Abstract
Alginates are natural polysaccharides that are extracted from brown seaweed varieties and it is widely used for their rheological properties. The main step in the extraction protocol of sodium alginate is alkaline extraction. Sodium alginate was produced by dipping the seaweed in 1% formaldehyde and 2.5% of sodium carbonate solution and properties were studied following the standard methods. The amount of sodium alginate yield was 31.7% in Sargassum wightii. The moisture content and the ash content were recorded at 16.82% and 5.20%, respectively. The viscosity and the gel strength were noted as 40 vcP, 4.54 × 10–2 kN with 0.1 M CaCl2 and 6.86 × 10–2 kN with 0.2 M CaCl2 respectively. This study of the extraction method and its properties reveal that Sargassum wightii brown seaweed species have a high affinity to extract the alginate.
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1 Introduction
Brown algae (Phaeophyta) cell wall has a fibrillar section formed of cellulose micro fibrils, which is embedded with acid polysaccharides, linked to each other by protein [1]. The acid polysaccharides are mainly composed of fucoidans (sulphated fucans) and alginic acid, which are helping to structural toughness, and flexibility to the algae [2]. The word “alginate” is a generic term meaning of the various derivatives of the alginic acid either occurred naturally or produced from the natural derivatives [3]. Alginate mainly consists of α-l guluronic acid (G) and β-d mannuronic acid (M) units [4,5,6]. Due to the rheological properties of these polysaccharides, it is widely used in various fields of industries [7].
Countries in Asia have a long history of seaweed farming for food and other industrial purposes [8]. Now it is widely spreading to the rest of the world. Due to this reason, most Asian counties are cultivating and collecting a wide variety of seaweed [9]. Alginate is extracted from brown seaweed and it has been widely used in many fields such as immobilization technology, tissue engineering, pharmaceutical industry, and food applications as a stabilizer, gelling agent, thickening agent, edible coating for some foods, and textile industry [10]. The alginate content of brown seaweed varies depending upon the environmental conditions such as salinity, temperature, wave-current, species, the season of harvesting, and method of extraction used, etc. [11, 12].
Sodium Alginate (SA) obtained from brown algae, signifies a biodegradable, non-toxic polymer and most versatile polysaccharide in nature. Sodium Alginate is a well-known polysaccharide in the food packaging industry and is used as edible films. However, the fragility and the high sensitivity to water remain of SA leads to difficulties of widespread food packaging applications. Therefore, SA mixed with other polysaccharides or protein to make the edible films and it becomes the most simple and attractive strategy for improving the properties [13]. Luis and his team investigated the effect of adding a low concentration of nano-SiO2 in the properties of the films based on SA and it has been reported with great success in improving mechanical and thermal properties. The film moisture content and water vapour barrier decreased due to the increase of nano SiO2 level [14]. According to the literature, SA extracted from this species has given promising yield and viscosity of the products [15].
Alginate is extracted from brown seaweed; by analytical method mainly focuses on the conversion of insoluble alginate present in the cell wall as magnesium and calcium alginate to a soluble form usually in sodium alginate [16]. The common extraction method of alginate has five steps: acidification, alkaline extraction, solid/liquid separation, precipitation, and drying [17]. During the acidification process, the seaweed becomes acidified and it is facilitated to alkaline extraction. Acidify seaweed are immersed in the sodium carbonate solution to convert the insoluble alginic acid into soluble sodium alginate [18]. The quantity of the yield is highly dependent on the volume of reactant, extraction time, and the brown seaweed species. The alkaline extraction time is influencing the rheological properties of the alginate and the reaction condition seems to favor bacterial growth and development. Vauchel et al. noted alginate degradation could occur due to bacterial development [1].
Among approximately 320 species of seaweed around the Sri Lankan coast, nearly 50–60 species have potential commercial importance. Brown seaweed such as Sargassum, has a great economic potential for the vast array of industries that have not yet been commercially utilized [19]. In the present study, we report on the extraction of alginates from brown algae species (Sargassum wightii) collected from the Southern coast of Sri Lanka. Through this study, we determine the optimum condition of the extraction method and evaluate their quality with commercially available alginate samples.
2 Material and methodology
2.1 Seaweed collection and drying
Sargassum wightii samples were collected from shallow seawater in the Southern coastal area, Sri Lanka. The samples were thoroughly washed with seawater, then cleaned with tap water to remove sands and other impurities. Finally, samples were washed with distilled water and dried under sunlight on a mesh, scattered in a layer that had a height of 4–5 cm for 12 h. The temperature and the time duration were recorded to determine the time, which was needed to remove the moisture content of seaweed until 20%.
2.2 Production of sodium alginate
McHugh et al. [17, 18] method was followed with slight modification to alginate extraction. Dried seaweed was dipped in 1% CaCl2 solution (AR, Sigma Aldrich, Germany) for 2 h and then again dipped in 1% formaldehyde solution (AR, Merck, Germany) for 6 h. Then the sample was washed with deionized water three times. Thereafter, samples were dipped in 5% HCl solution (AR, Sigma Aldrich, Germany) for 30 min and again washed with deionized water three times. Then prepared the 2.5% Na2CO3 solution (AR, Sigma Aldrich, German) and washed seaweed sample was dipped in this solution for 3 h. After 3 h, seaweed was removed from the solution by filtration and the filtrate was separated. Then ethanol (95%, AR, Sigma Aldrich, Germany) was added to the filtrate in a 2:3 ratio to precipitate fibrous alginic acid from the mixture. The mixture was stirred to complete the precipitation and precipitate was squeezed manually to remove the liquid phase. Finally, precipitation was dried in an oven (Memmert, UFE-500, United Kingdom) at 50 °C for 12 h and milled.
2.3 Yield
The yield is expressed as the weight percentage of alginate with the weight of the seaweed samples. Approximately 100 g of dried seaweed were taken for alginate extraction and the final yield was calculated as the weight percentage for 100 g of dried seaweed. The formaldehyde concentration (FA) and the Na2CO3 concentration were optimized to take the best yield.
2.4 Properties of sodium alginate
2.4.1 Water content and ash content
The water content was obtained by the gravimetric method by drying the sample of alginate at the temperature of 105 °C, overnight in the oven (Memmert, UFE-500, UK). The ash content was obtained by the both method are know as gravimetric by burning the alginate sample in muffle furnace (Carbolite GLM, United Kingdom) at the temperature of 250 °C for 12 h until it becomes ash. All the samples were replicated thrice (n = 3).
2.4.2 Insoluble matter test
Alginate sample (1 g) was dissolved in 5 mL of 1 M NaOH and magnetic stirring (Labtech, South Korea) for 30 min (n = 3). The mixture was filtered through a suction filter unit and filter paper was dried at 100 °C until the weight become constant.
2.4.3 Viscosity test
Viscosity was tested by Brookfield viscometer (Model BL, Tokimec Inc, Japan) with a number 2 needle at 60 rpm. Calculation of viscosity was done with the reading and the cofactor, which is relevant to needle number 2, and 60-rpm rotation speed with the following equation (n = 3).
2.4.4 Testing for gel strength
Extracted 2% (W/V) of the alginic acid solution was mixed with 0.1 M and 0.2 M CaCl2 solution while stirring to make the gel sample. Gel strengths were tested by using Instron Universal Tensile Tester (Model 4465, Instron Corporation, United Kingdom) with a 2 kN load and 150 mm/min position speed.
2.4.5 International commission on illumination (CIE) L.a.b values for colour determination
It is expressed colour of three values; L for perceptual lightness, a and b for the four unique colour of human vision known as red, green, blue and yellow. Formaldehyde percentage was optimized with two concentration levels (0.25%, 1%) for taking the colour of the yield. Both two concentration levels were compared with the samples extracted without formaldehyde (n = 3).
2.4.6 Metal analysis
Samples were grind using a domestic food blender and sieved, then 0.5 g of each sample mineralized in Teflon digestion vessels in a closed microwave accelerated system (CEM, MARS 6, USA) using 10 mL nitric acid (AR, Sigma, USA) as a reagent. Atomic absorption spectrophotometer (AAS) (Varian 240 FS, Varian Inc., Australia) was used to determine the mercury (Hg), cadmium (Cd), lead (Pb), arsenic (As), in the prepared samples. Vapour generation accessory (Varian VGA-77) with the closed-end cell was used for Hg determination. A graphite tube atomizer (Varian GTA-120) was used for Cd, As, and Pb. The calibration curves for all the metals were obtained with a series of standard solutions, which were prepared using the above mentioned standard solutions. All the samples were replicated thrice.
2.4.7 Statistical analysis
Statgraphics Centurion XVI v 16.1.15 (Manugistics Inc.Rockville, MD, USA) software was used for statistical evaluation (ANOVA) for comparing standard deviation and mean values, respectively.
3 Results and discussion
Drying of seaweed aims to reduce the water content of the mass, making it easy to handle and increasing the absorption of the chemicals during the extraction process. During the drying, process seaweed should not be subjected to the higher temperature for long periods due to degrading the alginate [20]. To minimize the yield loss, dried the seaweed for 8 h at 50 °C or sun drying for 12 h can be used. During the sun drying, the moisture content was reduced with time as follows (Table 1).
A Statistical evaluation was performed by comparing the standard deviation and average value of the moisture content of the seaweed with time. ANOVA was applied for comparison of the average moisture content and statistically significant difference (p = 0.000) between the means of the four variables at the 95% significant level. Multiple comparison procedure was applied to determine which means are significantly different from each other. All pairs showed a statistically significant difference at the 95% confidence level. Approximately 80% of the moisture content was removed after 12 h sun-drying process. The temperature under the sun drying has fluctuated from 30 to 50 °C. Previous researchers recorded the best moisture content in the seaweed for storage was less than 20% [21]. Due to that reason, we selected 12 h of sun-drying best for the removal of the moisture from seaweed.
According to the literature, drying is affected to leaching some compounds such as mannitol, laminarin, and forms brown pigments like fucoidan in the seaweed cells. These pigments are highly affect the purity and the colour of the final product. To avoid this issue, formaldehyde and hydrochloric acid treatment were used to remove the pigments from the sample. The seaweed was dipped in the 1% of CaCl2 solution for 2 h and the alginate was precipitated as calcium alginates [22]. McHugh et al. noted the calcium alginate is a fibrous material that can be readily separated on a metal screen, treated with chlorine to bleach the product. After being treated with dilute mineral acid it can be obtained alginic acid in fibrous forms. Alginic acid can be converted into sodium alginate by neutralizing it with alkaline [23].
The formaldehyde concentration (FA) and Na2CO3 concentrations were optimized to take the maximum yield. Formaldehyde was added in two concentrations (0.25%, 1%) and a blank test was run simultaneously. Some studies reported a lower concentration of FA (0.1%) and during the test, all other parameters were constant except the FA concentration [23]. The colour of the final product was determined with the international commission on illumination (ICI) L.a.b values. Table 2 shows the L.a.b values for different FA concentrations. Figure 1 shows the observed colour difference in the samples for different FA concentrations levels.
According to the ANOVA table of ‘L’, the p-value is less than 0.05 (95% confidence interval) and there was a significant difference between the three variables. In the application of multiple comparisons for individual samples, there was no significant difference between 0.25 and 1% FA samples. ANOVA table of the ‘a’, the p-value is less than 0.05, and three variables were significantly different. Base on the multiple comparisons there was no significant difference between 0.25% FA used to sample with and without FA used. ANOVA table for ‘b’, there was a significant difference between 3 variables but multiple comparisons for individual samples proved that there was no significant difference between FA used samples.
According to the L.a.b value, the best FA concentration is 1% due to the brownish-yellow in colour of the final product. The use of 5% HCl solution during the pre-extraction hydrolyzed the seaweed cell wall, reduced the impurities and made alginate for more easy extraction [24].
The use of Na2CO3 during extraction allows the separation of cellulose from the alginate-contained cell wall by increasing the yield [25]. Hence, the different concentrations of Na2CO3 (1.5, 2.0, 2.5, 3.0, 5.0 and 7.5%) were used in extraction process in order to select the optimum concentration. Figure 2 shows the yield % of the different concentration levels. The highest yield was found in the 2.5% Na2CO3 concentration level.
Parthiban et al. reported the maximum yield of sodium alginate found in the Sargassum species than other species and it was noted as 31.7% [3]. The highest moisture and ash content in the final product of our alginate was recorded as 16.82% and 5.2% respectively. Moisture content was approximately similar to the previously published value. Parthiban et al. noted the Padina sp. had higher ash content than Sargassum sp. Thallus of the Sargassum sp., which is not directly; connect to the bottom of the shore. But thallus of the Padina sp. directly contacts to the bottom of the shore. Due to that reason, there was low mineral content in their thallus of the Sargassum sp. The viscosity and the gel strength were also measured in the final product. The recorded viscosity and gel strength was 40 vcP, 4.54 × 10–2 kN with 0.1 M CaCl2 and 6.86 × 10–2 kN with 0.2 M CaCl2 respectively. The insoluble matter percentage by mass in the alginate was observed as 0.4%.
Under the trace metal content, we analysed the Hg, Cd, As, and Pb. Mercury was not detected in the final product (LOD-0.07 mg/kg) and the Pb, As and Cd concentrations were 2.11 mg/kg, 0.50 mg/kg, and 0.44 mg/kg respectively. The Southern coastal area in Sri Lanka is a very famous area for tourism and most of the industries are located in this area. The number of rivers mouth open to the Southern coastal area. It may be the reason for a considerable amount of some metal (eg., Pb) accumulating in the seaweed.
According to the specification of the Indian standard for alginic acid in food-grade (IS 7928:1993), they recommended the requirements need to be fulfilled to use for food-grade [26]. Table 3 shows the comparison of the final product with the Indian standard.
The result shows that the final product of alginate slightly deviated from the Indian specification. From the results mentioned above, the use of Sargassum wightii species collected from the Southern coastal area must be considered due to the high affinity to extract the alginate. Further studies are needed to determine the availability of the resources, purity, and microbiological parameters of the final products.
4 Conclusion
The results of the present study indicated that the alginate obtained at the laboratory level from the algae Sargassum wightii can be produced at the pilot level with the technology development. To better synthesis of alginate, it is necessary to apply 1% formaldehyde with 2.5% Na2CO3 for a higher yield. As a food additive, attention needs to be paid to the use of alginate with quality and safety. Algae are highly enriched with heavy metals, polychlorinated biphenyls (PCBs) and other environmental contaminants in seawater. In the terms of heavy metals, the present study reported lead, cadmium and arsenic. Therefore, to ensure the safety of seaweed utilization by strictly monitoring and controlling the environment of seaweed breeding and growth. In short, due to its properties such as viscosity, gel strength, insoluble matter, etc., alginic acid will expand its use. Developing new products using alginic acid will be a valuable and promising research direction.
Data availability
The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.
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The authors would like to acknowledge to, laboratory staff in Analytical Chemistry Laboratory, National Aquatic Resources Research and Development Agency (NARA) for their support.
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GDTMJ and BKKKJ equally contributed to the manuscripts. The design idea, plan, and statistical analysis of the research and wrote the manuscript. NAGS conducted the laboratory analysis. All authors read and approved the final manuscript.
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Jayasinghe, G.D.T.M., Jinadasa, B.K.K.K. & Sadaruwan, N.A.G. Pathway of sodium alginate synthesis from marine brown algae, Sargassum wightii from Sri Lanka. Discov Food 2, 2 (2022). https://doi.org/10.1007/s44187-021-00001-5
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DOI: https://doi.org/10.1007/s44187-021-00001-5