Next Article in Journal
New Polyketides from the Marine-Derived Fungus Letendraea Sp. 5XNZ4-2
Next Article in Special Issue
Effect of Carrageenans on Vegetable Jelly in Humans with Hypercholesterolemia
Previous Article in Journal
Novel Efficient Bioprocessing of Marine Chitins into Active Anticancer Prodigiosin
Previous Article in Special Issue
Health Functionality and Quality Control of Laver (Porphyra, Pyropia): Current Issues and Future Perspectives as an Edible Seaweed
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Diverse Applications of Marine Macroalgae

by
Adriana Leandro
1,
Leonel Pereira
1 and
Ana M. M. Gonçalves
1,2,*
1
MARE (Marine and Environmental Sciences Centre), Department of Life Sciences, Faculty of Sciences and Technology, University of Coimbra, 3004-517 Coimbra, Portugal
2
Department of Biology and CESAM, University of Aveiro, 3810-193 Aveiro, Portugal
*
Author to whom correspondence should be addressed.
Mar. Drugs 2020, 18(1), 17; https://doi.org/10.3390/md18010017
Submission received: 27 November 2019 / Revised: 18 December 2019 / Accepted: 22 December 2019 / Published: 24 December 2019
(This article belongs to the Special Issue Characterization of Bioactive Components in Edible Algae)

Abstract

:
The aim of this paper is to review the multiplicity of the current uses of marine macroalgae. Seaweeds are already used in many products and for different purposes, from food products to medicine. They are a natural resource that can provide a number of compounds with beneficial bioactivities like antioxidant, anti-inflammatory, anti-aging effects, among others. Despite studies directed in prospecting for their properties and the commodities already marketed, they could, surely, be even more researched and sustainably explored.

1. Marine Macroalgae Diversity and Ecology

The marine environment is home for many diverse organisms such as algae, molluscs, sponges, corals, tunicates. Currently, oceans are already considered the “lungs of the Earth” due to Cyanobacteria and other algae that live in seawater. In fact, these beings provide up to 80% of the atmospheric oxygen, which we rely on to breathe. Cyanobacteria are blue colored, aquatic, photosynthetic, and because they are bacteria, they usually are unicellular, but they often grow in colonies large enough to be seen. Cyanobacteria are prokaryotic organisms while algae are eukaryotic organisms. Algae are almost ubiquitous, between microscopic and macroscopic species, they can be found in every wet environment in land, in fresh water or in oceans [1].
In this review, the focus is the marine macroalgae or seaweeds, which are multicellular, macroscopic, eukaryotic, and autotrophic organisms. They are taxonomically organized in three large and distinct groups, based on the color of the thallus: Chlorophyta (green algae), Rhodophyta (red algae), and Ochrophyta – Phaeophyceae (brown algae). All of them accumulate starch in the interior of their cells as energy store, and other different polysaccharides of large molecular chain. The green algae produce ulvan and contain carotene and xanthophylls and chlorophylls a and b (what sustains the idea that they are the ancestors of the plants) as pigments. The red algae (most common in hot seas) have chlorophylls a and d and carotenoids and their staining is due to the presence of phycoerythrin (pigment) in their cells. In the brown algae are found the pigments fucoxanthin, chlorophylls a and c and carotenoids and, as reserve substances, oils, and polysaccharides (such as laminarin) [2,3].
Like plants in terrestrial land, seaweeds have similar ecological roles but in aquatic territory. Some macroalgae species may serve as bioindicators of the quality of water and some can do bioremediation by bioabsorption and bioaccumulation [4,5,6].
As other vegetables, seaweeds are primary producers, the base of the marine food chain, sustaining several benthic animal communities [7]. They also compete for light, nutrients, and space, in addition to the need of carbon dioxide and water to develop. Inclusively algae and plants produce the same storage compounds and use similar defence strategies against predators and parasites [2]. They have also developed effective mechanisms to survive many biotic threats, like bacteria, virus, or fungal infections. Because they are sessile organisms, seaweeds have evolved to live in variable, extreme, and hostile abiotic environmental and stress conditions, like temperature changes, salinity, environmental pollutants, or UV radiation exposure. That caused these beings to be able to produce a wide range of compounds called ‘secondary metabolites’, like pigments, vitamins, phenolic compounds, sterols, and other bioactive agents. Besides these, they also produce amino acids and proteins, saturated/unsaturated fatty acids and all kinds of polysaccharides which are directly implicated in the development, growth, or reproduction conditions to perform physiological functions. So, based on the production of these molecules, in addition to its ecological importance, marine macroalgae also have great importance at commercial level. That’s why, a few years ago, the interest in the cultivation and exploitation of macroalgae in the most varied forms increased. Seaweeds are already used in many countries for very different purposes, like industrial phycocolloids extraction or extraction of compounds with antiviral, antibacterial, or antitumor activity [8]. They can also be, directly or indirectly, used for human and animal nutrition (livestock) or farming (biofertilizers) [9].
Although there is still much to investigate and find out about these living beings, it is known that several of the substances they synthesize have great potential to be used in areas such as pharmaceutical, cosmetics and the food industry. As their interest, cultivation and applications increase, their value in the market rises too. It is estimated that in 2024 this value will exceed twice the achieved in 2017 (see Figure 1) [10].

2. Marine Macroalgae Applications

2.1. Human Food

Asian countries, especially China and Japan, are known for being large seaweed consumers for many centuries. The first records show that the harvesting of macroalgae, such as Laminaria spp., Undaria pinnatifida, Sargassum fusiforme (formerly Hizikia fusiforme) (commonly known as kombu, wakame, and hiziki, respectively), for human consumption was already carried out by people in China, at least from 500 B.C. [7]. While in Europe it occurred a thousand years later [9].
More than 600 species of edible seaweeds are categorized. Now it is recognized that edibles seaweeds have great nutritional content as they are a low caloric food, but rich in vitamins, minerals, and dietary fibers [7,9]. Their nutritive value may vary depending on the geographic location, season of the year, growth stage, part of the seaweed harvested, etc [11]. Thus, to assure the nutritional value of seaweeds, they need to be evaluated before being used as supplements.
Seaweeds draw from the sea an incomparable wealth of mineral elements, macro elements, and trace elements. They are known as an excellent source of vitamins and minerals, especially potassium and iodine (i.e., Palmaria palmata, Fucus vesiculosus, Laminaria sp.), and potentially good sources of proteins (i.e., red algae such as Pyropia tenera (formerly Porphyra tenera), Grateloupia filicina), long-chain polysaccharides (i.e., P. tenera) and soluble and insoluble dietary fibers (i.e., G. filicina, Chondrus crispus, Ulva lactuca) [12]. It was found that the ashes of edible seaweeds contained higher amounts of macrominerals (8.083–17.875 mg/100 g; Na, K, Ca, Mg) and trace elements (5.1–15.2 mg/100 g; Fe, Zn, Mn, Cu), than those reported for edible land plants. So edible brown and red seaweeds could be used as a food supplement to reach the recommended daily intake of some essential minerals and trace elements [13]. For example, the consumption of 10 g of the green alga Ulva lactuca provides 70% of the body’s daily magnesium requirements and over half of its iron requirements [12,13].
Macroalgae can be used like other vegetables, being equally or even more versatile than them. Sea vegetables, as they are known, could be commercialized and/or eaten in many forms, such as fresh, dried, in flakes, flour or powder, or incorporated in other food products (added-value products) (see Table 1).
The entire organism can be eaten freshly harvested or after dried and then re-hydrated and cooked [7,16]. They are already commercialized under multiple brands, and labeled with “fat-free”, “gluten-free”, “mineral rich”, “low carbohydrates”, and “low calories” [14,15,18,21]. There are natural and healthier substitutes of pasta or bacon (i.e., Himanthalia elongata, as spaghetti, and Palmaria palmata, as sea bacon, both from Seamore food company), the well-known nori sheets (genus Porphyra/Pyropia) to prepare sushi rolls or crispy thin snacks, and many other recipes such as wraps with Undaria pinnatifida (wakame) and H. elongata, or the laverbread, a paste prepared with boiled nori (also recognized as laver) [15,18] and in desserts like in innovative Spanish nougats with crushed nori algae [21]). Above all this nutritional value, macroalgae are donors of a number of great ‘side-effects’ acting as nutraceuticals. A study with Japanese children revealed that seaweeds intake in the diet was significantly negatively related to systolic blood pressure in girls and with diastolic blood pressure in boys. This study suggests that seaweeds have beneficial effects on blood pressure [22].
As we can see, macroalgae can be incorporated in food products after processed into flakes, flour, powder or even in more specific extracts. Their pigments, like carotenoids, are, in fact, one of the products of interest for the food industry [23]. Traditionally, carotenoids have been used in that industry due to their properties as natural color enhancers. However, those that are synthetically obtained are now suspected of being promoters of carcinogenesis and liver and renal toxicity. So, there is a strong market demand to replace them with natural pigments. Seaweeds are a great source of many pigments, especially β-carotene which besides its anticancer activity, has been reported that it is absorbed 10 times more easily by the body than the synthetic one [24].
Pigments are important in this industrial range, but there are some constitutes of algae that are even more, their hydrocolloids, such as carrageenan, alginic acids, and agar. These are the main constituents of red and brown algal cell walls and are widely used in several food industries (see Table 2).
Carrageenan is a natural phycocolloid and is one of the main additives used by the food industry, in many dairy products (e.g. yoghurts, flavoured milkshakes, flans, jellies, ice creams, and beers) and meat products (e.g. hams), as thickening, emulsifier or stabilizing agent [3,25,26]. Extracted from several families of the order Gigartinales. These polygalactans are sulfated and have a linear structure formed by galactose residues with alternating α (1–3) and β (1–4) bonds. Regulatory authorities (FDA) have established a minimum value for the molecular weight of the carrageenan to be used in food preparations. The commercial carrageenans usually range from 400 to 600 kDa, having the minimum of 100 kDa. This minimum value was established by the response to reports of highly degraded carrageenan-induced ulceration of the colon. There are three main varieties of carrageenan, differing in their sulfation degree. Kappa (κ)-carrageenan has one sulfate group per disaccharide, Iota (ι)-carrageenan has two sulfates and Lambda (λ)-carrageenan has three sulfates per disaccharide. The type of carrageenan selected is dependent on the desired finished product characteristics. Iota and kappa carrageenans are gelling carrageenans, while lambda is a thickening/viscosifier carrageenan [28].
Agar is other phycocolloid, composed of a variable combination of agarose and agaropectin, depending of the species and seasonal factors. Agarose, which is the primary component of agar, is a linear polymer of agarobiose, a disaccharide composed of D-galactose and 3,6-anhydro-L-galactopyranose. Agaropectin, which occurs usually in minor amounts, is a heterogeneous mixture of β-1,3-linked D-galactose which contains substituted sulfate and pyruvate moieties. Like carrageenan, agar has a similar application, so it also has gelling properties, but while carrageenan gels by both ionic and hydrogen bonds, agar gels only by hydrogen bonds. Extracted from several species of red algae, mainly the Gelidium sp., Gracilaria sp. and Pterocladiella sp., it is frequently used as thickener in food products and a vegetarian substitute for gelatine [7,9]. Currently, agar is also being used to develop a new biomaterial for packaging. Made from agar and other natural raw materials, these new wrappers are sustainable, biodegradable, and constitute an alternative to plastics [29].
Alginate is also a gelling agent found and extracted from brown seaweed (eg. Ascophyllum sp., Laminaria sp., Lessonia sp., Macrocystis sp.). In fact, it is the most abundant marine biopolymer and, next to cellulose, the most abundant biopolymer in the world. Alginate is a linear acidic polysaccharide that can be a homopolymer or a heteropolymer of β-d-mannuronate and/or α-l-guluronate [27]. It is used as a stabilizer in many food products like ice cream, yogurt, cream, and cheese. It is also used in the food industry as a thickener, emulsifier for sauces, dressings, and jam, and it needs no heat to gel. It is most commonly used with calcium lactate or calcium chloride in the spherification process, a technique performed in molecular cooking.

2.2. Livestock and Agriculture

The consumption of macroalgae is not only for humankind, but also for other animal species. European usage of seaweeds in animal husbandry has come since the time of the Romans. Countries such as Iceland, France, and Norway usually use them in domestic animal nutrition [30]. In fact, the first seaweed meal for animal feed was produced in Norway. It was made from brown seaweeds that were collected, dried, and milled [7].
Besides its direct uses as feed, macroalgae are already introduced in other type of feed as a nutritive additive, and as a nutraceutical compound. Currently the feeding of the animals is supplemented by algae to fill the deficiency in mineral pastures in the U.S.A., Australia and New Zealand. Seaweed meal, used principally as a vitamin and mineral supplement, is produced mainly from the kelps Ascophyllum nodosum, Fucus spp., Laminaria spp., Macrocystis spp. [30].
Extracts like macroalgae-derived sulfated polysaccharides are added to animal feed. It was proven that these meals can improve animal intestinal integrity and efficient immune response [31].
On the other hand, feeding seaweeds and macroalgal products has been shown to reduce enteric methane emission from rumen fermentation, [32] which makes this type of feeding a promising candidate as a biotic methane mitigation strategy in the largest milk or beef producing [33].
Moreover, seaweed and seaweed-derived products have been widely used in agriculture to improve crop production systems due to the existence of a number of plant growth-stimulating compounds [34,35,36]. Inclusively, since ancient times, they were traditionally used to fertilize the fields, they have long been used to augment plant productivity and food production in various regions of the world [30].
Seaweeds and their compounds can promote early seed germination, root and plant growth, confer tolerance to freezing, resistance to biotic stresses, and increase the plant nutrient absorption capacity [37,38]. For example, auxins, a plant hormone responsible for the vegetative growth, and auxin-like compounds were detected in some seaweeds [39].
However, the biostimulator potential of many of these compounds has not been fully exploited due to the lack of scientific data on growth factors present in seaweeds and their mode of action in affecting plant growth [36]. The effects are complex and dependent on the crop, the local environmental conditions and on the interactions of the algae species with the soil community [30]. Seaweeds’ extracts, like laminarin, have been shown to stimulate natural defence responses in plants and are involved in the induction of genes encoding various pathogenesis-related proteins with antimicrobial properties. Also, it has been demonstrated that alginate oligomers show growth-promoting effects on certain higher plant species [35].
Studies suggest that adding strongly polar degraded fucoidan, alginate, etc., to soils improves crumb structure and aeration, thus stimulating microorganisms and root systems which improves plant growth [40].
The current commercial extracts are manufactured mainly from the brown seaweeds Ascophyllum nodosum, Laminaria spp., Saccorhiza spp., Ecklonia maxima, Fucus spp., Sargassum spp., and Durvillaea spp., although other species such as Ulva intestinalis, Ulva lactuca, Codium sp. (Chlorophyta), Gelidium sp., and Chondrus crispus (Rhodophyta) are also used [30].

2.3. Cosmetics

The definition of cosmetic product, according to the European Commission, is: “Any substance or mixture intended to be placed in contact with the external parts of the human body (epidermis, hair system, nails, lips, and external genital organs) or with the teeth and the mucous membranes of the oral cavity with a view exclusively or mainly to cleaning them, perfuming them, changing their appearance, protecting them, keeping them in good condition, or correcting body odours” [41].
More recently, there is another category—the ‘cosmeceuticals’—which is attracting the industry’s attention and is of interest to the most attentive consumers. Despite still being without legal meaning nowadays, the industry continues to use this designation referring to a product that lies between the benefits of cosmetics and pharmaceuticals [42,43].
There is a growing demand for more natural cosmetics, those made with natural/organic ingredients, due to the benefits they offer, and the absence of many harmful chemicals which are present in conventional cosmetics products. Consequently, the cosmetic industry is rapidly expanding to meet these increased demands. Some of the key active-based natural ingredients used in cosmetics are extracted from marine organisms, like seaweeds (see Table 3).
Marine macroalgae are one of the most abundant sources of vitamins, minerals, amino acids, antioxidants, and essential fatty acids. Seaweeds are unique in containing bioavailable ingredients, meaning that its active, nutrient-rich compounds are more readily absorbed by the skin and the body. Because of its bioavailable nature, seaweeds provide a multitude of benefits including reducing the appearance of redness and blemishes, brightening, hydrating, re-mineralizing, reducing the appearance of sun damage, and firming skin [44,45,46].
Algae can be incorporated into these products as algal extracts of selected elements or, alternatively, pieces of dried seaweeds can be crushed and ground and incorporated into skin care products such as exfoliating lotions, face masks, face washes and soaps. Cosmetic products, such as creams and lotions, sometimes show on their labels that the contents include “marine extract”, “extract of alga”, “seaweed extract”, or similar [7,44]. Usually this means that one of the hydrocolloids extracted from seaweeds was added to the product. Alginate or carrageenan are water-binding agents, which means they help hold water onto the skin and hair, increasing the moisture balance [47]. Both can be found in multiple products like lotions, creams, shampoos, conditioners, and toothpastes [48].
Seaweeds can be used in two ways in cosmetics: they can either be a vehicle, serving as a stabilizing, emulsifying, or other type of agent necessary for product preparation; or as the active therapeutic ingredient in the product, for example in anti-aging skin treatments or after-sun skin care products [13,48,49].
Algae are rich in saturated and unsaturated fatty acids that are bioactive compounds. For example, palmitic acid and other fatty acids, that are present in large quantities in marine seaweeds, are used in cosmetics as emulsifiers, and its derivated ascorbyl palmitate is an antioxidant that is effective for anti-aging and anti-wrinkle effects [48,50].
Purified phlorotannins extracted from brown seaweeds are included in cosmetics, since these molecules have the role of preventing and slowing down the skin aging process, which is mainly associated with free radical damage and with the reduction of hyaluronic acid concentration [51].
Wang et al. [52] compared the moisture-absorption and retention properties of polysaccharides extracts from five different seaweed species [52]. Marine algae are reported to produce different polysaccharides, including alginates, ulvans, laminarans, and fucoidans [53]. These molecules usually contain large proportions of L-fucose and sulfate, together with minor amounts of other sugars such as xylose, galactose, mannose, and glucuronic acid [45]. In their study, Wang et al. [52] reported that the polysaccharides extracted from brown seaweed (more precisely the fucoidan obtained from the Saccharina japonica) exhibited the best moisture-absorption and retention capacity, while the green ones were the worst. This ability of polysaccharides is influenced by its sulfated content, molecular weight (length of chain), and by the type of algae that they are extracted from [52]. An example of it is a cosmetic, CODIAVELANE®, composed of propylene glycol, water, and Codium tomentosum extract. It is proven that it normalizes and balances skin’s moisture content by adding oligo-elements and increasing surface hydration [49].
A group of small water-soluble compounds, mycosporine-like amino acids (MAA), found in marine algae, is biologically relevant because of its photo-protective potential. In addition, its antioxidant and skin protective strategies raise the interest for possible pharmaceutical and cosmetic applications [54,55]. An extract of Asparagopsis armata (ASPAR’AGE™) containing this MAA molecules is already incorporated in some lotions with anti-aging properties [56].
Besides the numerous existing and marketed cosmetics and cosmeceuticals, there are many other seaweed extracts that are under investigation. Kamei et al. [57] discovered a compound from Sargassum macrocarpum, Sargafuran, that was bactericidal and completely killed Propionibacterium acnes by lysing bacterial cells [57]. The results suggest that this substance could be applied in new skin care cosmetics to prevent or improve acne.

2.4. Pharmaceutics

The overuse of antibiotics can lead to the development of resistant pathogenic bacteria. New antibiotics that are effective against new and resistant bacterial strains are needed. As previously mentioned, seaweeds have evolved to survive many environmental stresses and threats. Besides the predators/herbivores, they have to continuously face high concentrations of infectious and surface-fouling bacteria that are indigenous to ocean waters [8]. So, the macroalgae have evolved and developed certain mechanisms of defence like the production of bioactive compounds. Substances such as phlorotannins, polysaccharides, and peptides allow seaweeds to avoid bacterial invasion [8], and some have been investigated about other potential pharmacological effects (antiviral, antitumoral, immunogenic effects). One example is the peptide kahalalide F and its isomer, iso-kahalalide F, extracted from a green macroalga, Bryopsis pennata, which present cytotoxic effects and were used in anticancer clinical trials. Despite its great potential, this molecule is under modification tests to improve its water solubility, stability, and effectiveness [70].
Sometimes the extract used can be obtained from a mix of various algae species, and even of different seaweed groups. For example, there is a patent of green and/or brown seaweed extract for the treatment of type 2 diabetes and its complications. This has brown seaweeds such as Fucus vesiculosus or Ascophylum nodosum and green algae, selected from the group consisting of Cladophora sp., Monostroma sp., Ulva compressa (as Entoromorpha compressa), Codium sp., among others [71].
According to another study, methanolic extracts of some brown, red and green algae are effective at inhibiting the growth of pathogenic Gram-positive (Staphylococcus aureus, Micrococcus luteus, Enterococcus faecalis) and Gram-negative bacteria (Enterobacter aerogenes, Escherichia coli) [72]. The species were Corallina officinalis (Rhodophyta), Cystoseira barbata, Dictyota dichotoma, Halopteris filicina, Cladostephus spongiosus (Ochrophyta, Phaeophyceae), and Ulva rigida (Chlorophyta).
The seaweed-derived substances that received most attention from pharmaceutical companies are the sulfated polysaccharides (negatively charged sugar polymers due to the presence of sulfate groups). Sulfated polysaccharides are extracted from red algae (carrageenans and agarans), brown algae (e.g. fucoidans) and green algae (e.g. ulvans). Their value lies on their bioactivities, namely their antibacterial, antiviral activity, antitumoral, and immunomodulatory potential [8,70,72,73].
On the other hand, other polysaccharides, like alginate, are also used in pharmaceutical formulations as excipients. Alginate polymers have a wide potential in drug formulation due to their lack of toxicity and they can be tailor-made to suit the demands of applicants in both the pharmaceutical and biomedical areas. This brown seaweed—derived group of polymers owns a few characteristics that makes it useful as a formulation aid, both as a conventional excipient and more specifically as a tool in polymeric-controlled drug delivery [8,74], and it is commonly used as bio-adhesive in pharmaceutical applications [75]. Other application of alginate is in wound healing dressing due to the excellent swelling properties and biocompatibility [76]. In fact, not only the alginate, but seaweed extracts—like the Laminaria spp.—are being studied and used for the development of biodegradable wound care products, since they contain healing accelerator substances: alpha keto isovalerate, alpha keto glutarate, and alpha keto oxaloacate [77].
It has been demonstrated that alginate has therapeutic effects in mammalian systems such as anticoagulants and antitumor activities. Also containing alginate, there is some gastrointestinal formulations and protectors (i.e., Gaviscon), that neutralize the acids, prevents the contact of stomach contents with the oesophagus (reflux), and relieve symptoms of heartburn and indigestion [78].
Agar, which was initially used as a laxative agent in the preparation of medicines, in western countries [26], is now used as an ingredient in tablets and capsules, as well as in different types of emulsions. Like alginate, the main role of agar in the pharmaceutical industry is as an excipient.
The three main types (ι, κ, λ) of carrageenan form thermo-reversible gels in aqueous solutions and in the presence of cations. Therefore, they are used in pharmaceutical formulations for stabilization of disperse systems and viscosity modification [75]. In addition to its hydrating properties, it has also been found in some studies to block the growth of viruses like human papillomavirus, making it potentially even more protective in sexual lubricants (in which it is already included). Studies in vitro demonstrated that carrageenan, even when diluted a million-fold, presents activity against a range of common sexually transmitted HPV types that can cause cervical cancer and genital warts [47]. So, due to these properties, carrageenans might have a great interest in the composition of sexual lubricant. Also the polymer galactofuran (extracted from Undaria pinnatifida) was proven as an effective Herpes virus inhibitor [79].
Among polysaccharides, fucoidans were particularly studied as they showed interesting biological activities (anti-thrombotic, anti-coagulant, anticancer, anti-proliferative, and anti-inflammatory) [66,80,81,82].
Other group of small molecules (previously indicated in this article), the MAAs, have skin protective and wound healing effects. Like the porphyra-334 was able to suppress ROS (reactive oxygen species) production in human skin fibroblast cells [83]. Pigments isolated from seaweeds also have bioactivities. Like the fucoxanthin, obtained from Saccharina japonica (as Laminaria japonica), that has been reported to suppress tyrosinase activity in UVB-irradiated guinea pig and melanogenesis in UVB-irradiated mice. Oral treatment of fucoxanthin significantly suppressed skin mRNA expression related to melanogenesis, suggesting that fucoxanthin negatively regulated melanogenesis factor at transcriptional level [45].
Seaweed phlorotannin extracts from Ascophylum nodosum are reported to have potential in the treatment of diabetes [84] while those from Ecklonia cava are now marketed for potential health benefits due to their antioxidant activities [85]. These phlorotannins are phenols structurally different from those obtained from plants, since these are oligomers and polymers of phloroglucinol (1,3,5-tri-hhydroxybenzene) and the terrestrial ones are based on gallic acids or flavones [86]. The brown algal polyphenols were investigated in an SKH-1 hairless mouse skin model with UVB-induced skin carcinogenesis. This in vivo report demonstrated that both dietary feeding and topical treatment of brown algal polyphenols has suppressed cyclooxygenase-2 (COX-2) expression and cell proliferation [87]. These results suggest the role of brown algae polyphenols, phlorotannins, as potential cancer chemo-preventive agents against photo-carcinogenesis and other adverse effects of UVB exposure. That reveals these compounds may be used as active ingredients in drugs or cosmetic/cosmeceutical formulations, like in sunscreen or anti-aging creams [87].
Marine brown algae-derived phlorotannins have also been investigated for their human beneficial aspects that include hypoallergenic, anti-inflammatory, and hyaluronidase inhibitory activities. In vitro studies with the methanol extracts from marine brown algae Eisenia arborea have shown inhibition of histamine release from rat basophile leukaemia cells (RBL-2H3) sensitized with anti-dinitrophenyl (DNP) IgE and stimulated with DNP-BSA [88]. Shibata et al. [89] also studied some length-varied phlorotannins obtained from Ecklonia bicyclis (as Eisenia bicyclis) and Ecklonia kurome in their ability to inhibit hyaluronidase activity in vitro. In fact, they proved that those molecules have a stronger inhibitory effect on hyaluronidase than the well-known inhibitors catechins and sodium cromoglycate [89].

3. Conclusions

This review intended to demonstrate the versatility and the multiple applications of marine macroalgae.
Many products we consume or use daily contain seaweed extracts in their composition, such as ham, ice cream, bottled chocolate drinks, and toothpaste or deodorizers, although most people probably do not even imagine such thing. Nowadays, there is a growing interest in seaweeds due to the recognition of numerous new bioactive compounds. Antioxidants, antimicrobials, anti-inflammatory, anti-aging, anticancer, are just some of its amazing properties to use as pharmaceuticals, cosmeceuticals, nutraceuticals, or even in agriculture or feeding.
There is more and more awareness of sustainable use of natural resources, rather than synthetic and processed products with eventual harmful side effects to the consumer. All the growing interest in these potentialities led to the fostering of macroalgae production, as well as to do research on them. Seaweeds are a resource to maintain and preserve with unique properties.

Author Contributions

A.M.M.G. conceived and designed the idea; A.M.M.G. and L.P. contributed to the idea; A.L. wrote the paper; A.M.M.G. and L.P. contributed to the writing of the paper. All authors have read and agreed to the published version of the manuscript.

Funding

This work had the support of Foundation for Science and Technology (FCT), through the strategic projects UID/MAR/04292/2019 granted to MARE and UID/AMB/50017/2019 granted to CESAM. This research was also co-financed by the project MENU - Marine Macroalgae: Alternative recipes for a daily nutritional diet (FA_05_2017_011), funded by the Blue Fund under Public Notice No. 5—Blue Biotechnology.

Acknowledgments

This work was supported by Foundation for Science and Technology (FCT) through the strategic projects granted to MARE—Marine and Environmental Sciences Centre UID/MAR/04292/2019 and granted to CESAM Centro de Estudos do Ambiente e do Mar UID/AMB/50017/2019. This research was also co-financed by the project MENU—Marine Macroalgae: Alternative recipes for a daily nutritional diet (FA_05_2017_011), funded by the Blue Fund under Public Notice No. 5—Blue Biotechnology. Adriana Leandro thanks FCT for the financial support provided through the doctoral grant SFRH/BD/143649/2019 funded by National Funds and Community Funds through FSE. Ana M.M. Gonçalves acknowledges University of Coimbra for the contract IT057-18-7253.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Lewin, R.A.; Andersen, R.A. Algae. Encyclopedia Britannica. Algae. Available online: https://www.britannica.com/science/algae (accessed on 14 November 2019).
  2. Barsanti, L.; Gualtieri, P. Algae Anatomy, Biochemistry and Biotechnology; CRC Press: Boca Raton, FL, USA, 2014. [Google Scholar]
  3. Vidotti, E.C.; Rollemberg, M.; Do, C.E. Algas: Da economia nos ambientes aquáticos à biorremediação e à química analítica. Quim. Nova 2014, 27, 139–145. [Google Scholar] [CrossRef] [Green Version]
  4. Neveux, N.; Bolton, J.J.; Bruhn, A.; Roberts, D.A.; Ras, M. The Bioremediation Potential of Seaweeds: Recycling Nitrogen, Phosphorus, and Other Waste Products. Blue Biotechnol. 2018, 1, 217–239. [Google Scholar] [CrossRef]
  5. Yu, Z.; Robinson, S.M.C.; Xia, J.; Sun, H.; Hu, C. Growth, bioaccumulation and fodder potentials of the seaweed Sargassum hemiphyllum grown in oyster and fish farms of South China. Aquaculture 2016, 464, 459–468. [Google Scholar] [CrossRef]
  6. Henriques, B.; Lopes, C.; Figueira, P.; Rocha, L.; Duarte, A.; Vale, C.; Pardal, M.; Pereira, E. Bioaccumulation of Hg, Cd and Pb by Fucus vesiculosus in single and multi-metal contamination scenarios and its effect on growth rate. Chemosphere 2017, 171, 208–222. [Google Scholar] [CrossRef] [PubMed]
  7. Klnc, B.; Cirik, S.; Turan, G.; Tekogul, H.; Koru, E. Seaweeds for Food and Industrial Applications. Food Ind. 2013. [Google Scholar] [CrossRef] [Green Version]
  8. Shannon, E.; Abu-Ghannam, N. Antibacterial derivatives of marine algae: An overview of pharmacological mechanisms and applications. Mar. Drugs 2016, 14, 81. [Google Scholar] [CrossRef]
  9. Pereira, L. Edible Seaweeds of the World; CRC Press: Boca Raton, FL, USA, 2016. [Google Scholar] [CrossRef]
  10. Statista-The Statistic Portal. The Statistic Portal Value of the Seaweed Market Worldwide in 2017 and 2024 (in Billion U.S. Dollars). Available online: https://www.statista.com/ (accessed on 6 January 2019).
  11. Kim, S.K. Handbook of Marine Macroalgae: Biotechnology and Applied Phycology; Wiley-blackwell: Hoboken, NJ, USA, 2011. [Google Scholar] [CrossRef]
  12. Yuan, Y.V.; Westcott, N.D.; Hu, C.; Kitts, D.D. Mycosporine-like amino acid composition of the edible red alga, Palmaria palmata (dulse) harvested from the west and east coasts of Grand Manan Island, New Brunswick. Food Chem. 2009, 112, 321–328. [Google Scholar] [CrossRef]
  13. Rupérez, P. Mineral content of edible marine seaweeds. Food Chem. 2002, 79, 23–26. [Google Scholar] [CrossRef]
  14. Tangles, S. Kelp Noodles. Available online: https://kelpnoodles.com/ (accessed on 10 January 2019).
  15. Clearspring Clearspring. Authentic Japanese Specialities and Organic Fine Foods. Available online: www.clearspring.co.uk (accessed on 22 December 2018).
  16. ALGAplus. Tok de Mar. Available online: www.algaplus.pt (accessed on 20 January 2019).
  17. Beesweet. Available online: https://beesweet.pt/ (accessed on 7 January 2019).
  18. Food, S. Seamore Food. Available online: https://seamorefood.com (accessed on 16 December 2018).
  19. PortoMuiños. Seaweed. Available online: http://www.portomuinos.com (accessed on 21 January 2019).
  20. The Whole Foodies. Available online: https://thewholefoodies.com.au/ (accessed on 10 January 2019).
  21. Vicens, T. Torrons Vicens. Turrones Artesanales. Available online: https://www.vicens.com/ (accessed on 20 December 2018).
  22. Wada, K.; Nakamura, K.; Tamai, Y.; Tsuji, M.; Sahashi, Y.; Watanabe, K.; Ohtsuchi, S.; Yamamoto, K.; Ando, K.; Nagata, C. Seaweed intake and blood pressure levels in healthy pre-school Japanese children. Nutr. J. 2011, 10, 83. [Google Scholar] [CrossRef] [Green Version]
  23. Kristinsson, G.; Jónsdóttir, R. Novel Bioactive Seaweed Based Ingredients and Products; Norden: Heerup, Denmark; Nordic Innovation: Oslo, Norway, 2015. [Google Scholar]
  24. Christaki, E.; Bonos, E.; Giannenasa, I.; Florou-Paneria, P. Functional properties of carotenoids originating from algae. J. Sci. Food Agric. 2013, 93, 5–11. [Google Scholar] [CrossRef]
  25. Pereira, L.; Van De Velde, F. Portuguese carrageenophytes: Carrageenan composition and geographic distribution of eight species (Gigartinales, Rhodophyta). Carbohydr. Polym. 2011, 84, 614–623. [Google Scholar] [CrossRef] [Green Version]
  26. Armisen, R. World-wide use and importance of Gracilaria. J. Appl. Phycol. 1995, 7, 231–243. [Google Scholar] [CrossRef]
  27. Stiger-Pouvreau, V.; Bourgougnon, N.; Deslandes, E. Carbohydrates from Seaweeds. In Seaweed in Health and Disease Prevention; Elsevier Inc.: Amsterdam, The Netherlands, 2016. [Google Scholar] [CrossRef]
  28. Pereira, L.; Gheda, S.F.; Ribeiro-Claro, P.J.A. Analysis by Vibrational Spectroscopy of Seaweed Polysaccharides with Potential Use in Food, Pharmaceutical, and Cosmetic Industries. Int. J. Carbohydr. Chem. 2013, 7. [Google Scholar] [CrossRef]
  29. Talep, M. Desintegra Me. Available online: https://margaritatalep.com/ (accessed on 24 January 2019).
  30. Craigie, J.S. Seaweed extract stimuli in plant science and agriculture. J. Appl. Phycol. 2015, 23, 371–393. [Google Scholar] [CrossRef]
  31. OlmixGroup. Algimun. Available online: https://www.olmix.com/animal-care/algimun (accessed on 4 January 2019).
  32. Li, X.; Norman, H.; Kinley, R.; Laurence, M.; Wilmot, M.; Bender, H.; Nys, R.; Tomkins, N. Asparagopsis taxiformis decreases enteric methane production from sheep. Anim. Prod. Sci. 2018, 58, 681–688. [Google Scholar] [CrossRef]
  33. Pereira, L.; Bahcevandziev, K.; Joshi, N.H. Seaweeds as Plant Fertilizer. Agricultural Biostimulants and Animal Fodder; CRC Press: Boca Raton, FL, USA, 2019. [Google Scholar] [CrossRef]
  34. Nabti, E.; Jha, B.; Hartmann, A. Impact of seaweeds on agricultural crop production as biofertilizer. Int. J. Environ. Sci. Technol. 2017, 14, 1119–1134. [Google Scholar] [CrossRef]
  35. Khan, W.; Menon, U.; Subramanian, S.; Jithesh, M.; Rayorath, P.; Hodges, D.M.; Critchley, A.T.; Craigie, J.; Norrie, J.; Prithiviraj, B. Seaweed extracts as biostimulants of plant growth and development. J. Plant Growth Regul. 2009, 28, 386–399. [Google Scholar] [CrossRef]
  36. Tuchy, L.; Chowańska, J.; Chojnacka, K. Seaweed extracts as biostimulants of plant growth: Review. Chemik 2013, 67, 636–641. [Google Scholar]
  37. Fernandes, A.L.T.; Oliveira Silva, R. Avaliação do extrato de algas (Ascophyllum nodosum) no desenvolvimento vegetativo e produtivo do cafeeiro irrigado por gotejamento e cultivado em condições de cerrado. Enciclopédia Biosf. Cent. Científico Conhecer Goiânia 2011, 7, 147–157. [Google Scholar]
  38. Akila, N.; Jeyadoss, T. The potential of seaweed liquid fertilizer on the growth and antioxidant enhancement of Helianthus annuus L. Orient. J. Chem. 2010, 2, 19–23. [Google Scholar]
  39. Crouch, I.; van Staden, J. Evidence for the presence of plant growth regulators in commercial seaweed products. Plant Growth Regul. 1993, 13, 21–29. [Google Scholar] [CrossRef]
  40. Milton, R. Liquid seaweed as a fertilizer. Proc. Int. Seaweed Symp. 1964, 4, 428–431. [Google Scholar]
  41. Regulation (EC) No 1223/2009 of the European Parliament and of the Council on Cosmetic Products; European Union: Brussels, Belgium, 2009.
  42. Brandt, F.S.; Cazzaniga, A.; Hann, M. Cosmeceuticals: Current trends and market analysis. Semin. Cutan. Med. Surg. 2011, 30, 141–143. [Google Scholar] [CrossRef] [PubMed]
  43. Vermeer, B.J.; Gilchrest, B.A.; Friedel, S.L. A proposal for rational definition, evaluation, and regulation. Arch. Dermatol. 1996, 132, 337–340. [Google Scholar] [CrossRef] [PubMed]
  44. Osea Malibu. Non-Toxic Seaweed Skin Care. Available online: https://oseamalibu.com/ (accessed on 14 December 2018).
  45. Thomas, N.V.; Kim, S.K. Beneficial effects of marine algal compounds in cosmeceuticals. Mar. Drugs 2013, 11, 146–164. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Pereira, L. Seaweeds as Source of Bioactive Substances and Skin Care Therapy—Cosmeceuticals, Algotheraphy and Thalassotherapy. Cosmetics 2018, 5, 68. [Google Scholar] [CrossRef] [Green Version]
  47. Buck, C.B.; Thompson, C.D.; Roberts, J.N.; Müller, M.; Lowy, D.R.; Schiller, J.T. Carrageenan is a potent inhibitor of papillomavirus infection. PLoS Pathog. 2006, 2, 671–680. [Google Scholar] [CrossRef] [Green Version]
  48. Fabrowska, J.; Łȩska, B.; Schroeder, G. Freshwater Cladophora glomerata as a new potential cosmetic raw material. Chemik 2015, 69, 491–497. [Google Scholar]
  49. Majmudar, G. Compositions of Marine Botanicals to Provide Nutrition to Aging and Environmentally Damaged Skin. U.S. Patent 8318178, 27 November 2012. [Google Scholar]
  50. Yarnpakdee, S.; Benjakul, S.; Senphan, T. Antioxidant Activity of the Extracts from Freshwater Macroalgae (Cladophora glomerata) Grown in Northern Thailand and Its Preventive Effect against Lipid Oxidation of Refrigerated Eastern Little Tuna Slice. Turk. J. Fish. Aquat. Sci. 2018, 19, 209–219. [Google Scholar]
  51. Ferreres, F.; Lopes, G.; Gil-Izquierdo, A.; Andrade, P.B.; Sousa, C.; Mouga, T.; Valentão, P. Phlorotannin Extracts from Fucales Characterized by HPLC-DAD-ESI-MSn: Approaches to Hyaluronidase Inhibitory Capacity and Antioxidant Properties. Mar. Drugs 2012, 10, 2766–2781. [Google Scholar] [CrossRef] [Green Version]
  52. Wang, J.; Jin, W.; Hou, Y.; Niu, X.; Zhang, H.; Zhang, Q. Chemical composition and moisture-absorption/retention ability of polysaccharides extracted from five algae. Int. J. Biol. Macromol. 2013, 57, 26–29. [Google Scholar] [CrossRef] [PubMed]
  53. Wijesinghe, W.A.J.P.; Jeon, Y.-J. Biological activities and potential industrial applications of fucose rich sulfated polysaccharides and fucoidans isolated from brown seaweeds: A review. Carbohydr. Polym. 2012, 88, 13–20. [Google Scholar] [CrossRef]
  54. Hartmann, A.; Gostner, J.; Fuchs, J.E.; Chaita, E.; Aligiannis, N.; Skaltsounis, L.; Ganzera, M. Inhibition of collagenase by mycosporine-like amino acids from marine sources. Planta Med. 2015, 81, 813–820. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Chrapusta, E.; Kaminski, A.; Duchnik, K.; Bober, B.; Adamski, M.; Bialczyk, J. Mycosporine-Like Amino Acids: Potential Health and Beauty Ingredients. Mar. Drugs 2017, 15, 326. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  56. Drouart, C. SEPPIC. Ingredients and Formulas. Available online: https://www.seppic.com/ (accessed on 7 December 2018).
  57. Kamei, Y.; Sueyoshi, M.; Hayashi, K.; Terada, R.; Nozaki, H. The novel anti-Propionibacterium acnes compound, Sargafuran, found in the marine brown alga Sargassum macrocarpum. J. Antibiot. 2009, 62, 259–263. [Google Scholar] [CrossRef]
  58. Cabarry, C. SpecialChem-Connect, Innovate, accelerate. The Universal Selection Source: Cosmetics Ingredients 2018. Available online: https://cosmetics.specialchem.com/ (accessed on 5 December 2018).
  59. Bommers, M. La-Mer. My Skin—And What It Needs. Available online: https://www.la-mer.com/en/ (accessed on 6 December 2018).
  60. Ziaja. Focus on Skin. Available online: http://ziaja.co.uk/ (accessed on 12 December 2018).
  61. Lusalgae. We Innovate in Marine Biotechnology. Available online: http://www.lusalgae.pt/lusalgae_en.html (accessed on 12 December 2018).
  62. Demais, H.; Brendle, J.; Herve, D.; Anca, L.L.; Lurton, L.; Brault, D. Argiles Intercalées. FR2874912B1. Available online: https://patents.google.com/patent/FR2874912B1/fr (accessed on 13 December 2019).
  63. Algabase. Available online: http://www.algabase.com (accessed on 12 December 2018).
  64. Verdy, C.; Branka, J.E.; Mekideche, N. Quantitative assessment of lactate and progerin production in normal human cutaneous cells during normal ageing: Effect of an Alaria esculenta extract. Int. J. Cosmet. Sci. 2011, 33, 462–466. [Google Scholar] [CrossRef]
  65. Thalgo. La Beaute Marine. Available online: http://www.thalgo.com/ (accessed on 6 December 2018).
  66. Chizhov, A.O.; Dell, A.; Morris, H.R.; Haslam, S.M.; McDowell, R.A.; Shashkov, A.S.; Nifant’ev, N.E.; Khatuntseva, E.A.; Usov, A.I. A study of fucoidan from the brown seaweed Chorda filum. Carbohydr. Res. 1999, 320, 108–119. [Google Scholar] [CrossRef]
  67. Chizhov, A.O.; Dell, A.; Morris, H.R.; Haslam, S.M.; McDowell, R.A.; Shashkov, A.S.; Nifant’ev, N.E.; Khatuntseva, E.A.; Usov, A.I. Fucoidan-Containing Cosmetics. U.S. Patent 20060093566A1, 13 August 2000. [Google Scholar]
  68. Ach Brito-SPA Collection. Available online: https://www.achbrito.com/pt/ (accessed on 27 January 2019).
  69. Jeunesse, M. 7th Heaven. Available online: https://www.my7thheaven.com/ (accessed on 6 January 2019).
  70. Wang, B.; Waters, A.L.; Valeriote, F.A.; Hamann, M.T. An efficient and cost-effective approach to kahalalide F N-terminal modifications using a nuisance algal bloom of Bryopsis pennata. Biochim. Biophys. Acta Gen. Subj. 2015, 1850, 1849–1854. [Google Scholar] [CrossRef] [Green Version]
  71. Daniels, B.A. Seaweed Extract Composition for Treatment of Diabetes and Diabetic Complications. Available online: https://patents.google.com/patent/US20070082868A1/en (accessed on 13 December 2019).
  72. Taskin, E.; Ozturk, M.; Taskin, E.; Kurt, O. Antibacterial activities of some marine algae from the Aegean Sea (Turkey). African. J. Biotechnol. 2007, 6, 2746–2751. [Google Scholar]
  73. Vasconcelos, A.G.; Araújo, K.V. POLISSACARÍDEOS EXTRAÍDOS DE ALGAS MARINHAS E SUAS APLICAÇÕES BIOTECNOLÓGICAS: UMA REVISÃO. Revista Brasileira de Inovação Tecnológica em Saúde 2015, 5, 27–51. [Google Scholar] [CrossRef] [Green Version]
  74. Tønnesen, H.H.; Karlsen, J. Alginate in drug delivery systems. Drug Dev. Ind. Pharm. 2002, 28, 621–630. [Google Scholar] [CrossRef] [PubMed]
  75. Guo, J.H.; Skinner, G.W.; Harcum, W.W.; Barnum, P.E. Pharmaceutical applications of naturally occurring water-soluble polymers. Pharm. Sci. Technol. Today 1998, 1, 254–261. [Google Scholar] [CrossRef]
  76. Yanagibayashi, S.; Kishimoto, S.; Ishihara, M.; Murakami, K.; Aoki, H.; Takikawa, M.; Fujita, M.; Sekido, M.; Kiyosawa, T. Novel hydrocolloid-sheet as wound dressing to stimulate healing-impaired wound healing in diabetic db/db mice. Biomed. Mater. Eng. 2012, 22, 301–310. [Google Scholar] [CrossRef] [PubMed]
  77. Glynn, K.P.; Martin, A. Biodegradable Wound Care Products with Biocompatible Artificial Skin Treatment and Healing Accelerator. U.S. Patent Application No. 13/135646, 14 February 2013. [Google Scholar]
  78. Mandel, K.G.; Daggy, B.P.; Brodie, D.A.; Jacoby, H.I. Review article: Alginate-raft formulations in the treatment of heartburn and acid reflux. Aliment. Pharmacol. Ther. 2000, 14, 669–690. [Google Scholar] [CrossRef] [PubMed]
  79. Hemmingson, J.A.; Falshaw, R.; Furneaux, R.H.; Thompson, K. Structure and antiviral activity of the galactofucan sulfates extracted from Undaria pinnatifida (Phaeophyta). J. Appl. Phycol. 2006, 18, 185–193. [Google Scholar] [CrossRef]
  80. Church, F.C.; Meade, J.B.; Treanor, R.E.; Whinna, H.C. Antithrombin activity of fucoidan. The interaction of fucoidan with heparin cofactor II, antithrombin III, and thrombin. J. Biol. Chem. 1989, 264, 3618–3623. [Google Scholar] [PubMed]
  81. Kim, E.J.; Park, S.Y.; Lee, J.-Y.; Yoon, J.H. Fucoidan present in brown algae induces apoptosis of human colon cancer cells. BMC Gastroenterol. 2010. [Google Scholar] [CrossRef] [Green Version]
  82. Hsu, H.Y.; Takada, H.; Iha, M.; Nagamine, T. Attenuation of N-nitrosodiethylamine-induced liver fibrosis by high-molecular-weight fucoidan derived from Cladosiphon okamuranus. Oncotarget 2014. [Google Scholar] [CrossRef] [Green Version]
  83. Choi, Y.-H.; Yang, D.J.; Kulkarni, A.; Moh, S.H.; Kim, K.W. Mycosporine-Like Amino Acids Promote Wound Healing through Focal Adhesion Kinase (FAK) and Mitogen-Activated Protein Kinases (MAP Kinases) Signaling Pathway in Keratinocytes. Mar. Drugs 2015, 13, 7055–7066. [Google Scholar] [CrossRef] [Green Version]
  84. Zhang, J.; Ewart, H.S.; Barrow, J.K.S.; James, C. Ascophyllum Compositions and Methods. U.S. Patent Application No. 11/660275, 13 November 2008. [Google Scholar]
  85. Lee, B.-H.; Choi, B.-W.; Ryu, G.-S.; Kim, S.-K.; Shin, H.-C. Material Separated from Ecklonia cava, Method for Extracting and Purifying the Same and Use Thereof as Antioxidants. U.S. Patent 6384085, 12 December 2002. [Google Scholar]
  86. Shibata, T.; Kawaguchi, S.; Hama, Y.; Inagaki, M.; Yamaguchi, K.; Nakamura, T. Local and chemical distribution of phlorotannins in brown algae. J. Appl. Phycol. 2004, 16, 291–296. [Google Scholar] [CrossRef]
  87. Hwang, H.; Chen, T.; Nines, R.G.; Shin, H.; Stoner, G.D. Photochemoprevention of UVB-induced skin carcinogenesis in SKH-1 mice by brown algae polyphenols. Int. J. Cancer 2006, 119, 2742–2749. [Google Scholar] [CrossRef] [PubMed]
  88. Sugiura, Y.; Takeuchi, Y.; Kakinuma, M.; Amano, H. Inhibitory effects of seaweeds on histamine release from rat basophile leukemia cells (RBL-2H3). Fish. Sci. 2006, 72, 1286–1291. [Google Scholar] [CrossRef]
  89. Shibata, T.; Fujimoto, K.; Nagayama, K.; Yamaguchi, K.; Nakamura, T. Inhibitory activity of brown algal phlorotannins against hyaluronidase. Int. J. Food Sci. Technol. 2002, 37, 703–709. [Google Scholar] [CrossRef]
Figure 1. Value of the seaweed market worldwide in 2017 and 2024 (in billion U.S. dollars) [10].
Figure 1. Value of the seaweed market worldwide in 2017 and 2024 (in billion U.S. dollars) [10].
Marinedrugs 18 00017 g001
Table 1. Examples of seaweed-derived food products.
Table 1. Examples of seaweed-derived food products.
Seaweed speciesExtractProduct(s)Reference(s)
Chlorophyta (green seaweed)
Cladophora sp.Fresh or dry Sea vegetable [14]
Ulva (formerly Enteromorpha) sp.,
Monostroma sp.
Fresh or dry Sea vegetable[14]
Ulva pertusaFresh or drySea vegetable (known as green nori)[15]
Ulva rigidaFresh or dry Sea vegetable
Seasoning in ready to eat canned fish
Added to marine salt
[16]
Ochrophyta, Phaeophyceae (brown seaweed)
Fucus vesiculosusExtract 1
Fresh or dry
Incorporated in honey
Seasoning in ready to eat canned fish
Added to marine salt
[16,17]
Himanthalia elongataDry Sea vegetable
Pasta
[18,19]
Himanthalia elongata,
Undaria pinnatifida
Fresh or dry (whole or in flakes)
Sodium alginate extract
Wrap
Tartar with olives
Kelp noodles
[14,18,19,20]
Sargassum fusiformeFresh or drySea vegetable[15]
Undaria pinnatifidaFresh or drySea vegetable
Pasta
[14,19]
Rhodophyta (Red seaweed)
Chondrus crispusFresh or drySea vegetable [14,16]
Meristotheca papulosaFresh or drySea vegetable [14]
Palmaria palmataFresh or dry (whole or in powder)Sea vegetable
Bacon substitute
[16,18]
Pyropia spp.
(P. dioica, P. tenera, P. yezoensis),
Porphyra umbilicalis
Fresh or drySea vegetable
Nori sheets
Laverbread
Crispy nougat
Crispy thins/snacks
Added to marine salt
[15,16,19,21]
1 The extract/compound used in the product(s) is not specified in the reference.
Table 2. Phycocolloids utilized in food industries and its properties.
Table 2. Phycocolloids utilized in food industries and its properties.
Seaweed speciesCompoundProduct(s)PropertiesReference(s)
Rhodophyta (red seaweed)
Gigartina skottsbergiiCarrageenan:
[A] lota
[B] Kappa
[C] Lambda
yoghurts, flans, jellies,
ice creams,
meat products (ham)
[A] and [B]—gelling
[C]—thickening/viscosifier
[9,25,26]
Gelidium sp.,
Gracilaria sp.,
Pterocladiella sp.
Agarvegetal jellyGelling[7,9]
Ochrophyta, Phaeophyceae (brown seaweed)
Lessonia spp.,
Macrocystis sp.
Alginateyoghurts, ice creamsEmulsifying, Gelling, Stabilizer[27]
Table 3. Cosmetical products containing seaweed parts or extracts.
Table 3. Cosmetical products containing seaweed parts or extracts.
Seaweed species.ExtractProduct(s)PropertiesReference(s)
Chlorophyta (green seaweed)
Caulerpa lentilliferaExtract (Rich in unsaturated fatty acids and vitamin A and C)Hair and skin care products (shampoo, shower gel, soaps, lotions)Moisturizing; anti-aging; whitening/lightening agent[58]
Cladophora glomerataExtract (Rich in unsaturated fatty acids and polyphenols)Skin care products (emulsion, cream, lotion)Moisturizing; anti-aging [48,50]
Codium tomentosumExtract Codiavelane®Skin care products (creams, lotions)Anti-aging; moisturizing[49,52,59]
Monostroma sp.Extract (rich in water-soluble polysaccharides) Extract 1Skin care products (e.g. slimming and anti-cellulitis formulations)
Hair and nails care products (hair and nails growth)
Facial Mask
Moisturizing; anti-inflammatory agent; anti-aging[49]
Ulva compressa (as Enteromorpha compressa)Extract 1Skin care products (creams, lotions)Moisturizing[59,60]
Ulva lactucaHydrolysed extract Aosaine® (three-quarters of aosaine consists of amino acids very similar those responsible for the skin’s elasticity)Skin care products (creams, lotions)Anti-aging (anti-wrinkle and collagen stimulation)[49,56,58]
Ulva spp.Aqueous extract (rich in ulvans)
Extracts 1
Skin care product (creams, lotions)
Bath salts (thalassotherapy kit)
Moisturizing; whitening/lightening; antioxidative; chelating; anti-inflammatory; calming[61,62,63]
Ochrophyta, Phaeophyceae (brown seaweed)
Alaria esculentaExtract (rich in fatty acids and trace elements)Skin care products (creams, lotions)Moisturizing; anti-aging[59,64]
Ascophyllum nodosumExtract 1Skin care product (cream)Anti-ageing; skin softness and elasticity restoring[59]
Bifurcaria bifurcataExtract 1Bath salts, gel and facial mask (thalassotherapy kit)Exfoliant; detoxifying; nourishing[61]
Fucus serratusExtract 1Oral-care productProtecting agent (reduces gingivorrhagia)[58]
Fucus spiralisExtract 1Facial mask and (imperfection corrector) gelSkin purification; oiliness and pore dilatation reduction[65]
Fucus vesiculosusExtract (rich in muco-polysaccharides)Slimming and anti-cellulitis cosmetic formulations
Facial Mask
Skin softness and elasticity properties;
exfoliant; brightening; detoxifying
[49,58]
Halopteris scopariaExtract (rich in anti-oxidative polyphenols, cytokines and betaines)Skin care products (cream, lotion)Skin softness and elasticity restoring[59]
Sargassum fusiforme (as Hizikia fusiforme)Extract 1Skin care products (creams)Whitening/lightening;[58]
Laminaria digitataExtract (rich in trace elements, like iodine)Skin care products
(lotions, anti-cellulitis formulations)
Anti-aging (prevent lines and wrinkles. Collagen and elastin stimulation); anti-cellulitis; moisturizing[58,59,60]
Laminaria hyperboreaExtracts 1Skin care product (cream)
Facial masks
Anti-aging; moisturizing; anti-acne[59,65]
Laminaria ochroleucaExtract ANTILEUKINE 6™
Extracts 1
Hair and skin care products (body lotion, shampoo and conditioner)Anti-aging; sun-protector; anti-acne; moisturizing[56,59,65]
Saccharina latissima (as Laminaria saccharina)Extract (w/ hyaluronic acid and polysaccharides; sodium and potassium ions; phlorotannins (polyphenols))Skin care product (cream)Antioxidant; anti-aging; anti-blemishes[59]
Macrocystis pyriferaExtract (rich in polysaccharides) Extract 1Skin care product (anti-aging balm)Moisturizing; antioxidant; anti-aging; anti-blemishes[44,59]
Pelvetia canaliculataExtracts 1Hair and skin care products (creams, lotions, shampoo)Moisturizing; anti-aging (anti-wrinkle and collagen stimulation)[58,59]
Saccharina japonicaPolysaccharide extract (rich in fucoidan)Skin care products (anti-cellulitis formulations)Moisturizing; anti-aging; anticellulite[52,53,66]
Kjellmaniella crassifoliaFucoidan extractHair and skin care products (creams, lotions, shampoo)Moisturizing; anti-aging; nourishing; preventing hair loss[67]
Sargassum muticumExtract (rich in proteins)Skin care products (creams, lotions)Anti-aging (anti-wrinkle, antioxidant, and collagen stimulation. Reduce skin damage caused by UVB and chemical stress)[59]
Undaria pinnatifidaExtract 1
Powder, whole leaf and extract forms (rich in fucoidan)
Skin care products
(aromatherapy oil; face and body oil; body scrub)
Anti-aging (anti-wrinkle); whitening/lightening; moisturizing; nourishing[44,58,59]
Rhodophyta (red seaweed)
Asparagopsis armataExtract ASPAR’AGE™Skin care products (creams)Moisturizing; anti-aging[56]
Chondrus crispusExtracts 1
Powder
Hair and skin care products (lotions; creams; make-up removers; body scrub; shampoo; conditioner)
Lipsticks and deodorants
Algae and sea salt soap
Moisturizing; cleaning; exfoliant;
Emulsifier and thickener;
cleaning; exfoliant
[58,59,65,68]
Corallina officinalisExtract 1Skin care product (cream)Anti-redness[59]
Gelidium corneum (as Gelidium sesquipedale)Extract (rich in minerals, trace elements and amino acids)Skin care product (lotion)Skin softness and elasticity restoring[59]
Gigartina skottsbergiiPowder, whole leaf and extract 1
Extract (rich in polysaccharides, vitamins and minerals)
Bath and skin care products (mineral-rich seaweed bath soak)Moisturizing; whitening/lightening[44]
Gracilaria confertaExtract 1Skin care products (creams)Moisturizing; nourishing[58]
Palmaria palmataExtract 1Skin care products (Facial clarifier gels and emulsions)Skin clarification (reduction of pigmentation imperfections), and uniformization (skin grain homogenization)[65]
Pyropia tenera (as Porphyra tenera)Extract 1Skin care products (creams)Sun protector[58]
Porphyra umbilicalisExtract 1Skin care products (cream; facial scrub masks)Moisturizing; exfoliant; brightening; detoxifying[59,69]
Vertebrata lanosa (as Polysiphonia lanosa)Extract 1Skin care products (creams)Moisturizing; nourishing[52,65]
1 The extract/compound used in the product(s) is not specified in the reference.

Share and Cite

MDPI and ACS Style

Leandro, A.; Pereira, L.; Gonçalves, A.M.M. Diverse Applications of Marine Macroalgae. Mar. Drugs 2020, 18, 17. https://doi.org/10.3390/md18010017

AMA Style

Leandro A, Pereira L, Gonçalves AMM. Diverse Applications of Marine Macroalgae. Marine Drugs. 2020; 18(1):17. https://doi.org/10.3390/md18010017

Chicago/Turabian Style

Leandro, Adriana, Leonel Pereira, and Ana M. M. Gonçalves. 2020. "Diverse Applications of Marine Macroalgae" Marine Drugs 18, no. 1: 17. https://doi.org/10.3390/md18010017

APA Style

Leandro, A., Pereira, L., & Gonçalves, A. M. M. (2020). Diverse Applications of Marine Macroalgae. Marine Drugs, 18(1), 17. https://doi.org/10.3390/md18010017

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop