Submitted:
13 April 2024
Posted:
15 April 2024
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Abstract
Keywords:
1. Introduction
2. Materials and Methods
3. Mannosylerythritol Lipids Structure, Properties, and Production
4. Mannosylerythritol Applications Described in the Literature
4.1. Biomedical/Pharmaceutical Industry
4.2. Personal Care and Cosmetics
4.3. Agriculture
4.4. Food and Feed Industry
4.5. Environmental Responses
4.6. Others
5. Current and Future Perspectives About MELs in the Market

Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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| Application Area | Specification | Brief Description of the Results | MELs Used | References |
|---|---|---|---|---|
| Biomedical/ Pharmaceutics | Anti microbial activity |
▪ Both MELs were strongly active against gram-positive bacteria (Bacillus subtilis, Micrococcus luteus, Mycobacterium rhodoochrous, Staphylococcus aureus). | MEL-A 99% and MEL-B 99% |
[27] |
| ▪ MELs had antimicrobial activity against S. aureus and biofilm disruption activity. | MELs mixture | [18] | ||
| ▪ MEL-A inhibited the germination of Bacillus cereus spores. | MEL-A 80% | [28] | ||
| ▪ MEL-A inhibited planktonic cells and biofilm of S. aureus. | MEL-A 80% | [29] | ||
| ▪ MEL-B inhibited the growth of bovine mastitis causative S. aureus. | MEL-B | [30] | ||
| ▪ The combination of MEL-A with high hydrostatic pressure led to a higher bactericidal effect against Listeria monocytogenes (than the hydrostatic pressure alone). | MEL-A 80% | [31] | ||
| ▪ MELs inhibited the growth of E. coli and P. aeruginosa. The combination of MELs and antibiotics potentiated antibiotics’ efficiency. | NA | [32] | ||
| Application area | Specification | Brief description of the results | MELs used | References |
|
Biomedical/ Pharmaceutics (continuation) |
Antitumor |
▪ MELs induced the differentiation of Human Promyelocytic Leukemia cells HL60 and inhibited Protein Kinase C activity. | MELs mixture |
[33,34] |
| ▪ MELs inhibited Tyrosine Kinase activity, inhibiting proliferation and inducing the differentiation of Human Myelogenous Leukemia cells K562. | MELs mixture |
[35] | ||
| ▪ MEL-B reduced cell viability and induced death by apoptosis of B16F10 Mouse Melanoma cells. | MEL-B 95% Toyobo | [36] | ||
| ▪ MELs stimulated Tyrosinase activity and melanin production, leading to apoptosis and cell-differentiation of B16 Mouse Melanoma cells. |
NA | [37] | ||
| Anti- inflammatory |
▪ MELs inhibit the secretion of inflammatory mediators by Rat Basophilic Leukemia RBL-2H3 cells (a mast cell line). |
MEL-A and MEL-B | [38] | |
| Neural repair | ▪ MELs induce the outgrowth of neurites from and enhance the activity of acetylcholinesterase in PC12 pheochromocytoma cells. | MEL-A | [39,40] | |
| Genetic material transfection or drug- carrying |
▪ MEL-A increased the efficiency of gene transfection by cationic liposomes with a cholesterol derivative or DC-Chol. | MEL-A | [41,42,43] | |
| ▪ MEL-A-containing cationic liposome was able to deliver siRNA rapidly and directly. | MEL-A | [44] | ||
| ▪ MELs were used as stabilizing agents for silver and zinc oxide nanocomposites, gold nanoparticles and for silver and magnetic iron oxide nanocomposites synthesis, to be used in human liver cancer cells inhibition (HepG2). | NA | [45,46,47] | ||
| ▪ Nanoliposomes made of soybean lecithin and cholesterol, when incorporated with MEL-B, have enhanced stability to pH 3-7 and deliver amoxicillin for Helicobacter pylori infection treatment in vivo. | MEL-B, Toyobo | [48] | ||
| ▪ MEL-B nanomicelles successfully carried berberine for H. pylori biofilm disintegration and infection eradication. | MEL-B, Toyobo | [49] | ||
| Drug Delivery |
▪ Preparation of MELs nanomiceles for drug delivery (clarithromycin). It was shown that, by varying the pH, it is possible to control clarithromycin delivery (pH 1.2, in 2 h, 37.1% of drug was delivery, while, at pH 7.4, only 9.7% was released). | MELs mixture |
[50] | |
| Immunoglobulin purification |
▪ MEL-A shows high binding affinity towards HIgG, HIgA and HIgM. | MEL-A | [51,52] | |
| Application area | Specification | Brief description of the results | MELs used | References |
|
Cosmetics and personal care |
Formulation stabilization | ▪ Emulsification of pseudo-ceramide is stabilized by molecular association with MELs. | Damy chemicals | [53] |
| MELs stabilize the foaming, emulsification, and wetting properties of Sodium Lauryl Sulphate. | MELs mixture |
[54] | ||
| ▪ Coating cosmetics (lip primer, foundation and sunscreen) pigments with MELs, enhance their skin adhesion. | NA | [55] | ||
| Skin whitening |
▪ MELs inhibit melanogenesis via suppressing ERK-CREB-MiTF-tyrosinase signalling in human melanocytes and a three-dimensional human skin equivalent. | MELs from DKBIO, MEL-B 85% | [22] | |
| Hair growth promotion | ▪ MEL-A produced from soybean oil increases cultured Fibroblast cells and 3D Human Skin model cells viability and activates Human Papilla cells. | MEL-A 80.1% | [56] | |
| Damaged hair repair | ▪ MEL-A and MEL-B shown similar activity as ceramides for hair damage repair, and increase of hair flexibility. | MEL-A 99% MEL-B 90% | [57] | |
| Skin repair and moisturization |
▪ MELs ameliorate UVA-induced aquaporin-3 downregulation by suppressing c-Jun N-terminal kinase phosphorylation in cultured human keratinocytes. | MELs from DKBIO | [23] | |
| ▪ MEL-A had a recovery effect on SDS damaged skin cells | MEL-A | [58] | ||
| ▪ MEL-A and MEL-B produced with olive oil show activities similar to natural ceramides on the cell viability and SDS-induced damage repair of cultured human skin cells; MEL-B increased the water content in the stratum corneum and reduced water loss by perspiration. | MEL-A 100% MEL-B 100% |
[59] | ||
| ▪ MELs with carbon chains with 10 or more carbons exhibit better cell damage repair than a natural C18 ceramide, particularly MEL-D C10 (MELs purified by acetylation level and carbon chain size, see original paper) | MELs purified |
[60] | ||
| ▪ MEL-B protected both HaCaT and 3D skin cell models from UVB- and SDS-induced damage by up-regulating the expression of the skin barrier damage-associated key mRNA genes and proteins LOR, FLG, and TGM1 (MELs mixture 34.94% MEL-A, 28.46% MEL-B and 11.32% MEL-C). | MELs mixture. |
[19] | ||
| ▪ MEL-B liposomes increase skin permeability to water-soluble compounds (calcein) in mice. | MEL-B, Toyobo | [61] | ||
| Antioxidant | ▪ MEL-C has antioxidant activity through DPPH radical and superoxide anion scavenging and protection of cultured human fibroblast cells against H2O2-induced oxidative stress | MEL-C 80.7-92.5% | [21] | |
| Anti microbial |
▪ MELs have antimicrobial activity against Malassezia furfur, the yeast that causes dandruff. A shampoo formulated with MELs and SLS had increased anti-dandruff activity | NA | [62] | |
| Application area | Specification | Brief description of the results | MELs used | References |
| Bioremediation | Oil spills | ▪ MELs increase the bioavailability and biodegradation rate of n-alkanes, diesel, kerosene and crude oil (MELs mixture: 68% MEL-A, 28% MEL-B and -C and 4% MEL-D). | NA MELs mixture |
[63,64,65] |
| ▪ Patent using MELs as petroleum demulsifier agents | NA | [66] | ||
| Food | Nutrient carriers |
▪ MELs were used in the formulation of a stable anthocyanin nutrient carrier | NA | [67] |
| Food preservation |
▪ MEL-A enhances the rheological properties and water holding capacity of frozen dough, minimizing the freezable water content, while killing B. cereus cells and spores | MEL-A | [28,68,69] | |
| ▪ Emulsification of essential oils with MEL-B (Thymus vulgaris, Lippia sidoides and Cymbopogon citratus), leads to an enhance of essential oils’ antioxidant activity and preservation of antimicrobial activity. | MEL-B | [54] | ||
| Agriculture | Agro-spreader | ▪ MEL used as agrochemical spreader for biopesticides for hydrophobic plant surfaces (MELs mixture: 58% MEL-A, 25% MEL-B and 10% MEL-D). | MEL mixture | [70] |
| Wetting agent | ▪ MEL solutions showed good wetting ability on poorly wettable Gramineae plant surfaces. | MEL-A, MEL-B, MEL-C | [70] | |
| Biocide | ▪ MEL-Ag nanoparticles; activity against mosquito larvae and pupae | MELs mixture |
[71] | |
| Powdery mildew was suppressed on MEL-treated leaves. | MEL-A | [72] | ||
| ▪ MELs, combined with other ingredients, are used for nematodes control. | NA | [73] | ||
| ▪ MEL-B, biostimulant and phytotoxic effect on lettuce plant germination and growth for given concentrations. | MEL-B 95% Toyobo | [74] | ||
| Fuels additive |
▪ MEL-A enhances the fluidity of fuels at low temperatures. | MEL-A | [75] | |
| Others | Jet biofuel | ▪ MELs are used as precursors for fuel with lipid chains comprising 6 to 14 carbons production. | NA | [76] |
| Enhanced oil recovery | ▪ MEL-B can create emulsions with heavy oils. | MEL-B | [77] | |
| Detergent | ▪ MELs had stability over wide pH and temperature ranges and improved detergent efficiency in removing stains from fabric in a proportion of 1:1 (w detergent/w MELs) | MELs mixture |
[78,79] | |
| Ice prevention | Suppression of agglomeration and growth of ice particles | MEL-A | [80] |
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