Molecular weight data of the PCE Extract.
Ginseng has a long history of use as a traditional medicine; and it is one of the top selling medicinal herbs in the world. It is a multi-action herb with a wide range of pharmacological effects on the central nervous system, cardiovascular system and endocrine secretion, and the reproductive and immune systems . Ginseng is a deciduous, perennial plant of the Araliaceae family. There are two major species of ginseng: Panax ginseng and Panax quinquefolius; and the roots are primarily used for medicinal benefits. Ginseng’s wide range of pharmacological activities is believed to be due to the presence of a host of bioactive compounds. The primary ones are the ginsenosides, which are steroidal saponins conjugated to different sugar moieties and polysaccharides (PS) which account for 10-20% by weight of ginseng.
Polysaccharide components of ginseng have received much attention recently because of the emergence of different biological activities, such as immunomodulatory, antibacterial, anti-mutagenic, radioprotective, anti-oxidative, anti-ulcer, antidepressant, anti-septicaemic and anti-inflammatory activities . Specifically, the polysaccharide fraction of ginseng has been shown to have immunomodulatory effects in both preclinical and clinical studies [3-6], although they are poorly characterized.
Several polysaccharides have been identified in P. ginseng and P. notoginseng but these compounds, including arabinogalactan, pectins, and acidic polysaccharides, have been rarely studied in the North American species. They are made up of a complex chain of monosaccharides rich in L-arabinose, D-galactose, L-rhamnose, D-galacturonic acid, D-glucuronic acid and D-galactosyl residues . The actual structural characteristics and the heterogeneity of PS components are poorly understood due to a lack of methodologies for separation as well as quantitative and qualitative analysis.
Most studies have focused on Asian ginseng PS and mostly in vitro experimental models. In this chapter, we will focus on Panax quinquefolius (American ginseng). The use of gel permeation chromatography (GPC) with multiple detectors has provided enhanced resolution for phytochemical analysis. And we have used both in vivo and in vitro models to evaluate its immunomodulatory activity.
Ginseng. Four-year-old American ginseng roots collected in 2007 from five different farms in Ontario, Canada were provided by the Ontario Ginseng Growers Association. Ginseng extracts from each farm were prepared individually and combined to produce composite extracts which were used for phytochemical and pharmacological studies . The AQ extract has no detectable endotoxin contamination as determined by Limulus test.
2.1. Chemicals and biologicals
Sephadex G75 was purchased from GE Healthcare Bio-Sciences AB (Sweden). The Diethylaminoethyl (DEAE)-Cellulose and monosaccharide standards were purchased from Sigma (Oakville, Ontario). All other chemicals were of analytical grade and used as received. Cell culture medium and reagents were purchased from Gibco laboratories (USA). BD OptEIA ELISA kits tumour necrosis factor-α and interleukin-6 (BD Biosciences, USA). LPS from Escherichia coli and Griess reagent were purchased from Sigma-Aldrich (USA).
Animals. Adult male Sprague-Dawley rats (200–250g; Charles River, St. Constant, QC, Canada) were used. The Animal Ethics Review Committee of the Western University approved the study (Protocol No: 2009-070).
Preparation of the aqueous (AQ) and polysaccharide (PS) ginseng extracts. Dried ginseng root samples were shipped to Naturex (USA) for extraction. Samples were ground between ¼ and ½ inch and used to produce the AQ extract . Briefly, 4kg ground ginseng roots were soaked three times during five hours in 16L of water solution at 40°C. After extraction, the solution was filtered at room temperature. The excess solvent was then removed by a rotary evaporator under vacuum at 45°C. The three pools were combined and concentrated again until the total solids on a dry basis were around 60%. These concentrates were lyophilized with a freeze dryer (Labconco, USA) at -50°C under reduced pressure to produce the AQ ginseng extract in powder form. Yield of the powder extracts from the concentrates was about 66%. The yields of the final extract (mean ± standard deviation of % extractive) from the initial ground root were 41.74±4.92.
A solution of AQ extract in distilled water (10g/10mL) was prepared, and the crude PS was precipitated by the addition of four volumes of 95% ethanol. The PS fraction was collected by centrifugation at 350×g (Beckman Model TJ-6, USA) for 10 minutes and lyophilized to produce the crude PS extract.
To prepare the water soluble polysaccharide extract (WSPE), ginseng roots (500 g) were extracted with 7.0 L of MilliQ (EMD Millipore) water at 100 ºC for 4 h and filtered through sheets of glass fiber. The solid material was extracted twice under identical conditions. The filtrates were combined, then centrifuged to remove water insoluble materials and supernatants were concentrated (1.0 L) and precipitated by the addition of 95% ethanol (4 to 1 volumes). After centrifugation, the precipitate was washed and dried by solvent exchange, first using 95% ethanol, and then absolute ethanol. Crude water soluble polysaccharide extract (WSPE) was obtained with a 20.0 % yield (relative to dry weight of plant material) (Figure 1).
3.1. Chromatography of ginseng extracts
High performance liquid chromatography (HPLC) analysis for ginsenoside determination
HPLC analysis on the composition of ginsenosides in the AQ extracts (100mg/ml methanol) was performed with a Waters 1525 HPLC System with a binary pump and UV detector . A reversed-phase Inspire C18 column (100mm×4.6 mm, i.d. 5μm) purchased from Dikma Technologies (USA) was used for all chromatographic separations. Gradient elution consisted of [A] water and [B] acetonitrile at a flow of 1.3mL/min as follows: 0min, 80-20%; 0-60min, 58-42%; 60-70min, 10-90%; 70-80min, 80-20%. Absorbance of the eluates was monitored at 203nm.
Sephadex G-75 chromatography
AQ ginseng extract (500mg) was dissolved in 5mL distilled water and then fractionated by loading to a calibrated Sephadex G-75 column (47×2.5cm) equilibrated and eluted with distilled water mobile phase at 4°C with a flow rate of 1mL/min . Absorbance of the eluates was monitored at 230nm. Fractions were collected and lyophilized for the study of bioactivity distribution.
Preparation of the de-proteinated water soluble polysaccharide extracts (DWSPE)
WSPE (50 g) were re-dissolved in 1.5 L of MilliQ water and partitioned five times with Sevag reagent (1:4 n-butanol:chloroform, v/v, 500 mL each) to remove proteins . Polysaccharides were precipitated again by ethanol and dried by solvent exchange. This procedure yielded 46.0 g of the de-proteinated water soluble polysaccharide fraction (DWSPE). The procedure for the preparation of DWSPE from P. quinquefolius is shown in Figure 1.
Total fractionation of the DWSPE by ion exchange chromatography on DEAE-Cellulose
DWSPE fraction (20 g) was dissolved in MilliQ water (200 mL) and loaded on a DEAE-Cellulose column (10.0 X 20 cm, Cl-) pre-equilibrated with MilliQ water. The column was eluted first with 4.0 L of MilliQ water at a flow rate of 10 mL/min (4 bar column pressure) to obtain the unbound or neutral fraction (DWSPE-N) and then with 4.0 L of 0.5 M NaCl to obtain the bound or acidic fraction (DWSPE-A). The fractions were concentrated, dialyzed (cut off pore size of 2 KDa) against MilliQ water and freeze dried to give 15.0 g (13.8 %) of the DWSPE-N and 0.9 g (0.83 %) of the acidic fraction DWSPE-A. DWSPE-A (0.6 g) was dissolved in 50 mL MilliQ water and loaded on a DEAE-Cellulose column (10 X 20 cm, Cl-). The column was eluted by a stepwise gradient with 2.0 L of NaCl aqueous solutions (0.0, 0.1, 0.2, 0.3 and 0.5 M each) at a flow rate of 10 mL/min (4 bar column pressure). A total of 120 eluate fractions were collected (50 mL each), dialyzed and lyophilized (Figure 2).
High performance gel permeation chromatography-evaporative light scattering detection (HPGPC-ELSD) analysis
HPGPC was carried out at 40 ºC using a TSK-gel G-3000PWXL column (7.8 X 300 mm, TOSOH, Japan) connected to a HPLC system coupled with Diode Array and Evaporative Light Scattering Detectors (DAD-ELSD). The column was calibrated with standard dextrans (5 to 410 KDa range, Figure 7-B). Ten microliters of 20 mg/mL solutions of DWSPE, DWSPE-N and DWSPE-A were separately injected and eluted with HPLC grade water at a flow rate of 0.8 mL/min and monitored using ELSD with a temperature setting at 80 °C.
High performance gel permeation chromatography-multi-detector analysis
AQ and PS ginseng extracts were analysed at 40°C with TSK-gel PWXL G-4000PWXL column (7.8 X 300 mm, TOSOH, USA) connected to a Viscotek (Varian Instruments, USA) gel permeation chromatography system with Omnisec software (version 4.5, Viscotek, USA) for data acquisition. Solutions of AQ and PS extract (1mg/mL) were filtered with 0.2µm nylon filter and used for analysis. Each sample (100µl) was injected and eluted with 0.3M sodium chloride (NaCl) mobile phase at a flow rate of 1mL/min and monitored using a multiple detectors system for light scattering, refractive index and viscosity. Pullulan polysaccharide reference standard was analyzed as a positive control.
3.2. Analysis of the monosaccharides composition in WSPE by HPLC-ELSD
Carbohydrate analysis represents a challenge in analytical chemistry since neutral or acidic saccharides (mono, oligo and poly) have little UV activity. In our study, evaporative light scattering detection (ELSD) was used. The ELSD does not require the solutes of interest to have any optical properties; and the only requirement is that the eluent be more volatile than the solutes. WSPE (20 mg) was dissolved in 10 mL of 2N HCl solution and was boiled for 2 h. The hydrolyzed product was neutralized (pH 6-7) and centrifuged before analysis.
HPLC analysis was conducted using an 1100 series HPLC-DAD-ELSD system (Agilent Technologies Inc., Santa Clara, CA, USA). To enhance resolution of monosaccharides, analysis was performed using two separate columns (Figure 2). Glucose, galactose, arabinose, mannose and xylose were eluted using a Rezex RPM Monosaccharide PB+2 (8%) (Phenomenex, Torrance, California) column with a mobile phase of 100 % water (Chromasolv Plus, HPLC grade) isocratically at 80 °C and a flow rate of 0.6 mL/min. The ELSD temperature was set to 80 °C. Galacturonic acid and rhamnose content were examined using a Luna 5 μ NH2 100Å column (Phenomenex, Torrance, California) and eluted with a mobile phase of acetonitrile and water (80:20) at 40 °C and a flow rate of 3 mL/min. The ELSD temperature was set to 44 °C.
3.3. Pharmacological evaluation
3.3.1. In vivo study
Adult male rats (250-300 gm) were treated with 125 mg/kg of AQ extract or crude PS fraction dissolved in saline by gastric garvage (10 ml/Kg bwt) once daily for 3 or 6 consecutive days, and examined 24 hr after the last dose. Animals were anesthetized with i.m. injection (80 and 5 mg/kg b.wt. ketamine and xylazine, respectively) and the trachea was cannulated for lung bronchoalveolar lavage (BAL) with Dulbecco’s phosphate-buffered saline (PBS) to collect alveolar macrophages.
Blood was collected into heparinized tubes from rats by intracardiac puncture, samples were immediately centrifuged at 3000 rpm for 10 minutes and the plasma was separated, aliquoted and stored at -20 °C until use.
3.3.2. In vitro study
Rat alveolar macrophages were collected by BAL using cannulated 10-ml syringe with three 10ml washes of PBS. Fluid recovered from BAL was centrifuged at 1000 rpm for 5 minutes. Cells were cultured in RPMI-1640 medium supplemented with 10% Fetal Bovine Serum (FBS), 25mM HEPES, 2mM Glutamine, 100IU/ml penicillin and 100μg/ml streptomycin in 96-well tissue culture plates, at a density of 2×105 cells per well at 37°C maintained in a humidified incubator with 5% CO2.
Experiments to evaluate dose-related stimulation of inflammatory mediators profile in vitro were carried out by treating and incubating rat alveolar macrophages with 0, 50, 100 and 200μg/ml of ginseng extracts for 24 hours and washed before challenging with LPS (1μg/mL) was used as positive control. The 24 hours-production of NO, TNF-α and IL-6 in culture medium was determined.
To examine the direct inhibitory effect of ginseng extracts on LPS-stimulated immune function, we pre-treated the macrophages with 0, 50, 100 or 200μg/ml of ginseng extracts for 24 hours and washed before challenging with LPS (1 μg/ml). The 24-hour cytokine production induced by LPS was determined by measuring NO, TNF-α and IL-6 levels in the culture medium.
3.3. Quantification of NO, TNF-α and IL-6
TNF-α and IL-6 concentrations in supernatants from cultured cells and plasma were analyzed with ELISA . Samples were evaluated with rat cytokine-specific BD OptEIA ELISA kits (BD Biosciences, USA) according to the manufacturer’s protocol. NO production was analyzed as accumulation of nitrite in the culture medium. Nitrite in culture supernatants was determined with Griess reagent (Sigma-Aldrich, USA) as previously described .
3.4. Statistical analysis
In vivo and in vitro experiments were performed at least three separate times. All statistical analyses were performed with GraphPad prism 4.0a Software (GraphPad Software Inc., USA). Data were presented as the mean ± standard deviation (SD) of triplicates from three independent experiments. Data sets with multiple comparisons were evaluated by one-way analysis of variance (ANOVA) with Dunnett’s post-hoc test. P<0.05 was considered to be statistically significant.
Ginsenoside Compositon. AQ extract contained a total ginsenoside content of 13.87% dry weight of extract and showed characteristics of Panax quinquefolius with Rb1 and Re as the predominant ginsenosides, with no detectable Rf and minimal levels of Rg1 (Fig.3).
Crude PS extract. The yield of crude PS fraction by four volumes of 95% ethanol precipitation was 10 % dry weight of root materials. A representative G-75 chromatographic profile of the crude PS extract is shown in Figure 4 . The major PS peak (with a elution volume of 100 ML) had an estimated average molecular weight of 73kDa, while there were two minor, less well- resolved peaks (Fig 4 ).
Monosaccharide composition of the WSPE determined by HPLC-ELSD. Representative chromatograms showing individual monosaccharides in water soluble polysaccharide extract (WSPE) are shown in Figure 5 and 6. Glucose was found to be the major neutral monosaccharide present in WSPE with amounts ranging from 77 to 86 % (w/w). Galactose and arabinose were present in similar amounts with galactose being present at levels of 6.8 to 7.5 % (w/w) and arabinose being present at levels between 4.5 to 5.9 % (w/w). Galacturonic acid was also identified on WSPE at levels ranging from 8.7 to 9.5 % (w/w). Mannose and xylose were also monitored but were not detected in the sample.
Total fractionation of the DWSPE by ion exchange chromatography on DEAE-Cellulose. To further analyse the WSPE, the material was de-proteinated using the Sevag method, giving a DWSPE with a yield of 92% and the protein content yield of 1.8% (relative to the dry weight of WSPE). Fractionation of WSPE by a combination of anion-exchange on DEAE-cellulose and gel permeation chromatographies with a procedure shown in Figure 1 revealed the elution of a neutral fraction with water (N-DWSPE, 75 % relative to the dry weight of DWSPE) and an acidic fraction (A-DWSPE, 4.5%) with a 0.5 M NaCl solution (Figure 7). Both fractions presented a wide and complex molecular weight distribution ranging from 5 to 410 KDa. The acidic fraction A-DWSPE containing most likely uronic acids was subjected to a second fractionation by DEAE-cellulose chromatography.v
Secondary Fractionation with the A-DWSPE on DEAE-Cellulose column chromatography. The elution of 0.6 g of A-DWSPE on a DEAE-cellulose chromatography was carried out using a stepwise gradient of NaCl. With these elution steps, A-DWSPE was separated into six fractions (Figure 2): A-DWSPE-1 (F1-F20, 96 mg, 16 %), A-DWSPE-2 (F21-F40, 54mg, 9%), A-DWSPE-3 (F41-F60, 162 mg, 27%), A-DWSPE-4 (F61-F80, 120mg, 20%), A-DWSPE-5 (81-F100, 78mg, 13%) and A-DWSPE-6 (F101-F120, 60mg, 10%) corresponding to the elution with 0.0, 0.1, 0.2, 0.3, 0.4 and 0.5 M NaCl solutions, respectively.
In order to further analyze the unique NA ginseng polysaccharide samples, GPC with multiple detectors was utilized. Figure 8 shows the results of multiple pullulan polysaccharide standards ranging from 1800 Da to 1,050,000 Da. The utilized column gave good resolution of the individual standards over this range. Figure 8 shows the results of the multi-detector system containing 4 different detectors, i.e. refractive index (RI), right angle light scattering, low angle light scattering and viscometer. In Figure 9, the crude polysacchride extract is observed to have three major peaks with Mw values of 1092 kDa, 135 kDa and 12 kDa (Table 1). The major peak at 1092 kDa accounts for 66% of the weight fraction. Figure 9 shows the deproteinated polysaccharide fraction, in which the Mw values are largely unchanged (Table 1). However, the protein content fraction (PTF) contains only a small amount of carbohydrates with the majority of the high molecular weight fraction removed. The acid fraction contains 3 peaks, of generally lower Mw values, while the neutral fraction obtained from anionic exchange of DWSPE contains only one broad peak (Figure 9).
|RI area (mVmL)||5.84||2.03||1.03|
|Weight fraction (% of RI area)||65.6%||22.8%||11.6%|
5. Immunomodulatory activity
In vivo effect. Treatment with AQ extract for 3-6 days produced marked stimulation of alveolar macrophages as determined by increased production of NO and TNF- and IL-6 following culturing for 24 hrs, reaching activities that were 50-100% of the positive (LPS) control (Figure 10). This immunostimulatory effect was also reflected in the elevation of plasma TNF- and IL-6 levels of treated animals (Figure 11). However, the responsiveness of macrophages collected from ginseng treated animals to LPS stimulation ex vivo showed >50% to 100% reduction in NO, TNF-α and IL-6 production as compared to those non-ginseng treated controls, especially with 6 days of ginseng treatment (Figure 10). These data showed that orally administered AQ extract had both immuno-stimulatory and anti-inflammatory effect. Data presented in Figure 12 showed that this immunomodulatory activity could be extended to the PS extract on the basis of its effect on macrophage NO production and the LPS responsiveness.
In vitro effect
Both AQ, crude PS and acidic PS showed stimulation of NO and TNF-α production by alveolar macrophages in vitro (Figure 13). The magnitude of the response to PS was greater than those induced by acidic PS or AQ extract. Neutral PS was devoid of activity. The lack of concentration-dependent effect of PS was probably due to its high potency and inducing its maximum effect at the concentration studied. Data presented in Figure 14 showed how pretreatment with various extracts for 24 hrs altered the subsequent response to LPS challenge. Since prior LPS treatment was known to cause desensitization of subsequent response to LPS, this was used as a positive control to evaluate the immunosuppressive effect of ginseng extracts. It was apparent that PS was the most effective in reducing the NO and TNF-α response to LPS, while the AQ and acidic PS extracts were similar, and neutral PS was inactive.
Medicinal plants have been in use for human health for thousands of years, yet polysaccharides have only been recognized recently as a major contributor to the bioactivity of these traditional medicines. Polysaccharides from plant sources with immunomodulatory, anti-tumor, anti-viral, anti-bacterial, anti-inflammatory, anti-oxidant, and anti-diabetogenic activities have been reported [2, 9-15]. And a few polysaccharides, including lentinan, Astragalus polysaccharide, polyporus polysaccharide and Achyranthes bidentata polysaccharide have been licensed for clinical application in China . In Canada, a polysaccharide-enriched American ginseng extract (Cold Fx®) has been licensed in 2007 as a natural health product to ‘help reduce the frequency, severity and duration of cold and flu symptoms by boosting the immune system’ with an estimated annual sale of over $48M [4, 5]. Our findings on the paradoxical effects of AQ and PS extract on macrophage function in vivo may have significant implication in the use of American ginseng polysaccharides in several clinical applications.
The structure and biological activities of the polysaccharides from the roots, leaves and fruits of Panax ginseng have recently been reviewed by Sun . There is limited information on American ginseng. Our study in vitro has demonstrated the up-regulation of inflammatory mediators production by AQ and crude PS extracts in rat alveolar macrophages (Figure 13) which validated what we have previously reported [3 and 6]. In addition we have demonstrated specificity of PS in that acidic but not neutral species of the PS was bioactive. Following sub-acute oral administration, both PS and AQ extracts were also immuno-stimulatory based on elevation of plasma cytokine levels and increase in the function of alveolar macrophages ex vivo. The immuno-stimulatory dosage used in the present in vivo study was comparable to those proven to be effective for cardiovascular health and for protection against diabetic retinopathy, neuropathy and cardiomyopathy reported by other investigators using identical ginseng extracts and in the same animal species [17-19]. However, the magnitude of the immunostimulatory effect in vivo was smaller than the in vitro response. This may be related to the lower bioavailability of the orally-administered ginseng extract. The pharmacokinetics of oral ginseng PS is not known, but the recovery of major ginsenosides in plasma after oral administration was quite low . Result of our in vitro and in vivo studies was supportive of what was reported for CVT-E002 (a patented, poly-furanosyl-pyranosyl polysaccharide-rich extract of the root of North American ginseng): stimulation of normal mouse spleen cells and immunoglobulin G production as well as activation of peritoneal exudate macrophages leading to enhanced cytokine stimulation in treated mice.
In addition to the well-recognized immuno-stimulatory activity of ginseng, an anti-inflammatory effect was shown in the present study as reflected in the reduced responsiveness of alveolar macrophages collected from ginseng-treated animals to LPS challenges ex vivo (Figure 10). This apparent anti-inflammatory effect of ginseng PS is different from what we have previously reported for a specific component(s) of the alcoholic extract of American ginseng as well as the anti-inflammatory effects that have been ascribed to some ginsenosides and their metabolites [6, 21-22]. This potential anti-inflammatory mechanism is being validated by evaluating changes in LPS–induced inflammatory response following polysaccharide pretreatment in vivo in our on-going research. The intent is to determine whether ginseng PS causes desensitization of immune cells as reported for LPS . This action of ginseng, when proven, may be particularly relevant to bacterial infection and related toxicemia. An anti-inflammatory effect of ginseng polysaccharide has been reported by Zhao et al. using a model of auto-immune disease, as evidenced by the reduction in the expression of TNF-α and IFN-γ in lymphocytes in the enteric mucosal immune system of rats with collagen induced arthritis . In view of the diverse immunomodulatory effects of ginseng polysaccharide, the identification of specific polysaccharides with unique property and biological action will be of great interest.
It appears that AQ and PS ginseng extracts have a paradoxical effect on macrophage function: stimulation under normal condition, but reduction when the biological system is under a pro-inflammatory state. In the context of sepsis, AQ and PS immuno-stimulatory effect will be beneficial as a first line of defense during the initial infection stage of bacterial infection by rendering macrophages to be cytotoxic  whereas the immune-suppressive activity may be effective in antagonizing the cytokine storm at the later stages of infection by suppressing LPS activation of macrophages.
Carbohydrates analysis represents a major challenge in analytical chemistry since neutral or acidic saccharides (mono, oligo and poly) have little UV activity. The refractive index (RI) detector, which is commonly used in HPLC analysis, has issues with baseline stability and sensitivity. The ELSD used in the present study has the advantage of its independence of any optical properties in the solutes of interest. Our HPLC-based analysis allowed the measurement of 7 mono-saccharides within a 30 minute total run time. The monosaccharide composition of P. quinquefolius reported in this study was similar to that described previously  with the addition of galacturonic acid. The monosaccharide composition provides insight into the types of polysaccharides which may be found in P. quinquefolius. Polysaccharides structures in P. quinquefolius have not previously been thoroughly studied, though several polysaccharides have been isolated from P. ginseng and P. notoginseng. Glucose and galacturonic acid were the most prominent monosaccharides detected. Previously, polysaccharide fractions from P. ginseng with high levels of glucose have been determined to contain starch-like glucans and arabinogalactans and fractions with high levels of galacturonic acid have been shown to contain pectins with several linked galacturonic acid domains . It is possible that polysaccharides similar to these may be present in Ontario-grown American ginseng though further work will have to be done to characterize their structures.
Polysaccharides are very complex with a wide range of MW, varying monosaccharide composition and conformation (degree of branching or linearity), which contribute to their diverse structure and biological activities, these can also hamper the study of their structure–function relationships . The multi-detector GPC instrument provided additional information on the polysaccharide structure. This instrument uses Triple detection with a concentration detector (refractive index detector), viscometer and light scattering detector, with each detector providing different although complementary information . Pullulan standards of up to 1,000 kDa showed that the measured ginseng polysaccharide molecular weights for the crude, water soluble and deproteinated extracts are within the range of standards. The light scattering detector, which is based on fluctuations in interference between macromolecules (e.g. polysaccharides) scattering a coherent monochromatic laser beam, is considered an absolute detector for Mw values, confirming the reported values of Table 1. The viscometer is sensitive to branching effects, although the trace in Figure 9 shows no significant branching effect for the ginseng polysaccharides. The RI detector was rather sensitive to the carbohydrate fractions, showing 3 major polysaccharide components for each of the three measured extracts. The high molecular weight peak has a very low intensity for the PTF sample, indicating that the deproteination step removed the high molecular weight fraction. The neutral extract gave similar molecular weights as the acidic polysaccharide extract, although with a higher sample recovery.
7. Conclusions and future directions
Our study has revealed a paradoxical immunomodulatory effect of AQ and PS extracts isolated from Ontario-grown Panax quinquefolius. This activity may be relevant to clinical application involving bacterial infection and toxemia. Challenges in development of botanical polysaccharides for clinical application include lack of methodology for structure identification and characterization, isolation and purification, and product quality control, has been recognized . Our research will focus on the application of new methodologies to characterize the polysaccharide structures from ginseng and to elucidate the structure-biological activity relationship.