Journal of Antioxidant Activity

Journal of Antioxidant Activity

Journal of Antioxidant Activity

Current Issue Volume No: 1 Issue No: 4

Research Article Open Access Available online freely Peer Reviewed Citation

Antioxidant Properties of Red and Yellow Varieties of Cashew Apple, Nut and Husk (AnacardiumOccidentaleL.) Harvested in Mexico

1Escuela Nacional de Ciencias Biológicas-Instituto Politecnico Nacional. Department of Biophysics

2Escuela Nacional de Ciencias Biológicas-Instituto Politecnico Nacional Department of Biochemical Engineering.


Numerous studies have reported the health benefits of consuming fruits and vegetables that contain antioxidant properties. Within the group of fruits considered exotic, some are accessible and only consumed in their place of origin, such as soursop, noni, kiwi, pitahaya, and others. Anacardiumoccidentale, cashew, is a crop native to the Brazilian northeast that has excellent medicinal and nutritional properties. Because few studies have characterized cashew produced in Mexico, in the present work, the physicochemical properties and antioxidant capacity of cashew apple (red and yellow varieties) and its nut were studied. The content of total phenolic compounds and the antioxidant capacity were higher in the nut (174.19±20.98 GAE mg/100 g db) while cashew red pulp showed a superior value of the phenol content (159.75±12.91 GAE mg/100 g db) to that of yellow cashew pulp (151.9±5.23 GAE mg/100 g db). A high value was obtained for the TPC of the husk of cashew nut (74.30 mg GAE/g) compared with those of the kernel and false fruit. Red cashew presented a higher antioxidant capacity at 77.65 μmol Trolox/g and was superior to that of the kernel (38.52±2.9 μmol Trolox/g). Because cashew apple is usually discarded, a marmalade based on the pulp is proposed as an alternative for its conservation because it has a high content of phenolic compounds that is conserved for six weeks of shelf life.

Author Contributions
Received 29 Mar 2019; Accepted 30 May 2019; Published 05 Jun 2019;

Academic Editor: Vijay Bharti, DIHAR, DRDO, Ministry of Defence, Pin-901205, India.

Checked for plagiarism: Yes

Review by: Single-blind

Copyright ©  2019 Figueroa-Valencia M, et al.

Creative Commons License     This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Competing interests

The authors have declared that no competing interests exist.


Figueroa-Valencia M, Rosales-Martinez P, Santoyo-Tepole F, Ramos-Monroy O.A, García-Ochoa F et al. (2019) Antioxidant Properties of Red and Yellow Varieties of Cashew Apple, Nut and Husk (AnacardiumOccidentaleL.) Harvested in Mexico. Journal of Antioxidant Activity - 1(4):19-32.

Download as RIS, BibTeX, Text (Include abstract )

DOI 10.14302/issn.2471-2140.jaa-19-2747


In recent years, the natural antioxidants present in fruits and vegetables have been the objectives of several pharmaceutical studies and the relationship between the natural product consumption and reduction of the risk of oxidative-stress-induced diseaseswas established1. It has been reported that phenolic compounds have excellent antioxidant activity, acting as hydrogen donors, reducers and eliminator agents of free radicals2. They also have an adequate chemical structure for their antioxidant action, attracting free radicals and neutralizing dangerous reactive species of oxygen and metallic and chelator ions3. Because of their high reactivity, they are found in almost all cases combined with an organic acid, a sugar or even a polymer4. Thus, the United Nations Organization for Food, Agriculture/World Health Organization (FAO/OMS) recommends adequate balanced feeding, including fruits and vegetables, in general5, because they contain vitamins, essential micronutrients, fiber, vegetable proteins, and chemical compounds, as well as bioactive content that helps human metabolism to prevent diseases6.

Antioxidant compounds play a very important role in the control of numerous types of diseases related to oxidative stress. The use of some plant extracts with antioxidant properties has been reported, for example Zataria multiflora ethanolic extracts protects lung tissues from Cyclophosphamide-Induced(CP-induced) toxicity and suggest a role for oxidative stress in the pathogenesis of lung toxicity produced by CP in mice7. Another study also showed that Zatariaproduces a potent hepatoprotective role and could be a potent candidate to use concomitantly as a supplement agent against hepatotoxicity of CP for the patients undergoing chemotherapy8. Origanum vulgare ethanolic extract exerts a potent genoprotective effect against CP-induced genotoxicity in mice bone marrow, which might be possibly due to the scavenging of free radicals during oxidative stress conditions9. Hesperidin is a flavonone glycoside, belonging to the flavonoid family, which is widely found in Citrus species and acts as a potent antioxidant and anticancer agent because of the protection roles against oxidative stress10.

The cashew apple and their diverse biological activities have been described, as their potent antibacterial activity against Gram-positive bacteria11, moderate cytotoxic activity against several tumor cell lines12, and tyrosinase13, lipoxygenase14 and others inhibitory activities. These studies have evidence that antioxidants play an important role in reducing the risk of cancer15.

Other study reports the evaluation of antibacterial activity in vitro of different parts of two varieties of Anacardiumoccidentale L. on human pathogens. This study showed that there were variations in the capacities of extracts of the various plant parts to inhibit bacterial growth of the six experimental human pathogens (SEHP)16. This is due to the type and amount of bioactive compounds present in the extracts of the different parts of the fruit.

Regarding the fruit group, some are not of general consumption, they are common only in their origin region, and they also have significant antioxidant properties, including exotic fruits or superfruits, such as noni, lychee, pitaya, mangosteen and cashew, among others17,18. Peculiar characteristics of these fruits include their appearance, with a specific and different flavor from that of ordinary and universal fruits; most of them are consumed to quench thirst because of the high content of water; others have medicinal properties or high levels of fiber, indicating they are laxative and have good digestive properties19.

Tropical fruits are consumed naturally or in juices; the exotic varieties of fruits have unique textures and a mixture of sweet and sour taste and are beneficial to health because they contain vitamins (A, B and C) and minerals, such as calcium, iron, potassium, and magnesium20.

Cashew (Anacardiumoccidentale L.) is known commonly as anacardo, castaña of cajú, cashew or merey and is found in the Brazilian Northeast with excellent medicinal and nutritional properties. Currently, all of its components, false fruit or cashew apple and seed (Figure 1), are used in different areas, such as in elaborate candies, cosmetics, and even medications for different diseases21,22,23. The nut (known as Nut of India) of the fruit is valued because of its high content of proteins and essential oils24. The nutshell contains oil used in the manufacture of insecticides, waterproofing, and varnishes25. Cashew apple can also be consumed fresh or processed with various final products such as jam, juices, and wines. The vitamins, minerals, organic acids and carbohydrates in cashew apple are essential sources of nutrients. Nevertheless, these components of cashew apple are highly perishable; therefore, they require special care during storage, transportation and processing26.

Figure 1.Parts of Cashew (Anacardium occidentale L.)12,13
 Parts of Cashew (Anacardium occidentale L.)12,13

In Mexico, cashew is produced in some states of the country such as Campeche, Chiapas, Guerrero, and Veracruz27, where the consumption is mainly natural and the pulp is used to prepare beverages and artisan desserts. However, cashew fruit is overlooked and wasted to obtain only the nut, which has the maximum commercial value28.

Considering the few investigations about the characterization of cashew produced in Mexico, the objective of the present work was to study the physical, chemical and antioxidant properties of the apple or false fruit (cashew apple) and walnut of the red and yellow varieties. These were harvested in Guerrero, one of the states with the highest production. To obtain an alternative to conservation and avoid wasting of the false fruit, we proposed to make a commercial product such as a marmalade, exploiting its antioxidant properties.

Materials and Methods

Raw Material

Cashew (Anacardiumoccidentale) used was from the Costa Grande region located in the state of Guerrero. The cultivation area is at the south, southwest, and west of the country, as well as at the north in the Tierra Caliente region and part of Michoacán state. Cashew fruit must be harvested at an optimum state of maturation to have the nut in the best condition. The March-June 2015 harvest was transported under refrigeration conditions (4°C) to avoid fast over-mature or deterioration and was stored in the laboratory at -18°C until analysis. The sample preparation was as follows:

a. Pulp: cashew apple was cut into small slices and macerated. The flesh was obtained on a Whatman No. 40 filter paper and was used to obtain the juice, which determined the total phenol and antioxidant properties.

b. Nut peel (coarse): the thick skin of the nut was subjected to thermal treatment at 100°C for 1 hour in an electric oven to extract the kernel (the thick shell was not studied because it is inedible). The nut peel was considered an untreated sample.

c. Husk: the thin crust covering the kernel was separated manually using tip tweezers and then was macerated to obtain a fine powder that was also packaged and stored at 4°C for analysis.

d. Nut: the nut without the thin shell was macerated until a powder was obtained that was packaged in a flask and stored in refrigeration at 4°C to determine phenolic compounds and antioxidant activity.

e. Toasted Nut: the toasting process employed an electric oven, in which the whole nut was placed in a tray and exposed at 133°C for two hours, followed by storage until subsequent analysis.

Physicochemical parameters: the pH measurement of the pulp of cashew apple was performed according to standard procedures29. The acidity percentage was determined using the flesh of cashew apple according to standard procedures expressing the results as % of citric acid for being the one of greater proportion in the samples30. Soluble solids (°Brix) were determined using the juice of the pseudofruit31. The density (g/ml) of cashew apple juice was determined according to standard procedures32. The humidity (%) of cashew apple was assessed by applying the technique of Bidwell Sterling33 using standard procedures34.

Methanol Extract

Samples of cashew apple, nut, commercial nut and husk were previously milled and macerated. Next, 2 g of cashew apple, 2 g of nut, 2 g of commercial nut and 0.5 g of husk were taken and placed into flasks separately. The samples were then subjected to extraction in 100 % methanol (10 ml) for 24 h in the dark and room temperature, followed by filtration to obtain the extract.

Phenolic Compounds

The method used was described previously35: 200 μL of the extract was mixed with 0.1 ml of Folin-Ciocalteu reagent for 3 minutes at room temperature, followed by the addition of 2 mL of sodium carbonate (7.5 %) and 2.8 mL of water. The sample was incubated for 1 h in the dark, followed by measurement in a Spectrophotometer at a wavelength of 725 nm. A curve of gallic acid was used, and the results were expressed as milligram equivalents of gallic acid (GAE) per 100 grams of sample fresh and dry.

Antioxidant Capacity by DPPH

A modified previously reported method36 was used to determine the antioxidant properties. The reducing power of the samples was determined by the method described by Brand-Williams et al. (1995),37 for the inhibition of the stable radical 2,2-diphenyl-1-picrylhydrazyl (DPPH). The assay was performed by mixing 0.1 mL of methanolic extract from the samples with 3.9 ml of a methanol solution of DPPH (0.005 g DPPH/10 ml of methanol). After 30 minutes in the dark, the absorbance at 515 nm was measured using 100% methanol as a blank and methanol 80% as a control treated with DPPH. The percentage of inhibition with respect to the initial absorbance obtained for the methanolic solution of DPPH is expressed as micromoles of TEAC (antioxidant activity equivalent of TROLOX) per 100 g of fresh sample, based on the TEAC type curve.

Processing of Marmalade

The raw material fruit was washed at the select maturation stage of both varieties. The fruit was divided into quarters and 500 g of fresh fruit, 400 g of sugar and 600 g of water were mixed, using citric acid as a preservative, and the marmalade was obtained using an artisanal method as follows: 3 g of the white skin of a lemon was added to 50 mL of water, followed by heating in a microwave oven for one minute (0.17 % citric acid). This hot citric acid mixture was used in the marmalade.

The previous preparation of water, citric acid and fruit was heated at 50 °C until 65 °Bx was obtained. After cooling 50 g samples in jars, each underwent pasteurization (100°C for 30 min) to obtain a shelf life of 45 days stored under refrigeration conditions38.

Sensory Evaluation

The sensory evaluation was carried out using 50 untrained judges performing discriminative and affective tests. A sample comprised 30 ml at 25°C. Discriminative analysis was performed using a comparison by pairs: two samples, (1) marmalade of cashew and (2) mango marmalade of a commercial brand, were evaluated for their characteristics-flavor, acidity, color intensity, aroma and like or dislike perception. A descriptive test applied using a scale of attributes, in which two samples were used: (1) marmalade of cashew and (2) marmalade of mango of a commercial brand39.

Statistical analysis of the results was carried out with the MINITAB 17.0 Software to obtain the mean ± standard deviation of the data (n = 3), and the multiple comparisons of Tukey test to determine significant difference between the samples.

Results and Discussion

Physicochemical Tests

(Table 1) shows the results obtained for the physicochemical parameters of the red and yellow cashew varieties.

Table 1. Physicochemical parameters of cashew pulp (cashew apple)
Parameter Red Yellow
Ph 4.05±0.18a 4.602±0.115b
(°Brix) 11.55±1.1a 11.54±1.238 a
Density (g/ml) 1.301±0.009 a 1.290±0.01 a
Acidity* (citric acid %) 0.433±0.065 a 0.40±0.04 a
Humidity (%) 80 70

Means value ± σ (standard deviation) of n = 3. Means that do not share a letter are significantly different (α = 0.05) according to multiple comparisons of Tukey test

A significant difference in pH values was observed between red and yellow cashew apple, while °Brix, density and acidity did not show it. Studies40 showed pH values of 4.14 and 4.15 for the red and yellow cashew varieties, respectively, similar to that obtained in this study. Some studies reported the pH of the false fruit, varying from 4 to 5.5. Guerrero et al. (2008)25, performed the physicochemical characterization, of the nut and false fruit of Anacardiumoccidentale L. (merey) under dry conditions and obtained for the harvested product pH values 6.47±0.02 and 3.57±0.07 for the nut and false fruit, respectively. The soluble solids obtained from both varieties (11.55 °Bx) were in the range reported for samples of Anacardiumoccidentale L. of Brazil and oscillated between 6 and 13 ºBx41,42. However, Chávez (2009)40 obtained pH values of fruits from El Salvador of 8.5 and 10 °Bx for the red and yellow cashew varieties, respectively. Guerrero et al. (2008)25 reported a higher value (17°Bx) for false fruit. An increased concentration of total soluble solids (monosaccharide) exists because of polysaccharide hydrolysis (homopolysaccharide) during maturation41,43. Significant differences (with a level of confidence of 95%) were not observed in the density values between both varieties. Cashew red presented a higher percentage of acidity than that reported by Chavez (2009)40 at 0.36 % total acidity, but the variety of cashew used was not specified. Guerrero et al. (2008)25 reported a higher value of acidity in fruits of A. occidentale L. under dry conditions (1.42 %) than that observed under conditions of irrigation (0.32 %)44. False fruit pulp presented a lower acidity than that reported for samples harvested in Tanzania, Costa Rica, India and Brazil41,42. Rodríguez (2011)44 expressed values of acidity of 0.185 ±0.01% for malic acid of the juice of cashew fruit.

The values of humidity for cashew red and yellow were similar to those reported by Chávez (2009)40 who attributed the differences to the conditions of cashew harvest, mature stage, and origin. The physicochemical characteristics of the fruits vary depending on their maturity, handling, and origin (climatic conditions and soil, among others). Water supply is an essential influence of the physiological development of the fruit (preservation of nutrients) and determines the quality and quantity of the harvested product45. For the nut sample, only the humidity generated a value of 12.84 %. This value has not been reported.

Total Phenolic Compounds

The results of the total phenolic compounds obtained from extracts of different samples of cashew apple and nut are presented in Table 2.

Table 2. TPC and AA of pulp, nut and husk of cashew
Sample TPC (GAE mg/100 g db) AA (μmols Trolox/g db)
red cashew (pulp) 159.75±12.91 77.65±1
yellow cashew (pulp) 151.9±5.23 56.53±1.2
nut 174.19±20.98 38.52±2.9
toasted nut (133°C, 2 h) 96.80±9.48 ND
Husk 7430±730 1549.55±170
commercial nut ND 2.48±0.2
  Reported values (comparative purposes)  
nut (Ogunlade et al.49) 204.95±1.4 (raw) 50-53.21 (FRAP)
toasted nut (130°C, 33 min) (Chandreskara and Shahidi,50) 528±1.0 58.14±2.84 (defatted meal)
husk (testa) (130°C, 33 min)(Chandreskara and Shahidi50) 26905 ±977 (raw)34799±688 (defatted meal) --------

Mean ± standard deviation (n = 9). TPC: total phenolic compounds; AA: antioxidant activity; wb = wet base; db = dried base; ND = not determined.

Cashew Apple

Cashew red pulp showed a superior value of the phenol content to that of yellow cashew pulp. Rufino (2010)46 determined the content of phenols in non-traditional fruits from Brazil, reporting a value of 118±3.7 mg GAE/100 g wb for cashew (Cajú). Fruits such as Bacuri, Carnaúba, Gurguri, Jaboticaba have a wide range of values of 23.8±0.7 to 549±22.2 mg AG/100 g. A high variability in the content of phenolic compounds of cashew is shown in the literature because of their origin, soil difference cyclic conditions, seasonal growth, postharvest, storage and extraction methods of polyphenols47. Plants can activate polyphenol synthesis as a response to stress conditions such as injuries, pathogens, and low nutrient compounds48.

On the other hand, when comparing the content of total phenols obtained for the red cashew with that for other fruits, the fruit of cashew had a value close to red fruits, such as strawberry (205.4±2.1 mg GAE/100 g wb), pomegranate (328.7±2.5 mg GAE/100 g wb51, and was higher than that reported for saladette tomato (92.31 mg GAE/100 g wb)52.

Cashew Nut

The untreated nut sample showed a higher content of phenolic compounds. However, in the nut toasted at 133°C for two hours, the TPC was decreased. Ogunlade et al. (2014)49 and Chandrasekara50reported values of 204.95±1.4 and 114±0.47 (defatted meal) mg GAE/100 g db, respectively, for the nut of Anacardumoccidentale. The value of 528±1.0 was published for the nut treated at 130°C for 33 min50. This difference could be because, in the toasted process used in the present work, the samples were exposed to higher temperatures and more extended periods (133°C; 2 hrs), causing structural changes, such as isomerization and a reduced content of phenolic compounds53,54. Other causes of these differences could be because, in the present study, defatted samples were used that could modify the general composition53. However, Chandrasekara and Shahidi50 reported that, during heat treatment, the reaction between reducing sugars and amino acids, known as the Maillard reaction, can occur, leading to the formation of various byproducts, intermediate and brown pigments (melanoidins), which may contribute to the TPC, flavor, antioxidant activity and color of food. The value of the TPC of nut obtained in the present work (174.19±20.98 mg GAE/100 g db) was higher than that reported for almond, hazelnut and Macadamia nut at 114, 111 and 87 mg GAE/100 g (wb), respectively, but inferior to that reported for cashew nut (nut of India), 381 mg GAE/100 g (wb)55 (Figure 2).

Figure 2.Content of the total phenols of other oilseeds, expressed as mg equivalents of gallic acid (GAE) / 100 g55.
 Content of the total phenols of other oilseeds, expressed as mg equivalents of gallic acid (GAE) / 100 g55.

A high value was obtained for the TPC of the husk of cashew nut (74.30 mg GAE/g) compared with those of the kernel and false fruit. Other authors have reported a value of 269.05±9.77 GAE mg/g in a defatted meal50. The samples of cashew nut and skin had proteins and sugar, and the formation of MRPs during roasting is possible. Thus, the roasting condition, as well as the type of nut, affects the TPC values of the extracts of cashew skins50. Studies have reported high amounts of husk or cuticle of different nuts. Rosales et al. (2014)54 declared a value of 132.9 mg GAE/g for the peanut cuticle Virginia variety. The high amounts of TPC obtained in the husk sample of cashew compared with the fruit are because the husk is the external part of the nut and protects against stress conditions, synthesizing the highest amount of phenols in this structure56. Francisco & Resurrección (2009)57 reported that phenolic compounds in the outer layer of plants as shell, cuticle, and sheath are present in a high concentration to protect all internal materials as cotyledons. Some phenolic acids, although they are united with a covalent bond of polymers, are not soluble in water and other components of the cellular wall as arabinoxylanes58. Thermal treatment could set free antioxidants of low molecular weight that could be sub-units of polymers of high molecular weight59. Studying the skin or husk of nuts is important because several studies have reported that the husk has healing properties such as hypoglycemic, hypoglycemic, antihypertensive, astringent, antihelminthic, and anti-inflammatory properties56.

Antioxidant Capacity

(Table 2) shows the results of the antioxidant activity of the extracts of false cashew fruit and treated and untreated nut. Red cashew presented a higher antioxidant capacity at 77.65 μmol Trolox/g and was superior to that of the kernel. Additionally, red cashew had a higher content of TPC. The differences between red and yellow cashew can be attributed to the type and amounts of phenolic compounds present in each because they contain tannins, polyphenols, and carotenes55. Some studies have reported that cashew has different characteristics and amounts of phenolic acids, such as ferulic, gallic, ellagic, p-coumaric and syringic acids, as well as flavonoids, such as myricetin, catechin, epicatechin, and epigalocatequine59,60. Ogunlade et al. (2014)49 reported a value between 50 to 53.21 μmol Trolox/100 g for Anacardiumoccidentale nut but they used a FRAP method.

Comparing values of the antioxidant capacity obtained for cashew with that of a common fruit, such as red apple (Malus sylvestris), which contains 0.259 μmol TE/g59,or with an exotic fruit of a higher consumption, such as soursop, which contains 2.88 μmol TE/g61, cashew presented a higher antioxidant capacity than these fruits. It is essential to exploit the benefits of cashew apple and use it as a raw material in functional food processing.

(Table 2) presents the values of the nut extracts. The nut studied had 38.52±2.9 μmol TE/g sample, and the commercial nut value was lower at 2.48 μmol TE/g sample. These results could be due to processes such as toasting and salting that are used commercially; high-temperature processes and high salt content can produce structural changes in phenolic compounds and generate structures with a lower antioxidant capacity and storage time54,62. Chandrasekara50reported a higher value of 58.14±2.84 (μmols Trolox/g db, defatted meal) for the toasted nut (130°C, 33 min) of Anacardumoccidentale than the one obtained in the present study and may be the difference was because of the treatment time. The husk possesses a higher antioxidant capacity than other samples and is because it is the structure that protects the seed and is where the antioxidant compounds are synthesized in a greater proportion54.

Antioxidants isolated from foods and beverages, such as the cashew apple and its processedproducts, may be superior to non-natural products15,51.

By relating the phenolic compounds against the antioxidant capacity of the fruit, nut and husk by means of a linear regression. The coefficient of determination provides a value of 0.9725 for red cashew, 0.9383 for yellow cashew, 0.9857 for nut and 0.9241 for husk; these values indicate a good fit of the data towards the linear, which represents that there is a directly proportional relationship between the phenolic compounds and the antioxidant capacity.

Marmalade Shelf Life

(Figure 3) shows the pH and acidity of marmalade for 6 weeks. The pH value decreased at the end of the period, showing a value of 3.68; this value is a warranty of a good shelf life of the final product. This value is in the range reported for the pH of marmalades (3.25-3.75) to ensure microbiological safety38. The final acidity level was 0.35% (presenting 22.2 % of reduction), and, according to standards, is acceptable until a value of 1%. Those values have been reported in other marmalades such as mango-flavored marmalade with an acidity value of 0.5% or orange-flavored marmalade with a final acidity value of 1%; the acidity value of cashew marmalade is in the range of that for jams of other more common fruits38. This low reduction might be due to the process because of the addition of sugar and water, and the general change in composition. The thermal process could cause structural changes that caused the difference in the acidity63.

Figure 3.pH and acidity of marmalade during 6 weeks.
 pH and acidity of marmalade during 6 weeks.

Cashew is considered an acid fruit, giving the confidence of a final product with good quality38. The acidity of prepared marmalades (0.35 %) presented a significant difference in the acidity of fresh fruit (0.43 g citric acid/100 ml). In jams prepared with fruits, a lower value of acidity and low pH values give the advantage of the best shelf life; it must be considered that the addition of citric acid forms a gel, avoiding sugar crystallization and acting as a preservative agent64.

Rodríguez (2011)44 prepared a juice of cashew pulp and presented a pH value of 4.4, which was similar to that reported by other authors65,66. The acidity value, determined as the malic acid percentage, was 0.177 %. This value is outside the range of established norms in Brazil67 for the juice of false fruit of cashew, which sets values between 0.22 and 0.52 %.

(Figure 4) shows the °Bx and phenol variation for six weeks. The °Bx data follow a linear trend and a slope almost at 0, obtaining a final value of 63.41°Bx, and an acceptable amount of marmalades according to the norms31. The behavior observed of phenolic compounds showed a slight increase in the initial value of 106.25 mg GAE/mL to 114 mg GAE/mL (6.8 % of growth). The cause may be the slight changes in temperature and light during the storage time64,67. The °Brix value did not change during this period. Vera (2012)68 formulated marmalades of other fruits, such as the apricot, and evaluated the physicochemical properties during storage (6 weeks) to guarantee the shelf life of the product by 12 months under storage conditions at room temperature (37°C). De Oliveira et al. (2015)69 also prepared strawberry marmalade, and evaluating the content of phenolic compounds during 60 days of storage showed a decreased of 235.84±10.15 mg EAG/100 g to 226.57±12.42 mg EAG/100 g, similar behavior to that in the present work.

Figure 4.Behavior of phenols (mg AG/mL) and °Bx of cashew marmalade during 6 weeks.
 Behavior of phenols (mg AG/mL) and °Bx of cashew marmalade during 6 weeks.

Those results could suggest that some structural changes in the phenolic compounds can occur after 30 days. Klopotek et al. (2005)70 argued that the processing and storage conditions caused co-pigmentation and auto-association of molecules, reducing the number of hydroxyl groups available to react in the Folin-Ciocalteu colorimetric assay, apparently decreasing the concentration of total phenols. The release of monomers of polymeric polyphenols also showed the highest values of the content of total phenols using the Folin-Ciocalteu assay71. Thus, it could explain the apparent increase in the phenolic compounds during the last week of storage of marmalade elaborated in this work. Thus, marmalade processing is an alternative to preserve the properties of bioactive compounds present in cashew fruit72.

Diverse products derived from cashew have been developed as beverages. Rodríguez (2011)44 developed a juice with cashew apple and reported a total phenolic concentration of 2321 mg GAE/L, lower than the value reported by Melo et al. (2006)73in cashew juice of 2952.5 mg EAG/L, but higher that the value reported in the juice of common fruits, such as orange, which contain values of 620.7 to 630.5 mEq GAE/L74. For the above, the false fruit of cashew represents a good source of antioxidants (106.25 mg GAE/mL) compared with fruits of regular consumption.

Sensory Evaluation

A discriminative and descriptive test was applied using 20 untrained judges. The first test used comparison pairs to find differences between marmalade formulated for this work and a commercial brand. According to panelist perception, cashew marmalade presented a less acidic flavor than the mango marmalade of the retail brand. The results matched the physicochemical parameters, and no significant differences were found in the acidity content during the period of storage.

The panelists observed a similar color of marmalade of cashew (color characteristic) and mango. Regarding flavor, cashew marmalade was a slightly astringent; this result also matched those obtained for the physicochemical parameters (pH and acidity). According to the panelists, mango marmalade was more astringent than cashew marmalade. The cause may be that commercial jams used the highest amount of citric acid as a preservative; in cashew marmalade, the citric acid was obtained from a natural source and was at a lower concentration.

Attribute Scale

The second test consisted of describing attributes of flavor using a graphic scale; the objective was to evaluate the characteristics of cashew marmalade compared with mango marmalade of a commercial brand. The chart scale of taste used grading extremes: low astringent to extremely astringent. Cashew marmalade was evaluated as having a low astringent flavor, while mango marmalade had a high astringent flavor; the difference might be due to the high amount of preservative (citric acid). On the other hand, fruits such as cashew and mango have a content of different polyphenols, such as phenolic acids, which tend to contribute to the astringency and acidity in foods75,76.

Cashew marmalade presented a higher °Bx value (63.41) than that of mango marmalade (30.67 °Bx)38. According to sensorial analysis, cashew marmalade belongs to the group of jams, jellies, and marmalades, according to the values of Brix degrees established in the norm of CODEX75,76. The final product presented a good appearance at 45 days of storage and refrigeration.


Cashew harvested in Mexico has good functional properties, and the differences reported in the literature are due to its origin, weather conditions, and harvesting soil. As shown in this investigation, the content of total phenolic compounds was higher in the red variety of cashew apple than in the treated nut at 133°C. The antioxidant capacity of the false fruit cashew of the red variety was superior to that of the yellow one. In the elaborated marmalade, °Bx did not change and the pH and acidity slightly decreased, while the phenolic compounds showed a reduction of 6.8 % during six weeks of storage. According to sensory evaluation, cashew marmalade is a product with the correct color and flavor and a good odor. Thermic treatment modifies the antioxidant capacity and content of phenolic compounds of nut. Toasted nut, with its high content of antioxidant compounds, is a functional food that requires minimal processing and can be directly consumed.

The present work proposes focusing on the use of cashew apple, considering that only the nut is commercialized and the rest of the fruit is usually discarded.

Funding and Acknowledgments

The authors would like to thank the Research and Postgraduate Secretariat of the INSTITUTO POLITECNICO NACIONAL (SIP-IPN) for the financial support of this study.


  1. 1.Ros E, L C Tapsell, Sabaté J. (2010) Nuts and berries for heart health. Current atherosclerosis reports. 12(6), 397-406.
  1. 2.Lobo V, Patil A, Phatak A, Chandra N. (2010) Free radicals, antioxidants and functional foods: Impact on human health. Pharmacognosy reviews. 4(8), 118.
  1. 3.Galano A. (2015) Free Radicals Induced Oxidative Stress at a Molecular Level: The Current Status, Challenges and Perspectives of Computational Chemistry Based Protocols. , Journal of the Mexican Chemical Society 59(4), 231-262.
  1. 4.Oliveira L D L D, Carvalho M V D, Melo L. (2014) Health promoting and sensory properties of phenolic compounds in food. , RevistaCeres 61, 764-779.
  1. 5.Hartley L, Igbinedion E, Thorogood M, Clarke A, Stranges S et al. (2012) Increased consumption of fruit and vegetables for the primary prevention of cardiovascular diseases. The Cochrane Database of Systematic Reviews,2012(5). 1-13.
  1. 6.Socarrás S M M, A M Bolet. (2010) Alimentación saludable y nutrición en las enfermedades cardiovasculares. , Revista Cubana de Investigaciones Biomédicas 29(3), 353-363.
  1. 7.Habibi E, Shokrzadeh M, Ahmadi A, Chabra A, Naghshvar F et al. (2018) Pulmonoprotective Action of Zataria multiflora Ethanolic Extract on Cyclophosphamide-Induced Oxidative Lung Toxicity in. , Mice.Chinese Journal of Integrative Medicine 1-8.
  1. 8.Shokrzadeh M, Chabra A, Ahmadi A, Naghshvar F, Habibi E et al. (2015) Hepatoprotective effects of Zataria multiflora ethanolic extract on liver toxicity induced by cyclophosphamide in mice.Drug research. 65(04), 169-175.
  1. 9.Habibi E, Shokrzadeh M, Ahmadi A, Chabra A, Naghshvar F et al. (2015) Genoprotective effects of Origanum vulgare ethanolic extract against cyclophosphamide-induced genotoxicity in mouse bone marrow cells.Pharmaceutical biology. 53(1), 92-97.
  1. 10.Ahmadi A, Shadboorestan A. (2016) Oxidative stress and cancer; the role of hesperidin, a citrus natural bioflavonoid, as a cancer chemoprotective agent.Nutrition and Cancer. 68(1), 29-39.
  1. 11.Kubo I, Ochi M, P C Vieira, Komatsu S. (1993) Antitumor agents from the cashew (Anacardium occidentale) apple juice.Journal of Agricultural and Food Chemistry. 41(6), 1012-1015.
  1. 12.Itokawa H, Totsuka N, Nakahara K, Maezuru M, Takeya K et al. (1989) A quantitative structure-activity relationship for antitumor activity of long-chain phenols from Ginkgo biloba L.Chemistry. , Pharmacy Bulletin 37, 1619-1621.
  1. 13.Kubo I, Kinst-Hori I, Yokokawa Y. (1994) . Tyrosinase inhibitors from Anacardium occidentale fruits.Journal of Natural Products 57, 545-551.
  1. 14.Shobha S V, Ramadoss C S, Ravindranath B. (1994) Inhibition of soybean lipoxygenase-1 by anacardic acids, cardols and cardanols.Journal of Natural Products. 57, 1755-1757.
  1. 15.Kubo I, Masuoka N, T J Ha, Tsujimoto K. (2006) Antioxidant activity of anacardic acids.Food. , Chemistry 99(3), 555-562.
  1. 16.Belonwu D C, Ibegbulem C O, P C Chikezie. (2014) Systemic evaluation of antibacterial activity of Anacardium occidentale.The. , Journal of Phytopharmacology 3(3), 193-199.
  1. 17.Moo-Huchin V M, Moo-Huchin M I, R J Estrada-León, Cuevas-Glory L, I A Estrada-Mota et al. (2015) Antioxidant compounds, antioxidant activity and phenolic content in peel from three tropical fruits from Yucatan, Mexico. Food chemistry. 166, 17-22.
  1. 18.Aguirre B G. (2016) El marañón. , Botanical Sciences 11, 23-26.
  1. 19.Runjala S, Kella L. (2017) Cashew apple (Anacardium occidentale L.) therap eutic benefits, processing and product development: An over view. The Pharma Innovation, 6(7, Part D),260.
  1. 20.J L Illescas, Bacho O, Ferrer S. (2007) Análisis de los principales frutos tropicales comercializados. Distribución y consumo. 95, 33-85.
  1. 21.Rico R, Bulló M, Salas‐Salvadó J. (2016) Nutritional composition of raw fresh cashew (Anacardium occidentale L.) kernels from different origin. , Food science & nutrition 4(2), 329-338.
  1. 22.Din H H. (2016) The worldwide fruits. Disponible en línea en:.
  1. 23.Wait A J, Jamieson J I. (1986) The botany and cultivation of the cashew. The archives of the rare fruit council of Australia. Disponible en línea en:
  1. 24.Quijada Alvarado, P J, Gómez, J D, Navarro Herrera et al. (2016) Diseño, construcción y validación de un dispositivo extractor de la nuez de marañón (Doctoral dissertation, Universidad de El Salvador).
  1. 25.Guerrero R, Lugo L, Marín M, Beltrán O, Pinto G L de et al. (2008) Caracterización fisicoquímica del fruto y pseudofruto de Anacardium occidentale L.(merey) en condiciones de secano. Revista de la Facultad de. , Agronomía 25(1), 81-94.
  1. 26.Arrázola G, Alvis A, Osorio J. (2013) Clarificación combinada y evaluación sensorial de jugo de marañón (Anacardium occidentale L.). , Revista MVZ Córdoba 18.
  1. 27.Siap. (2012) Cierre de la producción agrícola por cultivo. Disponible en línea en:
  1. 28.Abreu F P De, Dornier M, A P Dionisio, Carail M, Caris-Veyrat C et al. (2013) Cashew apple (Anacardium occidentale L.) extract from by-product of juice processing: A focus on carotenoids. , Foodchemistry 138(1), 25-31.
  1. 29.NMX-F-317-S-1978.Determinación de pH en alimentos. Normas mexicanas. Dirección general de normas.
  1. 30.NMX-F-102-S-1978.Determinación de la acidez titulable en productos elaborados a partir de frutas y hortalizas. Norma Mexicana. Dirección general de normas.
  1. 31.Alimentos NMX-F-103-1982.Frutas y derivados. Determinación de grados Brix. Normas mexicanas. Dirección general de normas.
  1. 32.NMX-F-075-1987.Alimentos determinación de la densidad relativa en aceites y grasas vegetales o animales. Normas mexicanas. Dirección general de normas.
  1. 33.G L Bidwell, W F Sterling. (1925) . Preliminary Notes on the Direct Determination of Moisture. Industrial &EngineeringChemistry 17(2), 147-149.
  1. 34.Alimentos NMX-F-227-1982.Especias y condimentos. Determinación de humedad por destilación con disolvente. Norma Mexicana. Dirección general de normas.
  1. 35.V L Singleton, Orthofer R, R M Lamuela-. (1999) Analysis of total phenols and other oxidation substrates and antioxidants by means of folin-ciocalteu reagent. In Methods in enzymology Academic press 299, 152-178.
  1. 36.Iacopini P, Baldi M, Storchi P, Sebastiani L. (2008) Catechin, epicatechin, quercetin, rutin and resveratrol in red grape: Content, in vitro antioxidant activity and interactions. , Journal of Food Composition and Analysis 21(8), 589-598.
  1. 37.Brand-Williams W, M E Cuvelier, Berset C L W T. (1995) Use of a free radical method to evaluate antioxidant activity. LWT-Food science and Technology. 28(1), 25-30.
  1. 38.Coronado M, Roaldo H. (2001) Elaboración de mermeladas procesamiento de alimentos para pequeñas y microempresas agroindustriales. CIED. Lima Perú. 8-18.
  1. 39.Olivares La Madrid, P A, A S Valdiviezo, M L Uriburu, A N Ramón. (2015) Formulación de mermeladas dietéticas de arándano (Vaccinium Corymbosum L.) y mango (Mangífera Indica L.). , Diaeta 33(152), 7-11.
  1. 40.G J Chávez. (2009) Producción y caracterización del fruto marañón (Anacardium occidentale) ubicado en el corregimiento de Zapatosa municipio de. Tamalameque-Cesar. Colombia.pp1-6
  1. 41.K M Barbosa, Silva F A G A, eSilva Lima, S P. (2004) Peduncle and fruit yield, in six cropping seasons, of early dwarf cashew tree clones irrigated with different water regimes. , Rev.Bras.Frutic 26(3).
  1. 42.Pereira Toledo, C M, Correa H C T, Nietsche S, Ferreira da Mota et al. (2005) Caracterização físico-química de pedúnculos e castanhas de clones de cajueiro-anão precoce nas condições do norte de Minas Gerais. , Bragantia 64(2).
  1. 43.Rooban R, Shanmugam M, Venkatesan T, Tamilmani C. (2016) Physiochemical changes during different stages of fruit ripening of climacteric fruit of mango (Mangifera indica L.) and non-climacteric of fruit cashew apple (Anacardium occidentale L.). , Journal of Applied and Advanced Research 1(2), 53-58.
  1. 44.Rodríguez E A O. (2011) Elaboración de una bebida a base del fruto falso de marañon (Anacardium occidentale L.) adicionada con betalaínas. Tesis de maestría, Universidad Veracruzana. 93.
  1. 45.Stenzel N M C, Neves C S V J, C J Marur, Scholz M B D S, J C Gomes. (2006) Maturation curves and degree-days accumulation for fruits of'Folha Murcha'orange trees. , ScientiaAgricola 63(3), 219-225.
  1. 46.Rufino M S M, R E Alves, E S Brito, Pérez-Jiménez J, Saura-Calixto F et al. (2010) Bioactive compounds and antioxidant capacities of 18 non-traditional tropical fruits from Brazil.Food Chemistry. 121(4), 996-1002.
  1. 47.Barreto G P M, Souza A C R, Azeredo H M C, A Z Mercadante. (2007) Bioactive compounds and free radical scavenger activity in ingredients prepared from the waste of the cashew-apple nut industry.Alimentos eNutrição. 18(2), 207-213.
  1. 48.C E Bita, Gerats T. (2013) Plant tolerance to high temperature in a changing environment: scientific fundamentals and production of heat stress-tolerant crops. Frontiers in plant science. 4.
  1. 49.Ogunlade I, I A Awosanmi, O A. (2014) Antioxidant activity and total phenolic content of some nuts commonly consumed in South-Western Nigeria. , The Journal of Phytopharmacology 3(4), 248-253.
  1. 50.Chandrasekara N, Shahidi F. (2011) Antioxidative potential of cashew phenolics in food and biological model systems as affected by roasting. , Food Chemistry 129(4), 1388-1396.
  1. 51.Fragoso C I I, M, Ramos M O A, Hernández B M T, M P Rosales et al. (2019) Berries Harvested in Mexico and its Use to Prepare a Functional Drink Conserved By Ultrasonication. 8(2), 2-16.
  1. 52.Rodríguez D D I, C S Arellano, M P Rosales, O F García, López C MS. (2018) . Antioxidant Content in Skin And Seeds of Three Tomato Varieties (Solanum Lycopersicum) Grown in 2 Regions of Mexico. International Journal of Food and nutritional science 7(3), 1-14.
  1. 53.D J Soares, Vasconcelos P H M D, Camelo A L M, Longhinotti E, Sousa P H M D et al. (2013) Prevalent fatty acids in cashew nuts obtained from conventional and organic cultivation in different stages of processing. , Food Science and Technology (Campinas) 33(2), 265-270.
  1. 54.M P Rosales, C S Arellano, A L Dorantes, O F García, López C M S. (2014) . Comparison between Antioxidant Activities of Phenolic Extracts from Mexican Peanuts, Peanuts Skins, Nuts and Pistachios.Journal of the Mexican Chemical Society 58(2), 185-193.
  1. 55.Tiemi L, Lajolo F, Genovese M. (2010) Comparison of phenol content andantioxidant capacity of nuts.Ciênciae Tecnología de Alimentos. 30(1), 254-259.
  1. 56.A S Ribeiro, Estanqueiro M, M B Oliveira, Lobo Sousa, M J. (2015) Main benefits and applicability of plant extracts in skin care products. , Cosmetics 2(2), 48-65.
  1. 57.Francisco M L L D, Resurreccion A V A. (2009) Total phenolics and antioxidant capacity of heat-treated peanut skins. , Journal of Food Composition and Analysis 22(1), 16-24.
  1. 58.W M Dynkowska, M R Cyran, Ceglińska A. (2015) Soluble and cell wall‐bound phenolic acids and ferulic acid dehydrodimers in rye flour and five bread model systems: insight into mechanisms of improved availability. , Journal of the Science of Food and Agriculture 95(5), 1103-1115.
  1. 59.S M Jeong, S Y Kim, D R Kim, S C Jo, K C Nam et al. (2004) Effect of heat treatment on the antioxidant activity of extracts from citrus peels. , Journal of Agricultural and Food Chemistry 52(11), 3389-3393.
  1. 60.N G Taş, Gökmen V. (2017) Phenolic compounds in natural and roasted nuts and their skins: a brief review. , CurrentOpinioninFoodScience 14, 103-109.
  1. 61.G J Correa, Ortiz D, J E Larrahondo, M, Pachon H. (2012) Actividad antioxidante en guanábana (Annona muricata l.): una revisión bibliográfica. Boletín Latinoamericano y del Caribe de Plantas Medicinales y. , Aromáticas 11(2).
  1. 62.Rawson A, Patras A, B K Tiwari, Noci F, Koutchma T et al. (2011) Effect of thermal and no thermal processing technologies on the bioactive content of exotic fruits and their products: Review of recent advances. , FoodResearchInternational 44(7), 1875-1887.
  1. 63.S A Chacón. (2006) Manual de procesamiento de frutas tropicalesa escala artesanal. Frutales. El Salvador. 12-26.
  1. 64.Tamuno E N J, E C Onyedikachi. (2015) Effect of Packaging Materials, Storage Conditions on the Vitamin C and pH Value of Cashew Apple (Anacardium occidentale L.) Juice. , Journal of Food and Nutrition Sciences 3(4), 160-165.
  1. 65.Pereira C D Q, F C Lavinas, Lopes M L M, V L. (2008) Industrialized cashew juices: variation of ascorbic acid and other physicochemical parameters. , Food Science and Technology (Campinas) 28, 266-270.
  1. 66.CODEX S. (2005) STAN 247-2005. Codex Gen. Stand. Fruit Juices and Nectars. Rome: Food and Agriculture Organization.
  1. 67.Mgaya‐Kilima B, S F Remberg, B E Chove, Wicklund T. (2015) Physiochemical and antioxidant properties of roselle‐mango juice blends; effects of packaging material, storage temperature and time. , FoodScience&Nutrition 3(2), 100-109.
  1. 68.Vera R M N. (2012) Elaboración de mermelada light de durazno. Tesis Licenciatura Ingeniería en Alimentos, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile.
  1. 69.Oliveira P L D L De, C L Moretti, Chiarello M, Melo L. (2015) Influence of strawberry jam color and phenolic compounds on acceptance during storage.RevistaCeres,Viçosa. 62(3), 233-240.
  1. 70.Klopotek Y, Otto K, Böhm V. (2005) Processing strawberries to different products alters contents of vitamin C, total phenolics, total anthocyanins, and antioxidant capacity. , Journal of Agricultural and Food Chemistry 53(14), 5640-5646.
  1. 71.J C Sánchez-Rangel, Benavides J, J B Heredia, Cisneros-Zevallos L, D A Jacobo-Velázquez. (2013) The Folin–Ciocalteu assay revisited: improvement of its specificity for total phenolic content determination. , Analytical Methods 5(21), 5990-5999.
  1. 72.T M Rababah, M A Al‐, Kilani I, Yang W, M N Alhamad et al. (2011) Effect of jam processing and storage on total phenolics, antioxidant activity, and anthocyanins of different fruits. , Journal of the Science of Food and Agriculture 91(6), 1096-1102.
  1. 73.Melo M L P, G A Maia, Silva A P V, Oliveira G S F, R W Figueiredo. (1998) Caracterização físico-química da amêndoa da castanha de caju. (Anacardium occidentale L.) crua e tostada. Food Science and Technology (Campinas) 18(2), 184-187.
  1. 74.Y S Kumar, Varakumar S, Reddy O V S. (2012) Evaluation of antioxidant and sensory properties of mango (Mangifera indica L.) wine. , CyTA-Journal of Food 10(1), 12-20.
  1. 75.Dedehou E, Dossou J, Anihouvi V, M. (2016) A review of cashew (Anacardiumoccidentale L.) apple: Effects of processing techniques, properties and quality of juice. , AfricanJournalofBiotechnology 15(47), 2637-2648.
  1. 76.ALIMENTARIO CODEX.(CODEX STAN 296-2009) Norma general del Codex para las confituras jaleas y mermeladas.

Cited by (1)

  1. 1.Dheeraj , Srivastava Ananya, Mishra Anuradha, 2023, Mitigation of cashew apple fruits astringency, Environmental Sustainability, 6(3), 319, 10.1007/s42398-023-00276-7