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Review

Applications of Probiotic Constituents in Cosmetics

1
State Key Laboratory of Biobased Material and Green Papermaking, Qilu University of Technology, Shandong Academy of Science, Jinan 250353, China
2
School of Bioengineering, Qilu University of Technology, Shandong Academy of Science, Jinan 250353, China
3
Huaxi Biotechnology Co., Ltd., No. 678, Tianchen Road, Lixia District, Jinan 250000, China
4
Zhucheng Dongxiao Biotechnology Co., Ltd., Zhucheng 262200, China
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
Molecules 2023, 28(19), 6765; https://doi.org/10.3390/molecules28196765
Submission received: 8 August 2023 / Revised: 19 September 2023 / Accepted: 20 September 2023 / Published: 22 September 2023

Abstract

:
Over the past few decades, research on the benefits of beneficial microorganisms on skin health has expanded and attracted a lot of attention. Today, a wide range of probiotic products are becoming available. With their extensive component profiles and varied physiological effects, probiotics, as well as extracts of them, have a significant impact on cosmetics. However, the present boom in consumer interest in alternatives has broadened the probiotic industry’s research and development frontiers. Considering the foregoing, it should come as no surprise that probiotics are highly valued for their proven anti-aging, skin whitening, anti-inflammatory, and photoprotective effects. This review aims to compile information on probiotics’ properties, their extracts, and preparations used in cosmetics. It also further summarizes research and applications on probiotic fermentation to promote the use of probiotic fermentation products in cosmetics. Notably, this review also adds information on particular properties and mechanisms of action of probiotics, which fills a gap in the research and application of probiotics in skin treatment and care. Their antioxidant and anti-aging qualities have received particular consideration. This review provides a new basis for the broad application of probiotics in cosmetics.

1. Introduction

Cosmetics are described by the US Food and Drug Administration (FDA) as “products (excluding pure soap) used to cleanse, beautify, enhance attractiveness, or alter the appearance of the human body”. Products that care for skin, hair, and mouth meet this standard. Probiotics and postbiotics are two product categories connected to the microbiome developed by the International Cosmetic Regulatory (ICCR) Collaboration [1]. Probiotic is “a living microbe that, when administered in sufficient amounts, provides a health benefit to the host” [2]. Probiotic products must meet three essential criteria. (1) To use the strain for its intended purpose, it must be genetically and phenotypically described and supported by results from experiments published in peer-reviewed journals. (2) At the time of use, the product must have a quantity of live microorganisms similar to the product demonstrated in clinical studies to benefit the designated target site. (3) If people are the intended receivers, the delivery technique, dosage, and length of use should be determined through human studies [3,4]. The microbiological content of cosmetics is anticipated to be modest (less than 500 Colony-Forming Units/gram (CFUs/g) for eye products and less than 1000 CFUs/g for other products) for safety reasons. There can be no natural probiotic cosmetics if it is impossible to include live bacteria. They may still have advantageous components from probiotic strains, in any case. Metazoons, also called bacterial lysates, ferments, and filtrates, are “preparations of non-living microorganisms or their components that have health benefits for the target host [5].” They can also be applied to the skin and mucous membranes of the host. These criteria do not cover purified metabolites or components that are cell-free. Filtrates are not considered epigenetic if they do not have biological components. Bacterial lysates and ferments may fit into this category depending on their makeup. Safety, functionality, and technical utility have been identified as essential criteria for the selection of probiotic bacteria, according to the World Health Organization (WHO), the Food and Drug Administration (FDA), and the European Food Safety Authority (EFSA). Experiments can be used to determine if microbial strains meet the requirements mentioned above in vitro. It is possible to screen microorganisms for their potential as probiotic strains based on these selection criteria confirmed by in vitro experiments [1].
Figure 1 illustrates the main processes by which probiotics promote skin health. Probiotics have been demonstrated to possess a number of skin-beneficial features, including the ability to reduce skin inflammation, heal several skin conditions, and shield against allergic contact dermatitis. Additionally, they are essential for enhancing the skin barrier, promoting water absorption, and delaying the aging process of the skin [6]. These data offer a theoretical foundation for creating probiotic products.
More and more studies have proven that probiotics have many benefits for the skin. Figure 2 shows the effects of probiotics in terms of anti-aging, antioxidants, whitening, and anti-wrinkling, which have increased the addition of probiotics in cosmetics.
Probiotics have recently been used in common care items. These cosmetics, such as face creams, moisturizing lotions, tonics, body washes, hair products, and beauty masks, contain pieces of cell walls and inert bacteria. Since live bacteria cannot be found in cosmetics, several companies make probiotic skin care products and add some probiotics. Some people will include prebiotics (probiotic “food,” such as oligosaccharides, galactose oligosaccharides, and fructooligosaccharides), which can prevent the growth of dangerous bacteria from readjusting the makeup of the skin microbiome while supporting the growth of helpful bacteria [7]. Others will add bacteriocin (the “active products” of probiotics, metabolites, such as lactobacillus fermentation products and yeast fermentation product extracts) to skin care products in order to assist the skin in readjusting the micro-ecological balance because of its small molecules, good stability, high-temperature resistance, acid and alkaline opposition, and acid and alkaline resistance. Probiotic extracts are now utilized increasingly frequently in cosmetics; lactobacillus is the most common ingredient. Various goods are available because of the abundance of producers and cosmetic forms, and it is challenging to calculate their precise quantity because new items enter the market virtually every year. Table 1 provides examples of 35 cosmetic products using probiotics or probiotic fermentation broth.
Probiotics themselves and their extracts play an essential role in the cosmetic market. There is an increasing number of cosmetics containing probiotics, especially those using probiotic fermentation products. Therefore, there is a need for authors to provide a review to focus on probiotics in cosmetics. Currently, old review articles in the field do not detail the mechanism of action of probiotics in cosmetic applications. The present review describes, in detail, the two significant skin challenges, anti-aging and antioxidant, from in vitro and ex vivo experiments to the mechanism of action. Below are a few older review articles that have been published in this area. Jinyan Yu et al. [8] reviewed the effects of probiotics on skin whitening, moisturizing, anti-aging, improving skin wrinkles, and deodorizing, which provided a new rationale for the broad application of probiotics in skin care. The review by Scarlett Puebla-Barragan et al. [4] discussed the current market, regulatory aspects, and potential applications of probiotics in the personal care industry. Ting Gao et al. [9] reviewed the application and mechanism of probiotic-mediated gut microbiota in skin care, providing a new rationale for the wide application of probiotics in skin care. Marco Duarte et al. [10] conducted a study on some postbiotics derived from probiotics. The review focuses on what is currently known about these compounds, the benefits of their use, the main postbiotics products available on the market and the players, the main trends in production, and the production methods available. Arun Karnwal et al. [11] reviewed the application of microbial biosurfactants instead of chemical surfactants in existing cosmetic and personal skin care pharmaceutical formulations. Some of the previously published references mentioned above also mention probiotics’ antioxidant and anti-aging properties. However, concerning skincare rather than cosmetic applications, they describe microbial biosurfactants and postbiotics rather than probiotics and their extracts. The present review aims to collect information about probiotics and their extracts and formulations for cosmetic applications.
Twenty years ago, the terms probiotics, prebiotics, and microbiome were unknown in the cosmetics industry. Although chemistry is a foundational element of the cosmetics industry, it has not yet been properly applied to molecules that identify the advantages of microbial products. Given the growth of the microbiome area, it is essential that professionals with knowledge of microbiology and chemistry arise in order to guarantee that consumers receive high-quality cosmetics that adhere to the definitions of probiotics, prebiotics, etc. There is no question that the inclusion of probiotics in cosmetics could result in novel approaches to enhancing both look and health, which would provide regulatory difficulties for the entry of cosmetics into the health sector. While promoting regulatory improvements, we must insist on clinical validation, verification of product safety, and strict guidelines for handling, storing, and using items that contain microbes and their byproducts or cell walls. Unfounded assertions are useless to everyone, while scientific research yields goods that are very beneficial to human health and well-being.

2. Application of Probiotics in Anti-Aging Cosmetics

The two types of skin aging are natural aging and photoaging. The term “natural aging” describes the contribution of internal components in the body brought on by exposed and unexposed areas, most notably manifested by wrinkles and skin relaxation. Ultraviolet radiation can cause photoaging when it enters the skin, which is a significant contributor to aging skin changes and cancer of the skin [12]. Changes in skin-related microbial communities, elevated skin pH, aberrant reactive oxygen species (ROS) generation, decreased collagen levels, and altered immune response are characteristics of photoaged skin.
The current probiotic cosmetics offer anti-aging effects on skin tissues primarily through the following mechanisms, per studies on the physiology of skin and aging mechanisms: hydrating and mending skin barrier function, replenishing collagen and elastin in the skin, and antioxidants [13]. In Table 2, various research investigations on probiotics’ antioxidant and anti-aging effects are compiled.
With the intensification of the aging of society and the pursuit of youth, the share of anti-aging skin care products in the cosmetics market has gradually increased. Consumers’ demand for the safety and efficacy of anti-aging cosmetics has also promoted the continuous improvement and improvement of the research and development technology of anti-aging cosmetics.

2.1. Hydrate and Restore the Skin’s Barrier

Moisturizing and repairing the skin’s barrier function are two crucial steps anti-aging cosmetics must take to address the issue of aging skin. Dry skin, a crucial sign of aging, will result from a reduced epidermis barrier function. Natural moisturizing components in keratinocytes and sebum membranes, which shield the skin’s surface and keep water from evaporating, keep the skin moisturized. Deteriorated sebaceous membranes, impaired epidermal barriers, and finally drier skin are all symptoms of aging skin. In order to make anti-aging cosmetics more effective, substances with moisturizing and skin barrier repair properties might be incorporated. For instance, adding the bioactive substances Streptococcus thermophilus S244 and Streptococcus salivarium spp. to cosmetic formulae can result in the production of enzymes that hydrate the skin, reducing dryness and slowing the aging process [20]. Figure 3 displays the moisturizing and anti-aging properties of probiotics.
According to clinical trials, oral probiotics can enhance skin hydration and increase skin water content, which can reduce wrinkles. In hairless mouse epidermis, oral treatment of Bifidobacterium breve or Lactobacillus plantarum decreased UV-induced water loss [21,22]. It is possible to increase skin water content and decrease wrinkles by taking a L. plantarum lysate or heat-inactivated lactococcus lactis orally [24,25]. On this basis, Hiroko Nakai et al. [27] studied the local application of heat-inactivated Lactobacillus plantarum L-137 (HK L-137). They found that treating epidermal cells with the cell fluid of HK L-137 (preparation of HK L-137 [38]) could increase the content of hyaluronic acid (HA). The mechanism of its action is that HK L-137 induces the production of cytokine IFN-γ to activate the NFκB pathway through a synergistic effect with TNF-α to enhance the expression of hyaluronate synthase mRNA in fibroblasts, thus producing more HA to play a role in moisturizing and anti-wrinkling.
The barrier and water retention functions of a healthy stratum corneum depend heavily on ceramide. According to studies, Streptococcus thermophilus preparations with ultrasonic therapy can boost the amount of ceramide in the stratum corneum, enhancing the barrier function and keeping the stratum corneum flexible [39].

2.2. Antioxidation

The excessive attack of free radicals on biological tissues like chromosomes, mitochondria, cell membranes, and connective tissues would result in the body aging, claims the free radical theory of aging [18]. Unsaturated fatty acids in the skin will be impacted by high quantities of free radicals, leading to unstable lipid peroxidation that will eventually break down into malondialdehyde. Malondialdehyde will quickly attack proteins and phospholipids and react to create lipofuscin, a lipid–protein complex that builds up in cells and is a marker of cell aging. As a result, eliminating many ROS is essential for preventing aging.
The information indicates that superoxide dismutase (SOD), glutathione (GSH), vitamin E (VE), and coenzyme Q10 (Q10) are the primary active raw materials with antioxidant action. A biological antioxidant enzyme called SOD efficiently eliminates too many superoxide free radicals from the body. The primary function of VE in the body is as an antioxidant; on the one hand, it can eliminate free reactive oxygen radicals and stop the production of lipid peroxide. On the other hand, it can safeguard SOD and lessen the pace at which soluble collagen becomes insoluble. Similar to VE, coenzyme Q10 is a naturally occurring antioxidant made by the cell itself and one of the elements that make up the mitochondrial respiratory chain.
We are aware that ROS generated by UV irradiation can increase the expression level of matrix metalloproteinases (MMPs), leading to the induction of apoptosis. ROS are also known to contribute to skin aging and pigmentation. Experimental proof of the antioxidant activity of heat-killed Lactobacillus acidophilus KCCM12625P (AL) was provided by Hye Yeon Lim et al. [40]. In human keratinocytes and human dermal fibroblasts (HDFs) exposed to UV light, AL was discovered to regulate the levels of ROS and MMPs. AL is, therefore, a cosmetic component that has anti-aging properties. AL can also dilute UV-induced melanin and reduce UV-induced pigmentation in B16F10 murine melanoma cells at the same time. Additionally, research has shown that heat-inactivated Lactobacillus acidophilus can reverse UV-induced skin damage [41] and boost the antioxidant defenses of the skin [17], which is therapeutically employed to prevent wrinkle formation.
Through an experimental study, Xiaofang Zhang et al. [16] discovered the anti-wrinkle effect of heat-killed Lactobacillus rhamnosus (RL). After receiving RL, mouse skin fibroblasts’ antioxidant capacity was increased and their ROS content was decreased, and human epidermal melanocytes were also able to produce anti-melanin, which might be used as an anti-photoaging ingredient in cosmetics.
In the realm of antioxidant research, where the combination of probiotics and antioxidants has synergistic effects on one another, β-Nicotinamide Mononucleotide (NMN) and lactic acid bacteria (LAB) have been investigated more and more. The combination of NMN and Lactobacillus fermentum TKSN041 has been shown in studies to be able to increase the levels of SOD, catalase (CAT), and interleukin in the skin, reduce UV-induced oxidative damage to the skin, and improve the overall antioxidant capacity of the skin. It is anticipated to become a potent drug for the prevention and treatment of skin photoaging [42].
Probiotics can create metabolites such as probiotic peptides, organic acids, flavonoids, alcohols, and polyphenols after heating some bacterial components such as lipoteichoic acid, peptidoglycan, exopolysaccharides (EPS), and cell surface proteins. Human dermal fibroblasts’ oxidative damage and photoaging have been shown to be reduced by lipoteichoic acid, which is extracted from probiotics [15]. In normal dermal fibroblasts and mouse melanoma cells, heat-killed Lacticaseibacillus paracasei (PL) can reduce UV-B-related oxidative damage and photoaging [14]. MMP expression, as well as extracellular matrix-degrading enzymes, were enhanced by UVR irradiation. MMP-1 is an interstitial collagenase that breaks down collagen’s triple helix among the MMP family of enzymes. We discovered that MMP-1 expression was reduced by lipoteichoic acid that was extracted from the cell wall of L. plantarum. Additionally, it can encourage collagen synthesis and hinder its breakdown, which both aid in lowering ROS production [43]. The theoretical underpinnings for the creation of active ingredients in skin antioxidants and anti-photoaging treatments are provided by this evidence.

2.3. Other Anti-Aging Effects

Probiotics include bioactive compounds in their extracellular vesicles, which are beneficial for skin health and anti-aging. Lipopolysaccharides, for instance, are found in the extracellular vesicles of gram-negative bacteria [26], while lipoteichoic acid is found in the extracellular vesicles of gram-positive bacteria [44]. These chemicals have a wide range of response mechanisms at their disposal. According to Chan Song Jo et al.’s research [45], women in their 20s had an average of more L. plantarum in their skin than women in their 50s. Extracellular vesicles (EVs) secreted by L. plantarum were found to have a number of anti-aging properties. These characteristics include their ability to prevent the activity of MMP-1 and elastase, enhance skin elasticity, and preserve cell shape. Second, they raises the level of filaggrin mRNA expression, which is necessary for epidermal homeostasis and the preservation of skin barrier function. With age, the expression of filaggrin is usually decreased [28], which increases the composition of the extracellular matrix, which is conducive to maintaining cell morphology.
Additionally, studies in humans have shown that EVs can lessen photoaging and age-related pigmentation of eye wrinkles. EVs are thus a potent anti-aging ingredient for skin treatments. By concurrently inhibiting melanin development and enhancing UV-A absorption with the help of L. plantarum SM4 biotransformation, the inner shell of the chestnut can be used as a cosmetic material [46].

3. Using Probiotics to Whiten Skin and Get Rid of Freckles

The amount of melanin produced by pigmented cells in the epidermis and its distribution in the top layer of skin, where melanin is transferred and amplified by prolonged exposure to sunlight or ultraviolet radiation, determines the color of human skin.
The need for whitening goods among young people is rising in modern society. There are several diets, medications, and cosmetics on the market today that have whitening properties. Arbutin, kojic acid, and niacinamide are a few melanin-producing inhibitors that have recently been discovered and utilized as skin lighteners [47,48,49]. However, the usage of naturally occurring chemicals rather than chemically synthesized ones has drawn greater attention.

3.1. Tyrosinase Activity Inhibition

Numerous enzymes and chemical catalytic processes are involved in the formation of skin melanin. Tyrosinase is essential for the production of melanin. Tyrosinase activity can be inhibited to reduce melanin formation, lighten the skin, and produce the effect of whitening. Figure 4 shows the mechanism of action of tyrosinase inhibition by probiotics. Because of their low toxicity and high absorption, tyrosinase inhibitors generated by probiotics are regarded as promising potential skin whitening agents [50]. Recent years have seen a rise in the use of probiotics in whitening cosmetics, such as the lactic acid in LAB, which can directly reduce melanin formation by inhibiting tyrosine. They can also whiten skin by interfering with tyrosinase expression. Tyrosinase was likewise suppressed by the probiotic culture’s supernatant. The anti-tyrosinase effect was seen in the supernatant of Bifidobacterium IDCC 4201 and L. plantarum IDCC 3501, which decreased melanin synthesis and altered the expression of proteins involved in the melanin formation pathway. A potential tyrosinase inhibitor is phenylacetic acid’s metabolite. The generation of phenylacetic acid’s anti-melanin may be boosted by the synergistic interaction of other functional molecules in the supernatant of the probiotic culture medium. Consequently, a probiotic culture medium supernatant with a high phenyl lactic acid content has the potential to be used in food and medicine as an anti-melanogenic agent [29].
The meaning of the abbreviations in the chart is as follows: adrenocorticotropic hormone (ATH), a-melanocyte activator (a-MSH), basic fibroblast growth factor (BFGF), cyclic adenosine monophosphate (cAMP), endothelin vascular peptide-1 (ET-1), granulocyte-macrophage-activating factor (GM-SCF), melanin receptor-1 (MCR-1), prostatic enzyme E2 (PGE2), protein kinase A (PKA), protein kinase C (PKC), phospholipase C (PLC), stem cell factor (SCF), and adenylate cyclase (ATC).
There are currently chemicals used in cosmetics and pharmaceutical products that can inhibit the melanin synthetase tyrosinase in melanocytes. However, the majority of the compounds that are now on the market can only stop the production of melanin; they cannot get rid of melanin that has already been created and implanted. They are less effective at lowering the amount of melanin in the skin. Kimchi-derived Staphylococcus lactis PMC48 can destroy melanin, degrade melanin, and inhibit tyrosinase, according to Sukyung Kim et al. It is superior to current melanin production inhibition approaches and is anticipated to be highly valuable as a raw material for cosmetics and medications that break down melanin [30].

3.2. The Role of Lipoteichoic Acid

Lipoteichoic acid is the main component of the cell wall of gram-positive bacteria. The modulation of the gastrointestinal and immunological systems, skin moisturization, and photoaging are only a few of the many positive effects of lipoteichoic acid, which is obtained from L. plantarum. Lipoteichoic acid’s use in the management of pigmentation was investigated by Hye Rim Kim et al. By activating the ERK and PI3K/AKT pathways, it reduced tyrosinase activity in cells and hematopoietic enzyme expression. Lipoteichoic acid, which was discovered from L. plantarum, can, therefore, treat melanosis and be employed as a cosmetic bleaching agent [31]. The formation of anti-melanin is aided by the lipoteichoic acid of L. plantarum GMNL6, which also functions as a cosmetic regulating substance [51].

3.3. Other Whitening Effects

The volunteers’ skin hydration, skin tone, spots, wrinkles, UV spots, and porphyrin syndrome were all improved after using a cream containing L. plantarum [32]. Staphylococcus sphaerus extract, an anti-melanin-producing agent, can reduce the pigmentation caused by melanocytostimulus [33]. These probiotics produce substances that are widely used in both medicine and cosmetics.

4. Probiotics Used in Anti-Inflammatory Cosmetics

In light of the rapid expansion of oral probiotics, numerous topical probiotic formulations have been proposed to treat skin micro-ecological diseases and encourage immunological homeostasis by balancing skin microbiota [52]. To maintain the skin’s micro-ecological balance, they produce antibacterial and anti-inflammatory substances to stop pathogen invasion and the growth of opportunistic microorganisms [35].
Topical probiotics dramatically reduced the signs and symptoms of rosacea, atopic dermatitis, and acne in a few small-scale clinical studies. Although the exact mechanism is uncertain, probiotics are thought to have anti-inflammatory effects via promoting regulatory T cells, producing anti-inflammatory cytokines (such IL-10), competing with pathogens for nutrients, and aggregating and replacing pathogens. Probiotic strains with symbiotic skin microorganisms, like Lactobacillus, Bifidobacterium, and Streptococcus, have been linked to skin immune-modulating effects by preventing the development of biofilms, lowering cytokines that cause systemic inflammation, and directly competitively inhibiting binding sites [53].

4.1. Cutaneous Inflammation

In their studies, Ia Khmaladze et al. [34] found that Lactobacillus reuteri DSM 17938 and its lysates might reduce skin irritation brought on by UVB (ultraviolet B, wavelength 280 nm~320 nm, mid-frequency medium-wave) exposure. Bacteria that are detrimental to the skin (Staphylococcus aureus, Streptococcus pyogenes, Bacillus acnes, and Pseudomonas aeruginosa) are inhibited by live L. reuteri DSM 17938. It is possible to cure inflammatory skin diseases using this strain. Heat-killed Lactococcus lactis H61 water extract is mixed with cosmetic ingredients for topical application. The inflammation of skin cells brought on by UVB loss was shown to be reduced by its ability to block the angiotensin-converting enzyme (ACE) (topical administration of angiotensin-converting enzyme inhibitors may enhance photoaged skin [54]). Interleukin-8 (IL-8) levels caused by UV radiation were lowered in cells pretreated with the extract, which also absorbed electromagnetic radiation in the UVB range [36]. This demonstrates that the extract has a number of advantages, such as anti-inflammation of the skin and UV damage prevention. The Bifidobacterium longum (BL) lysate possesses anti-inflammatory properties. Adding the BL lysate to cosmetics can improve various parameters related to inflammation (such as vasodilation, edema, mast cell degranulation, and reduced TNF-α release). The local use of BL preparation promotes skin homeostasis and guards against adverse environmental impacts that cause skin sensitivity (cold in winter, dry air) [37].
Atopic dermatitis (AD), also known as atopic eczema, is a chronic inflammatory skin condition that frequently flares up and is characterized by dry, itchy skin [55]. An essential component in the pathophysiology of atopic dermatitis is the microbial environment. Extracellular vesicles released by bacteria have been identified to affect allergic inflammatory processes, according to recent investigations. It was shown that the extracellular vesicles formed from L. plantarum were effective in avoiding skin inflammation by comparing the makeup of bacteria-released extracellular vesicles between atopic dermatitis sufferers and healthy subjects [56].
In patients with AD, Staphylococcus aureus predominates the skin microbiota, and bacterial burden is correlated with disease severity. Staphylococcus aureus colonization in patients with AD can be decreased using heat-treated cosmetic lotions containing Lactobacillus johnsonii NCC 533 (HT La1) [19].
The composition of the stratum corneum’s lipids has a crucial role in how well the osmotic barrier and water retention capacity work. Ceramide [23] is the primary component of them. Recent research has revealed that aberrant skin function in AD patients may result from a decrease in the total amount of ceramide. The increase in ceramide levels may be attributed to the hydrolysis of sphingomyelin-by-sphingomyelin enzymes present in the bacterial extract, which were used in an experimental cream to inactivate S. thermophilus using ultrasound. This finding supports the contribution of these bacterial lysates to stratum corneum barrier function. The experimental cream’s topical use also reduced the erythema, scales, and pruritus associated with AD skin [57].

4.2. Acne

Acne is a long-lasting inflammatory skin condition that affects sebaceous glands and hair follicles. Skin rashes, including whiteheads, blackheads, pustules, papules, and cysts on the face, chest, back, and shoulders are the primary clinical symptoms. The main contributory factors to acne vulgaris are androgen, excessive keratosis at the opening of hair follicles and sebaceous glands, bacterial colonization, and increased sebum output. In some patients, endocrine and genetic disorders may also play a role. Studies suggest that probiotics may reduce acne. The demand for probiotic supplements and beauty products is surging. Hope exists for acne sufferers’ skin using home remedies, like probiotic supplements and cosmetics.
Most acne cosmetics have the potential to improve clinical results. The cleanser should be used by all acne sufferers; those containing benzoyl peroxide or azelaic acid/salicylic acid/triclosan showed the most effectiveness. Products for managing sebum that contain zinc or niacinamide aid in reducing excessive sebum production. Acne healing could be sped up with the use of cosmetics containing antibacterial and anti-inflammatory substances such ethyl lactate, phytosphingosine, niacinamide, or resveratrol. Topical comedolytic drugs can help the skin absorb topical pharmaceuticals and have comedolytic effects. Examples include retinal/glycolic acid and lactic acid. Finally, a specific moisturizer should be seriously considered by all acne sufferers.
In order to get rid of potential skin pathogens, normal human skin can release a variety of antibacterial compounds. A gram-positive bacteria called L. plantarum makes antimicrobial peptides that can reduce inflammation and strengthen the skin’s natural defenses against microorganisms. We examined how lactobacillus extract affects the skin’s barrier function, the number of chemical irritants it produces, the skin microbiota, and acne-related erythema. The findings indicated that lactobacillus extract could successfully cure mild acne lesions and minimize skin erythema, repair the skin barrier, and diminish the skin microbial community [58].
The local ultrasonic treated preparation of S. thermophilus can raise the level of ceramide in the stratum corneum and assist in the treatment of acne because the ceramide (plant sphingosine) in S. thermophilus has antibacterial and anti-inflammatory effects against Cutibacterium acnes [59]. Topical applications of Lactobacillus salivary LS01 and Bifidobacterium brevis BR03 can also be used to treat rosacea [60]. Probiotics administered topically can act as a barrier to stop acne caused by other skin-invading pathogens [61]. Figure 5 demonstrates the role of the above probiotics in acne treatment. To combat harmful microbes and reduce inflammation, probiotics have lately been added to everyday skincare products.

5. Application of Probiotic Fermentation

Probiotic fermentation is a recent finding that can alter the chemical structure of medications to improve epidermal absorption and lower toxicity for the best possible pharmacological effectiveness. The aqueous extract of Acanthopanax Korean root (AE), which has undergone fermentation by L. plantarum and Bifidobacterium bifidum, can lessen intracellular ROS brought on by UVB or H2O2. Acanthopanax Korean root also exhibited much stronger antioxidant and anti-aging properties than extracts made prior to fermentation [62]. After L. rhamnosus fermentation, patchouli leaf extract can enhance the skin’s ability to fend off photoaging. According to studies, the fermented extract can increase the skin’s levels of SOD and GSH while lowering ROS [63]. Treatment with L. rhamnosus fermented jasmine extract can significantly slow down collagen breakdown, premature aging, and skin cell aging brought on by UVB and H2O2 [64]. It can also prevent excessive ROS production, collagen degradation, and premature aging in dermal fibroblasts. A possible therapeutic agent for the prevention and treatment of skin photoaging is L. plantarum fermented blackberry, which can diminish the production of wrinkles and help human dermal fibroblasts resist photoaging [65]. In human skin fibroblasts, UV-induced MMP-1 production and collagen degradation are prevented by fermenting lavender extract with Pediococcus pentosaceus DK1 [66]. The physiological activity of fructus aurantii extract is greatly enhanced by deep fermentation with Lactobacillus brevis [67]. The antioxidant activity of HaCaT cells can be increased by pomegranate peel and schisandra extracts that have been fermented by Lactobacillus acidophilus and L. plantarum, respectively [68]. Lactobacillus helveticus can ferment whey and decrease the expression of MITF, which prevents tyrosinase from blocking melanin synthesis [69]. The photoaging of fibroblasts brought on by UVA (ultraviolet A, wavelength 400 nm~320 nm, low-frequency long-wave) can be lessened by rhodiola rosea fermented by L. plantarum [70]. These fermented extracts contain anti-aging (Figure 6) and skin-lightening properties that could increase the usage of probiotics in the beauty industry. Probiotics’ fermented by-products serve a variety of purposes as well. The Lactobacillus rhamnosus LRH113 strain’s fermentation supernatant exhibits whitening and moisturizing properties, and it has a great deal of promise for use in future maintenance products.

6. Conclusions and Prospects

The use of probiotics and their extracts in cosmetics is discussed in this research, encompassing several application areas such as anti-aging, antioxidant, whitening, and anti-inflammatory effects. It summarizes the progress of research on probiotic fermentation. This review also collects new findings on probiotic research in dermatologic therapy and skin care. The beneficial function of probiotics on the skin has been further demonstrated with the development of analytical tools and biological activity evaluation methodologies. Since topical administration of probiotics has no known sensitizing or stimulating effects, there is still much potential for research in this area.
Based on the research progress collected in this review on probiotics in the field of cosmetics. In future research, it is crucial to undertake probiotic fermentation-type bioactivity investigations in order to learn more about the connection between the manufacturing process and the biological effects attained. On the other hand, additional studies of all probiotic strains on human skin or people are required to corroborate the therapeutic advantages shown in in vitro models.
Indeed, there should be a lot more research conducted in the future about adding probiotic ingredients to cosmetics, and some of the unexplored areas of the field will slowly come to the attention of researchers.

Author Contributions

Conceptualization, T.W. and Z.X.; methodology, N.F.; software, J.L., Z.C. and F.G.; validation, J.D., T.W. and Z.X.; writing—original draft preparation, J.D.; writing—review and editing, J.D., T.W. and Z.X.; supervision, T.W., X.G. and Z.X.; funding acquisition, T.W., X.G. and Z.X. All authors have read and agreed to the published version of the manuscript.

Funding

This work was financially supported by the Key Research and Development Program of Shandong Province (grant No. 2020CXGC010602), the Science and Technology Support Plan for Young People in Colleges and Universities of Shandong Province (grant No. 2020KJE005), the Natural Science Foundation of Shandong Province (grant No. ZR2022MC059), the Key innovation Project of Qilu University of Technology (Shandong Academy of Sciences) (grant No. 2022JBZ01-06), the Natural Science Foundation of Shandong Province (grant No. ZR2023MC087), and the Basic Research of Pilot Project for the Integration of Science, Education and Industry, Qilu University of Technology, Shandong Academy of Sciences (grant No. 2022PY074).

Data Availability Statement

Data will be made available upon request.

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

FDAFood and Drug Administration
ICCRInternational Cosmetic Regulatory
CFUs/gColony-Forming Units/gram
WHOWorld Health Organization
FDAFood and Drug Administration
EFSAEuropean Food Safety Authority
S. thermophilusStreptococcus thermophilus
L. plantarumLactobacillus plantarum
HK L-137Heat-inactivated Lactobacillus plantarum L-137
HAHyaluronic acid
ROSReactive oxygen species
SODSuperoxide dismutase
GSHGlutathione
VEVitamin E
Q10Coenzyme Q10
MMPsMatrix metalloproteinases
ALLactobacillus acidophilus KCCM12625P
HDFHuman dermal fibroblasts
RLHeat-killed Lactobacillus rhamnosus
NMNβ-Nicotinamide Mononucleotide
LABLactic acid bacteria
CATCatalase
EPSExopolysaccharides
PLHeat-killed Lacticaseibacillus paracasei
EVsExtracellular vesicles
IL-10Interleukin 10
IL-8Interleukin 8
ACEAngiotensin-converting enzyme
BLBifidobacterium longum
ADAtopic dermatitis
HT La1Heat-treated cosmetic lotions containing Lactobacillus johnsonii NCC 533
AEAcanthopanax Korean root

References

  1. Hill, C.; Guarner, F.; Reid, G.; Gibson, G.R.; Merenstein, D.J.; Pot, B.; Morelli, L.; Canani, R.B.; Flint, H.J.; Salminen, S.; et al. Expert consensus document. The International Scientific Association for Probiotics and Prebiotics consensus statement on the scope and appropriate use of the term probiotic. Nat. Rev. Gastroenterol. Hepatol. 2014, 11, 506–514. [Google Scholar] [CrossRef] [PubMed]
  2. Bermudez-Brito, M.; Plaza-Díaz, J.; Muñoz-Quezada, S.; Gómez-Llorente, C.; Gil, A. Probiotic mechanisms of action. Ann. Nutr. Metab. 2012, 61, 160–174. [Google Scholar] [CrossRef] [PubMed]
  3. Telesetsky, A. UN Food and Agriculture Organization: Exercising Legal Personality to Implement the UN Convention on the Law of the Sea. In Global Challenges and the Law of the Sea; Springer International Publishing: Cham, Switzerland, 2020. [Google Scholar]
  4. Puebla-Barragan, S.; Reid, G. Probiotics in Cosmetic and Personal Care Products: Trends and Challenges. Molecules 2021, 26, 1249. [Google Scholar] [CrossRef] [PubMed]
  5. Gibson, G.R.; Hutkins, R.; Sanders, M.E.; Prescott, S.L.; Reimer, R.A.; Salminen, S.J.; Scott, K.; Stanton, C.; Swanson, K.S.; Cani, P.D.; et al. Expert consensus document: The International Scientific Association for Probiotics and Prebiotics (ISAPP) consensus statement on the definition and scope of prebiotics. Nat. Rev. Gastroenterol. Hepatol. 2017, 14, 491–502. [Google Scholar] [CrossRef] [PubMed]
  6. Kober, M.M.; Bowe, W.P. The effect of probiotics on immune regulation, acne, and photoaging. Int. J. Womens Dermatol. 2015, 1, 85–89. [Google Scholar] [CrossRef]
  7. Krutmann, J. Pre-and probiotics for human skin. J. Dermatol. Sci. 2009, 54, 1–5. [Google Scholar] [CrossRef]
  8. Yu, J.; Ma, X.; Wang, X.; Cui, X.; Ding, K.; Wang, S.; Han, C. Application and mechanism of probiotics in skin care: A review. J. Cosmet. Dermatol. 2022, 21, 886–894. [Google Scholar] [CrossRef]
  9. Gao, T.; Wang, X.; Li, Y.; Ren, F. The Role of Probiotics in Skin Health and Related Gut-Skin Axis: A Review. Nutrients 2023, 15, 3123. [Google Scholar] [CrossRef]
  10. Duarte, M.; Oliveira, A.L.; Oliveira, C.; Pintado, M.; Amaro, A.; Madureira, A.R. Current postbiotics in the cosmetic market-an update and development opportunities. Appl. Microbiol. Biotechnol. 2022, 106, 5879–5891. [Google Scholar] [CrossRef]
  11. Karnwal, A.; Shrivastava, S.; Al-Tawaha, A.; Kumar, G.; Singh, R.; Kumar, A.; Mohan, A.; Yogita; Malik, T. Microbial Biosurfactant as an Alternate to Chemical Surfactants for Application in Cosmetics Industries in Personal and Skin Care Products: A Critical Review. Biomed. Res. Int. 2023, 2023, 2375223. [Google Scholar] [CrossRef]
  12. Gilchrest, B.A. Skin aging and photoaging: An overview. J. Am. Acad. Dermatol. 1989, 21, 610–613. [Google Scholar] [CrossRef]
  13. Teng, Y.; Huang, Y.; Danfeng, X.; Tao, X.; Fan, Y. The Role of Probiotics in Skin Photoaging and Related Mechanisms: A Review. Clin. Cosmet. Investig. Dermatol. 2022, 15, 2455–2464. [Google Scholar] [CrossRef] [PubMed]
  14. Xu, J.; Zhang, X.; Song, Y.; Zheng, B.; Wen, Z.; Gong, M.; Meng, L. Heat-Killed Lacticaseibacillus paracasei Ameliorated UVB-Induced Oxidative Damage and Photoaging and Its Underlying Mechanisms. Antioxidants 2022, 11, 1875. [Google Scholar] [CrossRef] [PubMed]
  15. Vinderola, G.; Sanders, M.E.; Salminen, S. The Concept of Postbiotics. Foods 2022, 11, 1077. [Google Scholar] [CrossRef]
  16. Zhang, X.; Xu, J.; Ma, M.; Zhao, Y.; Song, Y.; Zheng, B.; Wen, Z.; Gong, M.; Meng, L. Heat-Killed Lactobacillus rhamnosus ATCC 7469 Improved UVB-Induced Photoaging via Antiwrinkle and Antimelanogenesis Impacts. Photochem. Photobiol. 2023. ahead-of-print. [Google Scholar] [CrossRef]
  17. Im, A.R.; Lee, B.; Kang, D.J.; Chae, S. Protective effects of tyndallized Lactobacillus acidophilus IDCC 3302 against UVB-induced photodamage to epidermal keratinocytes cells. Int. J. Mol. Med. 2019, 43, 2499–2506. [Google Scholar] [CrossRef] [PubMed]
  18. Bernstein, E.F. Reactive oxygen species activate the human elastin promoter in a transgenic model of cutaneous photoaging. Dermatol. Surg. 2002, 28, 132–135. [Google Scholar] [CrossRef]
  19. Blanchet-Réthoré, S.; Bourdès, V.; Mercenier, A.; Haddar, C.H.; Verhoeven, P.O.; Andres, P. Effect of a lotion containing the heat-treated probiotic strain Lactobacillus johnsonii NCC 533 on Staphylococcus aureus colonization in atopic dermatitis. Clin. Cosmet. Investig. Dermatol. 2017, 10, 249–257. [Google Scholar] [CrossRef]
  20. Elmahdy, A.; Maibach, H.I. Textbook of Aging Skin; Springer International Publishing: Cham, Switzerland, 2017. [Google Scholar]
  21. Ra, J.; Lee, D.E.; Kim, S.H.; Jeong, J.W.; Ku, H.K.; Kim, T.Y.; Choi, I.D.; Jeung, W.; Sim, J.H.; Ahn, Y.T. Effect of oral administration of Lactobacillus plantarum HY7714 on epidermal hydration in ultraviolet B-irradiated hairless mice. J. Microbiol. Biotechnol. 2014, 24, 1736–1743. [Google Scholar] [CrossRef]
  22. Ishii, Y.; Sugimoto, S.; Izawa, N.; Sone, T.; Chiba, K.; Miyazaki, K. Oral administration of Bifidobacterium breve attenuates UV-induced barrier perturbation and oxidative stress in hairless mice skin. Arch. Dermatol. Res. 2014, 306, 467–473. [Google Scholar] [CrossRef]
  23. Imokawa, G.; Abe, A.; Jin, K.; Higaki, Y.; Kawashima, M.; Hidano, A. Decreased level of ceramides in stratum corneum of atopic dermatitis: An etiologic factor in atopic dry skin? J. Investig. Dermatol. 1991, 96, 523–526. [Google Scholar] [CrossRef]
  24. Kim, H.; Kim, H.R.; Jeong, B.J.; Lee, S.S.; Kim, T.R.; Jeong, J.H.; Lee, M.; Lee, S.; Lee, J.S.; Chung, D.K. Effects of oral intake of kimchi-derived Lactobacillus plantarum K8 lysates on skin moisturizing. J. Microbiol. Biotechnol. 2015, 25, 74–80. [Google Scholar] [CrossRef] [PubMed]
  25. Kimoto-Nira, H.; Aoki, R.; Sasaki, K.; Suzuki, C.; Mizumachi, K. Oral intake of heat-killed cells of Lactococcus lactis strain H61 promotes skin health in women. J. Nutr. Sci. 2012, 1, e18. [Google Scholar] [CrossRef] [PubMed]
  26. Tulkens, J.; Vergauwen, G.; Van Deun, J.; Geeurickx, E.; Dhondt, B.; Lippens, L.; De Scheerder, M.A.; Miinalainen, I.; Rappu, P.; De Geest, B.G.; et al. Increased levels of systemic LPS-positive bacterial extracellular vesicles in patients with intestinal barrier dysfunction. Gut 2020, 69, 191–193. [Google Scholar] [CrossRef] [PubMed]
  27. Nakai, H.; Hirose, Y.; Murosaki, S.; Yoshikai, Y. Lactobacillus plantarum L-137 upregulates hyaluronic acid production in epidermal cells and fibroblasts in mice. Microbiol. Immunol. 2019, 63, 367–378. [Google Scholar] [CrossRef] [PubMed]
  28. McGrath, J.A.; Uitto, J. The filaggrin story: Novel insights into skin-barrier function and disease. Trends Mol. Med. 2008, 14, 20–27. [Google Scholar] [CrossRef]
  29. Shin, M.; Truong, V.L.; Lee, M.; Kim, D.; Kim, M.S.; Cho, H.; Jung, Y.H.; Yang, J.; Jeong, W.S.; Kim, Y. Investigation of phenyllactic acid as a potent tyrosinase inhibitor produced by probiotics. Curr. Res. Food Sci. 2023, 6, 100413. [Google Scholar] [CrossRef]
  30. Kim, S.; Seo, H.; Mahmud, H.A.; Islam, M.I.; Sultana, O.F.; Lee, Y.; Kim, M.; Song, H.Y. Melanin Bleaching and Melanogenesis Inhibition Effects of Pediococcus acidilactici PMC48 Isolated from Korean Perilla Leaf Kimchi. J. Microbiol. Biotechnol. 2020, 30, 1051–1059. [Google Scholar] [CrossRef]
  31. Kim, H.R.; Kim, H.; Jung, B.J.; You, G.E.; Jang, S.; Chung, D.K. Lipoteichoic acid isolated from Lactobacillus plantarum inhibits melanogenesis in B16F10 mouse melanoma cells. Mol. Cells 2015, 38, 163–170. [Google Scholar] [CrossRef]
  32. Tsai, W.H.; Chou, C.H.; Chiang, Y.J.; Lin, C.G.; Lee, C.H. Regulatory effects of Lactobacillus plantarum-GMNL6 on human skin health by improving skin microbiome. Int. J. Med. Sci. 2021, 18, 1114–1120. [Google Scholar] [CrossRef]
  33. Liu, W.S.; Kuan, Y.D.; Chiu, K.H.; Wang, W.K.; Chang, F.H.; Liu, C.H.; Lee, C.H. The extract of Rhodobacter sphaeroides inhibits melanogenesis through the MEK/ERK signaling pathway. Mar. Drugs 2013, 11, 1899–1908. [Google Scholar] [CrossRef] [PubMed]
  34. Khmaladze, I.; Butler, É.; Fabre, S.; Gillbro, J.M. Lactobacillus reuteri DSM 17938-A comparative study on the effect of probiotics and lysates on human skin. Exp. Dermatol. 2019, 28, 822–828. [Google Scholar] [CrossRef]
  35. Cogen, A.L.; Nizet, V.; Gallo, R.L. Skin microbiota: A source of disease or defence? Br. J. Dermatol. 2008, 158, 442–455. [Google Scholar] [CrossRef]
  36. Kimoto-Nira, H.; Sekiyama, Y.; Moriya, N. Towards application of water extract from heat-killed Lactococcus lactis H61 as a cosmetic ingredient. Lett. Appl. Microbiol. 2019, 68, 530–536. [Google Scholar] [CrossRef] [PubMed]
  37. Guéniche, A.; Bastien, P.; Ovigne, J.M.; Kermici, M.; Courchay, G.; Chevalier, V.; Breton, L.; Castiel-Higounenc, I. Bifidobacterium longum lysate, a new ingredient for reactive skin. Exp. Dermatol. 2010, 19, e1–e8. [Google Scholar] [CrossRef] [PubMed]
  38. Fujiki, T.; Hirose, Y.; Yamamoto, Y.; Murosaki, S. Enhanced immunomodulatory activity and stability in simulated digestive juices of Lactobacillus plantarum L-137 by heat treatment. Biosci. Biotechnol. Biochem. 2012, 76, 918–922. [Google Scholar] [CrossRef] [PubMed]
  39. Di Marzio, L.; Cinque, B.; De Simone, C.; Cifone, M.G. Effect of the lactic acid bacterium Streptococcus thermophilus on ceramide levels in human keratinocytes in vitro and stratum corneum in vivo. J. Investig. Dermatol. 1999, 113, 98–106. [Google Scholar] [CrossRef] [PubMed]
  40. Lim, H.Y.; Jeong, D.; Park, S.H.; Shin, K.K.; Hong, Y.H.; Kim, E.; Yu, Y.G.; Kim, T.R.; Kim, H.; Lee, J.; et al. Antiwrinkle and Antimelanogenesis Effects of Tyndallized Lactobacillus acidophilus KCCM12625P. Int. J. Mol. Sci. 2020, 21, 1620. [Google Scholar] [CrossRef]
  41. Im, A.R.; Lee, B.; Kang, D.J.; Chae, S. Skin Moisturizing and Antiphotodamage Effects of Tyndallized Lactobacillus acidophilus IDCC 3302. J. Med. Food 2018, 21, 1016–1023. [Google Scholar] [CrossRef]
  42. Zhou, X.; Du, H.H.; Ni, L.; Ran, J.; Hu, J.; Yu, J.; Zhao, X. Nicotinamide Mononucleotide Combined with Lactobacillus fermentum TKSN041 Reduces the Photoaging Damage in Murine Skin by Activating AMPK Signaling Pathway. Front. Pharmacol. 2021, 12, 643089. [Google Scholar] [CrossRef]
  43. Hong, Y.F.; Lee, H.; Jung, B.J.; Jang, S.; Chung, D.K.; Kim, H. Lipoteichoic acid isolated from Lactobacillus plantarum down-regulates UV-induced MMP-1 expression and up-regulates type I procollagen through the inhibition of reactive oxygen species generation. Mol. Immunol. 2015, 67, 248–255. [Google Scholar] [CrossRef] [PubMed]
  44. Matsuguchi, T.; Takagi, A.; Matsuzaki, T.; Nagaoka, M.; Ishikawa, K.; Yokokura, T.; Yoshikai, Y. Lipoteichoic acids from Lactobacillus strains elicit strong tumor necrosis factor alpha-inducing activities in macrophages through Toll-like receptor 2. Clin. Vaccine Immunol. 2003, 10, 259–266. [Google Scholar] [CrossRef] [PubMed]
  45. Jo, C.S.; Myung, C.H.; Yoon, Y.C.; Ahn, B.H.; Min, J.W.; Seo, W.S.; Lee, D.H.; Kang, H.C.; Heo, Y.H.; Choi, H.; et al. The Effect of Lactobacillus plantarum Extracellular Vesicles from Korean Women in Their 20s on Skin Aging. Curr. Issues Mol. Biol. 2022, 44, 526–540. [Google Scholar] [CrossRef]
  46. Kim, S.H.; Yoem, S.H.; Kim, J.H.; Hong, J.W.; Oh, Y.S.; Kim, J.W. Enhancement of TRP Gene Expression and UV Absorption by Bioconverted Chestnut Inner Shell Extracts Using Lactiplantibacillus plantarum. Molecules 2022, 27, 4940. [Google Scholar] [CrossRef] [PubMed]
  47. Boo, Y.C. Arbutin as a Skin Depigmenting Agent with Antimelanogenic and Antioxidant Properties. Antioxidants 2021, 10, 1129. [Google Scholar] [CrossRef] [PubMed]
  48. Saeedi, M.; Eslamifar, M.; Khezri, K. Kojic acid applications in cosmetic and pharmaceutical preparations. Biomed. Pharmacother. 2019, 110, 582–593. [Google Scholar] [CrossRef]
  49. Wohlrab, J.; Kreft, D. Niacinamide—Mechanisms of action and its topical use in dermatology. Skin Pharmacol. Physiol. 2014, 27, 311–315. [Google Scholar] [CrossRef] [PubMed]
  50. El-Nashar, H.A.S.; El-Din, M.I.G.; Hritcu, L.; Eldahshan, O.A. Insights on the Inhibitory Power of Flavonoids on Tyrosinase Activity: A Survey from 2016 to 2021. Molecules 2021, 26, 7546. [Google Scholar] [CrossRef]
  51. Liu, W.S.; Chen, M.C.; Chiu, K.H.; Wen, Z.H.; Lee, C.H. Amelioration of dextran sodium sulfate-induced colitis in mice by Rhodobacter sphaeroides extract. Molecules 2012, 17, 13622–13630. [Google Scholar] [CrossRef]
  52. Romagnani, S. Coming back to a missing immune deviation as the main explanatory mechanism for the hygiene hypothesis. J. Allergy Clin. Immunol. 2007, 119, 1511–1513. [Google Scholar] [CrossRef]
  53. Lopes, E.G.; Moreira, D.A.; Gullón, P.; Gullón, B.; Cardelle-Cobas, A.; Tavaria, F.K. Topical application of probiotics in skin: Adhesion, antimicrobial and antibiofilm in vitro assays. J. Appl. Microbiol. 2017, 122, 450–461. [Google Scholar] [CrossRef] [PubMed]
  54. Matsuura-Hachiya, Y.; Arai, K.Y.; Ozeki, R.; Kikuta, A.; Nishiyama, T. Angiotensin-converting enzyme inhibitor (enalapril maleate) accelerates recovery of mouse skin from UVB-induced wrinkles. Biochem. Biophys. Res. Commun. 2013, 442, 38–43. [Google Scholar] [CrossRef] [PubMed]
  55. Wüthrich, B. Clinical aspects, epidemiology, and prognosis of atopic dermatitis. Ann. Allergy Asthma Immunol. 1999, 83, 464–470. [Google Scholar] [CrossRef] [PubMed]
  56. Kim, M.H.; Choi, S.J.; Choi, H.I.; Choi, J.P.; Park, H.K.; Kim, E.K.; Kim, M.J.; Moon, B.S.; Min, T.K.; Rho, M.; et al. Lactobacillus plantarum-derived Extracellular Vesicles Protect Atopic Dermatitis Induced by Staphylococcus aureus-derived Extracellular Vesicles. Allergy Asthma Immunol. Res. 2018, 10, 516–532. [Google Scholar] [CrossRef] [PubMed]
  57. Di Marzio, L.; Centi, C.; Cinque, B.; Masci, S.; Giuliani, M.; Arcieri, A.; Zicari, L.; De Simone, C.; Cifone, M.G. Effect of the lactic acid bacterium Streptococcus thermophilus on stratum corneum ceramide levels and signs and symptoms of atopic dermatitis patients. Exp. Dermatol. 2003, 12, 615–620. [Google Scholar] [CrossRef] [PubMed]
  58. Muizzuddin, N.; Maher, W.; Sullivan, M.; Schnittger, S.; Mammone, T. Physiological effect of a probiotic on skin. J. Cosmet. Sci. 2012, 63, 385–395. [Google Scholar] [PubMed]
  59. Bowe, W.P.; Logan, A.C. Acne vulgaris, probiotics and the gut-brain-skin axis—Back to the future? Gut Pathog. 2011, 3, 1. [Google Scholar] [CrossRef]
  60. Fortuna, M.C.; Garelli, V.; Pranteda, G.; Romaniello, F.; Cardone, M.; Carlesimo, M.; Rossi, A. A case of Scalp Rosacea treated with low dose doxycycline and probiotic therapy and literature review on therapeutic options. Dermatol. Ther. 2016, 29, 249–251. [Google Scholar] [CrossRef]
  61. Kang, B.S.; Seo, J.G.; Lee, G.S.; Kim, J.H.; Kim, S.Y.; Han, Y.W.; Kang, H.; Kim, H.O.; Rhee, J.H.; Chung, M.J.; et al. Antimicrobial activity of enterocins from Enterococcus faecalis SL-5 against Propionibacterium acnes, the causative agent in acne vulgaris, and its therapeutic effect. J. Microbiol. 2009, 47, 101–109. [Google Scholar] [CrossRef]
  62. Park, M.J.; Bae, Y.S. Fermented Acanthopanax koreanum Root Extract Reduces UVB- and H2O2-Induced Senescence in Human Skin Fibroblast Cells. J. Microbiol. Biotechnol. 2016, 26, 1224–1233. [Google Scholar] [CrossRef]
  63. Shin, D.; Lee, Y.; Huang, Y.H.; Lim, H.W.; Jang, K.; Kim, D.D.; Lim, C.J. Probiotic fermentation augments the skin anti-photoaging properties of Agastache rugosa through up-regulating antioxidant components in UV-B-irradiated HaCaT keratinocytes. BMC Complement. Altern. Med. 2018, 18, 196. [Google Scholar] [CrossRef] [PubMed]
  64. Ho, C.C.; Ng, S.C.; Chuang, H.L.; Wen, S.Y.; Kuo, C.H.; Mahalakshmi, B.; Huang, C.Y.; Kuo, W.W. Extracts of Jasminum sambac flowers fermented by Lactobacillus rhamnosus inhibit H2O2—And UVB-induced aging in human dermal fibroblasts. Environ. Toxicol. 2021, 36, 607–619. [Google Scholar] [CrossRef] [PubMed]
  65. Kim, H.R.; Jeong, D.H.; Kim, S.; Lee, S.W.; Sin, H.S.; Yu, K.Y.; Jeong, S.I.; Kim, S.Y. Fermentation of Blackberry with L. plantarum JBMI F5 Enhance the Protection Effect on UVB-Mediated Photoaging in Human Foreskin Fibroblast and Hairless Mice through Regulation of MAPK/NF-κB Signaling. Nutrients 2019, 11, 2429. [Google Scholar] [CrossRef]
  66. Ha, J.H.; Kim, A.R.; Lee, K.S.; Xuan, S.H.; Kang, H.C.; Lee, D.H.; Cha, M.Y.; Kim, H.J.; An, M.; Park, S.N. Anti-Aging Activity of Lavandula angustifolia Extract Fermented with Pediococcus pentosaceus DK1 Isolated from Diospyros kaki Fruit in UVB-Irradiated Human Skin Fibroblasts and Analysis of Principal Components. J. Microbiol. Biotechnol. 2019, 29, 21–29. [Google Scholar] [CrossRef] [PubMed]
  67. Chen, C.Y.; Hu, C.Y.; Chen, Y.H.; Li, Y.T.; Chung, Y.C. Submerged fermentation with Lactobacillus brevis significantly improved the physiological activities of Citrus aurantium flower extract. Heliyon 2022, 8, e10498. [Google Scholar] [CrossRef] [PubMed]
  68. Liu, H.M.; Xu, P.F.; Cheng, M.Y.; Lei, S.N.; Liu, Q.L.; Wang, W. Optimization of Fermentation Process of Pomegranate Peel and Schisandra Chinensis and the Biological Activities of Fermentation Broth: Antioxidant Activity and Protective Effect against H2O2-induced Oxidative Damage in HaCaT Cells. Molecules 2021, 26, 3432. [Google Scholar] [CrossRef]
  69. Ikarashi, N.; Fukuda, N.; Ochiai, M.; Sasaki, M.; Kon, R.; Sakai, H.; Hatanaka, M.; Kamei, J. Lactobacillus helveticus-Fermented Milk Whey Suppresses Melanin Production by Inhibiting Tyrosinase through Decreasing MITF Expression. Nutrients 2020, 12, 2082. [Google Scholar] [CrossRef]
  70. Fu, H.; Zhang, Y.; An, Q.; Wang, D.; You, S.; Zhao, D.; Zhang, J.; Wang, C.; Li, M. Anti-Photoaging Effect of Rhodiola rosea Fermented by Lactobacillus plantarum on UVA-Damaged Fibroblasts. Nutrients 2022, 14, 2324. [Google Scholar] [CrossRef]
Figure 1. The primary processes by which probiotics promote skin health.
Figure 1. The primary processes by which probiotics promote skin health.
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Figure 2. The significant cosmetic properties of probiotics. (↑—Increased expression,↓—Reduced expression)The effect of probiotics on the free radicals is multidirectional and includes the direct quenching of reactive oxygen (ROS) and matrix metalloproteinases (MMPS) species; the enhancement of endogenic antioxidant enzyme production (SOD (superoxide dismutase) and glutathione); the inhibition of enzymes involved in ROS generation (glutathione S-transferase, microsomal monooxygenase, mitochondrial succinoxidase, or NADH oxidase); the protection and regeneration of antioxidant compounds (vitamin C or E).
Figure 2. The significant cosmetic properties of probiotics. (↑—Increased expression,↓—Reduced expression)The effect of probiotics on the free radicals is multidirectional and includes the direct quenching of reactive oxygen (ROS) and matrix metalloproteinases (MMPS) species; the enhancement of endogenic antioxidant enzyme production (SOD (superoxide dismutase) and glutathione); the inhibition of enzymes involved in ROS generation (glutathione S-transferase, microsomal monooxygenase, mitochondrial succinoxidase, or NADH oxidase); the protection and regeneration of antioxidant compounds (vitamin C or E).
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Figure 3. Anti-aging and moisturizing effects of probiotics. (A) Probiotics improve skin hydration; (B) probiotics reduce skin wrinkles.
Figure 3. Anti-aging and moisturizing effects of probiotics. (A) Probiotics improve skin hydration; (B) probiotics reduce skin wrinkles.
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Figure 4. Mechanism of action of probiotics to inhibit melanogenesis. Probiotics inhibit tyrosinase activity by producing tyrosinase inhibitors; probiotics inhibit tyrosinase activity by promoting the production of phenylacetic acid; probiotics destroy tyrosine by producing lactic acid; probiotics destroy melanin by producing substances that degrade melanin.
Figure 4. Mechanism of action of probiotics to inhibit melanogenesis. Probiotics inhibit tyrosinase activity by producing tyrosinase inhibitors; probiotics inhibit tyrosinase activity by promoting the production of phenylacetic acid; probiotics destroy tyrosine by producing lactic acid; probiotics destroy melanin by producing substances that degrade melanin.
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Figure 5. The role of probiotics in the treatment of acne. The main causes of acne are increased secretion of androgens, which contributes to an increased rate of sebaceous cell production; rapid multiplication of propionibacterium acnes; inflammatory reactions.
Figure 5. The role of probiotics in the treatment of acne. The main causes of acne are increased secretion of androgens, which contributes to an increased rate of sebaceous cell production; rapid multiplication of propionibacterium acnes; inflammatory reactions.
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Figure 6. Role of probiotic fermentation in anti-aging. (↑—Increased expression, ↓—Reduced expression).
Figure 6. Role of probiotic fermentation in anti-aging. (↑—Increased expression, ↓—Reduced expression).
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Table 1. Selected examples of cosmetic products containing probiotics. * The ingredient listed as “Bifida ferment lysate” corresponds to a lysate from Bifidobacterium longum reuter.
Table 1. Selected examples of cosmetic products containing probiotics. * The ingredient listed as “Bifida ferment lysate” corresponds to a lysate from Bifidobacterium longum reuter.
Product IDCosmetic Effects (Manufacturer′s Declaration)Type of ProductCosmetic
Ingredient List
1Skin feels soft, moisturized, and revitalized.
Restore skin barrier function and seal in moisture
on the skin’s surface.
Skin relief and a reduction in potential irritation.
LotionLactobacillus ferment
2Enhance wrinkles, unwind, and keep skin looking young.
Enhance wrinkles, unwind, and keep skin looking young.
LotionLactococcus ferment extract
Yeast cytolytic extract
3To stop dry air from the outside, stop water loss and create a water-locking barrier on the skin’s surface.LotionLactobacillus ferment hyaluronic acid
4Maintain the balance between the skin’s water and oil content.
Improved skin stability.
Revitalize and repair skin.
TonerBifida ferment lysate *
5Multidimensional repair of skin fragility and relieving skin discomfort.CreamAlteromonas Baumann ferment extract
6Adjust skin and facial flora, inhibit acne inflammation root, improve redness and sensitivity, and enhance skin defense.CreamLactobacillus extract
7Balance skin micro-ecological environment and repair the micro-ecological barrier.
Intensive moisture lock water and reduce skin moisture loss.
CreamLeuconostoc ferment filtrate
Prebiotics: pentavitin
8Balance skin flora and improve skin health.CreamLactobacillus/soymilk ferment filtrate
9Balance skin flora and improve skin health.CleanserLactobacillus/soymilk ferment filtrate
Candida bobicola/glucose/methyl Rapeseedate ferment
10Improve skin antioxidant capacity.CreamLactococcus ferment
Bacillus ferment
11Produce acne suppressor, help regulate the skin surface flora, and reduce the risk of acne.CreamBifidobacterium longum, lysate
12Repair skin barrier, and relieve redness and discomfort.MaskVitreoscilla ferment
13Promotes collagen regeneration and smoothes wrinkles.LotionBifidobacterium longum, lysate
Yeast extract
Lactococcus ferment
14Reduce skin redness and sensitivity.
Inhibiting skin oxidation factor.
SerumPITERATM
15Regulate skin flora, strengthen the micro-ecological barrier, and improve skin condition.LotionLactobacillus/soymilk ferment filtrate
Bifidobacterium longum, lysate
16Strengthen the skin barrier and improve the skin quality.
Strengthen the muscle base, firm the skin, and delicate skin.
Promote collagen regeneration.
SerumBifidobacterium longum, lysate
Yeast extract
Vitreoscilla ferment
17Repair the skin barrier.SerumBifidobacterium longum, lysate
Yeast extract
Lactobacillus
18Maintain skin micro-ecological balance
and adjust skin flora.
SerumLactobacillus/soymilk ferment filtrate
19Prevent the imbalance of micro-ecological barriers.
Balance bacteria symbiosis, improve skin redness.
SerumLactobacillus ferment lysate
20Enhance the outer strength of the skin.MaskLactobacillus
21After fermentation, lactic acid bacteria present a protective film to prevent water evaporation, water tender, and shining through the skin, and strengthen the skin cuticle.CreamLactococcus ferment lysate
Bifida ferment extract
22Activate skin micro-ecological activity and inhibit harmful bacteria reproduction, and the skin becomes soft and delicate.LotionLactobacillus
23Balance the micro-ecological barrier to help reduce repeated breakouts.
Balance water and oil, stabilize skin,
and maintain skin health.
Gel
Cream
Toner
Lactobacillus
Lactobacillus ferment
Lactococcus ferment lysate
Prebiotics: chicory root extract
24Make the skin moist and tender.
Maintain skin elasticity and permeability.
Cream
Cleansing
Original nourishing ingredient:
S.E. essence
Bifidobacterium/soybean ferment
Lactococcus/milk ferment
25Balance skin micro-ecology and make skin healthy and delicate.Serum
Cream
NATURAL RETM: Lactobacillus complex extract
26Stong microbial barrier.
Maintain the balance of bacteria and stabilize the healthy state of the skin.
Cleansing
Toner
Lactobacillus
Lactococcus ferment lysate
Lactobacillus/soymilk ferment filtrate
Saccharomyces/rice ferment filtrate
27Prebiotics: maintain skin micro-ecological health.
Biostime: provides an environment for probiotics to grow.
Serum
Cream
Inulin
Alpha-glucan oligosaccharide
Yeast ferment extract filtrate
Lactobacillus/soymilk ferment lysate
Lactobacillus/soybean extract ferment filtrate.
Lactobacillus/punica granatum feuit ferment extract
28Extracted from the fermentation of lactic acid bacteria, it helps to reduce the effects of toxins and maintain the balance and integrity of the skin microbiome.SerumLactococcus ferment extract
29Firming skin and energizing bacteria.SerumPlant-derived probiotics: chicory root
30Reduce skin redness, acne, and sunburn.
Restore skin elasticity.
SerumLactococcus lactis fermentation lysate
31Maintain and counterbalance facial symbiotic bacteria.
Help restore the dynamic balance of bacteria on the skin surface and create a stable skin microenvironment.
Cleaning
Serum
Cream
Lactobacillus/soymilk ferment filtrate
Lactobacillus
32Balance skin flora and prevent aging.SerumBifida ferment lysate
33Regulate skin pH.CleaningBifidobacterium longum, lysate
Lactobacillus ferment
Lactobacillus ferment lysate
Streptococcus thermophilus ferment
Lactobacillus/soybean extract ferment
34Maintain the balance of bacteria and stabilize the healthy state of the skin.SerumBifida ferment lysate
35Accelerate collagen regeneration and effectively improve skin fullness.CreamBifidobacterium longum, lysate
Table 2. Experimental in vitro and in vivo studies of the beneficial effects of probiotics and their active ingredients on the skin and their mechanisms of action-summary.
Table 2. Experimental in vitro and in vivo studies of the beneficial effects of probiotics and their active ingredients on the skin and their mechanisms of action-summary.
ActivityExperimental ModelType of Probiotics
/Active Constituent
Mechanism of Action/EffectReferences
In VitroIn Vivo/Ex Vivo
AntioxidantHuman dermal
fibroblast (HDF)
Lipoteichoic acid isolated from Lactobacillus plantarum(LTA)
-
LTA pretreatment
-
Inhibited MMP-1 expression.
-
Inhibited activation of extracellular signal-regulated kinases (ERK) and c-Jun N-terminal kinases (JNK).
-
Promoted type 1 procollagen synthesis and reduced the generation of ROS induced by UV irradiation.
[14]
Normal human dermal fibroblast (NHDF) cells
B16F10 murine
melanoma cells
Heat-killed Lacticaseibacillus
paracasei (PL)
-
Reduced DNA damage.
-
Alleviated UVB-induced oxidative damage.
-
Attenuated UVB-induced photoaging.
[15]
MurineNicotinamide mononucleotide
(NMN) combined with
Lactobacillus fermentum TKSN041
-
Improved murine skin damage caused by UVB irradiation and the protective mechanism.
-
Increased the protein expression levels of AMPK, IκB-α, SOD1, and CAT in the skin tissues and Ireduced protein expression of NF-κBp65.
[16]
Mouse skin fibroblast (MSF) cells
Human epidermal
melanocytes (HEM)
Heat-killed L. rhamnosus ATCC 7469 (RL)
-
Absorbed UVB and reduced DNA damage.
-
Downregulated MMP-1, 2, 3 expressions associated with MAPK signaling.
-
Reduced ROS content.
-
Suppressed tyrosinase and TYRP-2 activity and/or levels associating with PKA/CREB/MITF signaling.
[17]
Human keratinocytes
Human
dermal fibroblasts
B16F10 murine
melanoma cells
Tyndallized Lactobacillus acidophilus KCCM12625P (AL)
-
Induced anti-wrinkle effects by regulating wrinkle-related genes.
-
Reduced the mRNA expression of melanogenesis-related genes such as tyrosinase, TYRP-1, and TYRP-2.
[18]
Anti-agingHS68 cells
dermal fibroblast cells
Extracts of Jasminum sambac flowers fermented by
Lactobacillus rhamnosus
-
Enhance the viability of HS68 cells.
-
Remarkably attenuate the UVB/H2O2-induced excessive production of reactive oxygen species, degradation of collagen, and premature senescence.
-
Enhance the expression of antioxidant genes.
[19]
Streptococcus salivarium spp.
Streptococcus thermophilus S244
Significant increase in skin moisture
(immediate and long-term).
[20]
Hs68 cells
Human dermal
fibroblasts
Hairless miceAdministered vehicle or
L. plantarum HY7714
-
Oral supplementation (1 × 109 CFU, per day) for 8 weeks
-
Significant increase in ceramide level flow compared to the UVB group.
-
Suppressed the increased transepidermal water loss and decrease in skin hydration.
-
Improved the reduction in SPT mRNA levels and suppressed the increase in ceramidase mRNA levels caused by UVB.
-
Effectively rescued UVB-reduced procollagen expression through the inhibition of UVB-induced matrix metalloproteinase expression in human dermal fibroblasts.
-
Inhibited the number, depth, and area of wrinkles in hairless mouse skin.
[21,22]
Human foreskin
fibroblast (Hs68)
SKH-1
hairless mice
Fermented blackberry (FBB) by
L. plantarum JBMI F5
-FBB pretreatment
-FBB administration
-
Inhibited UVB-mediated type-1 procollagen degradation and (MMP)-1 and MMP-2 protein expression.
-
Suppressed NF-κB.
-
Activation and MAPK phosphorylation.
-
Diminished the wrinkle formation in dorsal skin and epidermal thickening in UVB-irradiated hairless mice.
[23]
HaCaT cellsSKH-1
hairless mice
Volunteers
Kimchi-derived
L. plantarum K8 lysates
-
Oral supplementation for 8 weeks
-
Oral supplementation experimental candy containing 2.1% L. plantarum K8 lysate
-
Increased hyaluronic acid content
-
Decreased epidermal thickening.
-
Reduced damage to barrier function.
-
Significant increase in hydration.
-
Decreases in horny layer thickness and TEWL value were observed on the face and forearm.
[24,25]
Double-blind,
placebo-controlled trial Japanese women
volunteers(aged 31–62 years)
8-week treatment
Heat-killed cells of Lactococcus lactis strain H61
-
Oral supplementation (60 mg per day) for 8 weeks
-
Decreased skin elasticity and melanin Content in the cheek.
-
Increased sebum content.
-
Apparent hair follicles and dryness of the throat at week 8 were higher in the overall H61 group than in the combined placebo group.
-
Marked improvements in self-surveyed skin elasticity.
[24,25]
UVB-irradiated normal human epidermal keratinocytes (NHEKs) Cosmetic preparation that contained Water extract from heat-killed L.lactis H61
-
Suppression of inflammation of the skin.
-
Absorbed electromagnetic radiation in the UVB range.
-
Inhibited the production of interleukin-8 induced by UVB.
-
Did not protect against hydrogen peroxide-induced cell damage.
[26]
Primary epidermal cellsHairless miceHeat-killed L. plantarum L-137
-
Suppressed the loss of water content in the stratum corneum.
-
Increased HA production.
[27]
Clinical trialsExtracellular vesicles (EVs) that were secreted from
L. plantarum of women in
their 20s (LpEVs)
-
Suppressed wrinkle formation and pigmentation.
[28]
Spot
removing and whitening
Cultures of Bifidobacterium bifidum IDCC4201 and Lactiplantibacillus plantarum IDCC 3501
-
Phenyllactic
-
Anti-tyrosinase.
-
Reduced melanin synthesis.
-
Altered protein expression associated with the melanogenesis pathway.
[29]
Kimchi-derived Pediococcus acidilactici PMC48
-
Degrades melanin.
-
Tyrosinase-inhibiting effect.
[30]
B16F10 mouse
melanoma cells
Lipoteichoic acid (LTA) isolated from
Lactobacillus plantarum (pLTA)
-
Inhibited melanogenesis.
-
Reduced the cellular activity of tyrosinase and the expression of tyrosinase family members in a dose-dependent manner.
-
Reduced the expression of microphthalmia-associated transcription factor (MITF).
[31]
Clinical observationL. plantarum-GMNL6
-
The external ointment
-
Enhanced collagen synthesis and the gene expression of serine palmitoyltransferase small subunit A.
-
Reduced melanin synthesis, the biofilm of Staphylococcus aureus, and the proliferation of cutibacterium acnes.
-
The syndromes of skin moisture, skin color, spots, wrinkles, UV spots, and porphyrins were improved.
[32]
Anti-melanogenic
signaling pathway in
α-melanocyte
stimulating hormone
(α-MSH)-treated B16F10 melanoma cells and zebrafish
Extracts of Rhodobacter sphaeroides (Lycogen™)
-
Inhibited the cellular melanin contents and expression of the melanogenesis-related protein, including microphthalmia-associated transcription factor (MITF) and tyrosinase.
-
Reduced phosphorylation of MEK/ERK without affecting phosphorylation of p38.
-
Decreased zebrafish melanin expression in a dose-dependent manner.
[33]
Anti-
inflammatory
Twenty-seven AD patients and six healthy control subjects
Staphylococcus
aureus-induced mouse AD models
Lactobacillus plantarum-derived extracellular vesicles
-
Administration
-
Reduced epidermal thickening and the IL-4 level.
-
Treatment prior to S. aureus EV treatment.
[34]
Ex vivo skin modelsLive and the lysate products of probiotic strain
Lactobacillus reuteri DSM 17938
-
Reduced proinflammatory IL-6 and IL-8.
-
Live.
-
Increased aquaporin 3 (AQP3) gene expression.
-
Had antimicrobial action against path-genic skin bacteria (staphylococcus aureus, streptococcus pyogenes M1, cutibacterium acnes AS12, pseudomonas aeruginosa).
-
The lysate-enhanced laminin A/B levels

in a healthy (unstimulated) state of RHE.
[35]
Human keratinocytesIn the forearm skin of 11 atopic dermatitis (AD) patients
stratum corneum
20 healthy elderly women.
An experimental cream containing sonicated Streptococcus thermophilus
-
2-week application of the cream 7d application of the cream
-
Increase in skin ceramide amounts.
-
Improvement of the signs and symptoms characteristic of AD skin.
-
Increase in skin ceramide amounts.
-
Improvement of lipid barrier and more effective resistance against xerosis.
[36]
Nerve cell cultures
in vitro
Ex vivo human skin explant model
Sixty-six female
volunteers
Bifidobacterium longum sp. extract (BL)
-
Either the cream with the bacterial extract at 10% (the face, arms, and legs twice a day for two months)
-
Significant improvement versus the placebo in variousparameters associated with inflammation.
-
Inhibited capsaicin-induced CGRP release by neurons.
-
Decrease in skin sensitivity at the end of the treatment.
-
Increase skin resistance.
-
Physical and chemical aggression compared to the group of volunteers increased skin resistance.
[37]
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Dou, J.; Feng, N.; Guo, F.; Chen, Z.; Liang, J.; Wang, T.; Guo, X.; Xu, Z. Applications of Probiotic Constituents in Cosmetics. Molecules 2023, 28, 6765. https://doi.org/10.3390/molecules28196765

AMA Style

Dou J, Feng N, Guo F, Chen Z, Liang J, Wang T, Guo X, Xu Z. Applications of Probiotic Constituents in Cosmetics. Molecules. 2023; 28(19):6765. https://doi.org/10.3390/molecules28196765

Chicago/Turabian Style

Dou, Jiaxin, Ning Feng, Fangyu Guo, Zouquan Chen, Jie Liang, Ting Wang, Xueping Guo, and Zhenshang Xu. 2023. "Applications of Probiotic Constituents in Cosmetics" Molecules 28, no. 19: 6765. https://doi.org/10.3390/molecules28196765

APA Style

Dou, J., Feng, N., Guo, F., Chen, Z., Liang, J., Wang, T., Guo, X., & Xu, Z. (2023). Applications of Probiotic Constituents in Cosmetics. Molecules, 28(19), 6765. https://doi.org/10.3390/molecules28196765

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