A Comprehensive Review on Nutraceuticals: Therapy Support and Formulation Challenges
Abstract
:1. Introduction
2. Nutraceuticals in Various Diseases
2.1. Nutraceuticals in Cardiovascular Diseases
2.1.1. Allicin and Alliin
2.1.2. Omega-3Fatty Acids
2.1.3. Soy Isoflavones
2.1.4. Proteins, Peptides and Amino Acids
2.1.5. Antioxidant Vitamins
2.1.6. Phytosterols
2.2. Nutraceuticals in Cancer Chemo- and Radiotherapy
2.2.1. Curcumin (Diferuloyl-Methane) from Turmeric (Curcuma Longa)
2.2.2. Ginger
2.2.3. Genistein
2.3. Nutraceuticals in the Treatment of Prostate Cancer (PCa)
2.3.1. Silibinin
2.3.2. Soy Isoflavones
2.4. Nutraceuticals for Skin Treatment
2.4.1. Bio-Active Peptides
2.4.2. Bio-Active Polysaccharides
2.4.3. Bio-Active Botanical Extracts
2.4.4. Carotenoids
2.5. Nutraceuticals as Specialized Medical Products
3. Formulations and Challenges Involved
- Challenges with various dosage forms;
- Approaches to deal with formulation challenges;
- Excipients selection.
3.1. Challenges in the Formulation of Nutraceuticals and Dietary Supplement
3.2. Approaches to Deal with Formulation Challenges
3.2.1. Liposomes and Nanoemulsions
3.2.2. Lipid-Based Carriers
3.2.3. Polysaccharide Matrices
3.3. Excipient Selection
4. Safety and Quality Control of Nutraceuticals
- (a)
- Ibutramine hydrochloride monohydrate is a drug molecule that works by inhibiting serotonergic and noradrenergic reuptake and shows effects as an anti-obesity drug, and is a common adulterant. In a study conducted with twenty-two samples of dietary supplements in China, eleven were found to be contaminated with phenolphthalein, N-mono-desmethylsibutramine, and sibutramine. In another similar study performed on fifteen samples in China, four of them contained sibutramine and N-di-desmethylsibutramine [159]. Further, it has also been reported that two pregnant women in Turkey lost their wombs due to consumption of adulterated Chinese herbal medicine “meizitanc” [160]. Sibutramine has also been reported as a solvent in slimming preparations. It has led to mania-like psychosis in two women in Hong Kong [161].
- (b)
- Fenfluramine is another dug that was used as an adulterant in Chinese traditional medicines and found in many slimming preparations. It caused primary pulmonary hypertension and valvular heart disease. This drug was withdrawn from market in 1997 [162].
- (c)
- In some weight control programs using an orexigens, diuretics, stimulants and laxative agents, it has been demonstrated that these products contain adulterants as ephedrine, norephedrine, caffeine and furosemide [163].
- (d)
- Morphological substitute usage is another common example of adulteration that may cause serious health issues. For example, Panax ginseng (Araliaceae), also known as “Asian or Korean ginseng”, is used as traditional medicine. It has been found to be adulterated with roots of Panax quinquefolius L. (American ginseng) and Eleutherococcus senticosusmaxim (Siberian ginseng), which may cause health problem [164,165]. Another similar example is Panax ginseng being used as adulterant in roots of Mandragora officinarum L. (Solanaceae) because they are morphologically similar, but have completely different pharmacological effects and phytochemistry [166]. Further, roots of Pfaffia panaculata (Mart.) Kuntze (Amaranthaceae), also known as “Brazilian ginseng or suma root”, morphologically resembles P. ginseng roots, but the phytochemical content is different and, hence, pharmacological action is also different [167].
- (e)
- Some other examples of physical similarity between species include the flower Anthemisnobilis L. and the chamomile, Matricaria chamomilla L. (Asteraceae), both of which are listed in the European Pharmacopoeia as therapeutic plants, as well as several other species in the family Asteraceae, such as Tanacetum parthenium (L.) Sch. Bip., Tanacetum cinerariifolium (Trevir.) Schultz Bip., Tripleurospermum callosum (Boiss. et Heldr.) E. Hossain, Bellis perennis L.and Leucanthemum vulgare L. Furthermore, the pharmacological activity differs depending on the phytoconstituents [168,169].
- (f)
- One of the serious intentional adulterations is use of peanut skin extract in different grape products. Grape seed-containing drugs are said to have very high bioactive polyphenols content and used in prevention of cardiovascular and neurodegenerative disorders. The peanut skin is used as it is widely available, is a high-volume byproduct and is very cheap compared to grape products. However, it is a potential allergen, which may cause serious concerns when used as adulterant, which has been reported in a study where tested products contained no detectable quantities of grape seed extract, but only peanut skin as adulterant [170].
- (g)
- One of the most important categories affected by adulteration is species containing essential oils (spices). As these spices are of high economic value and are export-oriented commodities, these are widely adulterated with natural and synthetic adulterants. One of the most commonly reported examples is adulteration of pure Lavandula angustifolia Mill. (Lamiaceae) oil with other species of same genus, which are almost six times cheaper. Essential oils from citrus are usually adulterated with sweet orange essential oil. Another quoted case is use of citronella oil (Cymbopogon winterianus), which is quite cheaper, as an adulterant in very high economic value essential oil from Melissa officinalis herb (balm oil). Melissa officinalis herb contains citronellal as the main constituent whereas citronella oil contains enantiomeric mixtures of citronellal [171,172].
- (h)
- Another intention of adulteration is to add to the industrial value to the product. For example, synthetic α-irone and β-irone is added to iris (Iris sp., Iridaceae) oil to enhance the commercial value of the product, linalyl acetate or linalool, as the olfactory quality of bergamot or lavender oil becomes improved [171,172]. Other similar cases are when vegetable oils are added to increase the weight of other products—for example, lemongrass oil is diluted with coconut oil and sandalwood oil with polyethylene glycol. Leaf cinnamon essential oil contains lesser quantity of cinnamaldehyde but has the same olfactory notes as those of cinnamon bark essential oil, and, therefore, it has been reported as adulterant. Cheaper petit-grain oil made from leaves is used as adulterant in neroli oil made from the flowers of Citrus aurantium L. spp. amara L. var. pumilia (Rutaceae) [171]. Another case study reports that samples of the dietary supplements containing the leaf extract of G. biloba, used for cerebrovascular diseases, tinnitus and Alzheimer’s type of dementia, were demonstrated to be adulterated with free flavonols and glycones (such as quercetin and kaempferol, respectively) as well as genistein, the isoflavone derivative [173]. In another case, abietic acid has been reported as an adulterant in a herbal preparation used for the treatment of psoriasis [174].
- (i)
- One potential hazardous adulteration that has harmful effects on human health is adulteration with allopathic drugs. The commonly used molecules in such types of adulterations are non-steroid anti-inflammatory drugs (NSAIDs), steroids, anti-diabetics and analgesics. For example, glibenclamide and metformin are reported in anti-diabeticherbal/botanical supplements [175,176,177]. In addition, it has been reported that herbal anti-diabetic remedies contain chlorpropamide, gliclazide, glimepiride, glipizide, pioglitazone, tolazamide and tolbutamide. Many analgesic compounds, including codeine, indomethacin, ketoprofen, morphine, oxyphenbutazone, paracetamol, phenylbutazone, diclofenac, dipyrone, ibuprofen, mefenamic acid, salicylamide and salicylic acid, are found in adulterated dietary supplements. It has been reported that herbal preparations contain anabolic steroids and hormones, such as rostendione, betamethasone valerate, betamethasone, clenbuterol, dexamethasone, flumethasone, hydrocortisone, prednisolone, prednisone, testosterone propionate, testosterone isocaproate, testosterone phenylpropionate and testosterone decanoate [178]. Another significant case that has been reported is adulteration with phosphodiesterase type-5 (PDE-5) inhibitor analogues, such as sildenafil citrate (Viagra®, Pfizer, New York, NY, USA), vardenafil hydrochloride (Levitra®, Bayer, Leverkusen, Germany), and tadalafil (Cialis®, Elli Lilly, Indianapolis, IN, USA), have been found in dietary supplements containing well-known natural constituents such as Panax ginseng L., Astragalus membranaceus (Fisch.) Bunge, Schizandra chinensis (Turcz.) Baill., Ginkgo biloba L., and many others. One of the possible consequences of such adulteration with prescription-only drugs such as phosphodiesterase type-5 (PDE-5) inhibitor analogues, which are contraindicated in men taking nitrates, may lead to unsafe drop in blood pressure. Such reported adulterations are homosildenafil in a food beverage; acetildenafil and hydroxyhomosildenafil in some other herbal products; vardenafil, sildenafil, tadalafil, and vardenafil in an herbal product sold in Hong Kong; benzamidenafil in herbal products; and thiosildenafil, a thioketone analogue of sildenafil, in herbal aphrodisiac supplements; nitroso-prodenafil, a prodrug of aildenafil, is also a reported adulterant, which is as carcinogenic as nitroso derivatives. Researchers examined 91 herbal items for the presence of PDE-5 inhibitors and found that 74 of them actually contained the PDE-5 inhibitor analogs, despite the fact that none of the labels mentioned the presence of a synthetic inhibitor. Eighteen of twenty-three herbal dietary supplements on the Dutch market tested positive for sildenafil or a comparable PDE-5 inhibitor in a similar investigation. [179,180].
5. Formulation Challenges
- (a)
- Garlic (alicin) exhibits a hypotensive property and a hypocholesterolemic effect, acts as an anti-inflammatory agent and possess anti-bacterial as well as anti-fungal properties. When it is administered with anticoagulants (such as warfarin), it may lead to increased bleeding. With hypoglycemic drugs, such asinsulin or glipizide, it may cause hypoglycemia. With protease inhibitors (such as indinavir or saquinavir), garlic decreases their blood levels and effectiveness [184,185].
- (b)
- Ginger is commonly used to treat various types of stomach problems—such as, to expel gas, formotion sickness, diarrhea, nausea (anti-emetic) and loss of appetite. It is also used in pain relief from arthritis, menstrual pain, upper respiratory tract infections—coughs and bronchitis. Ginger taken with anticoagulants may lead to risk of bleeding. If ingested with hypoglycemic drugs, such as insulin or glipizide, it may cause hypoglycemia. When co-administered with calcium channel blockers, ginger might reduce further or cause an irregular heartbeat [186,187].
- (c)
- Green tea (polyphenols) improves mental alertness and thinking. It is also used to treat a plethora of other medical conditions, including Crohn’s disease, Parkinson’s disease, cardiovascular disease, diabetes, hypotension, chronic fatigue syndrome (CFS), tooth decay, kidney stones and skin conditions. Consuming green tea with stimulant medications could have dangerous consequences, such as elevated heart rate and blood pressure. Bortezomib (Velcade) may not be as effective against some cancers if used with green tea. Consuming green tea may reduce the effectiveness of warfarin [188,189].
- (d)
- The leaf extract of Gingko biloba is effective in the treatment of Alzheimer’s disease and other forms of dementia, Raynaud’s syndrome, peripheral vascular disease, vertigo and dizziness, premenstrual syndrome (PMS) and improving color vision in people with diabetes. Ginkgo, when administered with anticoagulants/with NSAIDs, it may increase the risk of bleeding. When administered with anticonvulsants, it may reduce the effectiveness in preventing seizures [190,191].
- (e)
- Licorice has been used for various digestive system complaints such as stomach ulcers, heartburn, colic and chronic gastritis. It is also used for sore throat, bronchitis and in treating infections caused by bacteria or viruses [192]. Licorice is also used in an herbal form called Shakuyaku-kanzo to increase fertility in women. It is also used to treat prostate cancer and the skin disorders such aseczema, in combination with other herbs. It may make antihypertensive drugs less effective, as it may increase salt and water retention. When taken with anti-arrhythmic drugs, it may decrease their efficacy as it may increase the risk of an abnormal heart rhythm. In some cases, it decreases the levels of potassium as it increases urine formation. In such cases, the risk of digoxin toxicity also increases, if patient is on digoxin [193,194,195].
- (f)
- Kava root (kava-lactones) medicine, native to South Pacific, is used to calm anxiety, stress and to treat insomnia. It is also used in the treatment of attention deficit hyperactivity disorder (ADHD), depression, migraines and other headaches, chronic fatigue syndrome (CFS), epilepsy, psychosis, common cold and other respiratory tract infections, muscle pain, tuberculosis and cancer prevention. Kava is applied to the skin for some skin disorders such asleprosy, to promote wound healing. It is also used in urinary tract infections (UTIs), pain and swelling of the uterus, menstrual discomfort and hot flushes in women with menopause. It is also used as pain reliever in toothaches. When co-administered with barbiturates and benzodiazepines, it may prolong or intensify their effects [196,197].
- (g)
- Chamomile (tea extract) is used as tea or dietary supplement for stomach cramps, to treat irritation from chest colds. It is also used for slow healing wounds, abscesses, gum inflammation, and skin conditions such as eczema, chickenpox and diaper-rash. The risk of bleeding increases when it is co-administered with anti-coagulants. Iron absorption also reduces in the presence of tea extract. The pollen is allergic in some cases. If one is allergic to ragweed pollen, chamomile use must be prohibited [198,199].
6. Patent Literature
7. Conclusions and Future Prospects
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Santini, A.; Novellino, E. Nutraceuticals—Shedding Light on the Grey Area between Pharmaceuticals and Food. Expert Rev. Clin. Pharmacol. 2018, 11, 545–547. [Google Scholar] [CrossRef] [Green Version]
- Keservani, R.K.; Kesharwani, R.K.; Sharma, A.K.; Gautam, S.P.; Verma, S.K. Nutraceutical formulations and challenges. In Developing New Functional Food and Nutraceutical Products; Academic Press: New York, NY, USA, 2017; pp. 161–177. [Google Scholar]
- Fernandes, S.D.; Narayana, R.C.; Narayanan, A.V. The Emergence of India as a Blossoming Market for Nutraceutical Supplements: An Overview. Trends Food Sci. Technol. 2019, 86, 579–585. [Google Scholar] [CrossRef]
- Fogacci, F.; Fogacci, S. Cardiovascular Risk Factors Management in Pregnancy: A Role for Nutraceuticals? In Nutraceuticals and Cardiovascular Disease; Humana: Cham, Switzerland, 2021; pp. 245–253. [Google Scholar]
- Mazza, A.; Nicoletti, M.; Lenti, S.; Torin, G.; Rigatelli, G.; Pellizzato, M.; Fratter, A. Effectiveness and Safety of Novel Nutraceutical Formulation Added to Ezetimibe in Statin-Intolerant Hypercholesterolemic Subjects with Moderate-to-High Cardiovascular Risk. J. Med. Food 2021, 24, 59–66. [Google Scholar] [CrossRef] [PubMed]
- Colletti, A.; Cicero, A.F. Nutraceutical Approach to Chronic Osteoarthritis: From Molecular Research to Clinical Evidence. Int. J. Mol. Sci. 2021, 22, 12920. [Google Scholar] [CrossRef] [PubMed]
- Pandey, M.M.; Rastogi, S.; Rawat, A.K.S. Indian traditional ayurvedic system of medicine and nutritional supplementation. Evid.-Based Complement. Alternat. Med. 2013, 2013, 376327. [Google Scholar] [CrossRef] [Green Version]
- Ozdal, T.; Tomas, M.; Toydemir, G.; Kamiloglu, S.; Capanoglu, E. Introduction to nutraceuticals, medicinal foods, and herbs. In Aromatic Herbs in Food; Academic Press: New York, NY, USA, 2021; pp. 1–34. [Google Scholar]
- Da Costa, J.P. A Current Look at Nutraceuticals—Key Concepts and Future Prospects. Trends Food Sci. Technol. 2017, 62, 68–78. [Google Scholar] [CrossRef]
- Elkhalifa, A.E.O.; Alshammari, E.; Adnan, M.; Alcantara, J.C.; Awadelkareem, A.M.; Eltoum, N.E.; Ashraf, S.A. Okra (Abelmoschus Esculentus) as a Potential Dietary Medicine with Nutraceutical Importance for Sustainable Health Applications. Molecules 2021, 26, 696. [Google Scholar] [CrossRef]
- Chopra, A.S.; Lordan, R.; Horbańczuk, O.K.; Atanasov, A.G.; Chopra, I.; Horbańczuk, J.O.; Jóźwik, A.; Huang, L.; Pirgozliev, V.; Banach, M.; et al. The current use and evolving landscape of nutraceuticals. Pharmacol. Res. 2022, 175, 106001. [Google Scholar] [CrossRef]
- Chauhan, B.; Kumar, G.; Kalam, N.; Ansari, S.H. Current Concepts and Prospects of Herbal Nutraceutical: A Review. J. Adv. Pharm. Technol. Res. 2013, 4, 4–8. [Google Scholar]
- Hanssens, L.; Thiebaut, I.; Lefèvre, N.; Malfroot, A.; Knoop, C.; Duchateau, J.; Casimir, G. The clinical benefits of long-term supplementation with omega-3 fatty acids in cystic fibrosis patients—A pilot study. Prostaglandins Leukot. Essent. Fatty Acids 2016, 108, 45–50. [Google Scholar] [CrossRef]
- Miyata, H.; Yano, M.; Yasuda, T.; Yamasaki, M.; Murakami, K.; Makino, T.; Nishiki, K.; Sugimura, K.; Motoori, M.; Shiraishi, O.; et al. Randomized study of the clinical effects of ω-3 fatty acid–containing enteral nutrition support during neoadjuvant chemotherapy on chemotherapy-related toxicity in patients with esophageal cancer. Nutrition 2017, 33, 204–210. [Google Scholar] [CrossRef] [PubMed]
- Moradi, S.; Alivand, M.; KhajeBishak, Y.; AsghariJafarabadi, M.; Alipour, M.; Chilibeck, P.D.; Alipour, B. The effect of short-term omega-3 fatty acids supplementation on appetite in healthy men: A randomized double-blinded controlled clinical trial. Nutr. Clin. Metab. 2022, 36, 46–53. [Google Scholar] [CrossRef]
- Tungkasamit, T.; Chakrabandhu, S.; Samakgarn, V.; Kunawongkrit, N.; Jirawatwarakul, N.; Chumachote, A.; Chitapanarux, I. Reduction in severity of radiation-induced dermatitis in head and neck cancer patients treated with topical aloe vera gel: A randomized multicenter double-blind placebo-controlled trial. Eur. J. Oncol. Nurs. 2022, 59, 102164. [Google Scholar] [CrossRef] [PubMed]
- Hutchings, H.A.; Wareham, K.; Baxter, J.N.; Atherton, P.; Kingham, J.G.C.; Duane, P.; Thomas, L.; Thomas, M.; Ch’ng, C.L.; Williams, J.G. A randomised, cross-over, placebo-controlled study of Aloe vera in patients with irritable bowel syndrome: Effects on patient quality of life. ISRN Gastroenterol. 2011, 2011, 206103. [Google Scholar] [CrossRef] [Green Version]
- Murray, M.; Dordevic, A.L.; Cox, K.; Scholey, A.; Ryan, L.; Bonham, M.P. Twelve weeks’ treatment with a polyphenol-rich seaweed extract increased HDL cholesterol with no change in other biomarkers of chronic disease risk in overweight adults: A placebo-controlled randomized trial. J. Nutr. Biochem. 2021, 96, 108777. [Google Scholar] [CrossRef]
- Young, M.A.; Cook, J.L.; Webster, K.E. The effect of topical wheatgrass cream on chronic plantar fasciitis: A randomized, double-blind, placebo-controlled trial. Complement. Ther. Med. 2006, 14, 3–9. [Google Scholar] [CrossRef]
- Ben-Arye, E.; Goldin, E.; Wengrower, D.; Stamper, A.; Kohn, R.; Berry, E. Wheat grass juice in the treatment of active distal ulcerative colitis: A randomized double-blind placebo-controlled trial. Scand. J. Gastroenterol. 2002, 37, 444–449. [Google Scholar] [CrossRef]
- D’angelo, L.; Grimaldi, R.; Caravaggi, M.; Marcoli, M.; Perucca, E.; Lecchini, S.; Frigo, G.M.; Crema, A. A double-blind, placebo-controlled clinical study on the effect of a standardized ginseng extract on psychomotor performance in healthy volunteers. J. Ethnopharmacol. 1986, 16, 15–22. [Google Scholar] [CrossRef]
- Hou, J.H.; Shin, H.; Shin, H.; Kil, Y.; Park, M.K.; Lee, W.; Seong, J.Y.; Lee, S.H.; Cho, H.S.; Yuk, S.H.; et al. Influence of Panax ginseng formulation on skin microbiota: A randomized, split face comparative clinical study. J. Ginseng Res. 2022, 46, 296–303. [Google Scholar] [CrossRef]
- Lopresti, A.L.; Smith, S.J. An investigation into the anxiety-relieving and mood-enhancing effects of Echinacea angustifolia (EP107™): A randomised, double-blind, placebo-controlled study. J. Affect. Disord. 2021, 293, 229–237. [Google Scholar] [CrossRef]
- Awad, O.G.A.N. Echinacea can help with Azithromycin in prevention of recurrent tonsillitis in children. Am. J. Otolaryngol. 2020, 41, 102344. [Google Scholar] [CrossRef] [PubMed]
- Galanakis, C.M. The Food Systems in the Era of the Coronavirus (COVID-19) Pandemic Crisis. Foods 2020, 9, 523. [Google Scholar] [CrossRef] [Green Version]
- Lokhande, S.S. Role of Nutraceuticals in Various Diseases: A Comprehensive Review. Asian J. Pharm. Res. 2018, 8, 236–240. [Google Scholar] [CrossRef]
- Hopper, I.; Connell, C.; Briffa, T.; De Pasquale, C.G.; Driscoll, A.; Kistler, P.M.; Atherton, J.J. Nutraceuticals in Patients with Heart Failure: A Systematic Review. J. Card. Fail. 2020, 26, 166–179. [Google Scholar] [CrossRef] [PubMed]
- Natic, M.; Pavlovic, A.; Bosco, F.L.; Stanisavljevic, N.; Zagorac, D.D.; Aksic, M.F.; Papetti, A. Nutraceutical properties and phytochemical characterization of wild Serbian fruits. Eur. Food Res. Technol. 2019, 245, 469–478. [Google Scholar] [CrossRef]
- Mishra, S.S.; Behera, P.K.; Kar, B.; Ray, R.C. Advances in probiotics, prebiotics and nutraceuticals. In Innovations in Technologies for Fermented Food and Beverage Industries; Panda, S.K., Shetty, P.H., Eds.; Springer: Cham, Switzerland, 2018; pp. 121–141. [Google Scholar]
- Bordignon, R.; Volpato, A.; Glombowsky, P.; Souza, C.F.; Baldissera, M.D.; Secco, R.; Da Silva, A.S. Nutraceutical effect of vitamins and minerals on performance and immune and antioxidant systems in dairy calves during the nutritional transition period in summer. J. Therm. Biol. 2019, 84, 451–459. [Google Scholar] [CrossRef]
- Sokola-Wysoczanska, E.; Wysoczanski, T.; Wagner, J.; Czyz, K.; Bodkowski, R.; Lochynski, S.; Patkowska-Sokola, B. Polyunsaturated fatty acids and their potential therapeutic role in cardiovascular system disorders—A Review. Nutrients 2018, 10, 1561. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Amaro, H.M.; Guedes, A.; Preto, M.A.; Sousa-Pinto, I.; Malcata, F.X. Gloeothece sp. as a Nutraceutical Source—An improved method of extraction of carotenoids and fatty acids. Mar. Drugs 2018, 16, 327. [Google Scholar] [CrossRef] [Green Version]
- Patel, S. Emerging trends in nutraceutical applications of whey protein and its derivatives. J. Food Sci. Technol. 2015, 52, 6847–6858. [Google Scholar] [CrossRef] [Green Version]
- Rai, R.H.; Goyal, R.K.; Singh, R.B.; Handjiev, S.; Singh, J.; Darlenska, T.H.; Smail, M.M. Vitamins and minerals as nutraceuticals in cardiovascular diseases and other chronic diseases. In Functional Foods and Nutraceuticals in Metabolic and Non-Communicable Diseases; Academic Press: New York, NY, USA, 2022; pp. 651–670. [Google Scholar]
- Zhang, R.; Wu, W.; Zhang, Z.; Lv, S.; Xing, B.; McClements, D.J. Impact of Food Emulsions on the Bioaccessibility of Hydrophobic Pesticide Residues in Co-Ingested Natural Products: Influence of Emulsifier and Dietary Fiber Type. J. Agric. Food Chem. 2019, 67, 6032–6040. [Google Scholar] [CrossRef]
- Howes, M.J.R.; Perry, N.S.; Vásquez-Londoño, C.; Perry, E.K. Role of phytochemicals as nutraceuticals for cognitive functions affected in ageing. Br. J. Pharmacol. 2022, 177, 1294–1315. [Google Scholar] [CrossRef] [PubMed]
- Rajasekaran, A.; Kalaivani, M. Designer foods and their benefits: A review. J. Food Sci. Technol. 2013, 50, 1–16. [Google Scholar] [CrossRef] [Green Version]
- Ting, Y.; Jiang, Y.; Ho, C.T.; Huang, Q. Common delivery systems for enhancing in vivo bioavailability and biological efficacy of nutraceuticals. J. Funct. Foods 2014, 7, 112–128. [Google Scholar] [CrossRef]
- Puri, V.; Sharma, A.; Kumar, P.; Singh, I. Thiolation of biopolymers for developing drug delivery systems with enhanced mechanical and mucoadhesive properties: A review. Polymers 2020, 12, 1803. [Google Scholar] [CrossRef] [PubMed]
- Moyo, M.; Aremu, A.O. Nutritional, phytochemical and diverse health-promoting qualities of Cleome gynandra. Crit. Rev. Food Sci. Nutr. 2022, 62, 3535–3552. [Google Scholar] [CrossRef] [PubMed]
- Reboredo-Rodríguez, P.; Varela-López, A.; Forbes-Hernández, T.Y.; Gasparrini, M.; Afrin, S.; Cianciosi, D.; Battino, M. Phenolic compounds isolated from olive oil as nutraceutical tools for the prevention and management of cancer and cardiovascular diseases. Int. J. Mol. Sci. 2018, 19, 2305. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Gupta, R.C.; Srivastava, A.; Lall, R. Toxicity Potential of Nutraceuticals. In Computational Toxicology. Methods in Molecular Biology; Nicolotti, O., Ed.; Humana Press: New York, NY, USA, 2018; Volume 1800, pp. 367–394. [Google Scholar]
- Bischoff, K. Glucosinolates and Organosulfur Compounds. In Nutraceuticals in Veterinary Medicine; Gupta, R.C., Srivastava, A., Lall, R., Eds.; Springer: Cham, Switzerland, 2019; pp. 113–119. [Google Scholar]
- Patra, S.; Nayak, R.; Patro, S.; Pradhan, B.; Sahu, B.; Behera, C.; Bhutia, S.K.; Jena, M. Chemical diversity of dietary phytochemicals and their mode of chemoprevention. Biotechnol. Rep. 2021, 30, e00633. [Google Scholar] [CrossRef]
- Scicchitano, P.; Cameli, M.; Maiello, M.; Modesti, P.A.; Muiesan, M.L.; Novo, S.; di Studio Ipertensione, G. Nutraceuticals and dyslipidaemia: Beyond the common therapeutics. J. Funct. Foods 2014, 6, 11–32. [Google Scholar] [CrossRef]
- Chanda, S.; Tiwari, R.K.; Kumar, A.; Singh, K. Nutraceuticals inspiring the current therapy for lifestyle diseases. Adv. Pharmacol. Sci. 2019, 2019, 6908716. [Google Scholar] [CrossRef]
- Singh, J.; Sinha, S. Classification, regulatory acts and applications of nutraceuticals for health. Int. J. Pharma Bio Sci. 2012, 2, 177–187. [Google Scholar]
- Ashraf, S.; Ghufran Saeed, S.M.; Saify, Z.S.; Haider, S.; Sayed, S.A.; Ali, R.; Simji, S. Potential nutraceutical benefits of basmati rice bran oil as analgesic, anti-inflammatory and anti-arthritis. Pak. J. Pharm. Sci. 2019, 32, 2545–2551. [Google Scholar] [PubMed]
- Pei, Y.; Ai, T.; Deng, Z.; Wu, D.; Liang, H.; McClements, D.J.; Li, B. Impact of plant extract on the gastrointestinal fate of nutraceutical-loaded nanoemulsions: Phytic acid inhibits lipid digestion but enhances curcumin bioaccessibility. Food Funct. 2019, 10, 3344–3355. [Google Scholar] [CrossRef] [PubMed]
- De Franciscis, P.; Colacurci, N.; Riemma, G.; Conte, A.; Pittana, E.; Guida, M.; Schiattarella, A. A nutraceutical approach to menopausal complaints. Medicina 2019, 55, 544. [Google Scholar] [CrossRef] [Green Version]
- Wiggs, A.; Molina, S.; Sumner, S.J.; Rushing, B.R. A Review of Metabolic Targets of Anticancer Nutrients and Nutraceuticals in Pre-Clinical Models of Triple-Negative Breast Cancer. Nutrients 2022, 14, 1990. [Google Scholar] [CrossRef] [PubMed]
- Van der Burg, K.P.; Cribb, L.; Firth, J.; Karmacoska, D.; Mischoulon, D.; Byrne, G.J.; Berk, M. EPA and DHA as markers of nutraceutical treatment response in major depressive disorder. Eur. J. Nutr. 2019, 59, 2439–2447. [Google Scholar] [CrossRef]
- Melino, S.; Leo, S.; ToskaPapajani, V. Natural Hydrogen Sulfide Donors from Allium sp. as a Nutraceutical Approach in Type 2 Diabetes Prevention and Therapy. Nutrients 2019, 11, 1581. [Google Scholar] [CrossRef] [Green Version]
- Poli, A.; Visioli, F. Pharmacology of nutraceuticals with lipid lowering properties. High Blood Press. Cardiovasc. Prev. 2019, 26, 113–118. [Google Scholar] [CrossRef]
- Cicero, A.F.; Grassi, D.; Tocci, G.; Galletti, F.; Borghi, C.; Ferri, C. Nutrients and nutraceuticals for the management of high normal blood pressure: An evidence-based consensus document. High Blood Press. Cardiovasc. Prev. 2019, 26, 9–25. [Google Scholar] [CrossRef]
- Ripani, U.; Manzarbeitia-Arroba, P.; Guijarro-Leo, S.; Urrutia-Graña, J.; De Masi-De Luca, A. Vitamin C May Help to Reduce the Knee’s Arthritic Symptoms. Outcomes Assessment of Nutriceutical Therapy. Med. Arch. 2019, 73, 173. [Google Scholar] [CrossRef]
- Ward, W.E.; Chilibeck, P.D.; Comelli, E.M.; Duncan, A.M.; Phillips, S.M.; Robinson, L.E.; Stellingwerff, T. Research in nutritional supplements and nutraceuticals for health, physical activity, and performance: Moving forward. Appl. Physiol. Nutr. Metab. 2019, 44, 455–460. [Google Scholar] [CrossRef] [Green Version]
- Puri, V.; Sharma, A.; Kumar, P.; Singh, I.; Huanbutta, K. Synthesis and Characterization of Thiolated Gum Ghatti as a Novel Excipient: Development of Compression-Coated Mucoadhesive Tablets of Domperidone. ACS Omega 2021, 6, 15844–15854. [Google Scholar] [CrossRef] [PubMed]
- Granetzke, L.; Paolini, B.; Wells, R.E. Complementary and Alternative Approaches to Chronic Daily Headache: Part III—Nutraceuticals. In Chronic Headache; Green, M.W., Cowan, R., Freitag, F.G., Eds.; Springer: Cham, Switzerland, 2019; pp. 273–287. [Google Scholar]
- Barmherzig, R.; Rajapakse, T. Nutraceuticals and Behavioral Therapy for Headache. Curr. Neurol. Neurosci. Rep. 2021, 21, 33. [Google Scholar] [CrossRef] [PubMed]
- Zayed, A.; Serag, A.; Farag, M.A. Cynara cardunculus L.: Outgoing and potential trends of phytochemical, industrial, nutritive and medicinal merits. J. Funct. Foods 2020, 69, 103937. [Google Scholar] [CrossRef]
- Reklou, A.; Katsiki, N.; Karagiannis, A.; Athyros, V. Effects of lipid lowering drugs on arterial stiffness: One more way to reduce cardiovascular risk? Curr. Vasc. Pharmacol. 2020, 18, 38–42. [Google Scholar] [CrossRef] [PubMed]
- Caliceti, C.; Urao, N.; Rizzo, P.; Giuliano, M. New Trends in Antioxidant Compounds: A Precise Nutraceutical in Cardiometabolic Disorders. Oxid. Med. Cell. Longev. 2019, 2019, 4794563. [Google Scholar] [CrossRef] [PubMed]
- Bahorun, T.; Aruoma, O.I.; Neergheen-Bhujun, V.S. Phytomedicines, nutraceuticals, and functional foods regulatory framework: The African context. In Nutraceutical and Functional Food Regulations in the United States and around the World; Bagchi, D., Ed.; Academic Press: New York, NY, USA, 2019; pp. 509–521. [Google Scholar]
- Mannarino, M.R.; Bianconi, V.; Pirro, M. Commentary to the possible role of nutraceuticals in the prevention of cardiovascular disease. High Blood Press. Cardiovasc. Prev. 2019, 26, 259–261. [Google Scholar] [CrossRef] [PubMed]
- Porto, C.M.; da Silva, T.D.P.S.; Sougey, E.B. Contribuições da vitamina D no tratamento de sintomasdepressivos e fatores de risco cardiovascular: Protocolo de estudo para um ensaioclínicorandomizado, duplo-cego e controlado por placebo. Trials 2019, 20, 583. [Google Scholar] [CrossRef] [Green Version]
- Janabi, A.H.W.; Kamboh, A.A.; Saeed, M.; Xiaoyu, L.; BiBi, J.; Majeed, F.; Alagawany, M. Flavonoid-rich foods (FRF): A promising nutraceutical approach against lifespan-shortening diseases. Iran. J. Basic Med. Sci. 2020, 23, 140. [Google Scholar]
- Myung, S.K.; Kim, H.B.; Lee, Y.J.; Choi, Y.J.; Oh, S.W. Calcium supplements and risk of cardiovascular disease: A meta-analysis of clinical trials. Nutrients 2021, 13, 368. [Google Scholar] [CrossRef]
- Russell, C.; Keshavamurthy, S.; Saha, S. Nutraceuticals in the Management of Cardiovascular Risk Factors: Where Is the Evidence? Cardiovasc. Hematol. Disord. Drug Targets 2021, 21, 150–161. [Google Scholar] [CrossRef]
- Ruscica, M.; Penson, P.E.; Ferri, N.; Sirtori, C.R.; Pirro, M.; Mancini, G.J.; Sattar, N.; Toth, P.P.; Sahebkar, A.; Lavie, C.J.; et al. Impact of nutraceuticals on markers of systemic inflammation: Potential relevance to cardiovascular diseases—A position paper from the International Lipid Expert Panel (ILEP). Prog. Cardiovasc. Dis. 2021, 67, 40–52. [Google Scholar] [CrossRef]
- Chen, G.; Wang, H.; Zhang, X.; Yang, S.T. Nutraceuticals and functional foods in the management of hyperlipidemia. Crit. Rev. Food Sci. Nutr. 2014, 54, 1180–1201. [Google Scholar] [CrossRef] [PubMed]
- Chakraborty, R.; Roy, S. Angiotensin-converting enzyme inhibitors from plants: A review of their diversity, modes of action, prospects, and concerns in the management of diabetes-centric complications. J. Integr. Med. 2021, 19, 478–492. [Google Scholar] [CrossRef]
- Chan, W.J.J.; McLachlan, A.J.; Luca, E.J.; Harnett, J.E. Garlic (Allium sativum L.) in the management of hypertension and dyslipidemia—A systematic review. J. Herb. Med. 2020, 19, 100292. [Google Scholar] [CrossRef]
- Sobenin, I.A.; Myasoedova, V.A.; Iltchuk, M.I.; Zhang, D.W.; Orekhov, A.N. Therapeutic effects of garlic in cardiovascular atherosclerotic disease. Chin. J. Nat. Med. 2019, 17, 721–728. [Google Scholar] [CrossRef]
- Manson, J.E.; Cook, N.R.; Lee, I.M.; Christen, W.; Bassuk, S.S.; Mora, S.; D’Agostino, D. Marine n − 3 fatty acids and prevention of cardiovascular disease and cancer. N. Engl. J. Med. 2019, 380, 23–32. [Google Scholar] [CrossRef]
- Barry, A.R.; Dixon, D.L. Omega-3 fatty acids for the prevention of atherosclerotic cardiovascular disease. Pharmacotherapy 2012, 41, 1056–1065. [Google Scholar] [CrossRef]
- El-Beltagi, H.S.; Mohamed, A.A.; Mohamed, H.I.; Ramadan, K.; Barqawi, A.A.; Mansour, A.T. Phytochemical and Potential Properties of Seaweeds and Their Recent Applications: A Review. Mar. Drugs 2022, 20, 342. [Google Scholar] [CrossRef]
- Padhi, E.M.; Hawke, A.; Liu, R.; Zhu, H.; Duncan, A.M.; Tsao, R.; Ramdath, D.D. Tracking isoflavones in whole soy flour, soy muffins and the plasma of hypercholesterolaemic adults. J. Funct. Foods 2016, 24, 420–428. [Google Scholar] [CrossRef]
- Ohta, S.; Asanoma, M.; Irie, N.; Tachibana, N.; Kohno, M. Soy Phospholipids Exert a Renoprotective Effect by Inhibiting the Nuclear Factor Kappa B Pathway in Macrophages. Metabolites 2022, 12, 330. [Google Scholar] [CrossRef]
- Möller, N.P.; Scholz-Ahrens, K.E.; Roos, N.; Schrezenmeir, J. Bioactive peptides and proteins from foods: Indication for health effects. Eur. J. Nutr. 2008, 47, 171–182. [Google Scholar] [CrossRef] [PubMed]
- Liao, W.; Sun, G.; Xu, D.; Wang, Y.; Lu, Y.; Sun, J.; Xia, H.; Wang, S. The blood-pressure-lowering effect of food-protein-derived peptides: A meta-analysis of recent clinical trials. Foods 2021, 10, 2316. [Google Scholar] [CrossRef] [PubMed]
- Mannucci, C.; Casciaro, M.; Sorbara, E.E.; Calapai, F.; Di Salvo, E.; Pioggia, G.; Navarra, M.; Calapai, G.; Gangemi, S. Nutraceuticals against oxidative stress in autoimmune disorders. Antioxidants 2021, 10, 261. [Google Scholar] [CrossRef] [PubMed]
- Majeed, M.; Ahmad, F.; Mundkur, L.; Appian, S. Pharmacology of α-spinasterol, a phytosterol with nutraceutical values: A review. Phytother. Res. 2022, 36, 3681–3690. [Google Scholar] [CrossRef] [PubMed]
- Poli, A.; Marangoni, F.; Corsini, A.; Manzato, E.; Marrocco, W.; Martini, D.; Medea, G.; Visioli, F. Phytosterols, cholesterol control, and cardiovascular disease. Nutrients 2021, 13, 2810. [Google Scholar] [CrossRef] [PubMed]
- Schoeneck, M.; Iggman, D. The effects of foods on LDL cholesterol levels: A systematic review of the accumulated evidence from systematic reviews and meta-analyses of randomized controlled trials. Nutr. Metab. Cardiovasc. Dis. 2021, 31, 1325–1338. [Google Scholar] [CrossRef]
- Saldanha, S.N.; Tollefsbol, T.O. The role of nutraceuticals in chemoprevention and chemotherapy and their clinical outcomes. J. Oncol. 2012, 2012, 192464. [Google Scholar] [CrossRef] [Green Version]
- Tripathi, Y.B.; Tripathi, P.; Arjmandi, B.H. Nutraceuticals and cancer management. Front. Biosci. 2005, 10, 1607–1618. [Google Scholar] [CrossRef]
- Ranzato, E.; Martinotti, S.; Calabrese, C.M.; Calabrese, G. Role of nutraceuticals in cancer therapy. J. Food Res. 2014, 3, 18. [Google Scholar] [CrossRef] [Green Version]
- Arora, D.; Jaglan, S. Nanocarriers based delivery of nutraceuticals for cancer prevention and treatment: A review of recent research developments. Trends Food Sci. Technol. 2016, 54, 114–126. [Google Scholar] [CrossRef]
- Caponio, G.R.; Lippolis, T.; Tutino, V.; Gigante, I.; De Nunzio, V.; Milella, R.A.; Gasparro, M.; Notarnicola, M. Nutraceuticals: Focus on anti-inflammatory, anti-cancer, antioxidant properties in gastrointestinal tract. Antioxidants 2022, 11, 1274. [Google Scholar] [CrossRef] [PubMed]
- Caponio, G.R.; Cofano, M.; Lippolis, T.; Gigante, I.; De Nunzio, V.; Difonzo, G.; Noviello, M.; Tarricone, L.; Gambacorta, G.; Giannelli, G.; et al. Anti-Proliferative and Pro-Apoptotic Effects of Digested Aglianico Grape Pomace Extract in Human Colorectal Cancer Cells. Molecules 2022, 27, 6791. [Google Scholar] [CrossRef] [PubMed]
- Zhang, X.; Zhang, W.; Chen, F.; Lu, Z. Combined effect of chrysin and apigenin on inhibiting the development and progression of colorectal cancer by suppressing the activity of P38-MAPK/AKT pathway. IUBMB Life 2021, 73, 774–783. [Google Scholar] [CrossRef] [PubMed]
- Yoshida, T.; Maruyama, T.; Miura, M.; Inoue, M.; Fukuda, K.; Shimazu, K.; Shibata, H. Dietary intake of pyrolyzed deketene curcumin inhibits gastric carcinogenesis. J. Funct. Foods 2018, 50, 192–200. [Google Scholar] [CrossRef]
- Kotha, R.R.; Luthria, D.L. Curcumin: Biological, pharmaceutical, nutraceutical, and analytical aspects. Molecules 2019, 24, 2930. [Google Scholar] [CrossRef] [Green Version]
- Wong, A.S.; Che, C.M.; Leung, K.W. Recent advances in ginseng as cancer therapeutics: A functional and mechanistic overview. Nat. Prod. Rep. 2015, 32, 256–272. [Google Scholar] [CrossRef]
- Dariya, B.; Govardhanagiri, S.; Rajitha, B.; Aliya, S.; Alam, A.; Nagaraju, G.P. Curcumin and Genistein Enhance the Sensitivity of Pancreatic Cancer to Chemotherapy. In Breaking Tolerance to Pancreatic Cancer Unresponsiveness to Chemotherapy; Nagaraju, G.P., Ed.; Academic Press: New York, NY, USA, 2019; pp. 87–109. [Google Scholar]
- Hsiao, Y.C.; Peng, S.F.; Lai, K.C.; Liao, C.L.; Huang, Y.P.; Lin, C.C.; Chung, J.G. Genistein induces apoptosis in vitro and has antitumor activity against human leukemia HL-60 cancer cell xenograft growth in vivo. Environ. Toxicol. 2019, 34, 443–456. [Google Scholar] [CrossRef]
- Bhagirath, D.; Yang, T.L.; Dahiya, R.; Majid, S.; Saini, S. Epigenetics of Prostate Cancer and Novel Chemopreventive and Therapeutic Approaches. In Epigenetics of Cancer Prevention; Bishayee, A., Bhatia, D., Eds.; Academic Press: New York, NY, USA, 2019; pp. 287–308. [Google Scholar]
- Li, Y.; Ahmad, A.; Kong, D.; Bao, B.; Sarkar, F.H. Recent progress on nutraceutical research in prostate cancer. Cancer Metastasis Rev. 2014, 33, 629–640. [Google Scholar] [CrossRef] [Green Version]
- Mahira, S.; Kommineni, N.; Husain, G.M.; Khan, W. Cabazitaxel and silibinin co-encapsulated cationic liposomes for CD44 targeted delivery: A new insight into nanomedicine based combinational chemotherapy for prostate cancer. Biomed. Pharmacother. 2019, 110, 803–817. [Google Scholar] [CrossRef]
- Bakhshi, F.; Molavi, O.; Rashidi, M.R.; Shayanfar, A.; Amini, H. Developing a high-performance liquid chromatography fast and accurate method for quantification of silibinin. BMC Res. Notes 2019, 12, 743. [Google Scholar] [CrossRef] [Green Version]
- Zhang, H.Y.; Cui, J.; Zhang, Y.; Wang, Z.L.; Chong, T.; Wang, Z.M. Isoflavones and prostate cancer: A review of some critical issues. Chin. Med. J. 2016, 129, 341. [Google Scholar] [CrossRef] [PubMed]
- Blake, C.; Hansen, T.; Simmons, T.C.; Lephart, E.D. Long time exposure to soy/isoflavone-rich diet enhances testicular and prostate health in Long-Evans rats. J. Funct. Foods 2013, 5, 1494–1501. [Google Scholar] [CrossRef]
- Zhu, W.W.; Zhang, Y.; Tang, C.H. Maximizing cholesterol-lowering benefits of soy protein isolate by glycation with soy soluble polysaccharide. Food Hydrocoll. 2023, 135, 108131. [Google Scholar] [CrossRef]
- Chung, B.H.; Horie, S.; Chiong, E. The incidence, mortality, and risk factors of prostate cancer in Asian men. Prostate Int. 2019, 7, 1–8. [Google Scholar] [CrossRef]
- Pérez-Sánchez, A.; Barrajón-Catalán, E.; Herranz-López, M.; Micol, V. Nutraceuticals for skin care: A comprehensive review of human clinical studies. Nutrients 2018, 10, 403. [Google Scholar] [CrossRef] [Green Version]
- Chakrabarti, S.; Guha, S.; Majumder, K. Food-derived bioactive peptides in human health: Challenges and opportunities. Nutrients 2018, 10, 1738. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Iwaniak, A.; Darewicz, M.; Mogut, D.; Minkiewicz, P. Elucidation of the role of in silico methodologies in approaches to studying bioactive peptides derived from foods. J. Funct. Foods 2019, 61, 103486. [Google Scholar] [CrossRef]
- Oesser, S.; Schunk, M.; Proksch, E. Positive effect of fish-derived Bioactive Collagen Peptides on skin health. Nutrafoods 2020, 1, 127–133. [Google Scholar]
- Ozogul, F.; Cagalj, M.; Šimat, V.; Ozogul, Y.; Tkaczewska, J.; Hassoun, A.; Kaddour, A.A.; Kuley, E.; Rathod, N.B.; Phadke, G.G. Recent developments in valorisation of bioactive ingredients in discard/seafood processing by-products. Trends Food Sci. Technol. 2021, 116, 559–582. [Google Scholar] [CrossRef]
- Proksch, E.; Schunck, M.; Zague, V.; Segger, D.; Degwert, J.; Oesser, S. Oral intake of specific bioactive collagen peptides reduces skin wrinkles and increases dermal matrix synthesis. Skin Pharmacol. Physiol. 2014, 27, 113–119. [Google Scholar] [CrossRef]
- Hexsel, D.; Zague, V.; Schunck, M.; Siega, C.; Camozzato, F.O.; Oesser, S. Oral supplementation with specific bioactive collagen peptides improves nail growth and reduces symptoms of brittle nails. J. Cosmet. Dermatol. 2017, 16, 520–526. [Google Scholar] [CrossRef] [PubMed]
- Senni, K.; Pereira, J.; Gueniche, F.; Delbarre-Ladrat, C.; Sinquin, C.; Ratiskol, J.; Colliec-Jouault, S. Marine polysaccharides: A source of bioactive molecules for cell therapy and tissue engineering. Mar. Drugs 2011, 9, 1664–1681. [Google Scholar] [CrossRef] [Green Version]
- Shivangi, S.; Dorairaj, D.; Negi, P.S.; Shetty, N.P. Development and characterisation of a pectin-based edible film that contains mulberry leaf extract and its bio-active components. Food Hydrocoll. 2021, 121, 107046. [Google Scholar] [CrossRef]
- Singh, B.; Mal, G.; Sharma, D.; Gautam, S.K.; Kumar, M.; Solimene, U.; Marotta, F. Plant Polyphenols: The Futuristic Bioactive Therapeutics for Skin Care. In Polyphenols: Prevention and Treatment of Human Disease; Watson, R.R., Preedy, V.R., Zibadi, S., Eds.; Academic Press: New York, NY, USA, 2018; pp. 385–394. [Google Scholar]
- Oliviero, F.; Scanu, A.; Zamudio-Cuevas, Y.; Punzi, L.; Spinella, P. Anti-inflammatory effects of polyphenols in arthritis. J. Sci. Food Agric. 2018, 98, 1653–1659. [Google Scholar] [CrossRef] [PubMed]
- Aydin, S.; Bacanlı, M.; Anlar, H.G.; Çal, T.; Arı, N.; Bucurgat, U.U.; Basaran, N. Preventive role of Pycnogenol® against the hyperglycemia-induced oxidative stress and DNA damage in diabetic rats. Food Chem. Toxicol. 2019, 124, 54–63. [Google Scholar] [CrossRef] [PubMed]
- Raskovic, A.; Bukumirovic, N.; PautKusturica, M.; Milic, N.; Cabarkapa, V.; Borisev, I.; Mikov, M. Hepatoprotective and antioxidant potential of Pycnogenol® in acetaminophen-induced hepatotoxicity in rats. Phytother. Res. 2019, 33, 631–639. [Google Scholar]
- Ermakov, I.V.; Ermakova, M.; Sharifzadeh, M.; Gorusupudi, A.; Farnsworth, K.; Bernstein, P.S.; Isman, C. Optical assessment of skin carotenoid status as a biomarker of vegetable and fruit intake. Arch. Biochem. Biophys. 2018, 646, 46–54. [Google Scholar] [CrossRef]
- Conte, L.; Somacal, S.; Nichelle, S.M.; Rampelotto, C.; Robalo, S.S.; Roehrs, M.; Emanuelli, T. Short-Term Bixin Supplementation of Healthy Subjects Decreases the Susceptibility of LDL to Cu2+-Induced Oxidation Ex Vivo. J. Nutr. Metab. 2019, 2019, 9407069. [Google Scholar] [CrossRef] [Green Version]
- Patel, P.; Jethani, H.; Radha, C.; Vijayendra, S.V.N.; Mudliar, S.N.; Sarada, R.; Chauhan, V.S. Development of a carotenoid enriched probiotic yogurt from fresh biomass of Spirulina and its characterization. J. Food Sci. Technol. 2019, 56, 3721–3731. [Google Scholar] [CrossRef]
- Inbathamizh, L.; Prabavathy, D.; Sudha, S. Quality Assurance of Nutraceuticals and Their Approval, Registration, Marketing. Handb. Nutraceuticals Nat. Prod. Biol. Med. Nutr. Prop. Appl. 2022, 2, 337–360. [Google Scholar]
- Das, L.; Bhaumik, E.; Raychaudhuri, U.; Chakraborty, R. Role of nutraceuticals in human health. J. Food Sci. Technol. 2012, 49, 173–183. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Moorehead, R.A. Rodent Models Assessing Mammary Tumor Prevention by Soy or Soy Isoflavones. Genes 2019, 10, 566. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Rivellese, A.A.; Ciciola, P.; Costabile, G.; Vetrani, C.; Vitale, M. The possible role of nutraceuticals in the prevention of cardiovascular disease. High Blood Press. Cardiovasc. Prev. 2019, 26, 101–111. [Google Scholar] [CrossRef]
- Sut, S.; Baldan, V.; Faggian, M.; Peron, G.; DallAcqua, S. Nutraceuticals, a new challenge for medicinal chemistry. Curr. Med. Chem. 2016, 23, 3198–3223. [Google Scholar] [CrossRef]
- Assadpour, E.; Mahdi Jafari, S. A systematic review on nanoencapsulation of food bioactive ingredients and nutraceuticals by various nanocarriers. Crit. Rev. Food Sci. Nutr. 2019, 59, 3129–3151. [Google Scholar] [CrossRef]
- Augustin, M.A.; Sanguansri, L. Challenges in developing delivery systems for food additives, nutraceuticals and dietary supplements. In Encapsulation Technologies and Delivery Systems for Food Ingredients and Nutraceuticals; Garti, N., McClements, D.J., Eds.; Woodhead Publishing Ltd.: Sawston, UK, 2012; pp. 19–48. [Google Scholar]
- Alexander, M.; Lopez, A.A.; Fang, Y.; Corredig, M. Incorporation of phytosterols in soy phospholipids nanoliposomes: Encapsulation efficiency and stability. LWT 2012, 47, 427–436. [Google Scholar] [CrossRef]
- Chaudhari, S.P.; Dugar, R.P. Application of surfactants in solid dispersion technology for improving solubility of poorly water soluble drugs. J. Drug Deliv. Sci. Technol. 2017, 41, 68–77. [Google Scholar] [CrossRef]
- Soukoulis, C.; Bohn, T. A comprehensive overview on the micro-and nano-technological encapsulation advances for enhancing the chemical stability and bioavailability of carotenoids. Crit. Rev. Food Sci. Nutr. 2018, 58, 1–36. [Google Scholar] [CrossRef]
- Ghorbanzade, T.; Jafari, S.M.; Akhavan, S.; Hadavi, R. Nano-encapsulation of fish oil in nano-liposomes and its application in fortification of yogurt. Food Chem. 2017, 216, 146–152. [Google Scholar] [CrossRef]
- Tripathi, K.M.; Tran, T.S.; Kim, Y.J.; Kim, T. Green fluorescent onion-like carbon nanoparticles from flaxseed oil for visible light induced photocatalytic applications and label-free detection of Al (III) ions. ACS Sustain. Chem. Eng. 2017, 5, 3982–3992. [Google Scholar] [CrossRef]
- Da Pieve, S.; Calligaris, S.; Panozzo, A.; Arrighetti, G.; Nicoli, M.C. Effect of monoglyceride organogel structure on cod liver oil stability. Food Res. Int. 2011, 44, 2978–2983. [Google Scholar] [CrossRef]
- Horuz, T.İ.; Belibaglı, K.B. Nanoencapsulation by electrospinning to improve stability and water solubility of carotenoids extracted from tomato peels. Food Chem. 2018, 268, 86–93. [Google Scholar] [CrossRef] [PubMed]
- Ha, T.V.A.; Kim, S.; Choi, Y.; Kwak, H.S.; Lee, S.J.; Wen, J.; Ko, S. Antioxidant activity and bioaccessibility of size-different nanoemulsions for lycopene-enriched tomato extract. Food Chem. 2015, 178, 115–121. [Google Scholar] [CrossRef] [PubMed]
- Kaur, R.; Sharma, A.; Puri, V.; Singh, I. Preparation and characterization of biocomposite films of carrageenan/locust bean gum/montmorrillonite for transdermal delivery of curcumin. BioImpacts 2019, 9, 37. [Google Scholar] [CrossRef] [Green Version]
- Tsai, Y.M.; Jan, W.C.; Chien, C.F.; Lee, W.C.; Lin, L.C.; Tsai, T.H. Optimisednano-formulation on the bioavailability of hydrophobic polyphenol, curcumin, in freely-moving rats. Food Chem. 2011, 127, 918–925. [Google Scholar] [CrossRef]
- Temmerman, R.; Pot, B.; Huys, G.; Swings, J. Identification and antibiotic susceptibility of bacterial isolates from probiotic products. Int. J. Food Microbiol. 2003, 81, 1–10. [Google Scholar] [CrossRef]
- Maji, I.; Mahajan, S.; Sriram, A.; Medtiya, P.; Vasave, R.; Khatri, D.K.; Kumar, R.; Singh, S.B.; Madan, J.; Singh, P.K. Solid self emulsifying drug delivery system: Superior mode for oral delivery of hydrophobic cargos. J. Control. Release 2021, 337, 646–660. [Google Scholar] [CrossRef]
- Huanbutta, K.; Sriamornsak, P.; Singh, I.; Sangnim, T. Manufacture of 2D-printed precision drug-loaded orodispersible film prepared from tamarind seed gum substrate. Appl. Sci. 2021, 11, 5852. [Google Scholar] [CrossRef]
- Sangnim, T.; Huanbutta, K. Development of Astaxanthin orodispersible tablet for elderly prepared by Direct compression. Chonburi Hosp. J. 2020, 45, 33. [Google Scholar]
- Sangnim, T.; Sriamornsak, P.; Singh, I.; Huanbutta, K. Swallowing Gel for Patients with Dysphagia: A Novel Application of Chitosan. Gels 2021, 7, 108. [Google Scholar] [CrossRef]
- Papaspyridi, L.M.; Aligiannis, N.; Christakopoulos, P.; Skaltsounis, A.L.; Fokialakis, N. Production of bioactive metabolites with pharmaceutical and nutraceutical interest by submerged fermentation of Pleurotus ostreatus in a batch stirred tank bioreactor. Procedia Food Sci. 2011, 1, 1746–1752. [Google Scholar] [CrossRef] [Green Version]
- De Marco Castro, E.; Shannon, E.; Abu-Ghannam, N. Effect of fermentation on enhancing the nutraceutical properties of Arthrospira platensis (Spirulina). Fermentation 2019, 5, 28. [Google Scholar] [CrossRef] [Green Version]
- Jampilek, J.; Kos, J.; Kralova, K. Potential of nanomaterial applications in dietary supplements and foods for special medical purposes. Nanomaterials 2019, 9, 296. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Braithwaite, M.C.; Tyagi, C.; Tomar, L.K.; Kumar, P.; Choonara, Y.E.; Pillay, V. Nutraceutical-based therapeutics and formulation strategies augmenting their efficiency to complement modern medicine: An overview. J. Funct. Foods 2014, 6, 82–99. [Google Scholar] [CrossRef]
- Polia, F.; Pastor-Belda, M.; Martínez-Blázquez, A.; Horcajada, M.N.; Tomás-Barberán, F.A.; García-Villalba, R. Technological and biotechnological processes to enhance the bioavailability of dietary (poly)phenols in humans. J. Agric. Food Chem. 2022, 70, 2092–2107. [Google Scholar] [CrossRef]
- Vivarelli, S.; Costa, C.; Teodoro, M.; Giambò, F.; Tsatsakis, A.M.; Fenga, C. Polyphenols: A route from bioavailability to bioactivity addressing potential health benefits to tackle human chronic diseases. Arch. Toxicol. 2022, 1–36. [Google Scholar] [CrossRef]
- Babazadeh, A.; Ghanbarzadeh, B.; Hamishehkar, H. Phosphatidylcholine-rutin complex as a potential nanocarrier for food applications. J. Funct. Foods 2017, 33, 134–141. [Google Scholar] [CrossRef]
- Srinivasan, V.; Chavan, S.; Jain, U.; Tarwadi, K. Liposomes for Nanodelivery Systems in Food Products. In Nanoscience for Sustainable Agriculture; Pudake, R.N., Chauhan, N., Kole, C., Eds.; Springer: Cham, Switzerland, 2019; pp. 627–638. [Google Scholar]
- Khorasani, S.; Danaei, M.; Mozafari, M.R. Nanoliposome technology for the food and nutraceutical industries. Trends Food Sci. Technol. 2018, 79, 106–115. [Google Scholar] [CrossRef]
- Giavasis, I. Bioactive fungal polysaccharides as potential functional ingredients in food and nutraceuticals. Curr. Opin. Biotechnol. 2014, 26, 162–173. [Google Scholar] [CrossRef]
- Panda, S.; Latha, V.; Pattnaik, S.; Maharana, L.; Prasad, R. An Update On Various Excipients Employed for Orodispersible Tablets with A Special Focus On Superdisintegrants. Int. J. Pharm. Clin. Res. 2015, 7, 440–449. [Google Scholar]
- Dhanya, K.; Sasikumar, B. Molecular Marker Based Adulteration Detection in Traded Food and Agricultural Commodities of Plant Origin with Special Reference to Spices. Curr. Trends Biotechnol. Pharm. 2010, 4, 454–489. [Google Scholar]
- Bansal, S.; Singh, A.; Mangal, M.; Mangal, A.K.; Kumar, S. Food adulteration: Sources, health risks, and detection methods. Crit. Rev. Food Sci. Nutr. 2017, 57, 1174–1189. [Google Scholar] [CrossRef] [PubMed]
- Aballay, L.R.; Eynard, A.R.; Díaz, M.D.P.; Navarro, A.; Munoz, S.E. Overweight and obesity: A review of their relationship to metabolic syndrome, cardiovascular disease, and cancer in South America. Nutr. Rev. 2013, 71, 168–179. [Google Scholar] [CrossRef]
- Ali, S.; Shah, W.A.S.; Shah, M.A.; Zareef, M.; Arslan, M.; Hassan, M.; Ali, I.; Ali, M.; Ullah, S. Adulteration and Safety Issues in Nutraceuticals and Functional Foods. In Advances in Nutraceuticals and Functional Foods; Apple Academic Press: Palm Bay, FL, USA, 2022; pp. 79–103. [Google Scholar]
- Wang, D.; Man, R.; Shu, M.; Liu, H.; Gao, Y.; Luan, F. Detection of sibutramine and phenolphthalein in functional foods using capillary electrophoresis. Anal. Methods 2016, 8, 621–626. [Google Scholar] [CrossRef]
- Cayan, F.; Dilek, U.; Akbay, E.; Gen, R.; Dilek, S. Use of Chinese herbal medicine ‘meizitanc’ in pregnancy: Report of three cases. J. Obstet. Gynaecol. Res. 2009, 35, 801–803. [Google Scholar] [CrossRef] [PubMed]
- Chong, C.S.Y. Psychosis related to the use of sibutramine disguised as over-the-counter herbal weight loss remedies: A report of two patients. East Asian Arch. Psychiatry 2010, 20, 186. [Google Scholar] [PubMed]
- Pratiwi, R.; Dipadharma, R.H.F.; Prayugo, I.J.; Layandro, O.A. Recent Analytical Method for Detection of Chemical Adulterants in Herbal Medicine. Molecules 2021, 26, 6606. [Google Scholar] [CrossRef]
- Cianchino, V.; Acosta, G.; Ortega, C.; Martínez, L.D.; Gomez, M.R. Analysis of potential adulteration in herbal medicines and dietary supplements for the weight control by capillary electrophoresis. Food Chem. 2008, 108, 1075–1081. [Google Scholar] [CrossRef]
- Baek, S.H.; Bae, O.N.; Park, J.H. Recent methodology in ginseng analysis. J. Ginseng Res. 2012, 36, 119. [Google Scholar] [CrossRef]
- Kesanakurti, P.; Ragupathy, S.; Faller, A.C.; Shanmughanandhan, D.; Buongiorno, F.; Della Noce, I.; Lu, Z.; Zhang, Y.; Newmaster, S.G. Development of Hydrolysis Probe-Based qPCR Assays for Panax ginseng and Panax quinquefolius for Detection of Adulteration in Ginseng Herbal Products. Foods 2021, 10, 2705. [Google Scholar] [CrossRef]
- Lam, M.; Khoshkhat, P.; Chamani, M.; Shahsavari, S.; Dorkoosh, F.A.; Rajabi, A.; Maniruzzaman, M.; Nokhodchi, A. In-depth multidisciplinary review of the usage, manufacturing, regulations & market of dietary supplements. J. Drug Deliv. Sci. Technol. 2021, 67, 102985. [Google Scholar]
- Salvador, M.J.; Andreazza, N.L.; Pascoal, A.C.R.F.; Pereira, P.S.; França, S.C.; Zucchi, O.L.; Dias, D.A. Bioactive Chemical Constituents and Biotechnological Production of Secondary Metabolites in Amaranthaceae Plants, Gomphreneae Tribe. In Biotechnological Production of Plant Secondary Metabolites; Orhan, I.E., Ed.; Bentham Science: Sharjah City, United Arab Emirates, 2012; p. 124. [Google Scholar]
- Formisano, C.; Delfine, S.; Oliviero, F.; Tenore, G.C.; Rigano, D.; Senatore, F. Correlation among environmental factors, chemical composition and antioxidative properties of essential oil and extracts of chamomile (Matricaria chamomilla L.) collected in Molise South-central Italy. Ind. Crops Prod. 2015, 63, 256–263. [Google Scholar] [CrossRef]
- Orhan, I.E.; Senol, F.S.; Skalicka-Wozniak, K.; Georgiev, M.; Sener, B. Adulteration and safety issues in nutraceuticals and dietary supplements: Innocent or risky. In Nutraceuticals, Nanotechnology in the Agri-Food Industry; Grumezescu, A.M., Ed.; Academic Press: New York, NY, USA, 2016; pp. 153–182. [Google Scholar]
- Villani, T.S.; Reichert, W.; Ferruzzi, M.G.; Pasinetti, G.M.; Simon, J.E.; Wu, Q. Chemical investigation of commercial grape seed derived products to assess quality and detect adulteration. Food Chem. 2015, 170, 271–280. [Google Scholar] [CrossRef]
- Do, T.K.T.; Hadji-Minaglou, F.; Antoniotti, S.; Fernandez, X. Authenticity of essential oils. Trends Anal. Chem. 2015, 66, 146–157. [Google Scholar] [CrossRef]
- Peng, M.; Zhao, X.; Biswas, D. Polyphenols and tri-terpenoids from Olea europaea L. in alleviation of enteric pathogen infections through limiting bacterial virulence and attenuating inflammation. J. Funct. Foods 2017, 36, 132–143. [Google Scholar] [CrossRef]
- Shahrajabian, M.H.; Sun, W.; Cheng, Q. Ginkgo Biloba: A Famous Living Fossil Tree and an Ancient Herbal Traditional Chinese Medicine. Curr. Nutr. Food Sci. 2022, 18, 259–264. [Google Scholar] [CrossRef]
- He, Y.; Zhang, Y.; Lu, J.; Lin, R. Isolation and structural elucidation of abietic acid as the main adulterant in an herbal drug for the treatment of psoriasis. J. Pharm. Biomed. Anal. 2012, 66, 345–348. [Google Scholar] [CrossRef]
- Shao, J.W.; Jiang, J.L.; Zou, J.J.; Yang, M.Y.; Chen, F.M.; Zhang, Y.J.; Jia, L. Therapeutic potential of ginsenosides on diabetes: From hypoglycemic mechanism to clinical trials. J. Funct. Foods 2020, 64, 103630. [Google Scholar] [CrossRef]
- Garg, U.; Ferguson, A.M. Adulteration of herbal remedies with conventional drugs: Role of the clinical laboratory. In Efficacy, Toxicity, Interactions with Western Drugs, and Effects on Clinical Laboratory Tests; Dasgupta, A., Hammett-Stabler, C.A., Eds.; Wiley: Hoboken, NJ, USA, 2011; p. 369. [Google Scholar]
- Elkady, E.F.; El-Zaher, A.A.; Elwy, H.H.; Saleh, M.A. Validated liquid chromatographic method for simultaneous determination of metformin, pioglitazone, sitagliptin, repaglinide, glibenclamide and gliclazide-application for counterfeit drug analysis. J. Anal. Bioanal. Tech. 2015, 13, S13. [Google Scholar]
- Bogusz, M.J.; Hassan, H.; Al-Enazi, E.; Ibrahim, Z.; Al-Tufail, M. Application of LC–ESI–MS–MS for detection of synthetic adulterants in herbal remedies. J. Pharm. Biomed. Anal. 2006, 41, 554–564. [Google Scholar] [CrossRef]
- Campbell, N.; Clark, J.P.; Stecher, V.J.; Thomas, J.W.; Callanan, A.C.; Donnelly, B.F.; Kaminetsky, J.C. Adulteration of purported herbal and natural sexual performance enhancement dietary supplements with synthetic phosphodiesterase type 5 inhibitors. J. Sex. Med. 2013, 10, 1842–1849. [Google Scholar] [CrossRef] [PubMed]
- Reeuwijk, N.M.; Venhuis, B.J.; de Kaste, D.; Hoogenboom, L.A.P.; Rietjens, I.M.; Martena, M.J. Sildenafil and analogous phosphodiesterase type 5 (PDE-5) inhibitors in herbal food supplements sampled on the Dutch market. Food Addit. Contam. Part A 2013, 30, 2027–2034. [Google Scholar] [CrossRef] [PubMed]
- Kazlauskaite, J.A.; Ivanauskas, L.; Bernatoniene, J. Novel Extraction Method Using Excipients to Enhance Yield of Genistein and Daidzein in Trifolium pratensis L. Pharmaceutics 2021, 13, 777. [Google Scholar] [CrossRef] [PubMed]
- Choi, M.K.; Song, I.S. Pharmacokinetic Drug–Drug Interactions and Herb–Drug Interactions. Pharmaceutics 2021, 13, 610. [Google Scholar] [CrossRef]
- Bushra, R.; Aslam, N.; Khan, A.Y. Food-drug interactions. Oman Med. J. 2011, 26, 77–83. [Google Scholar] [CrossRef]
- Brankovic, S.; Radenkovic, M.; Kitic, D.; Veljkovic, S.; Ivetic, V.; Pavlovic, D.; Miladinovic, B. Comparison of the hypotensive and bradycardic activity of ginkgo, garlic, and onion extracts. Clin. Exp. Hypertens. 2011, 33, 95–99. [Google Scholar] [CrossRef]
- Shiju, T.M.; Rajesh, N.G.; Viswanathan, P. Renoprotective effect of aged garlic extract in streptozotocin-induced diabetic rats. Indian J. Pharmacol. 2013, 45, 18. [Google Scholar] [CrossRef]
- Haniadka, R.; Saldanha, E.; Sunita, V.; Palatty, P.L.; Fayad, R.; Baliga, M.S. A review of the gastroprotective effects of ginger (Zingiber officinale Roscoe). Food Funct. 2013, 4, 845–855. [Google Scholar] [CrossRef]
- Bhowmik, D.; Tripathi, K.K.; Chandira, M.R.; Kumar, K.P. Zingiber officinale the herbal and traditional medicine and its therapeutically importance. J. Pharmacogn. Phytochem. 2010, 2, 102–110. [Google Scholar]
- Chinchole, A.S.; Waghmare, P.V.; Poul, B.N.; Panchal, C.V.; Sonawane, L.V.; Chavan, D.V. Green tea as a wonderful and grateful drink for promoting health. Pharma Sci. Monit. 2014, 5, 1–9. [Google Scholar]
- Qadir, M.I. Role of green tea flavonoids and other related contents in cancer prevention. Crit. Rev. Eukaryot. Gene Expr. 2017, 27, 163–171. [Google Scholar] [CrossRef] [PubMed]
- Kandiah, N.; Ong, P.A.; Yuda, T.; Ng, L.L.; Mamun, K.; Merchant, R.A.; Nguyen, V.T. Treatment of dementia and mild cognitive impairment with or without cerebrovascular disease: Expert consensus on the use of Ginkgo biloba extract, EGb 761®. CNS Neurosci. Ther. 2019, 25, 288–298. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Mazumder, A.G.; Sharma, P.; Patial, V.; Singh, D. Ginkgo biloba L. attenuates spontaneous recurrent seizures and associated neurological conditions in lithium-pilocarpine rat model of temporal lobe epilepsy through inhibition of mammalian target of rapamycin pathway hyperactivation. J. Ethnopharmacol. 2017, 204, 8–17. [Google Scholar] [CrossRef] [PubMed]
- Yang, R.; Yuan, B.C.; Ma, Y.S.; Zhou, S.; Liu, Y. The anti-inflammatory activity of licorice, a widely used Chinese herb. Pharm. Biol. 2017, 55, 5–18. [Google Scholar] [CrossRef] [Green Version]
- Sadeghi, M.; Namjouyan, F.; Cheraghian, B.; Abbaspoor, Z. Impact of Glycyrrhiza glabra (licorice) vaginal cream on vaginal signs and symptoms of vaginal atrophy in postmenopausal women: A randomized double blind controlled trial. J. Tradit. Complement. Med. 2020, 10, 110–115. [Google Scholar] [CrossRef] [PubMed]
- Ring, M. Women’s health: Polycystic ovarian syndrome, menopause, and osteoporosis. Prim. Care-Clin. Off. Pract. 2017, 44, 377–398. [Google Scholar] [CrossRef]
- Sharma, A.; Puri, V.; Kakkar, V.; Singh, I. Formulation and Evaluation of Silymarin-Loaded Chitosan-Montmorilloite Microbeads for the Potential Treatment of Gastric Ulcers. J. Funct. Biomater. 2018, 9, 52. [Google Scholar] [CrossRef] [Green Version]
- Domínguez, F.; González-Trujano, E.; Gallardo, J.M.; Orozco-Suárez, S. Antidepressant medicinal plants and compounds used in traditional medicines in North America. In Herbal Medicine in Depression; Grosso, C., Ed.; Springer: Cham, Switzerland, 2016; pp. 381–431. [Google Scholar]
- Van, T.M.; Xuan, T.D.; Minh, T.N.; Quan, N.V. Isolation and purification of potent growth inhibitors from Piper methysticum root. Molecules 2018, 23, 1907. [Google Scholar] [CrossRef] [Green Version]
- Simões, D.; Miguel, S.P.; Ribeiro, M.P.; Coutinho, P.; Mendonça, A.G.; Correia, I.J. Recent advances on antimicrobial wound dressing: A review. Eur. J. Pharm. Biopharm. 2018, 127, 130–141. [Google Scholar] [CrossRef]
- Salehi, B.; Lopez-Jornet, P.; Pons-Fuster López, E.; Calina, D.; Sharifi-Rad, M.; Ramírez-Alarcón, K.; Martins, N. Plant-derived bioactives in oral mucosal lesions: A key emphasis to curcumin, lycopene, chamomile, aloe vera, green tea and coffee properties. Biomolecules 2019, 9, 106. [Google Scholar] [CrossRef]
- Xie, C.; Chen, H.; Jin, G.; Ren, S.; Lu, J. Pesticidal Disease Protecting and Nutrient Pesticide Fertilizer and Application Thereof and Pesticidal Disease Protecting and Nutrient Pesticide Fertilizer Slow Release Formulation and Application Thereof. U.S. Patent CN104193540A, 14 September 2016. [Google Scholar]
- Xie, C.; Chen, H.; Hu, J.; Jiang, Z.; Ren, S.; Road, S. Nutritional Disease-Preventing Pesticide Fertilizer and Application Thereof Nutritional Disease-Preventing Pesticide Fertilizer Slow Release Agent and Application. Thereof. Patent CN104262041A, 7 January 2015. [Google Scholar]
- Ming, C.; Wang, X.; Xie, L. Disease-Preventing Nutrient Bag and Manufacture Method. Thereof. Patent CN101371628A, 25 February 2009. [Google Scholar]
- DiPierro, G.; Steven, A.G. Bio-Synchronous Transdermal Drug Delivery for Longevity Anti Ageing Fatigue Management Obesity Weight Loss Weight Management Delivery of Nutraceuticals and the Treatment of Hyperglycemia Alzheimer’s Disease Sleep Disorders Parkinson’s Disease Aids Epilepsy Attention Deficit Disorder Nicotine Addiction Cancer Headache and Pain Control Asthma Angina Hypertension Depression Cold Flu and the Like. US Patent 9669199B2, 6 June 2017. [Google Scholar]
- Dipierro, G.; Giannos, S.A. Transdermal Delivery Techniques for Drugs, Nutraceuticals and Other Active Substances. WO2008054788A3, 8 May 2008. [Google Scholar]
- Mckee, D.; Karwic, A. Product and Method for Producing a Vehicle for Oral Administration of Nutraceuticals. EP1835818B1, 10 August 2011. [Google Scholar]
- Ghai, G.; Boyd, C.; Csiszar, K.; Ho, C.-T.; Rosen, R.T. Methods of Screening Foods for Nutraceuticals. U.S. Patent 5955269A, 21 September 1999. [Google Scholar]
- Ismail, M.; Al-Naqeeb, G. Cardio-Protective Effects of Nutraceuticals Isolated from Nigella Sativa Seeds. EP2349302A4, 8 August 2012. [Google Scholar]
- Celi, P.; Chen, S.E.; Chung, T.K.; DSM IP Assets BV. Combination of 25-Hydroxyvitamin D and Antioxidants/Anti-Inflammatories for Bovine Health. U.S. Patent 10,517,316, 31 December 2019. [Google Scholar]
- Angel, J.; Rangel, O. Phyto-Nutraceutical Synergistic Composition for Parkinson’s Disease. U.S. Patent 20080118583A, 22 May 2008. [Google Scholar]
- Ghosh, P.; Shen, B. Nutraceuticals for the Treatment Protection and Restoration of Connective Tissues. AU2005200614A1, 3 March 2005. [Google Scholar]
- LaPointe, A.T.; LaPointe, J.A. Nutraceutical with Tart Cherries and Method of Treatment Therewith. U.S. Patent 7,494,674, 24 February 2009. [Google Scholar]
- Vermeer, S.; Wick, A.B.; Westbie, S.; Kravenes, J.; Hurgus, L.J.; Wick, H. Pharmaceutical and Nutraceutical Products Comprising Vitamin K2. CN101534807A, 16 September 2009. [Google Scholar]
- Chatterjee, S.; Butler, M.S.; Somanadhan, B. Anti-Cholesterolemic Compounds and Methods of Use. U.S. Patent 20100063153A1, 11 March 2010. [Google Scholar]
- Evans, S.; Block, J.B. Process to Modulate Disease Risk with Doses of a Nutraceuticals. U.S. Patent 6630160B1, 7 October 2003. [Google Scholar]
- Sole, M.J.; Jeejeebhoy, K.N. Composition for Improvement of Cellular Nutrition and Mitochondrial Energetics. U.S. Patent 6,080,788, 27 June 2000. [Google Scholar]
- Alghamdi, S.S. Method and Composition for Treating Symptoms of Sickle Cell Disease. U.S. Patent 20160089411A1, 31 March 2016. [Google Scholar]
- Hobman, P.; Test, A.; McDonough, M.; Cox, B. The Use of Angiogenin and Angiogenin Agonist for Treating Diseases and Disorders. CN102088995B, 20 January 2016. [Google Scholar]
- Lundberg, B. Highly Refined Cellulose Nutraceutical Compositions and Methods of Use. U.S. Patent 20080193590A1, 14 August 2008. [Google Scholar]
- Kim, M.Y.; Park, B.Y.; Moon, C.H.; Park, E.K.; Kim, K.M.; Angiolab Inc. Composition Comprising Melissa Leaf Extract for Anti-Angiogenic and Matrix Metalloproteinase Inhibitory Activity. U.S. Patent 7,485,327, 3 February 2009. [Google Scholar]
- Kasper, L.H.; Ochoa-Reparaz, J. Nutraceutical Composition and Methods for Preventing or Treating Multiple Sclerosis. U.S. Patent 20110009360A1, 13 January 2011. [Google Scholar]
- Biy, K.V.; Biy, K.Q. Nutraceutical for the Prevention and Treatment of Cancers and Diseases Affecting the Liver. CN1822768A, 23 August 2006. [Google Scholar]
- Verlinden, S.F. Chalcones and Derivatives for Use in Medicaments and Nutraceuticals. U.S. Patent 17/261,129, 23 September 2021. [Google Scholar]
- Madhavi, D.L.; Kagan, D.I. Nutraceuticals Having Sustained Release for Improved Bioavailability and Method of Production. U.S. Patent 17/126,811, 22 April 2021. [Google Scholar]
- Do, T.C.; Yang, P. Nutraceuticals Supplement Composition for Regulating Metabolism and Anti-Aging. U.S. Patent 17/203,558, 23 September 2021. [Google Scholar]
- Mitchell, M.; Brandenburg, J.E. Process for Fractionation and Extraction of Herbal Plant Material to Isolate Extractives for Pharmaceuticals and Nutraceuticals. U.S. Patent 10,981,083, 20 April 2021. [Google Scholar]
- Ichim, T.E.; Ramos, F.; Veltmeyer, J.; Dixon, T.G. Prevention of Neuroinflammation Associated Memory Loss Using Nutraceutical Compositions. U.S. Patent 17/395,249, 10 February 2022. [Google Scholar]
- Gokhale, S.; Bhaduri, A. In Silico Methods for Obtaining Nutraceutical Compositions. U.S. Patent 11,270,791, 8 March 2022. [Google Scholar]
- Mollar, B.F.; Saiz, P.M. Multilayer Pharmaceutical or Nutraceutical Solid Dosage Forms Comprising Pyrimidine and/or Purine Derivatives and B Vitamins, Preparation and Uses Thereof. U.S. Patent 17/606,701, 26 May 2022. [Google Scholar]
- Vorderbruggen, M. Enhanced D Vitamin Nutraceutical Compositions and Methods for Making and Used Same. U.S. Patent 17/546,982, 16 June 2022. [Google Scholar]
Nutraceuticals | Bioactive Molecule | Dosage | Formulation | Duration of Study | Action | Population Size (Volunteers) | References |
---|---|---|---|---|---|---|---|
Omega-3 | Eicosapentaenoic acid (EPA) and Docosahexaenoic acid (DHA) | 60 mg/kg/day | Capsule | 12 months | Cystic fibrosis | 15 | [13] |
Omega-3 | Eicosapentaenoic acid (EPA) and Docosahexaenoic acid (DHA) | 900 mg in the omega-3 rich group and 250 mg in the omega-3 poor group | Capsule | 15 days | Reduction of chemotherapy-related toxicities | 61 | [14] |
Omega-3 | Eicosapentaenoic acid (EPA) and Docosahexaenoic acid (DHA) | 2000 mg/day | Capsule | 21 days | Appetite | 72 | [15] |
Aloe vera | aloe-emodin, aloin, aloesin, emodin, and acemannan | - | Gel | 2 months | Acute dermatitis | 120 | [16] |
Aloe vera | aloe-emodin, aloin, aloesin, emodin, and acemannan | 60 mL | Juice | 5 months | Irritable bowel syndrome | 110 | [17] |
Seaweed | polysaccharides, proteins, lipids and polyphenols | 2000 mg/d | Extract | 12 weeks | High-density lipoprotein (hdl) cholesterol | 34 | [18] |
Wheatgrass | vitamins, (A, B, C and E), minerals such as iron, calcium, magnesium, benzo(a)pyrene, ferulic, gallic, caffeic, syringic and p-coumaric acid | - | Cream | 12 weeks | Plantar fasciitis | 134 | [19] |
Wheatgrass | vitamins, (A, B, C and E), minerals such as iron, calcium, magnesium, benzo(a)pyrene, ferulic, gallic, caffeic, syringic and p-coumaric acid | 100 cc/day | Juice | 1 month | Active distal ulcerative colitis | 23 | [20] |
Ginseng | ginsenosides | 100 mg twice a day | Capsule | 12 weeks | Psychomotor functions | 16 | [21] |
Ginseng | ginsenosides | - | Hydrogel | 2 weeks | Skin homeostasis | 20 | [22] |
Echinacea | polysaccharides, glycoproteins, alkamides, cichoric acid, caftaric acid and chlorogenic acids | 20 mg or 40 mg twice a day | Powder | 6 weeks | Anti-anxiety and anti-depressant | 104 | [23] |
Echinacea | polysaccharides, glycoproteins, alkamides, cichoric acid, caftaric acid and chlorogenic acids | 5 mL | Oral Suspension | 6 months | Tonsillitis | 300 | [24] |
Nutraceuticals/ Dietary Supplements | Nutrients | Health Benefits |
---|---|---|
Water Soluble Vitamins | Vitamin C | Wound healing, Antioxidant |
Vitamin B1 | Carbohydrate metabolism, Neurological function | |
Vitamin B2 | Energy metabolism, Nerve function | |
Vitamin B3 | Brain function | |
Vitamin B6 | Convert proteins to energy | |
Vitamin B12 | Formation of RBC’s, Synthesis of amino acids Metabolism of fat, protein and carbohydrate | |
Folic acid | Formation of RBC’s, Formation of genetic material of cells | |
Pantothenic acid | Intraneuronal synthesis of acetylcholine Synthesis of cholesterol, steroids, and fatty acids | |
Fat Soluble Vitamins | Vitamin A | Cancer, Skin disorder, Healthy vision Antioxidant |
Vitamin D | Absorption of calcium, Formation of bones and teeth | |
Vitamin E | Boost immune system, Antioxidant | |
Vitamin K | Blood clotting | |
Minerals | Calcium | Maintaining bone strength, blood clotting |
Iron | Oxygen transport, Energy production | |
Magnesium | Healthy nerve and muscle function and bone function | |
Phosphorus | Phosphorylation process, Genetic material | |
Copper | Heart functioning, Iron absorption | |
Iodine | Functioning of thyroid gland | |
Chromium | Diabetes | |
Selenium | Antioxidant | |
Zinc | Sperm production, wound healing | |
Herbals | Aloe vera | Anti-inflammatory, Wound healing |
Evening primrose oil | Treatment of atopic eczema | |
Garlic | Anti-bacterial, Anti-fungal | |
Ginger | Carminative, Anti-emetic | |
Ginseng | Adaptogen | |
Green tea | Cell mediated immunity, Antioxidant |
Patent Number | Patent Title | Year | Reference |
CN104193540B | Fertilizer and insecticide use nutraceuticals disease prevention, disease prevention nutraceutical insecticidal fertilizer slow-release agent and the use thereof | 2016 | [200] |
CN104262041A | Nutritional disease-preventing pesticide fertilizer and application thereof, nutritional disease-preventing pesticide fertilizer slow release agent and application thereof | 2015 | [201] |
CN101371628A | Disease-preventing nutrient bag and manufacture method thereof | 2009 | [202] |
US9669199B2 | Bio-synchronous transdermal drug delivery for longevity, anti-ageing, fatigue management, obesity, weight loss, weight management, delivery of nutraceuticals and the treatment of hyperglycemia, Alzheimer’s disease, sleep disorders, Parkinson’s disease, aids, epilepsy, attention deficit disorder, nicotine addiction, cancer, headache and pain control, asthma, angina, hypertension, depression, cold, flu and the like | 2017 | [203] |
WO2008054788A3 | Transdermal delivery techniques for drugs, nutraceuticals and other active substances | 2008 | [204] |
EP1835818B1 | Product and method for producing a vehicle for oral administration of nutraceuticals | 2011 | [205] |
US5955269A | Methods of screening foods for nutraceuticals | 1999 | [206] |
EP2349302A4 | Cardio-protective effects of nutraceuticals isolated from nigella sativa seeds | 2012 | [207] |
US10517316B2 | Combination of 25-hydroxyvitamin D and antioxidants/anti-inflammatories for bovine health | 2016 | [208] |
US20080118583A1 | Phyto-nutraceutical synergistic composition for Parkinson’s disease | 2008 | [209] |
AU2005200614A1 | Nutraceuticals for the treatment, protection and restoration of connective tissues | 2005 | [210] |
US7494674B2 | Nutraceutical with tart cherries and method of treatment therewith | 2009 | [211] |
CN101534807A | Pharmaceutical and nutraceutical products comprising vitamin k2 | 2009 | [212] |
US20100063153A1 | Anti-cholesterolemic compounds and methods of use | 2010 | [213] |
US6630160B1 | Process to modulate disease risk with doses of a nutraceuticals | 2003 | [214] |
US6080788A | Composition for improvement of cellular nutrition and mitochondrial energetics | 2000 | [215] |
US20160089411A1 | Method and composition for treating symptoms of sickle cell disease | 2016 | [216] |
CN102088995B | The use of angiogenin and angiogenin agonist for treating diseases and disorders | 2016 | [217] |
US20080193590A1 | Highly refined cellulose nutraceutical compositions and methods of use | 2008 | [218] |
US20040009244A1 | Composition comprising melissa leaf extract for anti-angiogenic and matrix metalloproteinase inhibitory activity | 2004 | [219] |
US20110009360A1 | Nutraceutical Composition and Methods for Preventing or Treating Multiple Sclerosis | 2011 | [220] |
CN1822768A | Nutraceutical for the prevention and treatment of cancers and diseases affecting the liver | 2006 | [221] |
US20210292265A1 | Chalcones and derivatives for use in medicaments and nutraceuticals | 2021 | [222] |
US20210113554A1 | Nutraceuticals Having Sustained Release for Improved Bioavailability and Method of Production | 2021 | [223] |
US20210290722A1 | Nutraceuticals supplement composition for regulating metabolism and anti-aging | 2021 | [224] |
US10981083B2 | Process for fractionation and extraction of herbal plant material to isolate extractives for pharmaceuticals and nutraceuticals | 2021 | [225] |
US20220040248A1 | Prevention of Neuroinflammation associated Memory Loss Using Nutraceutical Compositions | 2022 | [226] |
US11270791B2 | In silico methods for obtaining nutraceutical compositions | 2022 | [227] |
US20220160744A1 | Multilayer pharmaceutical or nutraceutical solid dosage forms comprising pyrimidine and/or purine derivatives and b vitamins, preparation and uses thereof | 2022 | [228] |
US20220184100A1 | Enhanced d vitamin nutraceutical compositions and methods for making and used same | 2022 | [229] |
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
Puri, V.; Nagpal, M.; Singh, I.; Singh, M.; Dhingra, G.A.; Huanbutta, K.; Dheer, D.; Sharma, A.; Sangnim, T. A Comprehensive Review on Nutraceuticals: Therapy Support and Formulation Challenges. Nutrients 2022, 14, 4637. https://doi.org/10.3390/nu14214637
Puri V, Nagpal M, Singh I, Singh M, Dhingra GA, Huanbutta K, Dheer D, Sharma A, Sangnim T. A Comprehensive Review on Nutraceuticals: Therapy Support and Formulation Challenges. Nutrients. 2022; 14(21):4637. https://doi.org/10.3390/nu14214637
Chicago/Turabian StylePuri, Vivek, Manju Nagpal, Inderbir Singh, Manjinder Singh, Gitika Arora Dhingra, Kampanart Huanbutta, Divya Dheer, Ameya Sharma, and Tanikan Sangnim. 2022. "A Comprehensive Review on Nutraceuticals: Therapy Support and Formulation Challenges" Nutrients 14, no. 21: 4637. https://doi.org/10.3390/nu14214637