A Systematic Review of Phytochemistry, Pharmacological Activities and Therapeutic Applications of Curcuma Longa
Janvi Sanjay Choudhary, Sunila. A. Patil, Sunil. P. Pawar
P.S.G.V.P. Mandal’s College of Pharmacy, Shahada, Maharashtra, India, 425409.
*Corresponding Author E-mail: janvichoudhary5454@gmail.com
ABSTRACT:
Turmeric is a spice that comes from the rhizomes of Curcuma longa, which belongs to the ginger family, Zingiberaceae. Rhizomes are horizontal underground stems that produce shoots and roots. The spice is sometimes called ‘Indian saffron’ because of its bright color. The bright yellow color of turmeric mainly comes from fat-soluble, polyphenolic pigments called curcuminoids. Curcumin is the main curcuminoid in turmeric and is usually seen as its most active component. Other curcuminoids present in turmeric include demethoxycurcumin and bisdemethoxycurcumin. Besides being a spice and colorant, turmeric has been used for medicinal purposes in India for centuries. Recently, studies have shown that curcumin may have anti-inflammatory and anticancer properties, sparking renewed scientific interest in its potential to prevent and treat disease.
KEYWORDS: Anti-Inflammatory, Anti-Helicobacter pylori, Curcumin, Curcuma longa, Indian saffron and curcuminoids.
INTRODUCTION:
Turmeric (Curcuma longa), a medicinal plant from the Zingiberaceae family, has long been valued in Indian herbal practice1,2. Its primary bioactive compounds are curcuminoids—curcumin, demethoxycurcumin (DMC), and bisdemethoxycurcumin (BDMC)3,4. These yellow constituents are derived from the rhizomes of C. longa5,6. Curcumin, the most studied curcuminoid, is a small, lipophilic polyphenol that dissolves in organic solvents and remains stable under gastric acidity. Turmeric also contains volatile oils such as turmerone, atlantone, and zingiberone, as well as sugars, proteins, and resins7. Curcumin, chemically known as diferuloylmethane, exhibits keto–enol tautomerism depending on the solvent environment8,9.
Turmeric has been used for more than 4,000 years in Vedic traditions for culinary, medicinal, and ritual purposes.10 Curcumin is associated with antioxidant11, anti-inflammatory12, antimutagenic13, antimicrobial14, and other therapeutic activities15. Because it is poorly absorbed and rapidly metabolized, several strategies have been developed to improve its bioavailability, with piperine offering the most significant enhancement—up to a 2000% increase16,17. Curcumin is a key ingredient in the root extract of Curcuma longa. The yellow root contains curcumin and has been used as a flavoring and coloring agent in food and medicine throughout Asian countries.18 Turmeric roots typically contain over 3% curcumin, 1.4% DMC, and 1.2% BDMC19. Curcumin has shown protective effects in conditions such as osteopenia20 and osteoarthritis21, and is traditionally used for various inflammatory, infectious, hepatic, and digestive disorders10,22.
Plant Profile:
Common Names:
Saffron Indian; haldi (Hindi); Curcuma; Rhizoma cur-cumae.
Table No. 1 - Synonyms:
|
Sanskrit |
Ameshta |
|
English |
Indian saffron |
|
Hindi |
Haldi |
|
Telugu |
Haridra |
|
Tamil |
Ameshta |
Biological source:
Turmeric is the dried rhizome (underground stem) of the plant Curcuma longa linn., also known as Curcuma domestica Valeton belonging to the natural order Zingiberaceae.
Family: Zingiberaceae
Geographical Sources:
It is commonly found in Cambodia, China, India, Nepal, Indonesia, Madagascar, Malaysia, Philippines and Vietnam. Indian scenario: It is commonly found in West Bengal, Tamil Nadu, and Maharashtra and also in Madras.23
Table No. 2 - Taxonomy Scientific Name: Curcuma longa
|
Kingdom |
Plantae |
|
Sub-kingdom |
Tracheobionta [Vascular plants] |
|
Super division |
Spermatophyta |
|
Division |
Magnoliophyta [Flowering plants] |
|
Class |
Lilliopsida [monocotyledons] |
|
Subclass |
Zingiberidae |
|
Order |
Zingiberales |
|
Genus |
Curcuma L. curcuma |
|
Species |
Curcuma longa L |
Natural Habitate:
Curcumin is used analytically to determine boron by forming the red complex rosocyanine with boric acid and serves as a natural food colorant due to its intense yellow pigmentation.24
Chemical Constituents:
Turmeric contains bioactive polyphenolic curcuminoids, including curcumin (diferuloylmethane), demethoxycurcumin (DMC), bisdemethoxycurcumin (BDMC), and cyclocurcumin25. Curcumin (3–4%) imparts the yellow color, consisting mainly of curcumin I (94%), curcumin II (6%), and curcumin III (0.3%), with overall curcuminoids making up 2–5% of the rhizome26,27. Curcumin is the most extensively studied compound28. Turmeric also contains sesquiterpenes such as turmerone, atlantone, zingiberone, turmeronol, germacrone, and bisabolene, along with carbohydrates, proteins, resins, and caffeic acid29. Chemically, curcumin (C21H20O6, 368.385 g/mol) has two oxy-substituted aryl groups linked by a seven-carbon α, β-unsaturated β-diketone chain30 and is hydrophobic (log P 3.43), poorly soluble in water, and accumulates in hydrophobic regions such as cell membranes31,32. It acts as a reducing agent and antioxidant, scavenging reactive oxygen species (ROS) and supporting antioxidant systems more effectively than vitamin E.33 The α,β-unsaturated β-diketone moiety serves as both the hydrogen-donor and hydrolysis site, leading to rapid degradation in aqueous or alkaline conditions,34 although binding to polymers, cyclodextrins, lipids, or proteins improves solubility and stability. After oral intake, curcumin is metabolized into sulfate and glucuronide derivatives35, and its stability and bioavailability can be enhanced via encapsulation, chemical modification of reactive sites, or curcumin analogues, which require further clinical evaluation.36,37 and modifying the β-diketone to reduce the activity of the enolate Michael acceptor.38 Additionally, curcumin analogues further clinical studies are necessary to assess and confirm their potential benefits.
Fig No. 1 – Chemical Constituents of Turmeric.39
Pharmacological Properties:
1. Anti-Viral Activity:
Curcumin exhibits broad antiviral activity against viruses including HPV, influenza, HBV, HCV, adenovirus, coxsackievirus, human norovirus, RSV, and HSV-140–44. Curcumin-functionalized graphene oxide shows strong inhibition of RSV by inactivating the virus and blocking its attachment, providing preventive and therapeutic effects in a dose-dependent manner45. It also inhibits IMPDH, reducing guanine nucleotide levels needed for RNA and DNA synthesis, and interferes with viral entry and multiple stages of the viral life cycle. Curcumin demonstrates antiproliferative, antiviral, and antiparasitic activities.46
2. Anti-Inflammatory Activity:
Curcumin exhibits strong anti-inflammatory effects in acute and chronic models, comparable to phenylbutazone in acute tests but less effective in chronic ones.47,48 It has been shown to be safe in six human trials and may exert its effects by modulating transcription factors, cytokines, protein kinases, adhesion molecules, redox status, and inflammation-related enzymes49.
3. Depression and Anxiety:
In clinical trials, curcumin improved depression symptoms as measured by scales such as BAI, BDI, HAM-D17, HADS, BDI-II, and IDS-SR30. One trial showed reduced anxiety but no effect on depression, likely due to a shorter 30-day treatment. In some studies, curcumin also modulated biomarkers, lowering IL-1β and TNFα, increasing plasma BDNF, reducing salivary cortisol, and affecting urinary thromboxane B2, substance P, endothelin-1, and leptin, which may contribute to its antidepressant effects50.
4. Anti-Cancer:
Cancer arises from genetic and epigenetic changes, leading to cell death, uncontrolled growth, metastasis, and angiogenesis51,52. Curcumin has been studied for its anti-cancer effects, showing benefits in gastrointestinal, melanoma, genitourinary53,54, breast, and lung cancers 55,56. Research indicates that curcumin exerts anti-cancer activity both alone and in combination with conventional chemotherapy, improving treatment outcomes and managing related complications57–60.
5. Anti-Bacterial:
Curcumin exhibits antibacterial activity against various periodontopathic bacteria by inhibiting growth and reducing the activities of Porphyromonas gingivalis Arg- and Lys-specific proteinases (RGP and KGP). It also suppresses biofilm formation of P. gingivalis and Streptococcus gordonii in a dose-dependent manner, with 20µg/mL inhibiting P. gingivalis biofilms by over 80%. However, 100µg/mL does not affect Aggregatibacter actinomycetemcomitans. At higher concentrations, curcumin disrupts bacterial membranes, as observed in Escherichia coli.61,62
6. Anti-Fungal:
The study of adding curcumin powder to plant tissue culture showed that curcumin at 0.8 and 1.0g/L had significant inhibitory effects on fungal contamination.63 Reduced proteinase secretion and changes in membrane-related ATPase activity might also play important roles in the antifungal effects of curcumin.64 Discovering new anti-candida substances is essential because of the development of resistant strains against current antifungal drugs.65
7. Anti-Arthritis:
Rheumatoid arthritis (RA) is a chronic inflammatory disease that features an increase in the number of synovial fibroblasts. Curcumin has strong anti-inflammatory and anti-arthritic effects.66 It is thought that curcumin's antioxidant, antiproliferative, anti-inflammatory, and immunosuppressive properties help improve symptoms for patients with rheumatoid arthritis.67
8. Wound- Healing Activity:
It effectively fights wound infection and helps repair burn injuries in rats. The growth factors play a role in the wound healing process stimulated by curcumin.68 The ways curcumin aids in wound healing include:
1. Immunohistochemical localization of transforming growth factor-β1 showed an increase in wounds treated with curcumin compared to untreated wounds.
2. It helps modulate collagen and reduce reactive oxygen species.69
Extraction:
Purification of Curcumin, extracted from turmeric, has uses in different industries. There are two methods for extracting curcumin: conventional and modern. The conventional method involves using solvents, including Soxhlet extraction, maceration, and hydro-distillation. Soxhlet extraction was first developed in 1879 for lipid isolation, is widely used to extract bioactive compounds from plants due to its high efficiency70. For curcumin, common solvents include water, ethanol, and methanol. Ethanolic extraction yielded 88.96mg/g71, while acetone extraction produced 6.9% curcumin72. Maceration extraction is the method of extracting compounds through continuous stirring. Acetonic extraction results in about 50% of curcumin (Nurhadi et al., 2020).73
CONCLUSION:
Turmeric has long been valued in traditional Indian medicine, and its principal compound, curcumin, continues to attract scientific interest due to its interaction with multiple cellular targets. Although curcuminoids show notable pharmacological and chemopreventive activity in experimental studies, additional well-controlled clinical trials are needed to establish their therapeutic potential. Research is also focused on improving curcumin’s low bioavailability, with encapsulation methods offering promising solutions. Advances in extraction technology—such as microwave- and ultrasound-assisted techniques—provide faster, more efficient alternatives to traditional Soxhlet extraction. Future work will emphasize enhancing bioavailability and further refining these extraction approaches.
REFERENCES:
1. Panpatil VV, Tattari S, Kota N, Nimgulkar C and Polasa K. In-vitro evaluation on antioxidant and antimicrobial activity of spice extracts of ginger, turmeric and garlic. Journal of Pharmacognosy and Phytochemistry. 2013; 2(3): 143-148.
2. Pawar H, Karde M, Mundle N, Jadhav P and Mehra K. Phytochemical evaluation and curcumin content determination of turmeric rhizomes collected from Bhandara District of Maharashtra (India). Med. Chem. 2014; 4(8): 588-591.
3. Aggarwal BB, Kumar A and Bharti AC: Anticancer potential of curcumin. preclinical and clinical studies. Anticancer Research. 2003; 23(1/A): 363-398.
4. Majeed M, Murray F, Badmaev V. Turmeric and the Healing Curcuminoids, McGraw-Hill Education; 1999. p.122-127.
5. Bhutya R,. Ayurvedic medicinal plants of india, Vol. 1, Scientific Publishers, 2011.p.25-27
6. Salehi B, Zucca P, Sharifi-Rad M, Pezzani R. Phytotherapeutics in cancer invasion and metastasis. Phytotherapy Research. 2018; 32(8): 1425-1449.
7. Kharat M, Du Z, Zhang G and McClements DJ. Physical and chemical stability of curcumin in aqueous solutions and emulsions: Impact of pH, temperature and molecular environment. Journal of Agricultural and Food Chemistry. 2017; 65(8): 1525-1532.
8. Hewlings SJ and Kalman DS. Curcumin: a review of its effects on human health. Foods. 2017; 6(10): 92.
9. Panahi Y, Hosseini MS, Khalili N, Naimi E, Majeed M and Sahebkar A. Antioxidant and anti-inflammatory effects of Curcumin oid piperine combination in subjects with metabolic syndrome: a randomized controlled trial and an updated meta analysis. Clinical Nutrition. 2015; 34(6): 1101-1108.
10. Prasad S, Aggarwal B. Turmeric, The Golden Spice: From Traditional Medicine to Modern Medicine. 2011;. p. 13.
11. Rheim FA, Ragab AA, Hamdy HED and Hammam FM: Evaluation of DNA damage in-vivo by comet assay and chromosomal aberrations for pyrethroid insecticide and the antimutagenic: Role of curcumin. The Egyptian Journal of Hospital Medicine. 2015; 59: 172-181.
12. 1Gómez-Estaca J, Balaguer MP, López Carballo G, Gavara R and Hernández Muñoz P. Improving antioxidant and antimicrobial properties of curcumin by means of encapsulation in gelatin through electrohydrodynamic atomization. Food Hydrocolloids. 2017; 70: 313-320.
13. Noorafshan A and Ashkani-Esfahani S. A review of therapeutic effects of curcumin. Current Pharmaceutical Design. 2013; 19(11): 2032-2046.
14. Prasad S, Tyagi AK and Aggarwal BB. Recent developments in delivery, bioavailability, absorption and metabolism of curcumin: the golden pigment from golden spice. Cancer research and treatment. Official Journal of Korean Cancer Association. 2014; 46(1): 2.
15. Gupta SC, Patchva S and Aggarwal BB. Therapeutic roles of curcumin: lessons learned from clinical trials. AAPS Journal. 2013; 15(1): 195-218.
16. Hu S, Maiti P, Ma Q, Zuo X, Jones MR, Cole GM and Frautschy SA. Clinical development of curcumin in neurodegenerative disease. Expert Review of Neuro Therapeutics. 2015; 15(6): 629 637.
17. Rungseesantivanon S, Thenchaisri N, Ruangvejvorachai P and Patumraj S. Curcumin supplementation could improve diabetes-induced endothelial dysfunction associated with decreased vascular superoxide production and PKC inhibition. BMC Complementary and Alternative Medicine. 2010; 10: 57-57
18. Kocaadam, B., Şanlier, N. Curcumin, An active component of turmeric (Curcuma longa), and its effects on health. Crit. Rev. Food Sci. Nutr. 2017; 57, 2889–2895.
19. Li S, Chemical Composition and Product Quality Control of Turmeric (Curcuma longa L.). Pharmaceutical Crops. 2011; 5: 28-54.
20. Riva A, Franceschi F, Togni S, Eggenhoffner R, Giacomelli L, Health Benefits of Curcumin and Curcumin Phytosome in Bone Density Disorders. JSM Bone Marrow Res. 2017; 1: 77-79.
21. Henrotin Y, Priem F, Mobasheri A. Curcumin: a new paradigm and therapeutic opportunity for the treatment of osteoarthritis: curcumin for osteoarthritis management. SpringerPlus. 2013; 2(56): 13 17.
22. Staff T P, PDR for Herbal Medicines, Thomson PDR, 2004. p. 234.
23. Jaggi Lal. Turmeric, Curcumin and Our Life: A Review. Bulletin of Environment, Pharmacology and Life Sciences. 2012;(17):11-17.
24. Roshan Prasad Yadav and Gaur Tarun. Versatility of turmeric: A review the golden spice of life. Journal of Pharmacognosy and Phytochemistry. 2017;6(1):41-46.
25. Pfeiffer E, Hhle S, Solyom AS and Metzler M. Studies on the stability of turmeric constituents. J Food Enginee. 2003; 56:257-259.
26. 26.Sunghwan Kim, Paul A. Thiessen. Pubchem Open Chemistry Data Base. Nucleic Acids Res. 2016; 4: 44.
27. Priyadarsini, K.I. The chemistry of curcumin: from extraction to therapeutic agent. Molecules 2014; 19: 20091-20112.
28. Fanti F, Conti S, Campani L, Morace G, Dettori G, Polonelli L. Studies on the epidemiology of Aspergillus fumigatus infections in a university hospital. European journal of epidemiology. 1989; 5, 8-14.
29. Nelson KM, Dahli JL, Bisson, J, Graham J, Pauli GF, Walters, MA. The Essential Medicinal Chemistry of Curcumin. Journal of medicinal chemistry. 2017; 60: 1620 1637
30. Kumar D, Basu S, Parija L, Rout D, Manna S, Debata, PR. Curcumin and Ellagic acid synergistically induce ROS generation, International Journal of Research and Review (ijrrjournal.com) Vol.7; Issue: 1; January 2020 284 Surbhi Rathore et.al. Curcumin: A Review for Health Benefits International Journal of Research and Review (ijrrjournal.com) 285 Vol.7; Issue: 1; January 2020 DNA damage. Biomedicine & pharmacotherapy. 2016; 81: 31-37.
31. Sharma OP. Antioxidant activity of curcumin and related compounds. Biochemical pharmacology. 1976; 25: 1811-1812.
32. Goel A, Kunnumakkara AB, Aggarwal BB. Curcumin as "Curecumin": from kitchen to clinic. Biochemical pharmacology. 2008; 75: 787-809.
33. Jurenka, JS. Anti-inflammatory properties of curcumin, a major constituent of Curcuma longa: a review of preclinical and clinical research Alternative medicine review. a journal of clinical therapeutic. 2009; 14: 141-153.
34. Shishodia S, Sethi G, Aggarwal BB. Curcumin: getting back to the roots. Annals of the New York Academy of Sciences. 2005; 10(56): 206-217.
35. Priyadarsini, KI. Photophysics, photochemistry and photobiology of curcumin: Studies from organic solutions, bio-mimetics and living cells. J Photoch Photobioc. 2009; 10: 81-95.
36. Griesser M, Pistis V, Suzuki T, Tejera N, Pratt DA, Schneider C. Autoxidative and cyclooxygenase-2 catalyzed transformation of the dietary chemopreventive agent curcumin. The Journal of biological chemistry. 2011; 286: 1114-1124
37. Tamvakopoulos, C, Dimas K, Sofianos ZD. Metabolism and anticancer activity of the curcumin analogue, dimethoxycurcumin. Clinical cancer research: an official journal of the American Association for Cancer Research. 2007; 13: 1269-1277.
38. Robinson TP, Hubbard RB. Synthesis and biological evaluation of aromatic enones related to curcumin. Bioorganic & medicinalchemistry. 2005; 13: 4007-4013.
39. Sueth-Santiago V, Moraes JdBB, Sobral Alves ES, Vannier-Santos MA, Freire-de-Lima CG, Castro RN, et al. (2016) The Effectiveness of Natural Diarylheptanoids against Trypanosoma cruzi: Cytotoxicity, Ultrastructural Alterations and Molecular Modeling Studies. PLoS ONE 11(9): e0162926 ; Khanna, M.M. (1999). Turmeric - Nature's precious gift. Current Sci. 76(10): 1351-1356.
40. Gupta AP, Khan S, Manzoor MM, Yadav AK, Sharma G, Anand R and Gupta S: Anticancer curcumin: Natural analogues and structure-activity relationship. In Studies in Natural Products Chemistry, Elsevier. 2017; 54: 355-401.
41. Dulbecco P and Savarino V: Therapeutic potential of curcumin in digestive diseases. World Journal of Gastroenterology. 2013; 19(48): 9256.
42. Maheshwari RK, Singh AK, Gaddipati J and Srimal RC: Multiple biological activities of curcumin: a short review. Life Sciences. 2006; 78(18): 2081-2087.
43. Koohpar ZK, Entezari M, Movafagh A and Hashemi M. Anticancer activity of Curcumin on human breast adenocarcinoma: role of Mcl-1 gene. Iranian Journal of Cancer Prevention. 2015; 8(3): 2231.
44. SayerA. Yeast Is A Cause of Cancer And Turmeric Can Kill Both. Research Confirms. Research. 2015; 4(2): 339.
45. Zhang Q, Li D, Liu Y, Wang H,et al. Potential anticancer activity of curcumin analogs containing sulfone on human cancer cells. Archives of Biological Sciences. 2016; 68(1): 125-133. Surbhi Rathore et.al. Curcumin: A Review for Health Benefits
46. Siegel R, Ma J, Zou Z and Jemal A. Cancer statistics. A Cancer Journal For Clinicians. 2014; 64(1): 929.
47. Hilles AR and Mahmood S. A review on phytochemistry and pharmacological effects of Trigonella foenumgraecum. Advanced Herbal Medicine. 2016; 2(3): 61-67.
48. Naik SR, Thakare VN and Patil SR. Protective effect experimentally of induced curcumin on inflammation, hepatotoxicity and cardiotoxicity in rats: evidence of its antioxidant property. Experimental and Toxicologic Pathology. 2011; 63(5): 419-431.
49. Kim J, Lee HJ and Lee KW. Naturally occurring phytochemicals for the prevention of Alzheimer’s disease. Journal of Neurochemistry. 2010; 112(6): 1415-1430.
50. Panahi Y, Hosseini MS, Khalili N, Naimi E, Majeed M, Sahebkar A. Antioxidant and anti-inflammatory effects of curcuminoid-piperine combination in subjects with metabolic syndrome: a randomized controlled trial and an updated meta-analysis. Clinical nutrition. 2015; 34: 1101-1108.
51. Hanahan D, Weinberg RA. Hallmarks of cancer the next generation. Cell. 2011; 144(5): 646 -674.
52. Nakano K, VousdenKH, PUMA. A Novel proapoptotic gene, is induced. Molecular cell. 2001; 7(3): 683-694.
53. Duvoix A ,Blasius R, Delhalle S, Schnekenburger M, et al. Chemopreventive and therapeutic effects of curcumin. Cancer letters. 2003; 223(2): 181-190.
54. Anand P, Sundaram C, Jhurani S, Kunnumakkara AB, Aggarwal BB. Curcumin and Cancer: an “old-age” disease with an “age-old” solution. Cancer letters, 2008; 267(1): 133-164.
55. Bar-Sela G, Epelbaum R, Schaffer M. Curcumin as an anti-cancer agent: review of the gap between basic and clinical applications. Current medicinal chemistry. 2010; 17(3): 190-197.
56. Ravindran J, Prasad S, Aggarwal BB. Curcumin and cancer cells: how many ways can Curry kill tumor cells selectively. The AAPS journal. 2009; 11(3): 495-510
57. Bayomi SM, El-Kashef HA, El-Ashmawy MB, Nasr MN, El-Sherbeny MA, Abdel Aziz NI, et al. Synthesis and biological evaluation of new curcumin analogues as antioxidant and antitumor agents: Molecular modeling study. European Journal of Medicinal Chemistry. 2015; 101: 584-594.
58. Wilken R, Veena MS, Wang MB and Srivatsan ES. Curcumin: A review of anti cancer properties and therapeutic activity in head and neck squamous cell carcinoma. Molecular Cancer 2011; 10(1): 12-17.
59. Fiala M. Curcumin and omega-3 fatty acids enhance NK cell-induced apoptosis of pancreatic cancer cells but Curcumin inhibits interferon-γ production: benefits of omega-3 with Curcumin against cancer. Molecules. 2015; 20(2): 3020-3026.
60. Attari F, Zahmatkesh M, Aligholi H, Mehr SE, Sharifzadeh M, Gorji A, Mokhtari T, Khaksarian M and Hassanzadeh G: Curcumin as a double-edged sword for stem cells: dose, time and cell type-specific responses to Curcumin. DARU Journal of Pharmaceutical Sciences. 2015; 23(1): 33.
61. 61.Tsekova PB, Spasova MG, Manolova NE, Markova ND and Rashkov IB. Electrospun Curcumin -loaded cellulose acetate/polyvinylpyrrolidone fibrous materials with complex architecture and antibacterial activity. Materials Science and Engineering. 2017; 73: 206-214.
62. No DS, Algburi A, Huynh P, Moret A, Ringard M, Comito N, Drider D, Takhistov P and Chikindas ML. Antimicrobial efficacy of curcumin nanoparticles against Listeria monocytogenes is mediated by surface charge. Journal of Food Safety. 2017; 3(7) 21-27.
63. Yang XX, Li CM, Li YF, Wang J and Huang CZ. Synergistic antiviral effect of curcumin functionalized graphene oxide against respiratory syncytial virus infection. Nanoscale. 2017; 9(41): 16086-16092. 66. Buckley D, Fraser A, Huang G and Jiang X. Recovery Optimization and Survival of the Human Norovirus Surrogates Feline Calicivirus and Murine Norovirus on Carpet. Applied and Environmental Microbiology. 2017; 83(22): e01336-17.
64. Buckley D, Fraser A, Huang G and Jiang X. Recovery Optimization and Survival of the Human Norovirus Surrogates Feline Calicivirus and Murine Norovirus on Carpet. Applied and Environmental Microbiology. 2017; 83(22): e01336-17.
65. Kunnumakkara AB, Bordoloi D, Padmavathi G, Monisha J, Roy NK, Prasad S and Aggarwal BB. Curcumin the golden nutraceutical: multitargeting for multiple chronic diseases. British Journal of Pharmacology. 2017; 174(11): 1325-1348.
66. Kim J, Lee HJ and Lee KW. Naturally occurring phytochemicals for the prevention of alzheimer’s disease. Journal of Neurochemistry. 2010; 112(6): 1415-1430.
67. Ghosh N, Ghosh R and Mandal SC. Antioxidant protection a promising therapeutic intervention in neurodegenerative disease. Free Radical Research. 2011; 45(8): 888-905.
68. 68.Hussain Z, Thu HE, Ng SF, et al. Nanoencapsulation an Efficient and promising approach to maximize wound healing efficacy of curcumin:A review of new trends and state-of-the-art. Colloids and Surfae B. Biointerfaces. 2017; 150: 223 241.
69. Jackson JK, Higo T, Hunter WL and Burt HM. The antioxidants Curcumin and quercetin inhibit inflammatory processes associated with arthritis. Inflammation Research. 2006; 55(4): 168-175.
70. Dutta B. Study of secondary metabolite constituents and curcumin contents of six different species of genus Curcuma. Journal of Medicinal Plants Studies. 2015;3(5):116-119.
71. Patil SS, Bhasarkar S, Rathod VK. Extraction of curcuminoids from Curcuma longa: Comparative study between batch extraction and novel three phase partitioning. Preparative Biotechnology. Biochemistry and 2019;49(4):407-418.
72. Sahne F, Mohammadi M, Najafpour GD, Moghadamnia AA. Extraction of bioactive compound curcumin from turmeric (Curcuma longa l.) Via different routes: a comparative study. Pak. J. Biotechnol. 2016;13(3):173 180.
73. Nurhadi B, Saputra RA, Setiawati TA, Husein SN, Faressi FR, Utari CD, et al. Comparison of Curcuma domestica and Curcuma xanthorrhiza oleoresins extracted using maceration, Soxhlet, and ultrasound assisted extraction (UAE). IOP Conference Series: Earth and Environmental Science. 2020; 443(1): 012074.
|
Received on 13.03.2026 Revised on 23.04.2026 Accepted on 25.05.2026 Published on 04.07.2026 Available online from July 18, 2026 Asian J. Pharm. Tech. 2026; 16(3):266-270. DOI: 10.52711/2231-5713.2026.00038 ©Asian Pharma Press All Right Reserved
|
|
|
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. Creative Commons License. |
|