Graphical abstract
Keywords: Annatto, Bixin, Antibacterial activity, Anticancer activity, Textile dyeing
Abstract
Bixa orellana commonly known as annatto is one of the oldest known natural dye yielding plants native to Central and South America. Various parts of annatto have been widely used in the traditional medical system for prevention and treatment of a wide number of health disorders. The plethora of traditional uses has encouraged researchers to identify and isolate phytochemicals from all parts of this plant. Carotenoids, apocarotenoids, terpenes, terpenoids, sterols, and aliphatic compounds are main compounds found in all parts of this plant and are reported to exhibit a wide range of pharmacological activities. In recent years annatto has received tremendous scientific interest mainly due to the isolation of yellow–orange natural dye from its seeds which exhibits high biodegradability, low toxicity, and compatibility with the environment. Considerable research work has already been done and is currently underway for its applications in food, textile, leather, cosmetic, solar cells, and other industries. The present review provides up-to-date systematic and organized information on the traditional usage, phytochemistry and pharmacology of annatto. It also highlights its non-food industrial applications in order to bring more interest on this dye plant, identifies the existing gaps and provides potential for future studies. Studies reported in this review have demonstrated that annatto holds a great potential for being exploited as source of drugs and a potential natural dye. However, further efforts are required to identify extract biomolecules and their action mechanisms in exhibiting certain biological activities in order to understand the full phytochemical profile and the complex pharmacological effects of this plant.
Introduction
Bixa orellana L. commonly known as annatto belongs to the family Bixaceae. It is 3–6 m high bush native to Central and South America and is one of the oldest known natural dye yielding plants, Fig. 1. It was named after the Spanish conquistador Francisco de Orellana and has been used earlier for body painting, treatment for heartburn and stomach distress, sunscreen, and repelling insects, and to ward off evil [1]. Annatto has been used for centuries in many parts of the world for the prevention and treatment of a number of heath disorders such as constipation, fevers, heartburn, asthma, scabies, ulcers, diarrhea, stomach upset, skin diseases, measles, anecdotal treatment of diabetes, allergy, leprosy, infectious diseases, burns, measles, gonorrhea, diarrhea, asthma, angina, tumors, skin problems, and urinary infections (oral and topic) [2], [3]. The pulp from seeds of this plant has long been used topically by indigenous people to enhance the beauty of lips which has led to the origin of B. orellana’s nick name as lipstick tree [4]. Annatto has enormous number of applications in coloring and bleaching of dairy food products especially bakery products, cream deserts, butter milk deserts, rice flour, and corn starch [5], [6], [7]. Extensive research studies carried out in the last few decades have shown isolation of several different classes of phytoconstituents including carotenoids, apocarotenoids, sterols, aliphatic compounds, monoterpenes and sesquiterpenes, triterpenoids, volatile oils and other miscellaneous compounds from all parts of this plant [8], [9], [10]. These phytochemicals exhibit a wide range of pharmacological activities that include antibacterial, antifungal, antioxidant, anti-inflammatory, anticancer, enhanced gastrointestinal motility, neuropharmacological, anticonvulsant, analgesic, and antidiarrheal activities [11], [12], [13], [14], [15].
Fig. 1.
(a) Plant (b) leaves and flower, and (c) seeds and dye.
Modern investigations on this plant have revealed the presence of natural reddish-yellow dye in seeds of B. orellana. The fruit of the B. orellana tree consists of 10–50 seeds of the size of grape seeds covered with a thin layer of soft, slightly sticky vermilion pulp [16]. Seeds are characterized by substantial amount of carotenoid compounds mainly apocarotenoid bixin, nor-bixin and other less important cryptoxanthin, lutein, zeaxanthin, and methylbixin [17], [18], [19]. Numerous pieces of research have been conducted on B. orellana plant over the last few years; however, there is a paucity of comprehensive review articles on this potential natural dye plant [4], [6], [14]. Keeping in view the tremendous interest in this dye containing plant, we herein summarize up-to-date information on the phytochemistry, and biological activities of annatto. Finally this review also highlights its important industrial applications with critical analysis of the existing gaps and potential for future studies.
Method
An extensive and systematic review of the existing literature was collected from scientific journals, books, reports and worldwide accepted databases (Scopus, ScienceDirect, Scifinder, Medline, Springer, and Google Scholar) using different search key words such as annatto, B. orellana, phytochemistry, pharmacology, antibacterial activity and dye.
Phytochemistry
Phytochemical screening of Bixa orellana carried out so far has led to the isolation and identification of a number of structurally diverse chemical compounds. There are many chemical constituents including carotenoids, apocarotenoids, sterols, aliphatic compounds, monoterpenes and sesquiterpenes, triterpenoids, and other miscellaneous compounds that have been identified and isolated mostly from seeds, seed coats and leaves of this plant. In this part of the review, we describe the major chemical constituents, their structures and their isolation from different parts of this plant, Table 1.
Table 1.
Chemical constituents of Bixa orellana.
S. no. | Classification | Components | Plant part | References |
---|---|---|---|---|
Carotenoids | ||||
(1) | Methylhydrogen-(9′Z)-6,6′-diapocarotene-6, 6′-dioate (Bixin) | Seed coat | [22] | |
(2) | Lutein | Seeds | [19] | |
(3) | Zeaxanthin | Seeds | [19] | |
(4) | Dimethyl-(9Z,9′Z)-6,6′-diapocarotene-6,6′-dioate | Seed coat | [22], [24] | |
(5) | NorBixin | Seeds | [86] | |
(6) | Methyl (9′Z)-apo-6′-lycopenoate | Seed coat | [23] | |
(7) | Methyl-(7Z,9Z,9′Z)-apo-6′-lycopenoate | Seed coat | [23], [24] | |
(8) | Methyl-(9Z)-apo-8′-lycopenoate | Seed coat | [23] | |
(9) | Methyl-(all-E)-apo-8′-lycopenoate | Seed coat | [23] | |
(10) | Methyl-(all-E)-apo-6′-lycopenoate | Seed coat | [17] | |
(11) | Methyl (9Z)-10′-oxo-6,10′-diapocaroten-6-oate | Seeds | [24] | |
(12) | Methyl (9Z)-6′-oxo-6,5′-diapocaroten-6-oate | Seeds | [24] | |
(13) | Methyl (9Z)-6′-oxo-6,6′-dioapocarotene-6-oate | Seeds | [24] | |
(14) | Methyl-(4Z)-4,8-dimethyl-12-oxododecyl-2,4,6,8,10-pentaenoate | Seeds | [24] | |
(15) | 6-Geranylgeranyl-8′-methyl-6, 8′-diapocaroten-6, 8′-dioate | Seeds | [8] | |
(16) | 6-Geranylgeranyl-6′-methyl (9′Z)-6, 6′-diapocaroten-6,6′-dioate | Seeds | [8] | |
(17) | 6-Geranylgeranyl-6′-methyl-6,6′-diapocaroten-6, 6′-dioate | Seeds | [8] | |
(18) | Trans-bixin | Seeds | [103] | |
Terpenoids | ||||
(19) | Farnesylacetone | Seeds | [22] | |
(20) | Geranylgeranyl octadecanoate | Seeds | [22] | |
(21) | Geranylgeranyl formate | Seeds | [22] | |
(22) | δ-Tocotrienol | Seeds | [25] | |
(23) | β-Tocotrienol | Seeds | [25] | |
Terpenes | ||||
(24) | β-Humulene | Roots | [26] | |
(25) | α-Carpophyllene | Leaves and roots | [12], [26] | |
(26) | α-Copaene | Leaves and roots | [12], [26] | |
(27) | α-Elemene | Leaves | [12] | |
(28) | Cis-ocimene | Leaves | [12] | |
(29) | Tomentosic acid | Roots | [104] | |
Volatile compounds | ||||
(30) | (Z,E)- farnesyl acetate (11.6%) | Seed oil | [27] | |
(31) | Occidentalol acetate (9.7%) | Seed oil | [27] | |
(32) | Spathulenol (9.6%) | Roots, seed oil | [26], [27] | |
(33) | Ishwarane (9.1%) | Seed oil | [27], [105] | |
Other compounds | ||||
(34) | Acetic acid | Roots | [10] | |
(35) | 2-Butanamine | Roots | [10] | |
(36) | Pentanoic acid | Roots | [10] | |
(37) | Phenol | Roots | [10] | |
(38) | Pantolactone | Roots | [10] | |
(39) | Benzoic acid | Roots | [10] | |
(40) | Phytol | Leaves | [37] | |
(41) | Stigmasterol | Leaves | [37] | |
(42) | Sitosterol | Leaves | [37] | |
(43) | Leucocyanidin | Leaves | [28] | |
(44) | Ellagic acid | Leaves | [28] | |
(45) | Luteolin | Leaves | [28] | |
(46) | Apigenin | Leaves | [28] |
Carotenoids
The main compounds found in B. orellana plant are carotenoids and apocarotenoids. Several phytochemical studies have been performed on isolation and identification of carotenoids and apocarotenoids of various extracts. Most of the carotenoids have been isolated from seed and seed coats. Bixin (1) [methylhydrogen-(9′Z)-6,6′-diapocarotene-6,6′-dioate] is the major carotenoid compound present in B. orellana seed coat and accounts for 80% in addition to the presence of other carotenoids in trace amounts [20], [21]. Tirimanna identified and isolated β-carotene, cryptoxanthin, lutein (2), zeaxanthin (3), and methyl bixin (4) in addition to bixin and nor-bixin (5) from seeds by thin layer chromatography [19]. Chemical investigation of methanol seed extract has resulted in the identification of the apocarotenoids methyl bixin (dimethylhydrogen-(9′Z)-6,6′-diapocarotene-6,6′-dioate) (4) [22]. In a series of phytochemical investigations Mercadante et al. reported a number of apocarotenoids from B. orellana seed coat. In 1996, they successfully isolated methyl-9′Z-apo-6′-lycopenoate (6) from the seed coats [23].
Methyl-(7Z,9Z,9′Z)-apo-6′-lycopenoate (7), methyl-(9Z)-apo-8′-lycopenoate (8), methyl-(all-E)-apo-8′-lycopenoate (9), and methyl-(all-E)-apo-6′-lycopenoate (10) were also isolated from seed coat of B. orellana [17]. In 1997, six minor diapocarotenoids and one C14-carotenoid derivative were isolated from the seed coat and were named dimethyl-(9Z,9′Z)-6,6′-diapocarotene-6,6′-dioate (4), methyl-(9Z)-10′-oxo-6,10′-diapocaroene-6-oate (11), methyl-(9Z)-6′-oxo-6,5′-diapocaroene-6-oate (12), methyl-(9Z)-6′-oxo-6,6′-diapocaroene-6-oate (13), and methyl-(4Z)-4,8-dimethyl-12-oxododecyl-2,4,6,8,10-pentaenoate (14) [24]. In another study conducted two years later, 6-geranylgeranyl-8′-methyl-6,8′-diapocaroten-6,8′-dioate (15), 6-geranylgeranyl-6′-methyl(9′Z)-6,6′-diapocaroten-6,6′-dioate (16) and 6-geranylgeranyl-6′-methyl-6,6′-diapocaroten-6,6′-dioate (17) were also successfully obtained from seeds of B. orellana [8]. The chemical structures of isolated carotenoids are shown in Fig. 2.
Fig. 2.
Chemical structures of carotenoids.
Terpenoids and terpenes
Terpenoids mainly C20-terpene alcohol all-geranylgeraniol as a major chemical component in Bixa orellena were isolated by Jondiko and Pattenden. Other terpenes that were isolated and characterized for the first time include farnesylacetone (19), geranylgeranyl octadecanoate (20), geranylgeranyl formate (21), δ-tocotrienol (22) and β-tocotrienol (23) [22]. Frega et al. reported the presence of tocotrienols mainly δ-tocotrienol from lipid fraction of annatto seeds using thin-layer chromatography. Sesquiterpenes are also a major group of volatile compounds found in annatto extracts [25]. In one of the recent studies on annatto β-humulene (24) was the major compound present in annatto extract along with its isomer caryophyllene (25) which was present in smaller quantities. Several other sesquiterpenes found usually in water-soluble as well as in oil-soluble extracts include α-copaene (26), and α-elemene (27) [26]. Fig. 3, Fig. 4 depict the chemical structures for all the isolated terpenes and terpenoids.
Fig. 3.
Chemical structures of terpenoids.
Fig. 4.
Chemical structures of terpenes.
Volatile compounds (essential oils)
Table 1 presents a list of volatile compounds isolated from different parts of B. orellana. Up to now very few studies have been performed on the extraction and identification of volatile compounds from Bixa orellana. One hundred and seven compounds from oil and water soluble annatto extracts were detected by GC/MS in one of the recent studies carried by Galindo-Cuspinera et al. using dynamic headspace-solvent desorption technique. The main volatile compounds identified were pentanol and hexanol, 3-hexenol, nonanal, hexanal, and 2-heptenal, dimethylcyclohexane, dimethylhexane and 2-methylheptane, 3-penten-2-one, 3-octanone, 4-methyl-3-penten-2-one, 4-hydroxy-4-methyl-2-pentanone, 6-methyl-5-hepten-2-one, acetic acid, ethyl butyrate, 1,2-propanediol-2-acetate, 3-methylpyridine, p-xylene and toluene, δ-elemene, α-pinene, limonene, β-myrcene, eucalyptol, β-phellandrene, and terpinen-4-ol [26]. Pino and Correa detected thirty-five compounds from seed oil of this plant using GC/MS technique. The major components characterized from seed oil were (Z,E)-farnesyl acetate (30) (11.6%), occidentalol acetate (31) (9.7%), spathulenol (32) (9.6%) and ishwarane (33) (9.1%) [27]. Chemical structures are shown in Fig. 5, Fig. 6.
Fig. 5.
Chemical structures of volatile compounds.
Fig. 6.
Chemical structures of other compounds.
Other miscellaneous compounds
Table 1 lists some other miscellaneous compounds and their chemical structures are given in Fig. 6. GC/MS analysis showed the presence of six major components 2-butanamine (35), acetic acid, pentanoic acid (36), phenol (37), pantolactone (38) and benzoic (39) [10]. Three new flavone bisulfates have been found in the leaves of Bixa orellana. They have been identified as 7-bisulfates of epigenin and luteolin and 8-bisulfate of hypolaetin, confirmed by synthesis [28].
Pharmacodynamics and potential applications
Many pharmacological investigations have been initiated by researchers all over the globe over the past few decades due to varied ethnomedical uses of B. orellana. A wide range of biological activities has been described in the literature including antibacterial and antifungal activities, antioxidant and free radical scavenging activities, anti-inflammatory activity, anti-carcinogenic activity, enhanced gastrointestinal motility, and neuropharmacological and anticonvulsant activities through detailed observation with respect to its ethnomedical uses. An overview of pharmacological and therapeutic profile of B. orellana is described below in detail and briefly summarized in Table 2.
Table 2.
Pharmacological effects of Bixa orellana.
Pharmacological effects | Details | Extracts/compounds | Potency of extracts/compounds zone of inhibition (mm)/% Inhibition | MIC/dose level | In vitro/In vivo | References |
---|---|---|---|---|---|---|
Antibacterial and antifungal activity |
|
Ethanolic leaves and seeds extract | 21.50, 20.00, 19.50, 17.00, 19.00, 22.50, 22.00 (leave extract) and 20.00, 17.00, 19.00, 14.50, 19.00, 18.00, 20.00 (seed extract), respectively. | – | In vitro | [32] |
Ethanolic leave extract | 21.6 | 24 mg/mL | In vitro | [33] | ||
Ethanolic hypocotyls extract | 15.8 | |||||
Ethanolic root extract | 15.20 | |||||
Acetone extracts | 10-14 | – | In vitro | [14] | ||
DMSO extracts | >14 | |||||
Dichloromethane/ ishwarane | – | – | – | [37] | ||
Methanolic crude extract | 17 | – | In vitro | [3] | ||
Hexane extract | 2.0 mg/mL | |||||
95% ethanol leaves extract | 15–17 | 5 mg/mL | In vitro | [40] | ||
Antioxidant and free radical scavenging activity |
|
Ethyl acetate extract, composed of hypolaetin and caffeoyl acid derivative | 11.0, 1.0, 3.0 and 7.0, respectively | 3.0 μg/mL | In vitro | [42] |
Seed extract | 5.5–48.9% relative to ascorbic acid 2.9–41.5% | 0.25 and 2.5 μg/mL | In vitro | [44] | ||
Bixin | 33% | 2.5 or 5.0 mg/kg | In vitro | [45] | ||
Anti-inflammatory activity |
|
Aqueous extract | – | 150 mg/kg | In vitro | [46] |
Pretreatment of aqueous leaf extract | – | 50 mg/kg and 150 mg/kg | In vitro | [46] | ||
After treatment of leaf extract (lyophilized) | – | 50 mg/kg and 150 mg/kg | In vitro | [47] | ||
Leaf extract | – | 200 mg/kg and 400 mg/kg | In vitro | [48] | ||
Aqueous extract (2-butanamine, acetic acid, pentanoic acid, phenol, pantolactone and benzoic acid) | – | – | In vitro | [10] | ||
Bixin | 19% and 33.60% | 50 μg/mL | In vitro | [50] | ||
Anti carcinogenic activity |
|
Bixin | – | 33, 49, 45, and 39 μg/mL | – | [50] |
Methanol leaves extract | 52%, 57% and 53% | 500 mg/kg | In vitro | [52] | ||
Cis-bixin | – | 10–50 μM | In vitro | [53] | ||
Gastrointestinal motility |
|
Dichloromethane extract of the air-dried leaves (Ishwarane) | (88.38 ± 13.59%) | 25, 50, and 100 mg/kg | In vitro | [37] |
Ishwarane | 50 mg/kg | In vitro | [37] | |||
Methanol leaves extract | 79.55% | 125, 250 and 500 mg/kg 500 mg/kg | In vitro | [54] | ||
Neuropharmacological activity and Anticonvulsant activity |
|
Leaves extract | 500 mg/kg | In vitro | [54] | |
Leaves extract | 58.45 min (control group) | 250 and 500 mg/kg | – | [54] | ||
76.70 and 90.82 min | ||||||
Leaves extract | 7.33 and 10.68 min | 250 and 500 mg/kg | – | [54] | ||
Analgesic activity and Antidiarrheal activity |
|
Methanol leaves extracts | 43.60% | – | In vitro | [55] |
Methanol leaves extracts | – | 22.36 μg/mL | In vitro | [54] | ||
Other pharmacological effects |
|
Methanol extract | – | 500 mg/kg | In vitro | [58] |
Ethanol extracts | – | – | In vitro | [59], [60] | ||
Whole plant extracts (Root and leaf extract) | 6.0 and 17.40 | – | In vitro | [61] | ||
Antibacterial and antifungal activities
Inhibitory actions of the methanol leaf and seed extracts were tested against bacterial and fungal strains. Leaf (MIC = 1000 μg/ml) extracts were more effective and possessed antimicrobial activity against a wide variety of bacteria and fungi, showing greatest activity against Salmonella typhi (MIC = 31.25 μg/mL) and Acinetobacter species (MIC = 31.25 μg/mL) against 10 μg/disc Streptomycin (9 ± 0.3 mm and 20 ± 0.2 mm) used as control, and Trichophyton mentagrophytes and Trichophyton rubrum (18 ± 0.3 mm) against 10 μL/sample Amphotericin-B with 19 ± 0.3 mm and 32 ± 0.2 mm, respectively [29]. This was attributed to the presence of alkaloids in the leaf extract. Additionally, crude ethanol leaf extracts exhibited better antibacterial effects against P. aeruginosa (MIC 512 μg/mL) and B. cereus (MIC 4096 μg/mL) whereas MIC values of seed extract were 128 and 1024 μg/mL respectively, and results were compared to standard bacteriocin drug niacin [30]. Braga et al. studied activity of fruit extract against Cryptococcus neoformans with MIC value of 78.0 μg/mL compared to standard Amphotericin-B with MIC value of 0.078 μg/mL [31].
Ethanolic leaf and seed extracts of B. orellana showed broad spectrum antibacterial activity against Bacillus subtilis, Staphylococcus aureus, Streptococcus pyogenes, Salmonella typhi, Pseudomonas aeruginosa, Escherichia coli and Candida albicans; the zone of inhibition (mm) was 21.50, 20.00, 19.50, 17.00, 19.00, 22.50, 22.00 (leaves extract) and 20.00, 17.00, 19.00, 14.50, 19.00, 18.00, 20.00 (seed extract) compared to 10 mg/ml gentamycin with MIC values of 34.00, 30.00, 24.00, 19.50, 33.00, 31.00, respectively. The results provide scientific support for the use of B. orellana in traditional medicine particularly as a gargle for sore throats and oral hygiene [32]. Ethanolic leaves extracts showed in vitro antimicrobial activity against Bacillus pumilus followed by the extracts from root and hypocotyls with zone of inhibitions of 21.60, 15.80 and 15.20 for 24 mg/mL concentration, respectively [33]. Analysis of dried leaves showed that a sesquiterpenes (Bixaghane) along with ellagic acid, 7-bisulfate luteolin, 8-bisulfate hypoluteolin, 7-glucoside luteolin, and bixorellin accounts for the potent antimicrobial activity of this plant [34]. The major antimicrobial compounds in the B. orellana seed extract were identified as carotenoids (9′-cis-norbixin and all-trans-norbixin) by 1H NMR and screened by thin layer chromatography and bioautography followed by liquid chromatography/photodiode array/mass spectrometry (LC/PDA/MS) analysis [26]. In 2012, antibacterial activity of the ethanolic, methanolic, acetone and dimethyl sulphoxide extracts was evaluated against E. coli, K. pneumonia, P. aeruginosa, B. subtilis, B. cereus and S. aureus by disk diffusion assay. The antibacterial effects were more pronounced in acetone and DMSO extracts as compared to ethanol and methanol extracts with zone of inhibition 10–14 mm and >14 mm, respectively against 25 μg tetracycline used as standard [12]. The crude extract of B. orellana hairy roots was assessed for anti-plasmodium activity against malaria strains 3D7 and K1 and displayed antimalarial properties in the 15–20 μM range with no cytotoxicity at the measured concentrations in the mammalian cell lines utilized for this experiment (EC50 > 26 μM) [35].
Previous investigations demonstrated the antifungal activity of the essential oils obtained from leaf extract of this plant against a wide variety of fungal strains [36]. The antifungal activity of sesquiterpene ishwarane, isolated by dichloromethane extraction had an activity index of 0.3 against C. albicans and T. mentagrophytes [37]. Phytochemical investigation revealed that alkaloids, tannins, triterpenoids and anthraquinones are responsible for the antifungal activity. Hexane extract showed antifungal effects against Trychophyton mentagrophytes and Trychophyton rubrum with MIC value of >8.0 mg/mL [38], and the results are comparable to earlier studies of antifungal activity against Cryptococcus neoformans and Microsporum gypseum with MIC values of 8 and 2 mg/mL, respectively [39]. In addition to above, 95% ethanolic leaves extract (5 mg/mL) of B. orellana was examined for in vitro antifungal and antibacterial activities using agar diffusion and tube dilution methods with zones of inhibition of 15–17 mm for all the standard strains of Gram-positive bacteria including Bacillus subtilis, Staphylococcus aureus, and Streptococcus faecalis while showing slight action against Escherichia coli, Serratia marcescens, Candida utilis, and Aspergillus niger while chloramphenicol and phenol positive controls show 12–18 mm and 10–28 mm, respectively [40].
Antioxidant and free radical scavenging activities
Conrad et al. investigated free radical scavenging potentials of ethanolic leaf extract of B. orellana [41]. Results indicate that phytochemical present in B. orellana leaves is effective protecting agents against carbon tetrachloride induced intoxication of blood and liver to albino rats. In vitro scavenging activity of various organic and aqueous seed extracts was evaluated against reactive oxygen and nitrogen species and results were compared to bixin standards. The results showed that ethyl acetate extract, mainly composed of hypolaetin and caffeoyl acid derivative (PC) had significant antioxidant effects with IC50 value of 11.0, 1.0, 3.0, 7.0 and 3.0 μg/mL as compared to bixin standards with IC50 values of 3.0, 0.3, 1.0, 3.0 and 1.0 μg/mL against H2O2, HOCl, O2, NO, and ONOO− [42]. With increase in the polarity of the solvent, free radical scavenging activity of B. orellana extract increases which is in accordance with the presence of higher phenolic content in more polar solvents [43].
In vitro antioxidant activity of seed extract of B. orellana was tested via 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging activity and iron(III) oxide reducing power using ascorbic acid (vitamin C) as a reference standard. Results indicated that the percentage reduction ranged from 5.5% to 48.9% relative to ascorbic acid (2.9–41.5%) between concentrations range of 0.25 and 2.5 μg/mL. Similarly, iron(III) oxide reducing power shows good linear concentration-dependent relation (R2 = 0.9986) comparable with ascorbic acid (R2 = 0.9934). According to the authors activity may be due to the presence of tannins and flavonoids found in the preliminary analysis [44]. Pretreatment with bixin (2.5 or 5.0 mg/kg BW; 48, 24 h and 10 min) reduced the total number of chromosome aberrations by about 33%, inhibited the increase in lipid peroxidation, and inhibited renal glutathione depletion induced by cisplatin (5 mg/kg BW) [45].
Anti-inflammatory activity
The results of the inhibitory effect of aqueous extract (150 mg/kg) of B. orellana on histamine-induced paw edema in rat models showed reduced histamine-induced paw edema in a dose dependent manner [10]. Additionally, pretreatment of 50 mg/kg and 150 mg/kg of aqueous leaf extract could significantly decrease carageenan, histamine, serotonin and bradykinin induced acute and chronic rat paw edema [46]. After treatment with lyophilized leaf extract at dose levels of 50 mg/kg and 150 mg/kg inhibits bradykinin-induced inflammation. Also a decrease in nitric oxide production and vascular endothelial growth factor (VEGF) was observed indicating that the anti-inflammatory effect may be related to the reduction in reactive oxygen species [47]. The antiulcer effects of hydroalcoholic leaf extract were studied on rat liver damage induced by 96% ethanol. The leaf extract at doses of 200 mg/kg and 400 mg/kg produced partial gastroprotection [48].
Results from the inhibitory effect of aqueous extract of B. orellana leaves on paw inflammation induced by histamine in mice showed significant reduction in paw volumes and almost normalized peritoneal vascular permeability, suspected to be aided by the suppression of other permeability-regulating substances (NO and VEGF) [10]. GC/MS analysis showed the presence of six major components 2-butanamine, acetic acid, pentanoic acid, phenol, pantolactone and benzoic acid, although results from the studies by Ruiz and comes showed that low concentration of acetic acid (0.3 mg/mL) has been shown to inhibit histamine release from guinea pig lung mast cells when stimulated by both antigen (ovalbumin) and ionophore A23187 [49]. Additionally, bixin (50 μg/mL) from B. orellana was screened for COX-1 and COX-2 enzyme inhibitory activities showing 19% and 33.60% inhibition, respectively compared with ibuprofen (2.52 μg/mL), aspirin (180 μg/mL), Vioxx (1.67 μg/mL), and Celebrex (1.67 μg/mL), used as positive controls, giving 51, 78, 63, 0.7 and 40%, 99%, 32% and 82% inhibition, respectively [50].
Anticarcinogenic activity and cytotoxicity-
Extracts and compounds from B. orellana also possessed anticancer/antitumor effects. The main effective compound was thought to be bixin [50]. The cell proliferation inhibitory effects of bixin varied among tumor cell lines giving respective IC50 values of 33, 49, 45, and 39 μg/mL against colon, CNS, stomach, and lung cancer cell lines. Clastogenic and anticlastogenic activity of bixin from seeds of B. orellana was evaluated in order to assess the chromosomal damage induced by the clastogen cisplatin [51]. Methanol leaf extract (500 mg/kg, crude herb medicinal equivalent, 3 times/day) decreased carbon tetrachloride hepatic damage in Swiss albino rats. Decrease in the elevations of liver alanine aminotransferase (ALT), aspartate aminotransferase (AST) and cholesterol by 52%, 57% and 53%, respectively has been monitored and supported by histopathological examination of liver tissues [52].
Cis-bixin from dried annatto seeds induces cytotoxicity in a wide variety of tumor cell lines in an ex vivo myeloma model system with IC50 values of 10–50 μM, 24 h exposures, and selectively killed freshly collected patient multiple myeloma cells and highly drug-resistant multiple myeloma cell lines [53]. The cis-bixin induced cytotoxicity was thought to be induced by ROS in dose- and time-dependent manner as demonstrated by the inhibition of thioredoxin and thioredoxin reductase and fluorescence-activated cell sorting (FACS) assays using the cell-permeable dyes 5-(and-6) chloromethyl-2′,7′-dichlorodihydrofluorescein diacetate, acetyl ester or dihydroethidium.
Gastrointestinal motility
A bioactive sesquiterpene (ishwarane) was isolated from dichloromethane extract of the air-dried leaves of B. orellana by silica gel chromatography and identified by 1H and 13C NMR. At dose levels of 25, 50, and 100 mg/kg ishwarane was tested for gastrointestinal mobility. Results of the prophylactic assay showed the antitoxic property at 100 mg/kg. At a dose of 50 mg/kg ishwarane resulted in a more propulsive movement of the gastrointestinal tract (88.38 ± 13.59%) as compared to negative control (78.47 ± 10.61%) [36]. A methanol leaf extract (125, 250 and 500 mg/kg, 30 min) was found to delay the intestinal transit of charcoal meal in mice to a statistically significant level (P < 0.01) with 79.55% inhibition at a dose of 500 mg/kg [54].
Analgesic activity and hypoglycemic activity
Analgesia of isolated ishwarane from B. orellana leaves showed 47.93 ± 15.16% inhibition relative to diclofenac sodium as positive control 42.53 ± 37.75% in tail flick model and an inhibition of 60 ± 41.22% relative to positive control 56.84 ± 32.60% in acetic acid writhing assays [36]. Methanol leaf extract showed hypoglycemic effects (30.2%, P < 0.040) in Swiss Webster mice after 45 min of loading glucose using a modified oral glucose tolerance test [55].
Antidiarrheal activity
Results from the study by Shilpi et al. showed that the methanol leaf extract (125, 250 and 500 mg/kg BW) inhibited castor oil induced diarrhea in mice. Antidiarrheal activities were supported by a statistically significant decrease in the total number of stools (including wet stools) and dose-dependently the total number of faces and the total number of wet faces with IC50 value of 22.36 μg/ml [54].
Other pharmacological effects
Methanol extract showed potent activity against L. amazonensis isolated from a patient with diffuse cutaneous leishmaniasis with IC50 = 22 μg/mL [56]. Additionally further research findings on in vitro and in vivo effects of the essential oil (Ishwarane and geranylgeranoil) of B. orellana seeds showed potential activity against intracellular amastigote form with IC50 value of 8.5 μg/mL [57]. The effect of methanol extract of B. orellana leaves on diuretics was demonstrated in Wister rat models, and results showed that the extract at a dose level of 500 mg/kg possessed diuretic effect with a significant increase in urine volume (2.4 ± 0.02 ml) and levels of sodium (82 ± 3.07 mEq/L), potassium (12.3 ± 0.47 mEq/L) and chloride (71 ± 2.52 mEq/L) as compared to control group 0.7 ± 0.04 mL, 62 ± 2.01, 11.4 ± 1.90 and 56 ± 1.90, respectively [58]. Additionally, various extracts of this plant have been used to neutralize snake venom and prevents associated adverse effects [59] and prove its use in folk medicine. Also, ethanol extracts (LD50 = 44 μg) offer partial protection against the edema forming activity and lethality in mice against Bothrops atrox venom [60]. Root and leaf extract of this plant have been found to have potent antigonorrheal activity with zones of inhibition 6.0 mm and 17.40 mm respectively [61].
The foliage of Bixa is used to treat skin problems and hepatitis, and also used as aphrodisiac, antidysenteric, and antipyretic [62]. The binding of naringenin-7-O-glucoside isolated from the fruit shell of B. orellana with calf thymus DNA (ctDNA) and the influence of cyclomaltoheptaose (b-cyclodextrin, b-CD) on the binding were studied by absorption and fluorescence spectroscopic techniques [63].
Industrial uses of annatto dye
Before describing the potential industrial applications of annatto dye, we find useful to briefly explain how natural colorants including annatto have been reintroduced into textile coloration and other application fields. Since the introduction of synthetic dyes in 1856, use of natural colorants from plants had almost vanished [64], [65], [66]. However, during the past decade synthetic dyes especially those producing any of the banned aromatic amines upon their degradation were shown to possess some drawbacks mainly carcinogenicity and environmental pollution [67], [68]. Therefore, the desire for green labeled products has led to a renaissance in natural colorants for use in textiles, food, cosmetics, dye synthesizer solar cells and other application fields [69], [70], [7]. Currently, a number of colorants from plant sources such as orange peel [71], pomegranate peel [72], almond shell [73], gallnut [74], Hibiscus mutabilis [75], Terminalia arjuna [76], Terminalia catappa, Saraca asoca [77], Tectona grandis [78], tea, turmeric [79], betanin [80], madder [81], weld [82], henna [83], [84], and chestnut shell [85] have been investigated as potential candidates for sustainable coloration and functional finishing of different kinds of textile materials. Annatto is one such natural yellow–orange dye obtained from renewable resource such as Bixa orellana plant, causes less toxicity and generally exhibits better biodegradability and compatibility with the environment.
Currently, the European Union has authorized a vast number of natural colorants as food additives including annatto which is assigned E-number of E160b for use in a wide range of food commodities such as dairy products, flour confectionery, fish, soft drinks, meat products, snack foods, and dry mixes [64], [86]. Despite its numerous food applications it has shown huge potential in textile and leather sectors. Bixin (Cis-form) is the principle coloring compound present in annatto seeds. It is oil soluble diapocarotenoid with two carboxylic acid groups in its molecular structure one of which is esterified and accounts for more than 80% of total annatto pigments [87], [88]. Another carotenoid type water soluble coloring compound is nor-bixin which is derived from bixin by hydrolysis of the ester group [89], [90].
Numerous approaches are used to extract the pigment from dried annatto seeds among which direct extraction using oil, aqueous alkali, or indirect extraction with solvents has been commercially accepted methods of bixin and nor-bixin extraction [91]. In view of its emerging importance, new green techniques have been employed for the extraction of annatto dye from Bixa orellana seeds. Sinha and colleagues reported microwave-assisted extraction of yellow–red from seeds by investigating the effects of pH, extraction time and amount of annatto seeds using response surface methodology (RSM) and artificial neural network (ANN) based predictive methods [92]. Lately, Yolmeh et al. studied ultrasound method for extraction of annatto dye. They used a statistical approach based on response surface methodology to optimize the extraction conditions such as concentration of solvent, extraction time, duty cycle, and solvent-to-material and found that ultrasound technology offers much better results than conventional techniques [93].
Several researches have been undertaken on the dyeing of textiles with annatto. Reports are available in the literature on dyeing properties of bixin on synthetic textile materials such as nylon and polyester [94]. Likewise, annatto pigments have demonstrated better results after their application on natural fibers including wool, silk and cotton [95], [96]. Recently, annatto dyed wool post-treated with ammonia resulted in a variety of beautiful shades with variation in hue and tone [69]. In 2015, Selvi et al. investigated the dyeing potential of four plants found in Mexico including B. orellana [97]. Among all the plants studied B. orellana was found to be less toxic when used to dye cotton cloth and manta without a chemical mordant.
B. orellana has been successfully introduced in leather dyeing and finishing. For the first time Selvi and coworker studied the feasibility of using natural dye extract from B. orellana seeds for dyeing and finishing of leather. The leathers dyed using the annatto extract showed better coloring and satisfactory fastness properties and hence offer a viable option for commercial exploitations as a replacement for synthetic dyes and pigments [98]. In another research work, Siva and coworkers reported a study to discover the potential of pigment from B. orellana as an alternative tracking gel to bromophenol blue for electrophoresis [99]. Bromophenol blue is a synthetic dye and could produce allergic and toxic reactions. They observed encouraging results for annatto dye with the developed procedure being easy, practical and reliable.
Chemical structure is an important component for efficient functioning of any dye sensitized solar cell. Over the past fifteen years there has been interesting exploration of natural colorants from flowers, seeds, fruits and leaves as possible ecofriendly and low cost sensitizers [100], [101]. Recent research on annatto has resulted in utilization of its pigments as sensitizer for dye sensitized solar cells. Haryanto and coworkers studied the manufacture of dye sensitized solar cell (DSSC) using annatto seeds and found quite satisfactory efficiency of fabricated solar cells [102]. Likewise, Gomez–Ortiz studied the use of bixin and nor-bixin in dye-sensitized solar cells (DSCs) and obtained efficiencies of up to 0.53% by using bixin-sensitized TiO2 solar cells [70].
Conclusion and future perspectives
This review summarizes recent research into the phytochemistry and pharmacology of Bixa orellana plant. Many of the ethnopharmacological uses and biological activities have been validated by in vitro studies and in vivo models. Although studies conducted on annatto have confirmed its wide-range of biological activities, more rigorous research is further needed to explore individual chemical constituents and their action mechanisms in exhibiting certain biological and pharmacological activities in order to introduce this plant in pharmaceutical and other industries. Most of the studies have proved that annatto extracts have potent biological activities compared to standard drugs tested which further encourage scientists to deepen the investigations in order to develop safe and effective drugs from this plant in the near future.
Furthermore, in the last part this review has documented the presence of carotenoids mainly bixin and nor-bixin in annatto seeds which have yellow coloring properties. The utilization of the seed extract as natural colorant is of commercial value in USA and is permitted by FDA for use in food and drinks. It exhibits a high potential for use in a wide range of food commodities such as dairy products, flour confectionery, fish, soft drinks, meat products, snack foods, and dry mixes. Efforts have been made in the recent years to introduce this colorant in other non-food sectors such as dyeing industry and leather finishing and as a novel sensitizer for dye sensitized solar cells. For commercial utilization in non-food applications, more researches on annatto dye chemistry and extraction methods need to be further and preciously explored in order to exploit full potential of this natural dye plant.
Conflict of interest
The authors have declared no conflict of interest.
Compliance with Ethics Requirements
This article does not contain any studies with human or animal subjects.
Acknowledgments
Financial support provided by University Grants Commission, Govt. of India, New Delhi, through BSR Research Fellowship in Science for Meritorious Students (Shahid-ul-Islam) and (Luqman Jameel Rather) is thankfully acknowledged.
Biographies
Shahid-ul-Islam is a doctorial student doing research work in Dr. Faqeer Mohammad’s group at the Department of Chemistry, Jamia Millia Islamia (Central University), New Delhi, India. His research is focused on natural colorants, biopolymers, green chemistry, and functional textiles. He has numerous academic publications in International journals of high repute to his credit and has also contributed to several internationally recognized books published by John Wiley & Sons, Springer, and Studium Press LLC. His research papers are cited in well-reputed scientific journals published by Nature, The American Chemical Society, and The Royal Society of Chemistry. Additionally two of his papers appeared in ScienceDirect’s Top 25 hottest articles from the Journal of Cleaner Production in 2013, 2014 and 2015.
Luqman Jameel Rather is a PhD student working in the field of Natural dyes in Dr. Faqeer Mohammad’s group in Department of Chemistry Jamia Millia Islamia, New Delhi. He earned his M.Sc. Chemistry in 2010 from University of Kashmir, Srinagar. He qualified CSIR-NET in 2011. His research is focused on thermodynamic and kinetic adsorption studies of natural colorants on wool, and development of fluorescent textiles.
Faqeer Mohammad is a Senior Assistant Professor in the Department of Chemistry, at Jamia Millia Islamia, (A Central University), New Delhi, India. He received his M.Sc, M.Phil and Ph.D in 1975, 1979, and 1982, respectively, from Aligarh Muslim University, Aligarh, UP, India. During his PhD he was awarded with JRF and SRF Research Fellowships from UGC and CSIR. He has published numerous research articles, reviews and book chapters all in the journals of International repute. He has until now supervised 20 graduate M.Sc and 4 Ph.D theses. His research interests are in the field of natural dyes and their applications.
Footnotes
Peer review under responsibility of Cairo University.
References
- 1.Silva S.N.S., Amaral C.L.F., Reboucas T.N.H. Adoption of conservation practices on farm and selection of varieties by producers of annatto in the city of Vitoria da Conquista-BA. Rev Bras Agroecologica. 2010;5:106–113. [Google Scholar]
- 2.Correa MP. Dicionario das Plantas ´ Uteis do Brasil e das ´ Exoticas Cultivadas ´, vol. 4. Ministerio da Agricultura/IBDF, Rio ´ de Janeiro, Brasil; 1978.
- 3.Villar R., Calleja J.M., Morales C., Caceres A. Screening of 17 Guatemalan medicinal plants for platelet antiaggregant activity. Phytother Res. 1997;11:441–445. [Google Scholar]
- 4.Aher A.A., Bairagi S.M. Formulation and evaluation of herbal lipstick from colour pigments of Bixa orellana (Bixaceae) seeds. Int J Pharm Biol Sci. 2012;4:357–359. [Google Scholar]
- 5.Kang E.J., Campbell R.E., Bastian E., Drake M.A. Annatto usage and bleaching in dairy foods. J Dairy Sci. 2010;93:3891–3901. doi: 10.3168/jds.2010-3190. [DOI] [PubMed] [Google Scholar]
- 6.Venugopalan A., Giridhar P., Ravishankar G.A. Food, ethanobotanical and diversified applications of Bixa orellana L.: a scope for its improvement through biotechnological mediation. Ind J Fundament Appl Life Sci. 2011;1(4):9–31. [Google Scholar]
- 7.Scotter M. The chemistry and analysis of annatto food colouring: a review. Food Addit Contam. 2009;26:1123–1145. [Google Scholar]
- 8.Mercadante A.Z., steck A., pfander H. Three minor carotenoids from annatto (Bixa orellana) seeds. Phytochem. 1999;52:135–139. [Google Scholar]
- 9.Pino J.A., Correa M.T. Chemical composition of the essential oil from annatto (Bixa orellana L.) seeds. J Essent Oil Res. 2003;15:66–67. [Google Scholar]
- 10.Yong Y.K., Zakaria Z.A., Kadir A.A., Somchit M.N., Lian G.E.C., Ahmad Z. Chemical constituents and antihistamine activity of Bixa orellana leaf extract. BMC Complement Altern Med. 2013;13:32. doi: 10.1186/1472-6882-13-32. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Agner A.R., Bazo A.P., Ribeiro L.R., Salvadori D.M. DNA damage and aberrant crypt foci as putative biomarkers to evaluate the chemopreventive effect of annatto (Bixa orellana L.) in rat colon carcinogenesis. Mutat Res. 2005;582:146–154. doi: 10.1016/j.mrgentox.2005.01.009. [DOI] [PubMed] [Google Scholar]
- 12.Stohs S.J. Safety and efficacy of Bixa orellana (achiote, annatto) leaf extracts. Phytother Res. 2014;28(7):956–960. doi: 10.1002/ptr.5088. [DOI] [PubMed] [Google Scholar]
- 13.Ulbricht C., Windsor R.C., Brigham A., Bryan J.K., Conquer J., Costa D., Giese N., Guilford J., Higdon E.R., Holmes K., Isaac R., Jingst S., Kats J., Peery L., Rusie E., Savinainen A., Schoen T., Stock T., Tanguay-Colucci S., Weissner W. An evidence-based systematic review of annatto (Bixa orellana L.) by the natural standard research collaboration. J Diet Suppl. 2012;9(1):57–77. doi: 10.3109/19390211.2012.653530. [DOI] [PubMed] [Google Scholar]
- 14.Venugopalan A., Giridhar P. Bacterial growth inhibition potential of annatto plant parts. Asian Pac J Trop Biomed. 2012;2(3) S1879-82. [Google Scholar]
- 15.Vilar D.A., Vilar M.S.A., Accioly de Lima e Moura T.F., Raffin F.N., Rosa de Oliveira M., Franco C.L.O. Traditional uses chemical constituents and biological activities of Bixa orellana L. a review. Sci World J. 2014 doi: 10.1155/2014/857292. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Alonso J. Tratado de Fitofarmacosy Nutraceuticos. Corpus, Rosario, Argentina; 2004.
- 17.Mercadante A.Z., Steck A., Pfander H. Isolation and structure elucidation of minor carotenoids from annatto (Bixa orellana L.) seeds. Phytochem. 1997;46:1379–1383. [Google Scholar]
- 18.Rao P.G.P., Jyothirmayi T., Balaswamy K., Satyanarayana A., Rao D.G. Effect of processing conditions on the stability of annatto (Bixa orellana L.) dye incorporated into some foods. LWT – Food Sci Tech. 2005;38:779–784. [Google Scholar]
- 19.Tirimanna A.S.L. Study of the carotenoid pigments of Bixa orellana L. seeds by thin layer chromatography. Mikrochim Acta. 1981;II:11–16. [Google Scholar]
- 20.Lauro G.J. A primer on natural colours. Cereal Food World. 1991;36:949–953. [Google Scholar]
- 21.Preston H.D., Rickard M.D. Extraction and chemistry of annatto. Food Chem. 1980;5(1):47–56. [Google Scholar]
- 22.Jondiko I.J.O., Pattenden G. Terpenoids and an apocarotenoid from seeds of Bixa orellana. Phytochem. 1989;41:3159–3162. [Google Scholar]
- 23.Mercadante A.Z., Steck A., Rodriguez-Amaya D., Pfander H., Britton G. Isolation of Methyl (9′Z)-apo-6′-lycopenoate from Bixa orellana. Phytochem. 1996;41:1201–1203. [Google Scholar]
- 24.Mercadante A.Z., Steck A., Pfander H. Isolation and identification of new apocarotenoids from annatto (Bixa orellana) seeds. J Agric Food Chem. 1997;45:1050–1054. [Google Scholar]
- 25.Frega N., Mozzon M., Bocci F. Identification and estimation of tocotrienols in the annatto lipid fraction by gas chromatography-mass spectrometry. J Am Oil Chem Soc. 1998;75:1723–1727. [Google Scholar]
- 26.Galindo-Cuspinera V., Lubran M.B., Rankin S.A. Comparison of the volatile compounds in water- and oil-soluble annatto (Bixa orellana L.) extracts. J Agric Food Chem. 2002;50:2010–2015. doi: 10.1021/jf011325h. [DOI] [PubMed] [Google Scholar]
- 27.Pino J.A., Correa M.T. Chemical composition of the essential oil from annatto (Bixa orellana L.) seeds. J Essent Oil Res. 2011;15:66–67. [Google Scholar]
- 28.Harborne J.B. Flavonoid bisulphates and their co-occurrences with ellagic acid in the Bixaceae, Frankeniaceae and related families. Phytochemistry. 1975;14:1331–1337. [Google Scholar]
- 29.Selvi A.T., Dinesh M.G., Satyan R.S., Chandrasekaran B., Rose C. Leaf and Seed extracts of Bixa orellana L. exert anti-microbial activity against bacterial pathogens. J Appl Pharm Sci. 2011;1(09):116–120. [Google Scholar]
- 30.Viuda-martos M., Ciro-gómez G.L., Ruiz-navajas Y., Zapata-montoya J.E., Sendra E., Pérez-álvarez J.A. In vitro antioxidant and antibacterial activities of extracts from annatto (Bixa orellana L.) leaves and seeds. J Food Safety. 2012;32:399–406. [Google Scholar]
- 31.Braga F.G., Bouzada M.L.M., Fabri R.L., Matos M., Moreira F.O., Scio E. Antileishmanial and antifungal activity of plants used in traditional medicine in Brazil. J Ethnopharmacol. 2007;111:396–402. doi: 10.1016/j.jep.2006.12.006. [DOI] [PubMed] [Google Scholar]
- 32.Fleischer T.C., Ameade E.P.K., Mensah M.L.K., Sawer I.K. Antimicrobial activity of the leaves and seeds of Bixa orellana. Fitoterapia. 2003;74:136–138. doi: 10.1016/s0367-326x(02)00289-7. [DOI] [PubMed] [Google Scholar]
- 33.Castello M., Phatak A., Chandra N., Sharon M. Antimicrobial activity of crude extracts from plant parts and corrsponding calli of Bixa orellana L. Ind J Exp Bio. 2002;40:1378–1381. [PubMed] [Google Scholar]
- 34.Solkar LV, Kakkar KK, Chakre OJ. Bixa orellana L. in glossary in Indian medicinal with active principles In: Warrier PK, Nambiar VPK, Ramankutty, editors, vol. 126. Kerala India: Orient Longmann; 1992.
- 35.Zollo P.H., Biyiti L., Tchoumbougnang F., Menut C., Lamaty G., Bouchet P. Aromatic plants of tropical Central Africa Part XXXII Chemical composition and antifungal activity of thirteen essential oils from aromatic plants of Cameroon. Flavour Frag J. 1998;13:107–114. [Google Scholar]
- 36.Zhai B., Clark J., Ling T., Connelly M., Medina-Bolivar F., Rivas F. Antimalarial evaluation of the chemical constituents of hairy root culture of Bixa orellana L. Molecules. 2014;19:756–766. doi: 10.3390/molecules19010756. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Raga D.D., Espiritu R.A., Chien-Chang S., Ragasa C.Y. A bioactive sesquiterpene from Bixa orellana. J Nat Med. 2011;65:206–211. doi: 10.1007/s11418-010-0459-9. [DOI] [PubMed] [Google Scholar]
- 38.Garcia V.M.N., Gonzalez A., Fuentes M., Aviles M., Rios M.Y., Zepeda G. Antifungal activities of nine traditional Mexican medicinal plants. J Ethnopharmacol. 2003;87:85–88. doi: 10.1016/s0378-8741(03)00114-4. [DOI] [PubMed] [Google Scholar]
- 39.Caceres A., Lopez B., Gonzalez S., Berger I., Tada I., Maki J. Plants used in Guatemala for the treatment of protozoal infections. I. Screening of activity to bacteria, fungi and American trypanosomes of 13 native plants. J Ethnopharmacol. 1998;62(3):195–202. doi: 10.1016/s0378-8741(98)00140-8. [DOI] [PubMed] [Google Scholar]
- 40.Irobi O.N., Moo-Young M., Anderson W.A. Antimicrobial activity of annatto (Bixa orellana) extract. Inter J Pharmacognosy. 1996;34(2):87–90. [Google Scholar]
- 41.Conrad O.A., Dike I.P., Agbara U. In vivo antioxidant assessment of two antimalarial plants – Allamamda cathartica and Bixa orellana. Asian Pac J Trop Biomed. 2013;3:388–394. doi: 10.1016/S2221-1691(13)60082-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Chiste R.C., Mercadante A.Z., Gomes A., Fernandes E., Lima J.L.F.C., Bragagnolo N. In vitro scavenging capacity of annatto seed extracts against reactive oxygen and nitrogen species. Food Chem. 2011;127:419–426. doi: 10.1016/j.foodchem.2010.12.139. [DOI] [PubMed] [Google Scholar]
- 43.Cardarelli C.R., Benassi M.T., Mercadante A.Z. Characterization of different annatto extracts based on antioxidant and colour properties. LWT-Food Sci Technol. 2008;41:1689–1693. [Google Scholar]
- 44.Abayomi M., Adebayo A.S., Bennett D., Porter R., Shelly-Campbell J. In vitro antioxidant activity of Bixa orellana (Annatto) seed extract. J Appl Pharm Sci. 2014;4:101–106. [Google Scholar]
- 45.Silva C.R., Antunes L.M.G., Bianchi M.L.P. Antioxidant action of bixin against cisplatin-induced chromosome aberrations and lipid peroxidation in rats. Pharm Res. 2001;43:561–566. doi: 10.1006/phrs.2001.0822. [DOI] [PubMed] [Google Scholar]
- 46.Zuraini A., Somchit M.N., Hamid R.A., Sukradi S., Fazira A.J.S.E., Yong Y.K. Inhibitions of acute and chronic inflammations by Bixa orellana leaves extract. Planta Med. 2007;73:76. [Google Scholar]
- 47.Keong Y.Y., Arifah A.K., Sukardi S., Roslida A.H., Somchit M.N., Zuraini A. Bixa orellana leaves extract inhibits bradykinin-induced inflammation through suppression of nitric oxide production. Med Princ Pract. 2011;20:142–146. doi: 10.1159/000319907. [DOI] [PubMed] [Google Scholar]
- 48.Huamán O., Sandoval M., Arnao I., Béjar E. Antiulcer effect of lyophilized hydroalcoholic extract of Bixa orellana (annatto) leaves in rats. An Fac Med. 2009;70:97–102. [Google Scholar]
- 49.Ruiz C.M., Gomes J.C. Effects of ethanol, acetaldehyde, and acetic acid on histamine secretion in guinea pig lung mast cells. Alcohol. 2000;20:133–138. doi: 10.1016/s0741-8329(99)00065-8. [DOI] [PubMed] [Google Scholar]
- 50.Reddy M.K., Alexander-Lindo R.L., Nair M.G. Relative inhibition of lipid peroxidation, cyclooxygenase enzymes, and human tumor cell proliferation by natural food colors. J Agric Food Chem. 2005;53:9268–9273. doi: 10.1021/jf051399j. [DOI] [PubMed] [Google Scholar]
- 51.Antunes L.M.G., Pascoal L.M., Bianchi M.L.P., Dias F.L. Evaluation of the clastogenicity and anticlastogenicity of the carotenoid bixin in human lymphocyte cultures. Mut Res. 2005;585:113–119. doi: 10.1016/j.mrgentox.2005.04.006. [DOI] [PubMed] [Google Scholar]
- 52.Ahsan R., Islam K.M., Musaddik A., Haque E. Hepatoprotective activity of methanol extract of some medicinal plants against carbon tetrachloride induced hepatotoxicity in albino rats. Global J Pharmacol. 2009;3:116–122. [Google Scholar]
- 53.Tibodeau J.D., Isham C.R., Bible K.C. Annatto constituent Cis-Bixin has selective antimyeloma effects mediated by oxidative stress and associated with inhibition of Thioredoxin and Thioredoxin reductase. Antioxid Redox Signal. 2010;13:987–997. doi: 10.1089/ars.2009.2896. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Shilpi J.A., Taufiq-Ur-Rahman M., Uddin S.J., Alam M.S., Sadhu S.K., Seidel V. Preliminary pharmacological screening of Bixa orellana L. leaves. J Ethnopharmacol. 2006;108:264–271. doi: 10.1016/j.jep.2006.05.008. [DOI] [PubMed] [Google Scholar]
- 55.Quanico J.P., Amor E.C., Perez G.G. Analgesic and hypoglycemic activities of Bixa orellana, Kyllinga monocephala and Luffa acutangula. Philippine J Sci. 2008;137:69–76. [Google Scholar]
- 56.Braga F.G., Bouzada M.M., Fabri R.L., Matos M.O., Moreira F.O., Scio E. Antileishmanial and antifungal activity of plants used in traditional medicine in Brazil. J Ethnopharmacol. 2007;111:396–402. doi: 10.1016/j.jep.2006.12.006. [DOI] [PubMed] [Google Scholar]
- 57.Monzote L., García M., Scull R., Cuellar A., Setzer W.N. Antileishmanial activity of the essential oil from Bixa orellana. Phytother Res. 2014;28(5):753–758. doi: 10.1002/ptr.5055. [DOI] [PubMed] [Google Scholar]
- 58.Radhika B., Begum N., Srisailam K., Reddy V.M. Diuretic activity of Bixa orellanna Linn. leaf extracts. Ind. J Nat Prod Res. 2010;1(3):353–355. [Google Scholar]
- 59.Núñez V., Otero R., Barona J., Saldarriag M., Osorio R.G., Fonnegra R. Neutralization of the edema-forming, defibrinating and coagulant effects of Bothrops asper venom by extracts of plants used by healers in Columbia. Brazilian. J Med Bio Res. 2004;37:969–977. doi: 10.1590/s0100-879x2004000700005. [DOI] [PubMed] [Google Scholar]
- 60.Otero R., Nunez V., Jimenez S.L., Fonnegra R., Osorio R.G., Garcia M.E. Snakebites and ethnobotany in the northwest region of Colombia: part II: neutralization of lethal and enzymatic effects of Bothrops atrox venom. J Ethnopharmacol. 2000;71(3):505–511. doi: 10.1016/s0378-8741(99)00197-x. [DOI] [PubMed] [Google Scholar]
- 61.Cáceres A., Menéndez H., Méndez E., Cohobón E., Samayoa B.E., Jauregui E. Antigonorrhoeal activity of plants used in Guatemala for the treatment of sexually transmitted diseases. J Ethnopharmacol. 1995;48:85–88. doi: 10.1016/0378-8741(95)01288-o. [DOI] [PubMed] [Google Scholar]
- 62.Chandel U., Begum T., Syedy M. Pharmacological studies of annatto (Bixa orellana L.) Int J Phar Biomedi Res. 2014;1(1):1720. [Google Scholar]
- 63.Sameena Y., Sudha N., Murugesan G., Israel I.V.M.V. Isolation of Prunin from the fruit shell of Bixa orellana and the effect of <beta> cyclodextrin on its binding with calf thymus DNA. Carbohydrate Res. 2013;365(46):51. doi: 10.1016/j.carres.2012.10.003. [DOI] [PubMed] [Google Scholar]
- 64.Samanta A.K., Agarwal P. Application of natural dyes on textiles. Indian J Fibre Text Res. 2009;34:384–399. [Google Scholar]
- 65.Shahid M., Islam S., Mohammad F. Recent advancements in natural dye applications: a review. J Clean Prod. 2013;53:310–331. [Google Scholar]
- 66.Yusuf M., Ahmad A., Shahid M., Khan M.I., Khan S.A., Manzoor N. Assessment of colorimetric, antibacterial and antifungal properties of woolen yarn dyed with the extract of the leaves of henna (Lawsonia inermis) J Clean Prod. 2012;27:42–50. [Google Scholar]
- 67.Islam S., Shahid M., Mohammad F. Perspectives for natural product based agents derived from industrial plants in textile applications – a review. J Clean Prod. 2013;57:2–18. [Google Scholar]
- 68.Islam S., Faqeer M. Roadmap to sustainable textiles and clothing. Springer; Singapore: 2014. Emerging green technologies and environment friendly products for sustainable textiles; pp. 65–82. [Google Scholar]
- 69.Islam S., Rather L.J., Shahid M., Khan M.A., Mohammad F. Study the effect of ammonia post-treatment on color characteristics of annatto-dyed textile substrate using reflectance spectrophotometery. Ind Crops Prod. 2014;57:337–342. [Google Scholar]
- 70.Gómez-Ortíz N.M., Vázquez-Maldonado I.A., Pérez-Espadas A.R., Mena-Rejón G.J., Azamar-Barrios J.A., Oskam G. Dye-sensitized solar cells with natural dyes extracted from achiote seeds. Sol Energy Mater Sol Cells. 2010;94:40–44. [Google Scholar]
- 71.Hou X., Chen X., Cheng Y., Xu H., Chen L., Yang Y. Dyeing and UV-protection properties of water extracts from orange peel. J Clean Prod. 2013;52:410–419. [Google Scholar]
- 72.Benli H., Bahtiyari M.I. Combination of ozone and ultrasound in pretreatment of cotton fabrics prior to natural dyeing. J Clean Prod. 2015;89:116–124. [Google Scholar]
- 73.İşmal Ö.E., Yıldırım L., Özdoğan E. Use of almond shell extracts plus biomordants as effective textile dye. J Clean Prod. 2014;70:61–67. [Google Scholar]
- 74.Zhang B., Wang L., Luo L., King M.W. Natural dye extracted from Chinese gall – the application of color and antibacterial activity to wool fabric. J Clean Prod. 2014;80:204–210. [Google Scholar]
- 75.Haddar W., Ticha M.B., Guesmi A., Khoffi F., Durand B. A novel approach for a natural dyeing process of cotton fabric with Hibiscus mutabilis (Gulzuba): process development and optimization using statistical analysis. J Clean Prod. 2014;68:114–120. [Google Scholar]
- 76.Vankar P.S., Shanker R., Verma A. Enzymatic natural dyeing of cotton and silk fabrics without metal mordants. J Clean Prod. 2007;15:1441–1450. [Google Scholar]
- 77.Baliarsingh S., Behera P.C., Jena J., Das T., Das N.B. UV reflectance attributed direct correlation to colour strength and absorbance of natural dyed yarn with respect to mordant use and their potential antimicrobial efficacy. J Clean Prod. 2015;102:485–492. [Google Scholar]
- 78.Prusty A.K., Das T., Nayak A., Das N.B. Colourimetric analysis and antimicrobial study of natural dyes and dyed silk. J Clean Prod. 2010;18:1750–1756. [Google Scholar]
- 79.Ghaheh F.S., Mortazavi S.M., Alihosseini F., Fassihi A., Nateri A.S., Abedi D. Assessment of antibacterial activity of wool fabrics dyed with natural dyes. J Clean Prod. 2014;72:139–145. [Google Scholar]
- 80.Guesmi A., Ladhari N., Hamadi N.B., Msaddek M., Sakli F. First application of chlorophyll-a as biomordant: sonicator dyeing of wool with betanin dye. J Clean Prod. 2013;39:97–104. [Google Scholar]
- 81.Shams-Nateri A. Reusing wastewater of madder natural dye for wool dyeing. J Clean Prod. 2011;19:775–781. [Google Scholar]
- 82.Mirjalili M., Nazarpoor K., Karimi L. Eco-friendly dyeing of wool using natural dye from weld as co-partner with synthetic dye. J Clean Prod. 2011;19:1045–1051. [Google Scholar]
- 83.Ali S., Hussain T., Nawaz R. Optimization of alkaline extraction of natural dye from Henna leaves and its dyeing on cotton by exhaust method. J Clean Prod. 2009;17:61–66. [Google Scholar]
- 84.Yusuf M., Shahid M., Khan S.A., Khan M.I., Islam S., Mohammad F. Eco-dyeing of wool using aqueous extract of the roots of indian madder (Rubia cordifolia) as natural dye. J Nat Fibers. 2013;10:14–18. [Google Scholar]
- 85.Zhao Q., Feng H., Wang L. Dyeing properties and color fastness of cellulase-treated flax fabric with extractives from chestnut shell. J Clean Prod. 2014;80:197–203. [Google Scholar]
- 86.Scotter M.J., Wilson L.A., Appleton G.P., Castle L. Analysis of annatto (Bixa orellana) food coloring formulations. 1. Determination of coloring components and colored thermal degradation products by high-performance liquid chromatography with photodiode array detection. J Agric Food Chem. 1998;46:1031–1038. [Google Scholar]
- 87.Annatto (Bixa orellana L.): its cultivation, preparation and usage. Inter J Trop Agri 1990;8:80–88.
- 88.Sekar N. Annatto colourants. Colourage. 2004;51:67. [Google Scholar]
- 89.Ramamoorthy S., Dossa F.P., Kundu K., Satyanarayana V.S.V., Kumar V. Molecular characterization of bixin-An important industrial product. Ind Crop Prod. 2010;32:48–53. [Google Scholar]
- 90.Chao R.R., Mulvaney S.J., Sanson D.R., Hsieh F., Tempesta M.S. Supercritical CO2 extraction of annatto (Bixa orellana) pigments and some characteristics of the color extracts. J Food Sci. 1991;56:80–83. [Google Scholar]
- 91.Sinha K., Chowdhury S., Saha P.D., Datta S. Modeling of microwave-assisted extraction of natural dye from seeds of Bixa orellana (Annatto) using response surface methodology (RSM) and artificial neural network (ANN) Ind Crops Prod. 2013;41:165–171. [Google Scholar]
- 92.Yolmeh M., Najafi M.B.H., Farhoosh R. Optimisation of ultrasound-assisted extraction of natural pigment from annatto seeds by response surface methodology (RSM) Food Chem. 2014;155:319–324. doi: 10.1016/j.foodchem.2014.01.059. [DOI] [PubMed] [Google Scholar]
- 93.Gulrajani M.L., Gupta D., Maulik S.R. Studies on dyeing with natural dyes Part 1-Dyeing of annatto on nylon and polyester Indian. J Fibre Text Res. 1999;24:131–135. [Google Scholar]
- 94.Das D., Maulik S.R., Bhattacharya S.C. Dyeing of wool and silk with Bixa orellana. Indian J Text Res. 2007;32:366–372. [Google Scholar]
- 95.Savvidis G., Zarkogianni M., Karanikas E., Lazaridis N., Nikolaidis M., Tsatsaron E. Digital and conventional printing and dyeing with the natural dye annatto: optimisation and standardisation processes to meet future demands. Color Tech. 2013;129:55–63. [Google Scholar]
- 96.Chan-Bacab M.J., Sanmartín P., Camacho-Chab J.C., Palomo-Ascanio K.B., Huitz-Quimé H.E., Ortega-Morales B.O. Characterization and dyeing potential of colorant-bearing plants of the Mayan area in Yucatan Peninsula, Mexico. J Clean Prod. 2015;91:191–200. [Google Scholar]
- 97.Selvi A.T., Aravindhan R., Madhan B., Rao J.R. Studies on the application of natural dye extract from Bixa orellana seeds for dyeing and finishing of leather. Ind Crops Prod. 2013;43:84–96. [Google Scholar]
- 98.Siva R., Mathew G.J., Venkat A., Dhawan C. An alternative tracking dye for gel electrophoresis. Curr Sci. 2008;94:765–767. [Google Scholar]
- 99.Ludin N.A., Mahmoud A.M.A., Mohamad A.B., Kadhum A.A.H., Sopian K., Karim N.S.A. Review on the development of natural dye photosensitizer for dye-sensitized solar cells. Renew Sust Energy Rev. 2014;31:386–396. [Google Scholar]
- 100.Zhou H., Wu L., Gao Y., Ma T. Dye-sensitized solar cells using 20 natural dyes as sensitizers. J Photochem Photobiol. 2011;219:188–194. [Google Scholar]
- 101.Haryanto D.A., Landuma S., Purwanto A. Fabrication of dye-sensitized solar cell (DSSC) using annato seeds (Bixa orellana Linn) AIP Conf Proc. 2014;1586:104–108. [Google Scholar]
- 102.Galindo-Cuspinera V., Rankin S.A. Bioautography and chemical characterization of antimicrobial compound(s) in commercial water-soluble annatto extracts. J Agric Food Chem. 2005;53:2524–2529. doi: 10.1021/jf048056q. [DOI] [PubMed] [Google Scholar]
- 103.Andersonw S.G., Nair M.G., Chandra A., Morrison E. Supercritical fluid carbon dioxide extraction of annatto seeds and quantification of trans-bixin by high pressure liquid chromatography. Phytochem Anal. 1997;8:247–249. [Google Scholar]
- 104.Schneidere W.P., Aron E.L., Hinman J.W. Occurrence of Tomentosic acid in extracts of Bixa orellana. J Org Chem. 1965;30:2856–2857. doi: 10.1021/jo01019a519. [DOI] [PubMed] [Google Scholar]
- 105.Lawrence B.M., Hogg J.W. Ishwarane in Bixa orellana leaf oil. Phytochemistry. 1973;12:2995. [Google Scholar]