanga, Western Cape | Least concern | [68] |
| Lippia javanica | Lemon bush | Verbenaceae | Leaves, roots, stem, twigs | Myrcene, carvone, piperitenone, Ipsenone, Linalool, Limonene, Ocimenone, p-cymene, Sabinene, Tagetenone | Colds, wounds, insect repellent, bronchitis, skin disorders, and asthma | Anticancer, antidiabetic, antimalarial, antimicrobial, antioxidant | Eastern Cape, Free State, Gauteng, KwaZulu-Natal, Limpopo, Mpumalanga, North West. | Least concern, not threatened | [69,70] |
| Pelargonium graveolens | Rose geranium | Geraniaceae | Leaves | citronellol, geraniol, citronellyl formate, geranyl formate, iso-menthone, linalool, guaiadiene 6,9, and germacrene D | Diarrhea, urinary stones, liver problems, heavy menstrual flows, and is also helpful for detoxification | antiviral, astringent relaxant, analgesic, and anti-inflammatory | Eastern Cape, Limpopo, Mpumalanga, and Western Cape | Least concern. | [71] |
3.1. Lippia javanica

3.2. Pelargonium graveolens
3.3. Agathosma betulina

3.4. Cymbopogon citratus
3.5. Artemisia afra
3.6. Leonotis leonurus

3.7. Helichrysum odoratissimum

4. Nanoencapsulation Applications
4.1. Medicine
4.2. Food
4.3. Agriculture
4.4. Antimicrobial Resistance
5. Mechanism of Action
Toxicity of Nanocarriers
6. Challenges and Limitations
6.1. Socio-Economic and Production Challenges
6.2. Scientific Challenges
7. Conclusions and Recommendations
7.1. Conclusions
7.2. Recommendations
7.3. Future Studies
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
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| Plant Material | Plant Species | Method | Size | Encapsulation Efficiency (%) | Application | Reference |
|---|---|---|---|---|---|---|
| Plant oil | A. afra | Polymer-coated liposomes | 8.269 ± 0.796 µm | 18.7 | Medicine | [125] |
| Crude extract | C. citratus | CuO NPs | 55 nm | Not reported | Agriculture | [126] |
| Plant extract | C. citratus | Ag NPs | 47 nm | Not reported | Medicine | [127] |
| Plant extract | C. citratus | Ag NPs | ~35 nm | Not reported | Agriculture | [128] |
| Plant oil | C. citratus | Nanoemulsion | 10–100 nm | Not reported | Medicine | [129] |
| Plant oil | C. citratus | Liposome | 200 nm | Not reported | Medicine | [130] |
| Plant oil | Geranium | Alginate beads | Not reported | Not reported | Food | [131] |
| Plant extract | H. odoratissimum | ZnO NPs | 144.6 ± 2.60 nm | Not reported | Agriculture | [132] |
| Plant extract | L. leonurus | Nanostructured lipid carriers | 220 nm | Not reported | Medicine | [133] |
| Plant extract | L. leonurus | Chitosan nanoparticles | 31–65 nm | Not reported | Food | [134] |
| Plant oil | P. graveolens | chitosan-cinnamic acid nanogel | Not reported | 30.3 ± 1.77–38.4 ± 1.37% | Agriculture | [135] |
| Plant oil | P. graveolens | Nanoemulsion | 164 nm | Not reported | Medicine | [136] |
| Plant oil | P. graveolens | Nanoemulsion | 30.99 nm | Not reported | Agriculture | [137] |
| Plant oil | P. graveolens | Nanoemulsion | 553 nm | Not reported | Medicine | [138] |
| Plant oil | P. graveolens | Solid lipid nanoparticles | 50–170 nm | ̴ 74.93–93.46% | Agriculture | [139] |
| Plant oil | Pelargonium × ssp | chitosan microparticles | 2–3 μm | 35.2–58.5% | Medicine | [19] |
| Nanocarrier | Common Materials | Biotolerance | Major Toxicity Mechanisms | Advantages | Toxicity Concerns | Application | Reference |
|---|---|---|---|---|---|---|---|
| Liposomes | Phospholipids | Remarkably high | Harmless. Can trigger an immunological response in some cases. | Imitates biological membranes, biodegradable | Degradation, Lipid peroxidation | Essential oil encapsulation | [175,176] |
| Solid Lipid NPs | Nonpolar, hydrophobic lipids (Fatty acids, Triglycerides) | High | Surfactants can induce a cyclic cytotoxic reaction, e.g., lipid oxidation. | Stable, controlled release; low toxicity | Nucleation, limited encapsulation ability | Agriculture, pharmaceuticals and cosmetics | [177,178] |
| Nanostructured Lipid Carriers (NLCs) | Combination of solid and liquid lipids | High | Identical to SLNs; however, lower toxicity due to improved lipid structure | Stable, Improved encapsulation | Surfactants can cause irritation at high concentrations | Drug delivery, nutraceuticals | [179,180] |
| Polymeric NPs | Polyethylene glycol, Poly(lactic-co-glycolic acid), alginate, chitosan | Moderate-high (dependent on polymer) | Membrane disruption (cationic polymers) | Tunable properties | Cytotoxicity | Nanoencapsulation of EOs and drug delivery | [181] |
| Chitosan NPs | Chitosan | High | A strong positive charge can disrupt a membrane. | Antimicrobial, biodegradable | Possible cytotoxicity at high concentrations | Antimicrobial preparations and agriculture | [182,183] |
| Nanoemulsions | Oil, water, surfactants | High | Surfactant toxicity | Easy to prepare, efficient dissolution rate for hydrophobic substances | Concentration of surfactant determines stability | EO delivery, food, and cosmetics | [177,184,185] |
| Dendrimers | Poly(amidoamine), Polypropylene Imine (PPI) dendrimers | Moderate | The strong interaccumulation between a nanocarrier and a cell membrane or a cytotoxic surface group can lead to toxicity. | High encapsulation, controlled structure | Surface-dependent toxicity | Drug delivery and gene transfer | [178,179] |
| Metallic NPs | Ag, Au, ZnO | Low-moderate | DNA damage, ROS generation, and mitochondrial dysfunction. | Highly potent | Environmental residue, high cytotoxicity | Antibacterial coatings and sensors | [181] |
| Silica NPs | Mesoporous silica | Moderate | Tissue-level stress response, Oxidative stress. | Porous | Environmental persistent | Catalysts and drug delivery | [185,186] |
| Research Priority | Key Research Needs | Potential Impact for Food Systems |
|---|---|---|
| Clinical validation | Conduct preclinical and clinical studies to confirm safety, efficacy, and dosage of nanoencapsulated essential oils, particularly for antimicrobial and metabolic health applications | Scientific validation supporting nutraceutical and functional food development. |
| Toxicology and safety assessment | Evaluate nanotoxicity, long-term safety, and environmental impacts in food matrices, soil ecosystems, and aquatic environments. Develop standardized safety protocols | Safer application of nano-enabled preservatives and increased regulatory acceptance |
| Phytochemical standardization | Establish standardized extraction methods and perform detailed phytochemical profiling to identify active compounds and chemotypes | Consistent quality and reproducibility of essential oil-based ingredients |
| Food preservation and packaging | Develop nanoencapsulated EO-based preservatives and antimicrobial active packaging. Assess shelf-life extension and sensory impacts in real food matrices | Reduced food spoilage, improved shelf life, and natural alternatives to synthetic preservatives |
| Agricultural and Pest Management Applications | Develop nanoformulated essential oil-based biopesticides and evaluate their effectiveness within integrated pest management systems | Sustainable crop protection alternatives to synthetic agrochemicals. |
| Sustainable Cultivation and Conservation | Develop cultivation protocols for key species and investigate environmental influences on oil yield and chemical composition. Promote domestication of high-value aromatic plants. | Sustainable supply of essential oil resources and conservation of biodiversity |
| Regulatory and commercialization pathways | Develop regulatory guidelines, quality standards, and value chain models to support commercialization of EO-based nano-products. | Market-ready products, enhanced industry uptake, and rural economic development |
| Indigenous knowledge integration | Document traditional uses of aromatic plants and integrate ethnobotanical knowledge into scientific innovation frameworks | Ethical innovation and inclusive value chains benefiting local communities |
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© 2026 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.
Share and Cite
Wutu, O.S.; Mpambani, B.; Naidoo, C.M. Applications of Selected Nanoencapsulated Indigenous Essential Oils in Medicine, Food, and Agriculture: A Review. Foods 2026, 15, 1942. https://doi.org/10.3390/foods15111942
Wutu OS, Mpambani B, Naidoo CM. Applications of Selected Nanoencapsulated Indigenous Essential Oils in Medicine, Food, and Agriculture: A Review. Foods. 2026; 15(11):1942. https://doi.org/10.3390/foods15111942
Chicago/Turabian StyleWutu, Ongeziwe Sinazo, Babalwa Mpambani, and Clarissa Marcelle Naidoo. 2026. "Applications of Selected Nanoencapsulated Indigenous Essential Oils in Medicine, Food, and Agriculture: A Review" Foods 15, no. 11: 1942. https://doi.org/10.3390/foods15111942
APA StyleWutu, O. S., Mpambani, B., & Naidoo, C. M. (2026). Applications of Selected Nanoencapsulated Indigenous Essential Oils in Medicine, Food, and Agriculture: A Review. Foods, 15(11), 1942. https://doi.org/10.3390/foods15111942

