Optimization of extraction process and investigation of antioxidant effect of polysaccharides from the root of Limonium sinense Kuntze
Xinhui Tang^{1}, Lifang Yan^{2}, Jing Gao^{3}, Haiyan Ge^{3}, Haidong Yang^{3}, Na Lin^{3}
^{1} Jiangsu Provincial Key Laboratory of Coastal Wetland Bioresources and Environmental Protection, Yancheng Teachers University, Yancheng  224002, People's Republic of China ^{2} Jiangsu Provincial Key Laboratory of Coastal Wetland Bioresources and Environmental Protection, Yancheng Teachers University, Yancheng  224002; School of Pharmacy, Jiangsu University, Zhenjiang  212013, People's Republic of China ^{3} School of Pharmacy, Jiangsu University, Zhenjiang  212013, People's Republic of China
Date of Submission  31Jan2011 
Date of Decision  13Mar2011 
Date of Web Publication  25Aug2011 
Correspondence Address: Jing Gao School of Pharmacy, Jiangsu University, Zhenjiang, 212013 People's Republic of China
Source of Support: None, Conflict of Interest: None  Check 
DOI: 10.4103/09731296.84225
Abstract   
Objective: To optimize the extraction technology for polysaccharides from the root of Limonium sinense (Girard) Kuntze, Plumbaginaceae and evaluate the antioxidant capacity of polysaccharides from L. sinense (LSEP) Materials and Methods : Onesinger factor and response surface methodology(RSM) were established to extract the polysaccharides from L. sinense. Then, the 1,1diphenyl2picrylhydrazyl free radical, hydroxyl radical(.OH), and 2,2'Azinobis(3ethylbenzothiazoline6sulfonic acid) diammonium salt free radical assays were established to measure the antioxidant capacity of the LSEP in vitro. Results: According to analysis, extraction temperature significantly affected extraction yield. The optimum extraction conditions for LSEP were as follows: extraction temperature, 95°C; ultrasonic time 50 minutes; and dosage liquor ratio, 1: 12. Under these conditions, the experimental yield of crude LSEP was 12.80±0.19% which was well matched with the predicted models. The antioxidant capacity data suggested that LSEP has strong antioxidant activity. Conclusion: Onesinger factor and RSM were used to extract of LSEP are simple and feasible and LSEP could be developed as a nutraceutical agent for itsstrong antioxidant activity. Keywords: Antioxidant activities, optimization extraction, polysaccharide, response surface methodology
How to cite this article: Tang X, Yan L, Gao J, Ge H, Yang H, Lin N. Optimization of extraction process and investigation of antioxidant effect of polysaccharides from the root of Limonium sinense Kuntze. Phcog Mag 2011;7:18692 
How to cite this URL: Tang X, Yan L, Gao J, Ge H, Yang H, Lin N. Optimization of extraction process and investigation of antioxidant effect of polysaccharides from the root of Limonium sinense Kuntze. Phcog Mag [serial online] 2011 [cited 2021 Aug 5];7:18692. Available from: http://www.phcog.com/text.asp?2011/7/27/186/84225 
Introduction   
Limonium sinense (Girard) Kuntze, Plumbaginaceae, is a kind of herb mainly distributed along seashores and salts marshes in southern China, Ryukyus (Japan), and western Taiwan of China, and has been used traditionally for treating bleeding, piles, fever, hepatitis, diarrhea, bronchitis, and other disorders. ^{[1]} The hepatoprotective effect of L. sinense against carbon tetrachloride and Dgalactosamine intoxication in rats was reported ^{[2]} and the mechanism underlying its hepatoprotective effects was found to be related to the mitochondrial protection. ^{[3],[4],[5]} Recently, obvious antitumor activity and immune modulation effect of L. sinense were also found. ^{[6]} And, the polysaccharides, which are known as compound to possess numerous biological activities, are one of the most abundant components in L. sinense. However, there was no report about the optimization of extraction conditions for polysaccharides from L. sinense (LSEP).
Response surface methodology (RSM) is an effective tool for optimizing the process, especially when many factors and interactions affect desired response. It has been successfully used for optimizing complex process, extraction technology, conditions of enzyme reaction, and so on. ^{[7],[8],[9]} The advantage of RSM is that it can reduce the number of experimental trials and evaluate the interactions between multiple parameters, which are less laborious and timeconsuming than other optimizing process, and more effective and precise than many approaches.
In this paper, we aim to optimize the production process of LSEP from the L. sinense Kuntze root by RSM, employing a the BoxBehnken design (BBD) (3 factors and 3 levels) to study the effects of extraction temperature, ultrasonic time, and ratio of material to water on the crude extract of LSEP from the root of L. sinense Kuntze. And then, the antioxidant activities were assayed by testing the scavenging abilities on hydroxyl radicals, 1, 1diphenyl2picrylhydrazyl (DPPH), and 2,2'Azinobis(3ethylbenzothiazoline6sulfonic acid) diammonium salt (ABTS) radicals.
Material and Methods   
Materials
The whole plant of L. sinense (Girard) Kuntze, Plumbaginaceae, was collected from the Yancheng Sea Beach in Jiangsu, P. R. China, and identified by Mr. Yu Yanqiu (Jiangsu Provincial Key Laboratory of Coastal Wetland Bioresources and Environmental Protection, Yancheng Teachers University) in December 2008. The root of L. sinense was washed and oven dried at 60°C until the moisture level was constant. Dglucose was from Amresco Inc. All other reagents were of analytical grade.
Extraction and determination of crude polysaccharides from L. sinense
The root of L. sinense were dried, crushed, and extracted under the ratio of it to water (1 : 81 : 16), ultrasonic time (2080 minutes), extracting time (15 hours), temperature (60100°C), and extraction times (14 times). The combined extraction were centrifuged at 5 000 r/minutes for 15 minutes, precipitated with 95% ethanol, ^{[8]} and then precipitated by the addition of dehydrated alcohol to a final concentration of 80 % (v/v). The precipitates (LSEP) collected by centrifugation (2 000 g for 10 minutes, at 20°C) were washed by dehydrated alcohol for three times and dried under reduced pressure. Sugar content was measured by phenolsulfuric method using Dglucose as a standard. The purity of LSEP is calculated as the sugar content of extraction/dried crude polysaccharide weight.
Experimental design and statistical analysis
After determining the preliminary range of the extraction variables through a singlefactor test, a central composite design (CCD) with four independent variables (X1, extraction temperature; X2, ultrasonic time; X3, ratio of material to distilled water) at three levels was performed for statistical calculation, and the variables were coded according to
Where, ψ_{i} is a coded value of the variable; X_{i} the actual value of variable; X_{0} the actual value of the X_{i} on the center point; and ≥X_{i} the step change value. The range of independent variables and their levels are presented in [Table 1], which was based on the results of preliminary experiments. The extraction yield of LSEP was the dependent variables. As seen from [Table 2], the complete design consisted of 15 experimental points, and the experiment was carried out in a random order.  Table 1: Independent variables and their levels used in the response surface design
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 Table 2: Response surface central composite design (uncoded) and results for extraction yield of LSEP
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Data from the CCD were analyzed by multiple regressions to fit the following quadratic polynomial model.
Y represents the response function. β_{k0} is an intercept. Where, β_{ki} , β_{kii} , and β_{kij} are the coefficients of the linear, quadratic, and interactive terms, respectively. And, accordingly, xi and x_{j} represent the coded independent variables, respectively. The fitted polynomial equation is expressed as surface and contour plots in order to visualize the relationship between the response and experimental levels of each factor and to deduce the optimum conditions. ^{[10]} The analysis of variance tables were generated and the effect and regression coefficients of individual linear, quadratic, and interaction terms were determined. The regression coefficients were then used to make statistical calculation to generate dimensional and contour maps from the regression models. SAS (Version 8.0, USA) software package was used to analyze the experimental data. P values of less than 0.05 were considered to be statistically significant.
Assays for antioxidant activities
1, 1diphenyl2picrylhydrazyl radical scavenging assay
The free radical scavenging activity of the polysaccharides was measured by DPPH test according to the method of Shimada with some modifications. ^{[11]} Solution of DPPH in methanol (0.2 mmol/l) was prepared daily before Ultraviolet (UV) measurements. 0.1 ml of the polysaccharides of different addition quantities (10100 μg/ml) in methanol was thoroughly mixed with 3.9 ml of freshly prepared DPPH. The mixture was shaken well, allowed to stand for 30 minutes in the dark, and the absorbance was then measured at 517 nm against a blank. Lower absorbance of the reaction mixture indicated higher free radicalscavenging activity, which was analyzed from the graph plotted of inhibition percentage against compound concentration. V_{C} was used as positive control. The experiment was carried out in triplicate. The capability to scavenge the DPPH radical was calculated using the following equation:
Scavenging rate (%) = [1  (A_{i} A_{J}) / A_{0}] × 100
Where, A_{0} is the absorbance of DPPH solution without sample; A_{i} is the absorbance of the test sample mixed with DPPH solution; and A_{J} is the absorbance of the sample without DPPH solution.
2,2'Azinobis(3ethylbenzothiazoline6sulfonic acid) diammonium salt radical scavenging assay
For ABTS assay, the procedure followed the method of Du et al.^{[12]} with some modifications. The stock solutions included 7 mmol/l ABTS+ solution and 2.45 mmol/l potassium per sulfate solution. The working solution was then prepared by mixing the two stock solutions in equal quantities and allowing them to react for 12 hours at room temperature in the dark. The solution diluted with methanol to obtain an absorbance at 734 nm was 0.70 ± 0.02 using the spectrophotometer. Fresh ABTS+ solution was prepared for each assay. LSEP (0.1 ml) were allowed to react with 3.9 ml of the ABTS+ solution for 6 minutes in a dark condition. Then, the absorbance was taken at 734 nm using the spectrophotometer.
Scavenging rate (%) = [1  (A_{i} A_{J}) / A_{0}] × 100
Where, A_{0} is the absorbance of ABTS solution without sample; A_{i} is the absorbance of the test sample mixed with ABTS solution; and A_{J} is the absorbance of the sample without ABTS solution.
Hydroxyl radical scavenging assay
The assay was measured by the method of RosalesCastro M ^{[13]} with a minor modification. Polysaccharides were dissolved in deionized water at the concentration of 0.1 to 1 mg/ml. The sample solution (2 ml) was mixed with 6 mmol/l of FeSO4 solution (2 ml) and 6 mmol/l H_{2} O_{2} (2 ml) was then added to the reaction solution. The reaction solution was incubated for 10 minutes in room and then added 6 mmol/l of salicylic acid (2 ml) and incubated for 30 minutes. The absorbance of the mixture was measured at 510 nm against blank. The capability to scavenge hydroxyl radical was calculated using the following equation:
Scavenging rate (%) = [1(A_{i} A_{J})/A_{0}] ×100
Where, A_{0} is the absorbance of mixture solution without sample; A_{i} is the absorbance of the test sample mixed with reaction solution; and A_{J} is the absorbance of the test sample without salicylic acid.
Statistical analysis
All the data were shown in . Statistical significance was analyzed by oneway analysis of variance (ANOVA). P value <0.05 was considered statistically significant.
Results and Discussion   
Optimization of extraction conditions
Effect of ratio of material to water on the extraction yield of polysaccharides from L. sinense
The yield of LSEP effected by different ratio of material to water from 1 : 8 to 1 : 16 was shown in [Figure 1]a, while other extraction variables were set as follows: ultrasonic time, 20 minutes; extraction time, 2 hours; extraction temperature, 100°C; and number of extraction, 2 times. The extraction yields of the polysaccharides increased with the ratio increasing from 1 : 8 to 1 : 16, and then it tended to go steady. The more water was used, the more ethanol was exploited to precipitate LSEP. Therefore, extraction ratio 1 : 10 to 1 : 14 was favorable for polysaccharides production.  Figure 1: Effect of different extraction parameters on the yield of LSEP (ratio of material to water; ultrasonic time; extraction time; extraction temperature, and number of extraction)
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Effect of ultrasonic time on the yield of polysaccharides from L. sinense
The yield of LSEP affected by different ultrasonic time (20, 40, 60, and 80 minutes) was shown in [Figure 1]b, when other extraction variables were set as follows: ratio of material to water, 1 : 12; extraction time, 2 hours; extraction temperature, 100°C; and number of extraction, 2 times. The yield of LSEP reached a maximum when the ultrasonic time was 60 minutes. After this point, the yield of LSEP started to a descending with increasing the ultrasonic time. This situation maybe due to the polysaccharide hydrolyses under some temperature with long ultrasonic time. Therefore, ultrasonic time range of 40 to 80 minutes was adopted in this experiment.
Effect of extraction time on the yield of polysaccharides from L. sinense
The yield of LSEP affected by different extraction time (1, 2, 3, and 4 hours) was shown in [Figure 1]c, while other experimental conditions were as follows: ratio of material to water, 1 : 12; ultrasonic time, 20 minutes; extraction temperature, 100°C; and number of extraction, 2 times. The extraction yields of the polysaccharides increased with the increasing extraction time, and then it tended to go steady; however, considering the time and the economic benefits, the extraction time of 2 hours was selected as the optimal in the present experiment.
Effect of temperature on the yield of polysaccharides from L. sinense
As shown in [Figure 1]d, the effect of temperature on extraction yield was investigated. Different extraction temperature was set at 60, 70, 80, 90, and 100°C, while the other factors were set as follows: ratio of material to water, 1 : 12; ultrasonic time, 20 minutes; extraction time, 2 hours; and number of extraction, 2 times. The yield of LSEP increased with the increasing temperature and reached the peak value at 100°C, while the color is deepened from the extracted solution when the temperature was above 100°C. It is speculate that high temperature may affect the polysaccharide structure and activity, i.e., and the temperature (more than 100°C) easily decomposed polysaccharides to monosaccharide, which can impact the extraction rate. Therefore, 90100°C was considered to be optimal extraction temperature in this experiment.
Effect of extraction number on the yield of polysaccharides from L. sinense
The yield of LSEP affected by different number of extraction (14 times) was shown in [Figure 1]e, while other experimental conditions were as follows: ratio of material to water, 1 : 12; ultrasonic time, 20 minutes; extraction time, 2 hours; extraction temperature, 100°C. The yield of LSEP unexpectedly gets the point when number of extraction is from 1 to 3 times; however, the yield of LSEP no longer obviously changed with the increasing number of extraction. However, considering the economic benefits and the time, 2 times was selected as the optimal extraction number in the present experiment.
According to the singleparameter study, we adopted extraction temperature of 80 to 100°C; ultrasonic time, 20 to 60 minutes; and ratio of material to water, 1 : 10 to 1 : 14 for RSM experiments.
Predicted model and statistical analysis
The design material and the corresponding results of RSM experiments to determine the effects of the three independent variables including extraction temperature (X_{1}); ultrasonic time (X_{2}); and ratio of material to water (X_{3}) are shown in [Table 3]. By employing multiple regression analysis on the experiment data, the predicted model was obtained by the following secondorder polynomial function:
 Table 3: Regression analysis analyzed by oneway analysis of variance for responses surface quadratic model analysis of variance table (Practical sum of squaresType)
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The fit statistics of extraction yield (Y) for the selected quadratic predictive model is shown in [Table 3]. The dependent variable and the independent variables were highly significant (R^{2} = 0.9624), which indicated this experimental method is reliable. It suggests the regression equation can instead of the true test to analyze the experimental results. The ANOVA analysis is also shown in [Table 3]. P value is 0.0046 and the P values were used as a tool to check the significances of each coefficient. The smaller the P value was, the more significant the corresponding coefficient was. ^{[14]} It can be seen that the variable with the largest effect was the interaction effects of extraction temperature to ultrasonic time (X_{1} × X_{2}), followed by the linear terms of extraction time (X_{1} , X_{1} × X_{1} , and X_{3} × X_{3}). The other term coefficients (X_{2} , X_{3} , X_{1} × X_{3} , X_{2} × X_{3} , and X_{2} × X_{2}) were not influential (P>0.05).
Response surface plot and contour plot
3D response surface and 2D contour plots were the graphical representations of regression function. They showed the type of interactions between two tested variables and the relationship between responses and experiment levels of each variable. Different shapes of the contour plots indicated different interactions between the variables. Circular contour plot indicated that the interactions between the corresponding variables were negligible, while elliptical contour plot indicated otherwise. In the present study, the response surface and contour plots were obtained by using SAS version 8.0 and are presented in [Figure 2]. As shown in [Figure 2]a, when extraction temperature (X_{1}) was fixed, ultrasonic time (X_{2}) and ratio of material to water(X_{3}) demonstrated quadratic effects on the extraction yields. The elliptical contour plot shown in [Figure 2]d indicated that the mutual interactions between ultrasonic time and ratio of material to water were significant. [Figure 2]b and [Figure 2]e show that when ultrasonic time (X_{2}) was fixed, the variations of yields were negligible with the extraction time increase. [Figure 2]c shows that when ratio of material to water (X_{3}) was fixed and ultrasonic time kept at lower level, the yield increased at first and then decreased with the increase of temperature (X_{1}). From [Figure 2]f, it indicated that the mutual interactions between temperature and ultrasonic time were much significant. By analyzing the plots, the predicted values (13.5%) of the tested variables for polysaccharides lied in the following condition: extraction temperature, 95°C; ultrasonic time, 50 minutes; and ratio of material to water, 1 : 12. In the optimal conditions, the experiment yield of crude LSEP was 13.0 %, which agreed with the predicted value. Therefore, the results indicated suitability of the model employed and the success of RSM in optimizing the extraction conditions.  Figure 2: (ac) Response surface plots for the effects of (a) ultrasonic time and ratio of material to water; (b) extraction temperature and ratio of material to water; (c) extraction temperature and ultrasonic time on the yield of polysaccharide; (df) Contour plots for the effects of (d) ultrasonic time and ratio of material to water; (e) extraction temperature and ratio of material to water; (f) extraction temperature and ultrasonic time on the yield of polysaccharide
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Verification of predictive model
The suitability of the model equations for predicting optimum response values was tested under the following conditions: extraction temperature, 95°C; ultrasonic time, 50 minutes; and ratio of material to water, 1 : 12. This set of conditions was determined to be optimum by the RSM optimization approach and was also used to validate experimentally and predict the values of the responses using the model equation. A mean value of 12.80 ± 0.19 (%) (n = 3), obtained from real experiments, demonstrated the validation of the RSM model, indicating that the model was adequate for the extraction process.
Antioxidant activity analysis
Oxidation is essential to many organisms for the production of energy in biological processes. ^{[15]} Reactive oxygen species, ^{[13]} in the forms of superoxide anion (.O_{2}^{}), hydroxyl radical (.OH), and hydrogen peroxide (H_{2} O_{2}), are generated by normal metabolic processes or from exogenous factors and agents that can easily initiate the peroxidation of membrane lipids, leading to the accumulation of lipid peroxides. ^{[16]} Polysaccharides have exhibited strong antioxidant properties and can be developed as novel potential antioxidants. ^{[17]} Antioxidant activities of LSEP were assayed by using the models of scavenging DPPH, ABTS, and hydroxyl radicals.
Scavenging activity of 1, 1diphenyl2picrylhydrazyl radicals
In the DPPH test, the antioxidants are able to reduce the stable DPPH radical to the yellowcolored diphenylpicrylhydrazine. The scavenging ability of the samples is shown in [Figure 3]. [Figure 3]a shows that the scavenging rate of LSEP on the DPPH radical increased dosedependently and up to 97% at a dose of 80 μg/ml, which is similar to 100 μg/ml V_{C}.  Figure 3: Antioxidant effect of LSEP against different kind of free radicals. (a) scavenging activity of 1, 1diphenyl2picrylhydrazyl radicals; (b) scavenging activity of 2,2'Azinobis(3ethylbenzothiazoline6sulfonic acid) diammonium salt radicals; (c) scavenging activity of hydroxyl radicals; data are presented as mean values (n = 3)
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Scavenging activity of 2,2'Azinobis(3ethylbenzothiazoline6sulfonic acid) diammonium salt radicals
The scavenging ability of the samples on ABTS radicals is shown in [Figure 3]. [Figure 3]b shows that the scavenging effects of LSEP on the ABTS radicals increased in a concentrationdependent manner. The scavenging effects of 600 μg/ml LSEP (97 %) was higher than those of 100 g/ml V_{C} (60%), which suggested that LSEP had a strong antioxidant activity.
Scavenging activity of hydroxyl radicals
The scavenging effect of LSEP on hydroxyl radicals is shown in [Figure 3]c. The scavenging effect of LSEP increased with increasing concentration. The scavenging rate of 1 mg/ml LSEP was 70%, which is similar to the effect of V_{C} (1 mg/ml).
Conclusions   
The singlefactor experiments and BBD along with RSM were applied for optimizing extraction LSEP in this study. The optimal conditions for the production of polysaccharide were as follows: extraction temperature, 95°C; ultrasonic time, 50 minutes; and ratio of material to water, 1 : 12. In the optimal conditions, the experiment yield of LSEP was 12.80 ± 0.19 (%), which was agreed with the predicted value. The experimental conditions allow a fast and costsaving process in extraction of polysaccharide from the root of L. sinense Kuntze. And, at the same time, LSEP showed obvious scavenging activities on DPPH, ABTS, and hydroxyl radicals, which indicated that LSEP had antioxidant activity against various reactive oxygen species (ROS) and could be developed in the near future.
Acknowledgement   
This work was financially supported by the Natural Science Fund of Jiangsu Province (No. BK2009172), the Natural Science Foundation of Education Department of Jiangsu Province (Key Project No. 07KJA18017), the Natural Science Research Foundation of Jiangsu Province Higher Education (No. 08KJB360011), and the "333 Project" Funding for the Jiangsu Province.
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[Figure 1], [Figure 2], [Figure 3]
[Table 1], [Table 2], [Table 3]
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