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. 2014 Jun 23;2014:857292. doi: 10.1155/2014/857292

Traditional Uses, Chemical Constituents, and Biological Activities of Bixa orellana L.: A Review

Daniela de Araújo Vilar 1, Marina Suênia de Araujo Vilar 1, Túlio Flávio Accioly de Lima e Moura 2, Fernanda Nervo Raffin 2, Márcia Rosa de Oliveira 3, Camilo Flamarion de Oliveira Franco 4, Petrônio Filgueiras de Athayde-Filho 5, Margareth de Fátima Formiga Melo Diniz 1, José Maria Barbosa-Filho 1,*
PMCID: PMC4094728  PMID: 25050404

Abstract

Bixa orellana L., popularly known as “urucum,” has been used by indigenous communities in Brazil and other tropical countries for several biological applications, which indicates its potential use as an active ingredient in pharmaceutical products. The aim of this work was to report the main evidence found in the literature, concerning the ethnopharmacology, the biological activity, and the phytochemistry studies related to Bixa orellana L. Therefore, this work comprises a systematic review about the use of Bixa orellana in the American continent and analysis of the data collected. This study shows the well-characterized pharmacological actions that may be considered relevant for the future development of an innovative therapeutic agent.

1. Introduction

The use of natural compounds of mineral, animal, or plant origin in food products, cosmetics, and drugs began long ago. There are written records of ancient Egyptian and Chinese civilizations that have made use of these products. Nowadays, there has been a return to the search for products called “natural,” which in fact never ceased to exist. The analysis of the composition of many drugs shows that almost 50% of those in clinical use are derived from natural compounds. Furthermore, not only plants but also plant byproducts are widely used as preservatives and flavoring and coloring agents in various food and cosmetic preparations [1].

Bixa orellana is a plant native to Brazil but grows in other regions of South and Central America. It is grown in tropical countries such as Peru, Mexico, Ecuador, Indonesia, India, Kenya, and East Africa [2].

The seeds of this plant produce one of the dyes most frequently used worldwide, not only in food products but also in the textile, paint, and cosmetic industries. Its use has been stimulated due to the ban on the use of synthetic dyes in food and cosmetics, where it is one of the few accepted by the World Health Organization (WHO), since, in addition to being nontoxic, it does not seem to change the food value [3]. Another interesting fact is that 70% of all natural coloring agents consumed worldwide are derived from annatto [4].

Annatto first spread in the form of food coloring, also known as paprika, a condiment widely used in cooking to enhance the color of food. Today, however, its use has spread into many segments of industrial production. Thus, it is now applied on the skin—in the form of makeup and sunscreen—and there is research proving that its use brings health benefits, which makes producers thankful for cultivating it [5, 6]. Therefore, in the continuation of our research on bioactive molecules from various species of different plant families [722], we offer this compilation of the traditional uses, chemical constituents, and biological activities of Bixa orellana.

The aim of this review is to highlight the biological and phytochemical studies that have been published about Bixa orellana in South and Central America and try to correlate these studies with the popular uses of this plant in those regions, as well as to evaluate whether its chemical composition can support the reported biomedical properties related to Bixa orellana.

2. Materials and Methods

In this work, the biological activities and compounds isolated from Bixa orellana were searched using the database of the Web of Science, Scielo, and the University of Illinois in Chicago NAPRALERT (acronym for “NAturalPRoducts ALERT”). The data were updated in April 2014, using “Bixa orellana, chemical, and bixin” as keywords for this review. The references found in the survey were later consulted for details about the models or mechanisms of bioassays used to test the extracts of Bixa orellana.

3. Botanical

The annatto tree belongs to the family Bixaceae and the genus Bixa. Despite the existence of several species, the most common in our country is Bixa orellana L., named after Francisco Orellana, who was the first European to navigate the Amazon [23].

According to Revilla [58], B. orellana is a small tree or shrub measuring from 3 to 5 meters in height, sometimes reaching a height of 10 meters. The trunk is short, measuring 20–30 cm in diameter, with dark gray bark with lenticels in vertical rows. The leaves are alternate, 10 to 20 cm long and 5 to 10 cm wide, sharp, green on both sides, and with extended petioles.

According to Oliveira et al. [59], seeds measure 0.3–0.5 cm in length and 0.2-0.3 cm in diameter, and their shape varies from pyramidal to almost conical. The number of seeds per capsule varies according to the author: Alonso [60] found that each bivalvar capsule may contain from 30 to 60 seeds, on average.

The seeds are considered the plant part of commercial importance, since the pericarp (layer that surrounds the seeds) contains the pigments that have wide industrial application. About 80% of this pigment is the carotenoid known as bixin, which has the dye property and can be extracted with vegetable oils or chemical bases. Depending on the cultivar and climatic conditions of the region, the bixin content can vary from 1 to 6% in the seed aril. The remainder is composed of other dyes and inert substances of minor importance [61].

4. Use in Traditional Medicine

Annatto is a native plant from South America, more specifically of the Amazon region. The popular name “urucum” comes from the Tupi word “ru-ku,” which means “red.” In Brazil, this plant is commonly known as urucum, urucu, açafrão, açafroa, and açafroeira-da-terra. It is known by other popular names in other countries: atolé, achiote, and bija (Peru and Cuba); axiote (Mexico); achiote, achote, anatto, bija, and santo-domingo (Puerto Rico); bixa (Guyana); analto (Honduras); guajachote (El Salvador); onotto and onotillo (Venezuela); achiote and urucu (Bolivia); urucu (Argentina); roucou (Trinidad); roucou and koessewee (Suriname); and annatto (United States). The wide dissemination of its use in those regions is related to the growing demand for natural dyes by many pharmaceutical, cosmetic, textile, and especially food industries [57].

According to Côrrea [27], seeds urucum supplies seeds that have been used as a condiment as well as laxative, cardiotonic, hypotensive, expectorant, and antibiotic. In addition, it has anti-inflammatory activity for bruises and wounds and has been used for the treatment of bronchitis and for wound healing purposes. Oil is also obtained from this plant. The infusion of the leaves has been shown to be effective against bronchitis, sore throat, and eye inflammation. The pulp, which includes the seed, is used for soft drinks and febrifuge. Moreover, it can provide valuable dyeing materials such as yellow (orellin) and red (bixin) substances, with the latter constituting a crystallized active ingredient.

In the food industry, it is used to color butter, margarine, mayonnaise, sauces, mustard, sausage, soup, juice, ice cream, bakery products, macaroni, and cheese, where it is commonly called “do reino” (of the kingdom), coming from Holland. It is also widely used in the printing industry and dye manufacturing. Many Aborigines use annatto for dyeing, where the dye is naturally obtained as a mixture and used to color ceramics and other vases for domestic use. In addition, most endogenous people use this dye on their skin to beautify themselves during religious rituals and mainly to protect themselves from ultraviolet radiation and from mosquitoes that infest forests [49]. The bast provides fibers for rough cordage, and the powder resulting from grinding the seeds has been used as an aphrodisiac. Finally, the infusion of cold buds serves to wash inflamed eyes, whereas the decoction of the leaves has been used for antiemetic therapy during pregnancy [27] (Table 1).

Table 1.

Traditional uses of annatto in American countries.

Country/use Plant part References
Argentina
 Antipyretic/cardiotonic/antidiarrheal Seeds [24]
 Antidiarrheal/dyes/condiment Seeds [25]
Brazil
 Body paint Seeds [26]
 Insect repellent Seeds [27]
 Condiment/food coloring Seeds [27]
 Antipyretic Seeds [26]
 Antipyretic/laxatives/burns Seeds [28]
 Malaria Seeds [26]
Colombia
 Snakebite Leaves [29]
 Aphrodisiac Seeds [30]
Cuba
 Aphrodisiac Seeds [31]
Guatemala
 Gonorrhea/dysentery Leaves [32]
 Hepatitis Leaves [33]
 Dysentery Leaves [34]
 Blood diseases Leaves [35]
 Gonorrhea Roots [32]
 Diabetes Roots [36]
Honduras
 Aromatic/food coloring Seeds [37]
 Pain/digestive/dysentery Leaves [38]
Jamaica
 Diabetes Seeds [39]
Nicaragua
 Respiratory and pulmonary disorders/diarrhea/diuretic/burns Leaves + seeds [40]
 Labor pains Seeds [41]
 Cough/cold/diuretic/diarrhea/burns/labor pains Seeds [40]
Paraguay
 Insecticide/repellent Seeds [42]
 Diabetes Seeds [39]
Peru
 Aphrodisiac/aphrodisiac/diuretic/antidisenteria/astringent Fruits [34]
 Antipyretic/skin problems Leaves [33]
 Alcoholic hepatitis/worms Roots [33]
 Antipyretic/aphrodisiac/dysentery/astringent/stomach Seeds [34]
Trinidad and Tobago
 Diuretic Leaves [43]
 Diabetes Roots [44]
 Diabetes Roots [45]

Thus, despite the different culture and traditions among the countries in South and Central America, several of the popular uses of Bixa orellana are the same, for example, antipyretic, aphrodisiac, antidiarrheal, antidiabetic, and insect repellent.

5. Chemical Compounds

Bixin, a red-colored carotenoid, is the pigment present in high concentration in the annatto seed aril. It is the main substance responsible for the dyeing characteristics of seeds, where its concentration can be as high as 5.0%. However, different seeds may have levels less than 2.0%, and because their commercial value is based on the bixin percentage, levels higher than 2.5% are usually required for export [61].

Bixin was isolated for the first time from the seeds of Bixa orellana in 1875 and in 1961 its complete chemical structure and stereochemistry were determined by 1H and 13C-NMR. Bixin belongs to the small class of natural apocarotenoids, whose formation occurs by the oxidative degradation of C40 carotenoids (Table 2).

Table 2.

The main carotenoids from the seeds of Bixa orellana.

Carotenoid Country of isolation Physical aspect References
Apo-ψ-carotene, 9′Z-6′-ol Brazil Oil [46]
Beta carotene Brazil 183°C [47]
Suriname [48]
Bixin Brazil 198°C [4951]
Peru [52]
Dominican Rep. [53]
Suriname [48]
USA [54]
Z-Carotene Brazil Oil [46]
Cryptoxanthin Suriname 173°C [48]
Dimethyl-(9Z)-6,6′-diapocarotene-6,6′-dioate Brazil Oil [52]
Dimethyl-(9Z,9′Z)-6,6′-diapocarotene-6,6′-dioate Brazil Oil [50]
Phytoene Brazil Oil [46]
Phytofluene Brazil Oil [46]
Geranylgeraniol Brazil Oil [52]
Lutein Suriname 196°C [48]
Methyl-(9Z)-10′-oxo-6,10′-diapocarotene-6-oate Brazil Oil [50]
Methyl-(9Z)-6′-oxo-6,5′-diapocarotene-6-oate Brazil Oil [50]
Methyl-(9Z)-8′-oxo-6,8′-diapocarotene-6-oate Brazil Oil [50]
Methyl-(9′Z)-apo-6′-lycopenoate Brazil Oil [46]
Methyl-(7Z,9Z,9′Z)-apo-6′-lycopenoate Brazil Oil [55]
Methyl-(9Z)-apo-8′-lycopenoate Brazil Oil [46]
Methyl-(all-E)-apo-8′-lycopenoate Brazil Oil [46]
Neurosporene Brazil Oil [46]
Norbixin Brazil 300°C [52]
Trans-bixin Jamaica 195°C [56]
Zeaxanthin Suriname 215°C [48]

Source: [57].

Bixin consists of a chain of 25 carbons and has the molecular formula C25H30O4 (MW = 394.51). It has a carboxylic acid and methyl ester group at the ends of the chain. Bixin occurs in nature as 16-Z (cis), but during the extraction process it isomerizes resulting in the 16-E form (trans), which is called isobixin (Figure 1).

Figure 1.

Figure 1

Chemical structure of some pigments of annatto.

Many other carotenoids (C19, C22, C24, C25, C30, and C32) occur in Bixa orellana but constitute a minor percentage of the pigments. The major oily constituent of annatto seeds is geranylgeraniol, representing 1% of dry seeds. Norbixin (Figure 1) is a demethylated derivative of bixin and although it is a naturally occurring compound, it is almost always referred to as a saponification product of bixin. This is the form used for commercial purposes [62].

Currently, more than two dozen substances have been isolated from the seeds of Bixa orellana. Besides bixin and norbixin, other compounds such as isobixin, beta-carotene, cryptoxanthin, lutein, zeaxanthin, orellin, bixein, bixol, crocetin, ishwarane, ellagic acid, salicylic acid, threonine, tomentosic acid, tryptophan, and phenylalanine have been found in the seeds of annatto. In addition, the following compounds, in their respective concentrations, are found in these seeds: 40 to 45% cellulose, 3.5 to 5.5% sugars, 0.3 to 0.9% essential oils, 3% fixed oils, 1.0 to 4.5% pigments, and 13 to 16 % proteins and alpha and beta-carotene, as well as tannins and saponins [63, 64].

Mercadante et al. [50, 65] isolated eight apocarotenoids from annatto seeds: methyl (7Z, 9Z, 9′Z)-apo-6′-lycopenoate, methyl (9Z)-apo-8′-lycopenoate, methyl 1(all-E)-apo-8′-lycopenoate, methyl (all-E)-8-apo-beta-carotene-8′-oate, methyl (all-E)-apo-6′-lycopenoate, 6-geranylgeranyl-8′- methyl-6,8′diapocaroten-6-8′dioate, 6′-geranylgeranyl-6′-methyl-(9Z)-6,6′-diapocaroten-6-6′-dioate, and 6-geranylgeranyl-6′-methyl-6-6′-diapocaroten-6-6′-dioate.

More than 100 volatile compounds have been detected in aqueous and organic extracts, where 50 of these have already been identified (e.g., bornyl acetate, -caryophyllene, copaene, -cubebene, (+)-cyclosativene, geranyl phenylacetate, 1-heptanetiol, 3-methylpyridine, 4-methylpyridine γ-elemene, β-humulene, isoledene, β-pinene, seline-6-en-4-ol, δ-selinene, (−)-spathulenol, and (+)-ylangene) [66].

Because annatto is a rich source of carotenoids it is of great commercial importance. In fact, the therapeutic properties of annatto (e.g., antioxidant and hypoglycemic) have been attributed to its high levels of carotenoids [6769]. Table 2 lists some of these compounds.

The pigments in annatto seeds can be extracted by mechanical processes through grinding the seeds and by physical-chemical methods using solvents or enzymes [46]. The solvent extraction can be performed using three basic methods: alkaline extraction (NaOH or KOH solutions), which results in the conversion of bixin to norbixin; extraction with oil (soybean, corn); and extraction using organic solvents (hexane, chloroform, ethanol, acetone, or propylene glycol), which results in the purest form of pigments.

Barbosa-Filho et al. [49] studied the seeds of four types of annatto cultivated in Paraíba State, Brazil, namely, “cascaverde” (“green peel”), “cascavermelha” (“red bark”), “bico de calango” (“lizard beak”), and “grãopreto”(“black grain”), with respect to their oil (material extracted with hexane) and solid (material extracted with chloroform) contents, and also pure bixin, which was obtained by successive recrystallization from the chloroform fraction. Pure bixin appears as red-purple crystals with a melting point of 196–198°C. The different concentrations found for the oil fraction, chloroform extract, and bixin are as follows: red bark 5.8%, lizard beak 5.1%, green peel 4.9%, and black grain 4.6%. Red bark shows the highest yield for both solvent fractions, and the bixin amount is around 1%. This species has been reported as the most used in folk medicine. On the other hand, black grain shows negligible amounts of bixin.

6. Biological Activity

Table 3 shows data found in 38 studies performed with annatto in 15 different countries in the American countries. To obtain the extracts and fractions tested, several plant parts were used, such as leaf, root, seed, shoot, and even the whole plant. The data surveyed were classified according to the pharmacological activity tested.

Table 3.

Biological activities of extracts of annatto in American countries.

Country
biological activity
Part used Type of extract Organism tested Model tested Dose
used
Activity References
Argentina
 Antibacterial LE EtOH Bacillus subtilis In vitro 5 mg/mL Inactive [70]
Escherichia coli In vitro 5 mg/mL Inactive [70]
Micrococcus luteus In vitro 5 mg/mL Inactive [70]
Pseudomonas aeruginosa In vitro 5 mg/mL Inactive [70]
Staphylococcus aureus In vitro 5 mg/mL Inactive [70]
 Antifungal LE EtOH Aspergillus niger In vitro 5 mg/mL Inactive [70]
Candida albicans In vitro 5 mg/mL Inactive [70]
 Antiviral SE EtOH Virus Herpes simplex 1 Cell culture 0.78 mg/mL Inactive [71]
 Insecticidal AP MeOH Insect Sitophilus oryzae 5% Inactive [71]
Brazil
 Antimalarial SE CHCl3 Mouse Plasmodium berghei 100 mg/kg Inactive [26]
 Antioxidant SE EtOH In vitro DPPH assay 0.1 g L−1 Active [6]
 Insect repellent SE Petr. eth Hamster Lutzomyia longipalpis 1 g/L Active [72]
SE EtOH Mosquito Aedes aegypti 18.2 mg/mL Active [6]
 Molluscicidal SE EtOH Conch Biomphalaria glabrata 10,000 ppm Inactive [73]
 Mutagenic Powder Mouse Bone marrow cells 10,670 ppm Inactive [67]
 Toxicity SE Powder Rat In vivo 500 mg/kg Inactive [74]
 Antileishmanial LE/RO EtOH Leishmania amazonensis In vitro 0,12–2,5 mg/mL Active [75]
 Antileishmanial SE OE Leishmania amazonensis In vitro 10/50/100/500/1000 μg/mL Active [76]
  Hyperlipidemia SE H2O Mouse In vitro 400 and 800 mg/kg Active [77]
Colombia
 Snakebite LE EtOH Mouse Bothrops atrox LD50 > 260 μg/animal Active [29]
Costa Rica
 Anti-inflammatory RO EtOH Rat Paw edema/carrageenan 100 mg/kg Inactive [78]
Cuba
 Positive inotropic effect AP H2O Guinea pig Isolated atrium 320 μL Inactive [79]
 Antimalarial SE Plasmodium gallinaceum/falciparum In vivo/in vitro 500 mg/kg Active [80]
 Cytotoxic SE EtOH Tumor cells In vitro 3,9–250 mg/mL Active [81]
Ecuador
 Antifungal LE MeOH Aspergillus niger In vitro 10 mg/disk Inactive [82]
Candida albicans In vitro 10 mg/disk Inactive [82]
Cryptococcus neoformans In vitro 10 mg/disk Inactive [82]
Fusarium oxysporum In vitro 10 mg/disk Inactive [82]
Neurospora crassa In vitro 10 mg/disk Inactive [82]
Penicillium purpurogenum In vitro 10 mg/disk Inactive [82]
Trichophyton mentagrophytes In vitro 10 mg/disk Active [82]
Guatemala
 Antibacterial LE Various Escherichia coli In vitro 50 μL/disk Inactive [83]
Pseudomonas aeruginosa In vitro MIC > 10 mg/mL Inactive [83]
Salmonella typhi In vitro MIC > 10 mg/mL Inactive [83]
Shigella dysenteriae In vitro 50 μL Inactive [83]
Staphylococcus aureus In vitro MIC > 10 mg/mL Inactive [83]
 Antifungal LE H2O Aspergillus flavus In vitro MIC > 10 mg/mL Inactive [84]
Candida albicans In vitro MIC > 10 mg/mL Inactive [84]
Microsporum gypseum In vitro MIC > 10 mg/mL Inactive [84]
 Antigonorrheal LE EtOH Neisseria gonorrhea In vitro 50 μL/disk Active [32]
 Antitrypanosomal LE EtOH Trypanosoma cruzi In vitro MIC > 1 mg/mL Inactive [83]
 Cytotoxic LE H2O Crustacean Artemia salina LC50 > 1,000 ppm Inactive [83]
 Inhib. of platelet aggregation SE / In vitro Thrombin aggregation IC50 0.795 mg/mL Inactive [35]
Hawaii
 Contraceptive RO / Mouse / 0.2 mL/animal Inactive [85]
Jamaica
 Hypoglycemic SE CHCl3 Dog 1 g Active [39]
H2O Dog 200 mL/animal Active [39]
 Antioxidant SE EtOH In vitro In vitro 0.25 and 2.5 μg/mL Active [86]
Mexico
 Allergenic SE Oil Human 25 μL/ person Active [87]
Paraguay
 Insecticidal SE Petr. ether Insect Rhodnius neglectus 50 μg Inactive [42]
Puerto Rico
 Molluscicidal TP H2O Conch Lymnaea cubensis LD100 > 1 M ppm Inactive [88]
Dominican Republic
 Cytotoxic SE EtOH Cell culture Molt 4 cells 200 μg/mL Inactive [89]
Trinidad and Tobago
 Antibacterial SE EtOAc Escherichia coli In vitro 1,000 μg/mL Inactive [90]
Pseudomonas aeruginosa In vitro 1,000 μg/mL Inactive [90]
USA
 Anticonvulsant RA EtOH Mouse Seizures/electroshock 100 mg/kg Inactive [91]
Rat Seizures/pentylenetetrazole 400 mg/kg Inactive [91]
 Antimalarial SE CHCl3 Chicken Plasmodium gallinaceum 388 mg/kg Inactive [92]
 Mutagenic SE MeOH Salmonella typhimurium 100 mg/plaque Inactive [93]
H2O In vitro Placental trophoblasts 100 mg/plaque Inactive [93]
 Hypotensive RA EtOH Rat 50 mg/kg Active [93]
 Toxicity RA H2O Mouse LD50 > 700 mg/kg Inactive [92]

LE: leaf; AP: aerial part; TP: total plant; RO: root; SE: seed; /: not given; LD50: 50% lethal dose; IC50: concentration that inhibits 50% of the effect; MIC: minimum inhibitory concentration.

Among the twenty-one activities tested, those with the largest number of studies performed were antifungal activity (12), antibacterial activity (12), antimalarial activity (6), and mutagenic activity (3). Cytotoxic activity and toxicity have been little studied, with three and two studies, respectively. Pharmacological activities have been evaluated in animal models (22 preclinical studies), human models (1 clinical study), cell cultures (2 studies), and in vitro tests (32 studies).

Antifungal activity has been investigated in one country in Central America (Guatemala) and in two countries in South America (Ecuador and Argentina) using eleven different fungal strains [70, 82, 84].

Freixa et al. [82] conducted a study in Ecuador to assess the antifungal activity of extracts from the dried leaves of the annatto tree in response to 7 fungi species, obtaining satisfactory antifungal activity against Trichophyton mentagrophytes trains. In Guatemala, three different strains were used to evaluate antifungal activity, with no satisfactory activity being observed [84].

The extracts of annatto leaves have been evaluated for antibacterial activity against 8 different bacterial strains (Bacillus subtilis, Escherichia coli, Micrococcus luteus, Pseudomonas aeruginosa, Staphylococcus aureus, Salmonella typhi, Shigella dysenteriae, and Staphylococcus epidermidis), showing no activity.

Antimalarial activity has been determined against Plasmodium gallinaceum, Plasmodium lophurae, and Plasmodium berghei. Although the studies conducted previously in the United States did not show significant results [92], Valdés et al. (2011) reported a moderate activity of the seed extracts of Bixa orellana against Plasmodium berghei and falciparum.

7. Mutagenic and Cytotoxic Activities

No significant effect was observed when extracts of annatto seeds were tested for mutagenic activity in studies performed in the United States and Brazil [67, 93].

Extracts obtained from annatto seeds and leaves have been tested in cell cultures and the brine shrimp assay, respectively, and have been found to lack cytotoxicity in either model used. These experiments were carried out in Guatemala and the Dominican Republic [83, 89].

On the other hand, a study performed in Cuba with 10 medicinal plants that were active in inhibiting human lung carcinoma cell growth showed that the ethanolic extract of Bixa orellana presented cytotoxicity at concentrations below 100 μg/mL [81].

8. Toxicological Activities

Currently, concerns about the effect of synthetic dyes on human health are incontestable, making people increasingly choose those of natural origin, believing that they are devoid of toxic effects. This is not entirely true, because even a medication from a natural source can be a poison, depending on the dose that is administered. The failure to require in-depth data related to toxicological and chemical analyses for the registration of food additives derived from natural sources [67, 74] certainly makes the information about possible unwanted effects and/or pharmacological activities resulting from their use, much rarer than expected in view of the importance of the topic. In Brazil, the use of annatto is so widespread that its safety is not even questioned.

Paumgartten et al. [91] evaluated the toxicity of annatto extracts in rats. Doses up to 500 mg/kg body weight/day were introduced directly into the stomach of pregnant rats to evaluate the effect on the mother and fetus, and no adverse effects were found for either. The annatto extract did not induce an increase in the incidence of visible external, visceral, or skeletal anomalies in the fetuses. Therefore, the study suggested that the annatto extract was not toxic to rats nor was it embryotoxic. Studies performed in Brazil by Alves de Lima et al. [67], where extracts of annatto were mixed with the food of male rats, showed that the concentrations tested had no mutagenic or antimutagenic activity in their bone marrow cells. A parallel toxicity study conducted by Hagiwara et al. [74] showed that 0.1% annatto extract administered for thirteen weeks in the feed of male and female rats did not show any adverse effects. However, when higher doses were administered (0.3 and 0.9%), the authors noticed an increase in liver weight as well as changes in blood chemistries, including increase in alkaline phosphatase, phospholipids, and total protein, as well as albumin and albumin/globulin ratio.

Hagiwara et al. [74] also evaluated extracts of annatto for liver carcinogenicity in rats and found no evidence of liver tumors, even when given to animals at a high dose of 200 mg/kg body weight/day, compared to an acceptable dose of 0.0 to 0.065 mg/kg/day, thus indicating that the danger of a hepatocarcinogenic effect in humans may be absent or negligible.

A toxicity test was performed with extracts obtained from both plant seeds and shoots, and no significant effect was observed. The experiments were performed in the United States using mice as the animal model and it was found that the LD50 was greater than 700 mg/kg [92].

9. Correlation between the Biological Activities, Phytochemistry, and the Traditional Uses of Bixa orellana

Table 1 shows that many of the traditional uses of Bixa orellana are the same in several countries of South and Central America, which suggests its effectiveness as a therapeutic agent. Extracts of Bixa orellana showed biological activities such as antioxidant, hypotensive, molluscicide, and antimalarial against A549 cells for carcinoma of the lung, allergy, hypoglycemic, antifungal, antioxidant, insect repellent, antigonococcal, and antivenom serum and some of them are in accordance with the traditional use; for example, in Brazil it is used to extract the seeds with purpose repellent insecticide and antimalaria and scientific studies in the same country with the Lutzomyia longipalpis insect repellent action and prove a study in Cuba proved the pharmacological action for antimalarial activity when tested against Plasmodium berghei. Some of them are in accordance with the traditional use; for example, seed extracts have been used in Brazil and Cuba as insect repellent and antimalarial. Antioxidant and insect repellent activities can be attributed to the carotenoids and the essential and fixed oils, respectively.

Despite the previous reports about the presence of components with anti-inflammatory properties, such as salicylic acid, lutein, polyphenols, and tannins, this activity has not yet been proven for Bixa orellana extracts. Similarly, the plant's essential and fixed oils have shown antibacterial properties, although this activity has not been proven too.

In general, the data obtained in this review do not allow correlations between the biologic activities tested in vitro or in vivo with the compounds identified in this species. However, taking into account the related activities such as the antiparasitic effect and the lack of mutagenic and cytotoxicity activity, it is possible to consider Bixa orellana as a potential source for the development of phytopharmaceutical products.

In conclusion, the studies discussed in this review represent a rich database around the Bixa orellana activities and its potential uses, which evokes the feasibility of phytopharmaceuticals to treat some diseases whenever an antioxidant, hypotensor, or hypoglycemiant activity is necessary.

Although the commercial exploitation of this species is well established, there are very few studies on its pharmacological effects. Considering the need for developing a safe and effective product, more studies should be performed in order to confirm other biological activities supported by the popular uses of Bixa orellana.

Acknowledgments

The authors are grateful to CNPq/PRONEX/FAPESQ and CAPES for financial support and to the NAPRALERT Database of the University of Illinois, USA, for the literature on Bixa orellana. A. Leyva helped in editing the English language of the paper.

Conflict of Interests

The authors declare that they have no conflict of interests.

References

  • 1.Perecin MB, Bovi OA, Maia NB. Pesquisa com plantas aromáticas, medicinais corantes: o papel do Instituto Agronômico. O Agronômico. 2002;54:21–24. [Google Scholar]
  • 2.Elias MEA, Schroth G, Macêdo JLV, Mota MSS, D'Angelo SA. Mineral nutrition, growth and yields of annatto trees (Bixa orellana) in agroforestry on an Amazonian Ferralsol. Experimental Agriculture. 2002;38(3):277–289. [Google Scholar]
  • 3.Bastos ARR, Carvalho JG, Assis RP, Filho ABC. Marcha de absorção de nutrientes em urucum ( Bixa orellana L.) tipo cultivado piave vermelha em fase de viveiro. Cerne. 1999;5:76–85. [Google Scholar]
  • 4.Thomas EP, Colvin M, Rosen SB, Zuccarini C, Petzer S. Buffalo, NY, USA: Medical Research Council; 2005. HIV prevalence study and costing analysis undertaken for the development of an HIV/AIDS workplace strategy for buffalo city municipality. [Google Scholar]
  • 5.Franco CF. O Agronegócio do urucum na região Nordeste. 1 Reunião Nacional da Cadeia Produtiva de Urucum, CD-Rom, 2007.
  • 6.Giorgi A, De Marinis P, Granelli G, Chiesa LM, Panseri S. Secondary metabolite profile, antioxidant capacity, and mosquito repellent activity of Bixa orellana from Brazilian Amazon region. Journal of Chemistry. 2013;2013:10 pages.409826 [Google Scholar]
  • 7.Silva JS, Moura MD, Oliveira RAG, Diniz MFF, Barbosa-Filho JM. Natural product inhibitors of ovarian neoplasia. Phytomedicine. 2003;10(2-3):221–232. doi: 10.1078/094471103321659988. [DOI] [PubMed] [Google Scholar]
  • 8.Sousa FCF, Melo CTV, Citó COM, et al. Plantas medicinais e seus constituintes bioativos: uma revisão da bioatividade e potenciais benefícios nos distúrbios da ansiedade em modelos animais. Revista Brasileira de Farmacognosia. 2008;18:642–654. [Google Scholar]
  • 9.Quintans LJ, Jr., Almeida JRGS, Lima JT, et al. Plants with anticonvulsant properties—a review. Revista Brasileira de Farmacognosia. 2008;18:798–819. [Google Scholar]
  • 10.Falcão HDS, Leite JA, Barbosa-Filho JM, et al. Gastric and duodenal antiulcer activity of alkaloids: a review. Molecules. 2008;13(12):3198–3223. doi: 10.3390/molecules13123198. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Falcão HS, Mariath IR, Diniz MFFM, Batista LM, Barbosa-Filho JM. Plants of the American continent with antiulcer activity. Phytomedicine. 2008;15(1-2):132–146. doi: 10.1016/j.phymed.2007.07.057. [DOI] [PubMed] [Google Scholar]
  • 12.Mariath IR, Falcão HDS, Barbosa-Filho JM, et al. Plants of the American continent with antimalarial activity. Revista Brasileira de Farmacognosia. 2009;19(1):158–192. [Google Scholar]
  • 13.Hon JER, Soares PM, Melo CL, et al. Atividade farmacológica da monocrotalina isolada de plantas do gênero Crotalaria . Revista Brasileira de Farmacognosia. 2010;20:453–458. [Google Scholar]
  • 14.Almeida RN, Navarro DS, Barbosa-Filho JM. Plants with central analgesic activity. Phytomedicine. 2001;8(4):310–322. doi: 10.1078/0944-7113-00050. [DOI] [PubMed] [Google Scholar]
  • 15.Jesus NZT, Falcão HS, Gomes IF, et al. Tannins, peptic ulcers and related mechanisms. International Journal of Molecular Sciences. 2012;13(3):3203–3228. doi: 10.3390/ijms13033203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Rocha LG, Almeida JRGS, Macêdo RO, Barbosa-Filho JM. A review of natural products with antileishmanial activity. Phytomedicine. 2005;12(6-7):514–535. doi: 10.1016/j.phymed.2003.10.006. [DOI] [PubMed] [Google Scholar]
  • 17.Lima GRM, Montenegro CA, Almeida CLF, Athayde-Filho PF, Barbosa-Filho JM, Batista LM. Database survey of anti-inflammatory plants in South America: a review. International Journal of Molecular Sciences. 2011;12(4):2692–2749. doi: 10.3390/ijms12042692. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.De Lira Mota KS, Dias GEN, Pinto MEF, et al. Flavonoids with gastroprotective activity. Molecules. 2009;14(3):979–1012. doi: 10.3390/molecules14030979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Souto AL, Tavares JF, da Silva MS, de Diniz MFFM, de Athayde-Filho PF, Barbosa Filho JM. Anti-inflammatory activity of alkaloids: an update from 2000 to 2010. Molecules. 2011;16(10):8515–8534. doi: 10.3390/molecules16108515. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Silva FL, Fischer DCH, Tavares JF, Silva MS, de Athayde-Filho PF, Barbosa-Filho JM. Compilation of secondary metabolites from Bidens pilosa L. Molecules. 2011;16(2):1070–1102. doi: 10.3390/molecules16021070. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Filho JR, de Sousa Falcão H, Batista LM, Filho JMB, Piuvezam MR. Effects of plant extracts on HIV-1 protease. Current HIV Research. 2010;8(7):531–544. doi: 10.2174/157016210793499204. [DOI] [PubMed] [Google Scholar]
  • 22.Barbosa-Filho JM, Alencar AA, Nunes XP, et al. Sources of alpha-, beta-, gamma-, delta- and epsilon-carotenes: a twentieth century review. Revista Brasileirta de Farmacogn. 2008;18(1):135–154. [Google Scholar]
  • 23.Silva SNS, Amaral CLF, Rebouças TNH. Adoption of conservation practices on farm and selection of varieties by producers of annatto in the city of Vitoria da Conquista-BA. Revista Brasileira de Agroecologica. 2010;5:106–113. [Google Scholar]
  • 24.Bandoni AL, Mendiondo ME, Rondina RVD, Coussio JD. Survey of Argentine medicinal plants. I. Folklore and phytochemical screening. Lloydia. 1972;35(1–4):69–80. [PubMed] [Google Scholar]
  • 25.Garcia GH, Campos R, de Torres RA, et al. Antiherpetic activity of some Argentine medicinal plants. Fitoterapia. 1990;61(6):542–546. [Google Scholar]
  • 26.Brandao MGL, Grandi TSM, Rocha EMM, Sawyer DR, Krettli AU. Survey of medicinal plants used as antimalarials in the Amazon. Journal of Ethnopharmacology. 1992;36(2):175–182. doi: 10.1016/0378-8741(92)90018-m. [DOI] [PubMed] [Google Scholar]
  • 27.Corrêa MP. Dicionário das Plantas Úteis do Brasil e das Exóticas Cultivadas. Vol. 4. Rio de Janeiro, Brasil: Ministério da Agricultura/IBDF; 1978. [Google Scholar]
  • 28.Hirschmann GS, de Arias AR. A survey of medicinal plants of minas gerais, Brazil. Journal of Ethnopharmacology. 1990;29(2):159–172. doi: 10.1016/0378-8741(90)90052-u. [DOI] [PubMed] [Google Scholar]
  • 29.Otero R, Fonnegra R, Jiménez SL, et al. Snakebites and ethnobotany in the northwest region of Colombia. Part I: traditional use of plants. Journal of Ethnopharmacology. 2000;71(3):493–504. doi: 10.1016/s0378-8741(00)00243-9. [DOI] [PubMed] [Google Scholar]
  • 30.Garcia-Barriga H. Flora Medicinal de Colombia. Vol. 2. Bogota, Colombia: Universidad Nacional; 1975. [Google Scholar]
  • 31.Roig y Mesa JT. Plantas Medicinales, Aromaticas o Venenosas de Cuba. Havana, Cuba: Ministério de Agricultura; 1945. [Google Scholar]
  • 32.Cáceres A, Menéndez H, Méndez E, et al. Antigonorrhoeal activity of plants used in Guatemala for the treatment of sexually transmitted diseases. Journal of Ethnopharmacology. 1995;48(2):85–88. doi: 10.1016/0378-8741(95)01288-o. [DOI] [PubMed] [Google Scholar]
  • 33.Duke JA, Martinez RV. Amazonian Ethnobotanical Dictionary. Boca Raton, Fla, USA: CRC Press; 1994. [Google Scholar]
  • 34.Ramirez VR, Mostacero LJ, Garcia AE, et al. Vegetales Empleados en Medicina Tradicional Norperuana. Trujillo, Peru: Banco Agrario del Peru, Universidad Nacional de Trujillo; 1988. [Google Scholar]
  • 35.Villar R, Calleja JM, Morales C, Caceres A. Screening of 17 Guatemalan medicinal plants for platelet antiaggregant activity. Phytotherapy Research. 1997;11:441–445. [Google Scholar]
  • 36.Giron LM, Freire V, Alonzo A, Caceres A. Ethnobotanical survey of the medicinal flora used by the Caribs of Guatemala. Journal of Ethnopharmacology. 1991;34(2-3):173–187. doi: 10.1016/0378-8741(91)90035-c. [DOI] [PubMed] [Google Scholar]
  • 37.Lentz DL. Medicinal and other economic plants of the Paya of Honduras. Economic Botany. 1993;47(4):358–370. [Google Scholar]
  • 38.Lentz DL, Clark AM, Hufford CD, et al. Antimicrobial properties of Honduran medicinal plants. Journal of Ethnopharmacology. 1998;63(3):253–263. doi: 10.1016/s0378-8741(98)00100-7. [DOI] [PubMed] [Google Scholar]
  • 39.Morrison EY, West ME. The effect of Bixa orellana (Annatto) on blood sugar levels in the anaesthetized dog. West Indian Medical Journal. 1985;34(1):38–42. [PubMed] [Google Scholar]
  • 40.Coe FG, Anderson GJ. Screening of medicinal plants used by the Garífuna of eastern Nicaragua for bioactive compounds. Journal of Ethnopharmacology. 1996;53(1):29–50. doi: 10.1016/0378-8741(96)01424-9. [DOI] [PubMed] [Google Scholar]
  • 41.Barrett B. Medicinal plants of Nicaragua's Atlantic Coast. Economic Botany. 1994;48(1):8–20. [Google Scholar]
  • 42.Schmeda-Hirschmann G, de Arias AR. A screening method for natural products on triatomine bugs. Phytotherapy Research. 1992;6(2):68–73. [Google Scholar]
  • 43.Simpson GE. Folk medicine in Trinidad. The Journal of American Folklore. 1962;75(298):326–340. [Google Scholar]
  • 44.Mahabir D, Gulliford MC. Use of medicinal plants for diabetes in Trinidad and Tobago. Revista Panamericana de Salud Publica. 1997;1(3):174–179. doi: 10.1590/s1020-49891997000300002. [DOI] [PubMed] [Google Scholar]
  • 45.Ayensu ES. Medicinal plants of the West Indies. Unpublished Manuscript, 1978. [Google Scholar]
  • 46.Mercadante AZ, Steck A, Rodriguez-Amaya D, Pfander H, Britton G. Isolation of methyl 9′Z-APO-6′-lycopenoate from Bixa Orellana . Phytochemistry. 1996;41(4):1201–1203. [Google Scholar]
  • 47.Angelucci E, Arima HK, Kumagai EA, Annatto I. Preliminary data of the chemical composition. Coletanea do Instituto de Tecnologia de Alimentos. 1980;11:89–96. [Google Scholar]
  • 48.Tirimanna ASL. Study of the carotenoid pigments of Bixa orellana L. Seeds by thin layer chromatography. Mikrochimica Acta. 1981;76(1-2):11–16. [Google Scholar]
  • 49.Barbosa-Filho JM, Silva-Filho RN, Lira BF, et al. Teor de bixina em quatro variedades de Bixa orellana L. cultivadas na Paraíba. Revista Brasileira de Farmacognosia. 1998;7-8:41–47. [Google Scholar]
  • 50.Mercadante AZ, Steck A, Pfander H. Isolation and structure elucidation of minor carotenoids from annatto (Bixa orellana L.) seeds. Phytochemistry. 1997;46(8):1379–1383. [Google Scholar]
  • 51.Prentice-Hernandez C, Rusig O. Annatto (Bixa orellana L.) extract obtained using ethyl alcohol as a solvent. Arquivos de Biologia e Tecnologia. 1992;35:63–74. [Google Scholar]
  • 52.Mercadante AZ. Composition of carotenoids from annatto. ACS Symposium Series. 2001;775:92–101. [Google Scholar]
  • 53.Scotter MJ, Wilson LA, Appleton GP, 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. Journal of Agricultural and Food Chemistry. 1998;46(3):1031–1038. doi: 10.1021/jf9901845. [DOI] [PubMed] [Google Scholar]
  • 54.Degnan AJ, von Elbe JH, Hartel RW. Extraction of annatto seed pigment by supercritical carbon dioxide. Journal of Food Science. 1991;56:1655–1659. [Google Scholar]
  • 55.Mercadante AZ, Steck A, Pfander H. Isolation and identification of new apocarotenoids from annatto (Bixa orellana) seeds. Journal of Agricultural and Food Chemistry. 1997;45(4):1050–1054. [Google Scholar]
  • 56.Anderson SG, Nair MG, Chandra A, Morrison E. Supercritical fluid carbon dioxide extraction of annatto seeds and quantification of trans-bixin by high pressure liquid chromatography. Phytochemical Analysis. 1997;8:247–249. [Google Scholar]
  • 57.Barbosa-Filho JM. Bixa orellana: Retrospectiva de usos populares, atividades biológicas, fitoquímica e emprego na fitocosmética, no continente americano. João Pessoa, Brazil: Simpósio Brasileiro do Urucum—SIMBRAU; 2006. [Google Scholar]
  • 58.Revilla J. Plantas da Amazônia: Oportunidades Econômicas e Sustentáveis. 2nd edition. Manaus: Programa de Desenvolvimento Empresarial e Tecnológico; 2001. [Google Scholar]
  • 59.Oliveira F, Akisue G, Akisue MK. Farmacognosia. São Paulo, Brazil: Atheneu; 1996. [Google Scholar]
  • 60.Alonso J. Tratado de Fitofármacos y Nutracêuticos. Rosário, Argentina: Corpus; 2004. [Google Scholar]
  • 61.Franco CO, Fabri EG, Barreiro Neto M, Manfiolli MH, Harder MNC, Rucker NC. Urucum: Sistema de Produção para o Brasil. João Pessoa, Brazil: Emepa-Pb, Apta; 2008. [Google Scholar]
  • 62.Venugopalan PA, Giridhar GA, Ravishankar AG. Food, Ethanobotanical and diversified applications of Bixa orellana L.: a scope for its improvement through biotechnological mediation. Indian Journal of Fundamental and Applied Life Sciences. 2011;1:9–31. [Google Scholar]
  • 63.Taylor L. Herbal Secrets of the Rainforest. 2nd edition. Rocklin, Calif, USA: Sage Press; 2002. [Google Scholar]
  • 64.Oliveira JS. Caracterização, Extração e Purificação por Cromatografia de Compostos de Urucum (Bixa orellana L.) [tesis doctoral en Ingeniería Químic] Florianópolis, Brazil: Universidade Federal de Santa Catarina; 2005. [Google Scholar]
  • 65.Mercadante AZ, Steck A, Pfander H. Three minor carotenoids from annatto (Bixa orellana) seeds. Phytochemistry. 1999;52(1):135–139. [Google Scholar]
  • 66.Galindo-Cuspinera V, Lubran MB, Rankin SA. Comparison of volatile compounds in water- and oil-soluble annatto (Bixa orellana L.) extracts. Journal of Agricultural and Food Chemistry. 2002;50(7):2010–2015. doi: 10.1021/jf011325h. [DOI] [PubMed] [Google Scholar]
  • 67.Alves de Lima RO, Azevedo L, Ribeiro LR, Salvadori DMF. Study on the mutagenicity and antimutagenicity of a natural food colour (annatto) in mouse bone marrow cells. Food and Chemical Toxicology. 2003;41(2):189–192. doi: 10.1016/s0278-6915(02)00208-9. [DOI] [PubMed] [Google Scholar]
  • 68.Lima LRP, Oliveira TT, Nagem TJ, et al. Bixina, norbixina e quercetina e seus efeitos no metabolismo lipídico de coelhos. Brazilian Journal of Veterinary Research and Animal Science. 2001;38:196–200. [Google Scholar]
  • 69.Fontana JD, Mendes SV, Persike DS, Peracetta LF, Passos M. Carotenóides: cores atraentes e ação biológica. Biotecnologia Ciência & Desenvolvimento. 2000;2:p. 13. [Google Scholar]
  • 70.Penna CA, Radice M, Gutkind GO, et al. Antibacterial and antifungal activities of some Argentinean plants. Fitoterapia. 1994;65(2):172–174. [Google Scholar]
  • 71.Broussalis AM, Ferraro GE, Martino VS, Pinzón R, Coussio JD, Alvarez JC. Argentine plants as potential source of insecticidal compounds. Journal of Ethnopharmacology. 1999;67(2):219–223. doi: 10.1016/s0378-8741(98)00216-5. [DOI] [PubMed] [Google Scholar]
  • 72.Rojas de Arias A, Schmeda-Hirschmann G, Falcao A. Feeding deterrency and insecticidal effects of plant extracts on Lutzomyia longipalpis. Phytotherapy Research. 1992;6(2):64–67. [Google Scholar]
  • 73.Pinheiro MS, Rouquayrol MZ. Molluscicidal activity of plants from Northeast Brazil. Revista Brasileira de Pesquisas Médicas e Biológicas. 1974;7:389–394. [PubMed] [Google Scholar]
  • 74.Hagiwara A, Imai N, Ichihara T, et al. A thirteen-week oral toxicity study of annatto extract (norbixin), a natural food color extracted from the seed coat of annatto (Bixa orellana L.), in Sprague-Dawley rats. Food and Chemical Toxicology. 2003;41(8):1157–1164. doi: 10.1016/s0278-6915(03)00104-2. [DOI] [PubMed] [Google Scholar]
  • 75.Almeida CR, Silva RB, Marques MJ, Chavasco JK. Evaluation of antiparasitic activity of hydroethanolic extracts from root, stem and leaf of Bixa orellana L. on Leishmania amazonensis samples. Revista da Universidade Vale do Rio Verde. 2012;10(2):384–391. [Google Scholar]
  • 76.Lopes MV, Desoti VC, Caleare ADO, Ueda-Nakamura T, Silva SO, Nakamura CV. Mitochondria superoxide anion production contributes to geranylgeraniol-induced death in leishmania amazonensis. Evidence-Based Complementary and Alternative Medicine. 2012;2012:9 pages. doi: 10.1155/2012/298320.298320 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Ferreira JM, Sousa DF, Dantas MB, et al. Effects of Bixa orellana L. seeds on hyperlipidemia. Phytotherapy Research. 2013;27(1):144–147. doi: 10.1002/ptr.4675. [DOI] [PubMed] [Google Scholar]
  • 78.Benoit PS, Fong HHS, Svoboda GH, Farnsworth NR. Biological and phytochemical evaluation of plants. XIV. Antiinflammatory evaluation of 163 species of plants. Lloydia. 1976;39(2-3):160–171. [PubMed] [Google Scholar]
  • 79.Carabajal D, Casaco A, Arruzazabala L, Gonzalez R, Fuentes V. Pharmacological screening of plant decoctions commonly used in Cuban folk medicine. Journal of Ethnopharmacology. 1991;33(1-2):21–24. doi: 10.1016/0378-8741(91)90155-7. [DOI] [PubMed] [Google Scholar]
  • 80.Valdés AFC, Martínez JM, Rodríguez DA, Lizama RS, Gaitén YG. Actividad antimalárica de un extracto hidroalcohólico de Bixa orellanaL. Revista Cubana de Medicina Tropical. 2011;63:181–185. [PubMed] [Google Scholar]
  • 81.García AD, Sánchez HR, Lizama RS. Citotoxicidad de extractos de plantas medicinales sobre la línea celular de carcinoma de pulmón humano A549. Revista Cubana de Farmácia. 2011;45:101–108. [Google Scholar]
  • 82.Freixa B, Vila R, Vargas L, Lozano N, Adzet T, Canigueral S. Screening for antifungal activity of nineteen Latin American plants. Phytotherapy Research. 1998;12(6):427–430. [Google Scholar]
  • 83.Cáceres A, López B, González 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. Journal of Ethnopharmacology. 1998;62(3):195–202. doi: 10.1016/s0378-8741(98)00140-8. [DOI] [PubMed] [Google Scholar]
  • 84.Caceres A, Cano O, Samayoa B, Aguilar L. Plants used in Guatemala for the treatment of gastrointestinal disorders. 1. Screening of 84 plants against enterobacteria. Journal of Ethnopharmacology. 1990;30(1):55–73. doi: 10.1016/0378-8741(90)90017-n. [DOI] [PubMed] [Google Scholar]
  • 85.Matsui AS, Hoskin S, Kashiwagi M, et al. A survey of natural products from Hawaii and other areas of the Pacific for an antifertility effect in mice. Internationale Zeitschrift fur Klinische Pharmakologie, Therapie, und Toxikologie. 1971;5(1):65–69. [PubMed] [Google Scholar]
  • 86.Abayomi M, Adebayo AS, Bennett D, Porter R, Campbell JS. In vitro antioxidant activity of Bixa orellana (Annatto) seed extract. Journal of Applied Pharmaceutical Science. 2014;4(2):101–106. [Google Scholar]
  • 87.Dunham NW, Allard KR. A preliminary pharmacologic investigation of the roots of Bixa orellana . Journal of the American Pharmacist Associantion. 1960;49:218–219. [PubMed] [Google Scholar]
  • 88.Medina FR, Woodbury R. Terrestrial plants molluscicidal to lymnaeid hosts of Fasciliasis hepatica in Puerto Rico. Journal of Agricultura of the University of Puerto Rico. 1979;63:366–376. [Google Scholar]
  • 89.Weniger B, Jiang Y, Oulad-Ali A, Italiano L, Beck JP, Anton R. Biological effects of bixin and Bixa orellana extracts on lymphoid cells in culture. Planta Medica. 1993;59(7, article A680) [Google Scholar]
  • 90.Chariandy CM, Seaforth CE, Phelps RH, Pollard GV, Khambay BPS. Screening of medicinal plants from Trinidad and Tobago for antimicrobial and insecticidal properties. Journal of Ethnopharmacology. 1999;64(3):265–270. doi: 10.1016/s0378-8741(98)00130-5. [DOI] [PubMed] [Google Scholar]
  • 91.Paumgartten FJR, Carvalho RR, Araújo IB, et al. Evaluation of the developmental toxicity of annatto in the rat. Food and Chemical Toxicology. 2002;40(11):1595–1601. doi: 10.1016/s0278-6915(02)00133-3. [DOI] [PubMed] [Google Scholar]
  • 92.Spencer CF, Koniuszy FR, Rogers EF, et al. Survey of plants for antimalarial activity. Lloydia. 1947;10(3):145–174. [Google Scholar]
  • 93.Mikkelsen H, Larsen JC, Tarding F. Hypersensitivity reactions to food colours with special reference to the natural colour annatto extract (butter colour) Toxicological Aspects of Food Safety. 1978;1:141–143. doi: 10.1007/978-3-642-66896-8_16. [DOI] [PubMed] [Google Scholar]

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