Aim: The present study aimed to assess the efficacy of a nutraceutical ingredient, SelectSIEVE^® Rainbow, based on botanical extracts, in ameliorating cellulite-derived skin imperfections and microcirculation. The nutritional supplement contained a mixture of Oryza sativa (L.), Citrus sinensis (L.) Osbeck, Ananas comosus (L.) Merr, and Actinidia chinensis Planch; all ingredients were botanicals that can be used in food supplements. Results: In vitro studies showed the high capacity of the supplement to have an anti-inflammatory, antioxidant, and hypolipidemic effect, accompanied by an interesting proteolytic activity. The randomized double-blind placebo-controlled clinical trial, carried out on 60 women during an 8-week treatment period, confirmed the in vitro study results. SelectSIEVE^® Rainbow showed a whole-body shaping activity, with a reduction of the waist, hip, and tight circumference of 0.8, 0.65 and 0.72 cm, respectively. It also showed a reduction of subcutaneous fat mass of 1.24 mm and body weight, with an average of 0.7 kg and positive peaks of −2.9 kg. Skin health and appearance were also improved: +5.4% skin elasticity, +5.5% skin tonicity and +5.7% skin draining. Finally, the dermatological evaluation of the cellulite score and microcirculation showed an improvement in 57% and 60% of the subjects enrolled in the studies. Conclusions: This first study provides interesting inputs on the effectiveness of the nutraceutical complex standardized in polyphenols, anthocyanins and proteolytic enzymes to counteract cellulite blemishes and improve local microcirculation. The positive response encourages deeper studies and further investigation.

People with self-reported sensitive skin may reluctantly use performing anti-ageing skin care products as it could elicit skin discomfort. We thus aimed to design and test an anti-ageing skin care routine that is suitable for people reporting sensitive skin. Key principles for developing products for sensitive skin were applied and formulas were screened for their mildness in vitro using the Reconstructed Human Epidermis ET50 method. Anti-ageing efficacy and mildness was evaluated during a clinical study in China, with 33 female volunteers aged 40–65 years, with sensitive skin. The anti-ageing benefits were measured using Primos 3D, the cutometer and clinical evaluation. Hallmarks for sensitive skin such as skin hydration, skin barrier, skin redness and response to lactic acid were also measured. The ET50 method yielded values suggesting moderate to mild expected irritancy effect in vivo for most of them, and non-irritating effect for the serum. During the clinical study, no physical or functional signs of discomfort were reported with twice-daily usage of the routine. Instrumental evaluation of Wrinkle depth, skin elasticity/firmness, skin hydration, skin barrier and skin redness revealed improvement at 4 and 8 weeks. Clinical evaluation evidenced skin smoothness, skin suppleness and radiance improvements. The skin was less reactive to lactic acid stimuli, while the sensitive skin burden was lowered according to the dermatological quality of life index. Lastly, a separate investigation suggested the potential relief aspect of such routines to alleviate discomforts from mask wearing. With the right formulation design, the benefits of layering products from a routine can be made accessible to people with sensitive skin while simultaneously alleviating the burden of sensitive skin.

Dietary interventions represent an interesting alternative to pharmacological treatments for improving the quality of life (QoL) of subjects suffering from gastroesophageal reflux disease (GERD). This randomized, double-blind, placebo-controlled study aimed to evaluate the efficacy of a food supplement (FS) containing a probiotic strain, bioactive peptides, and vitamins in relieving heartburn/dyspeptic symptoms in subjects with mild-to-moderate GERD. Fifty-six adult participants were randomly assigned to receive the placebo or the active FS for 28 days. Subjects were asked to record daily the frequency and intensity of heartburn episodes and the intake of over- the-counter (OTC) medications. GERD-QoL and self-assessment questionnaires were also completed every two weeks and at the end of the treatment, respectively. FS was effective in achieving a progressive and significant reduction of heartburn frequency and severity, with an intergroup significant difference at the end of the treatment period. FS group also reported a reduction in the OTC medication intake, whereas placebo administration did not modify the OTC intake. Results from the QoL and self-assessment questionnaires showed that FS administration achieved a progressive and statistically significant intragroup and intergroup improvement in the QoL score and a higher positive response with respect to the placebo treatment.

Background: Acne is a multifactorial inflammatory skin disease affecting the quality of life of acne prone subjects. Several therapeutic approaches are currently used to counteract this condition, mostly having side effects. As acne development has been recently linked to skin and gut dysbiosis, acting on both aspects could represent an alternative and promising approach to ameliorate the acne clinical signs. Material and Methods: A cosmetic product, containing Ectoin, and a food supplement, containing probiotics, were formulated as a combined treatment to target both gut and skin microbiota and evaluated for the improvement of skin appearance on acne prone adult subjects. Eighty male and female subjects, showing acne clinical signs, were assigned to 4 groups to receive the following products: the cosmetic product containing Ectoin + a placebo food supplement, the combined treatment, a cosmetic reference product, specifically formulated for counteracting acne, + a placebo food supplement, the cosmetic reference product + the food supplement with probiotics. Acne lesions, skin sebum content, pH and moisturization were monitored. Results: Clinical evaluations of active acne lesions and comedones, skin complexion evenness and skin inflammatory status were carried out. The combined treatment resulted as effective as the cosmetic reference product in ameliorating the instrumental parameters, and more effective in the dermatological assessment of skin complexion evenness and inflammatory status. Conclusion: The combined treatment proposed, formulated to target both gut and skin microbiota, resulted effective in ameliorating acne clinical signs and could represent a valid alternative to conventional acne management.

Belight^3TM, a nutricosmetic formulation containing polyphenol-rich extracts, has previously been demonstrated to be safe and effective in brightening skin color and dark spots in a clinical study involving Asian volunteers. The aim of this study was to investigate the efficacy of this formulation in lightening dark spots in a Caucasian population, which is characterized by lighter skin pigmentation and greater visibility of hyperpigmentation, as well as to determine whether the supplementation increased sensitivity to UV exposure. A randomized, double-blind, placebo-controlled clinical study was conducted on 66 male and female participants with skin phototype I to III, all exhibiting facial hyperpigmentation. The color of selected dark spots was assessed using spectrophotometry to measure the L* value of the CIELab color space and the Individual Typology Angle (ITA). L* and ITA levels of dark spots were significantly increased after 6 and 12 weeks of Belight^3TM treatment (respectively by +1.2% and +2.5% for L* and by 12.1% and 22.5% for ITA), and this lightening effect was significantly higher than the placebo after 12 weeks (p < 0.05 for L*; p < 0.001 for ITA). Clinical evaluation of skin complexion evenness and dark spot visibility were also improved in subjects receiving the Belight^3TM treatment, achieving a significant difference with the placebo after 12 weeks. No changes in MED or skin redness were observed during this study. This study confirmed the safety and efficacy of Belight^3TM in lightening dark spots in a Caucasian population without increasing UV sensitivity.