Curcumin, a Compound from Natural Sources, a True Scientific Challenge – A Review

Zorka Stanić1
1Faculty of Science, University of Kragujevac, Kragujevac, Serbia

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Darvesh AS, Aggarwal BB, Bishayee A (2012) Curcumin and liver cancer: a review. Curr Pharm Biotechnol 13:218–228

Oliveira MR, Jardim FR, Setzer WN, Nabavi SM, Nabavi SF (2016) Curcumin, mitochondrial biogenesis, and mitophagy: exploring recent data and indicating future needs. Biotechnol Adv 34:813–826

Nabavi SF, Daglia M, Moghaddam AH, Habtemariam S, Nabavi SM (2013) Curcumin and liver disease: from chemistry to medicine. Compr Rev Food Sci F 13:62–77

Perrone D, Ardito F, Giannatempo G, Dioguardi M, Troiano G, Russo LL, Lillo A, Laino L, Muzio LL (2015) Biological and therapeutic activities, and anticancer properties of curcumin (review). Exp Ther Med 10:1615–1623

Stanic Z, Girousi S (2012) Electrochemical investigation of some biological important compounds correlated to curcumin. In: Sasaki J, Kichida M (eds) Curcumin: biosynthesis, medicinal uses and health benefits. Nova Science Publisher, New York, pp. 39–79

Siviero A, Gallo E, Maggini V, Gori L, Mugelli A, Firenzuoli F, Vannacci A (2015) Curcumin, a golden spice with a low bioavailability. J Herb Med 5:57–70

Mehanny M, Hathout RM, Geneidi AS, Mansour S (2016) Exploring the use of nanocarrier systems to deliver the magical molecule; curcumin and its derivatives. J Control Release 225:1–30

Wang YJ, Pan MH, Cheng AL, Lin LI, Ho YS, Hsieh CY, Lin JK (1997) Stability of curcumin in buffer solutions and characterization of its degradation products. J Pharm Biomed  Anal 15:1867–1876

Sharma RA, Gescher AJ, Steward WP (2005) Curcumin: the story so far. Eur J Cancer 41:1955–1968

Jovanovic SV, Steenken S, Boone CW, Simic MG (1999) H-atom transfer is a preferred antioxidant mechanism of curcumin. J Am Chem Soc 121:9677–9681

Bernabé-Pineda M, Ramírez-Silva MT, Romero-Romo M, González-Vergara E, Rojas-Hernández A (2004) Determination of acidity constants of curcumin in aqueous solution and apparent rate constant of its decomposition. Spectrochim Acta A Mol Biomol Spectrosc 60:1091–1097

Tønnesen HH, Másson M, Loftsson T (2002) Studies of curcumin and curcuminoids. XXVII. Cyclodextrin complexation: solubility, chemical and photochemical stability. Int J Pharm 244:127–135

Ravindranath V, Chandrasekhara N (1981) Metabolism of curcumin – studies with [3H] curcumin. Toxicology 22:337–344

Ghosh S, Banerjee S, Sil PC (2015) The beneficial role of curcumin on inflammation, diabetes and neurodegenerative disease: a recent update. Food Chem Toxicol 83:111–124

Pari L, Murugan P (2007) Changes in glycoprtein components in streptoyocin–nicotinamide induced type 2 diabetes: influence of tetrahydrocurcumin from Curcumin longa. Plant Foods Hum Nutr 62:25–29

Stanić Z, Voulgaropoulos A, Girousi S (2008) Electroanalytical study of the antioxidant and antitumor agent curcumin. Electroanal 20:1263–1266

Masek A, Chrzescijanska E, Zaborski M (2013) Characteristics of curcumin using cyclic voltammetry, UV–Vis, fluorescence and thermogravimetric analysis. Electrochim Acta 107:441–447

Weber WM, Hunsaker LA, Abcouwer SF, Deck LM, Jagt JDV (2005) Anti-oxidant activities of curcumin and related enones. Bioorg Med Chem 13:3811–3820

Derochette S, Serteyn D, Mouithys-Mickalad A, Ceusters J, Deby-Dupont G, Neven P, Franck T (2015) EquiNox2: a new method to measure NADPH oxidase activity and to study effect of inhibitors and their interactions with the enzyme. Talanta 144:1252–1259

Vajragupta O, Boonchoong P, Watanbe H, Tohda M, Kummasud N, Sumanont Y (2003) Manganese complexes of curcumin and its derivatives: evaluation for the radical scavenging ability and neuroprotective activity. Free Radic Biol Med 35:1632–1644

Liu Y-M, Lee K (2009) Modifications of the curcumin method enabling precise and accurate measurement of seawater boron concentration. Mar Chem 115:110–117

Margar SN, Rhyman L, Ramasami P, Sekar N (2016) Fluorescent difluoroboron-curcumin analogs: an investigation of the electronic structures and photophysical properties. Spectrochim Acta A 152:241–251

Chaicham A, Kulchat S, Tumcharern G, Tuntulani T, Tomapatanaget B (2010) Synthesis, photophysical properties, and cyanide detection in aqueous solution of BF2-curcumin dyes. Tetrahedron 66:6217–6223

Patra D, Malaeb NN (2011) Fluorescence modulation of 1,7-bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione by silver nanoparticles and its possible analytical application. Luminescence 27:11–15

Ponnuvel K, Banuppriya G, Padmini V (2016) Highly efficient and selective detection of picric acid among other nitroaromatics by NIR fluorescent organic fluorophores. Sensor Actuat B-Chem 234:34–45

Pourreza N, Golmohammadi H (2015) Application of curcumin nanoparticles in a lab-on-paper device as a simple and green pH probe. Talanta 131:136–141

Xu G, Wang J, Si G, Wang M, Xue X, Wu B, Zhou S (2016) A novel highly selective chemosensor based on curcumin for detection of Cu2+ and its application for bioimaging. Sensor Actuat B-Chem 230:684–689

Raj S, Shankaran DR (2016) Curcumin based biocompatible nanofibers for lead ion detection. Sensor Actuat B-Chem 226:318–325

Pourreza N, Golmohammadi H (2014) Green colorimetric recognition of trace sulfide ions in water samples using curcumin nanoparticle in micelle mediated system. Talanta 119:181–186

Yue Y, Yin C, Huo F, Chao J, Zhang Y (2014) The application of natural drug-curcumin in the detection hypochlorous acid of real sample and its bioimaging. Sensor Actuat B-Chem 202:551–556

Saithongdee A, Praphairaksit N, Imyim A (2014) Electrospun curcumin-loaded zein membrane for iron(III) ions sensing. Sensor Actuat B-Chem 202:935–940

Ojani R, Raoof J-B, Zamani S (2012) A novel voltammetric sensor for amoxicillin based on nickel–curcumin complex modified carbon paste electrode. Bioelectrochemistry 85:44–49

Serpi C, Stanić Z, Girousi S (2010) Electroanalytical study of the interaction between dsDNA and curcumin in the presence of copper(II). Talanta 81:1731–1734

Serpi C, Stanić Z, Girousi S (2010) Electroanalytical study of the interaction between double stranded DNA and antitumor agent curcumin. Anal Lett 43:1–16

Serpi C, Stanić Z, Girousi S (2013) Adsorptive transfer voltammetry applied to the study of chromium-induced DNA damage in the presence of curcumin. Int J Environ An Ch 93:543–552

Gupta SC, Patchva S, Aggarwal BB (2013) Therapeutic roles of curcumin: lessons learned from clinical trials. AAPS J 15:195–218

Neiman DC, Cialdella-Kam L, Knab AM, Shanely RA (2012) Influence of red pepper spice and turmeric on inflammation and oxidative stress biomarkers in overweight females: a metabolomics approach. Plant Foods Hum Nutr 67:415–421

Prasad S, Tyagi AK, Aggarwal BB (2014) Recent developments in delivery, bioavailability, absorption and metabolism of curcumin: the golden pigment from golden spice. Cancer Res Treat 46:2–28

Li J, Shin GH, Lee IW, Chen X, Park HJ (2016) Soluble starch formulated nanocomposite increases water solubility and stability of curcumin. Food Hydrocoll 56:41–49

Kumar A, Kaur G, Kansal SK, Chaudhary GR, Mehta SK (2016) Enhanced solubilization of curcumin in mixed surfactant vesicles. Food Chem 199:660–666

Shah BR, Li Y, Jin W, An Y, He L, Li Z, Xu W, Li B (2016) Preparation and optimization of Pickering emulsion stabilized by chitosan-tripolyphosphate nanoparticles for curcumin encapsulation. Food Hydrocoll 52:369–377

Righeschi C, Bergonzi MC, Isacchi B, Bazzicalupi C, Gratteri P, Bilia AR (2016) Enhanced curcumin permeability by SLN formulation: the PAMPA approach. Food Sci Technol-LWT 66:475–483

Pinheiro AC, Coimbra MA, Vicente AA (2016) In vitro behaviour of curcumin nanoemulsions stabilized by biopolymer emulsifiers - effect of interfacial composition. Food Hydrocoll 52:460–467

Borrin TR, Georges EL, Moraes ICF, Pinho SC (2016) Curcumin-loaded nanoemulsions produced by the emulsion inversion point (EIP) method: an evaluation of process parameters and physico-chemical stability. J Food Eng 169:1–9

Delmar K, Bianco-Peled H (2016) Composite chitosan hydrogels for extended release of hydrophobic drugs. Carbohydr Polym 136:570–580

Tan C, Xie J, Zhang X, Cai J, Xia S (2016) Polysaccharide-based nanoparticles by chitosan and gum arabic polyelectrolyte complexation as carriers for curcumin. Food Hydrocoll 57:236–245

Mutalik S, Suthar NA, Managuli RS, Shetty PK, Avadhani K, Kalthur G, Kulkarni RV, Thomas R (2016) Development and performance evaluation of novel nanoparticles of a grafted copolymer loaded with curcumin. Int J Biol Macromol 86:709–720

Huang Y-C, Kuo T-H (2016) O-carboxymethyl chitosan/fucoidan nanoparticles increase cellular curcumin uptake. Food Hydrocoll 53:261–269

Zhou M, Wang T, Hu Q, Luo Y (2016) Low density lipoprotein/pectin complex nanogels as potential oral delivery vehicles for curcumin. Food Hydrocoll 57:20–29

Rao PJ, Khanum H (2016) A green chemistry approach for nanoencapsulation of bioactive compound – curcumin. Food Sci Technol-LWT 65:695–702

Zou L, Zheng B, Zhang R, Zhang Z, Liu W, Liu C, Xiao H, McClements DJ (2016) Enhancing the bioaccessibility of hydrophobic bioactive agents using mixed colloidal dispersions: curcumin-loaded zein nanoparticles plus digestible lipid nanoparticles. Food Res Int 81:74–82

Pan Y, Tikekar RV, Wang MS, Avena-Bustillos RJ, Nitin N (2015) Effect of barrier properties of zein colloidal particles and oil-in-water emulsions on oxidative stability of encapsulated bioactive compounds. Food Hydrocoll 43:82–90

Zou L, Zheng B, Liu W, Liu C, Xiao H, McClements DJ (2015) Enhancing nutraceutical bioavailability using excipient emulsions: influence of lipid droplet size on solubility and bioaccessibility of powdered curcumin. J Funct Foods 15:72–83

Li M, Gao M, Fu Y, Chen C, Meng X, Fan A, Kong D, Wang Z, Zhao Y (2016) Acetal-linked polymeric prodrug micelles for enhanced curcumin delivery. Colloid Surface B 140:11–18

Laokuldilok N, Thakeow P, Kopermsub P, Utama-ang N (2016) Optimisation of microencapsulation of turmeric extract for masking flavor. Food Chem 194:695–704

Mokrani A, Krisa S, Cluzet S, Costa GD, Temsamani H, Renouf E, Mérillon J-M, Madani K, Mesnil M, Monvoisin A, Richard T (2016) Phenolic contents and bioactive potential of peach fruit extracts. Food Chem 202:212–220

Salahuddin P, Fatima MT, Abdelhameed AS, Nusrat S, Khan RH (2016) Structure of amyloid oligomers and their mechanisms of toxicities: targeting amyloid oligomers using novel therapeutic approaches. Eur J Med Chem 114:41–58

Temba BA, Fletcher MT, Fox GP, Harvey JJW, Sultanbawa Y (2016) Inactivation of Aspergillus flavus spores by curcumin-mediated photosensitization. Food Control 59:708–713

Liu X, Zhu L, Gao X, Wang Y, Lu H, Tang Y, Li J (2016) Magnetic molecularly imprinted polymers for spectrophotometric quantification of curcumin in food. Food Chem 202:309–315

Osorio-Tobón JF, Carvalho PIN, Barbero GF, Nogueira GC, Rostagno MA, Meireles MAA (2016) Fast analysis of curcuminoids from turmeric (Curcuma longa L.) by high-performance liquid chromatography using a fused-core column. Food Chem 200:167–174

Lu W, Kelly AL, Miao S (2016) Emulsion-based encapsulation and delivery systems for polyphenols. Trends Food Sci Technol 47:1–9

Faraj AA, Shaik AS, Ratemi E, Halwani R (2016) Combination of drug-conjugated SWCNT nanocarriers for efficient therapy of cancer stem cells in a breast cancer animal model. J Control Release 225:240–251

Mau L-P, Cheng W-C, Chen J-K, Shieh Y-S, Cochran DL, Huang R-Y (2016) Curcumin ameliorates alveolar bone destruction of experimental periodontitis by modulating osteoclast differentiation, activation and function. J Funct Foods 22:243–256

Kao H-H, Wu C-J, Won S-J, Shin J-W, Liu H-S, Su C-L (2011) Kinase gene expression and subcellular protein expression pattern of protein kinase C isoforms in curcumin-treated human hepatocellular carcinoma Hep 3B cells. Plant Foods Hum Nutr 66:136–142