Table 2.
Advantages and disadvantages of purification methods of polysaccharides.
| Sr. no | Methods | Advantages | Disadvantages |
|---|---|---|---|
| 1 | Graded precipitation | Easy-to-operate; often used firstly. | Unable to obtain homogeneous polysaccharide fractions. |
| 2 | Salting-out method | Cost-effective. | Low efficiency; easy to form co-precipitation. |
| 3 | Metal coordination | Good specificity. | It is not easy to find a proper coordination reagent. |
| 4 | Quaternary ammonium salt precipitation | Often used to purify acidic polysaccharides and neutral high-MW polysaccharides; good selectivity. | Need to accurately adjust/control ionic strength and pH of the solution. |
| 5 | Column chromatography: | ||
| i. Cellulose column | Purity of the eluate is high. | Low flow rate; long time-consuming. | |
| ii. Anion exchange column | Most widely used; fit for purifying various acidic/neutral polysaccharides and mucopolysaccharides. | Sometimes the height of column bed may change when pH of buffer changes. | |
| iii. Gel column | Principle of molecular sieve; often used to further purify polysaccharides. | The ionic strength of eluent should not be less than 0.2 mol/L. | |
| iv. Affinity column | High efficiency; easy-to-operate. | Difficult to find a proper ligand for a given polysaccharide. | |
| 6 | Ultracentrifugation | Good efficiency. | High requirement for equipment; mostly used for semi-micro preparation of polysaccharide. |
| 7 | Ultrafiltration | Principle of molecular sieve. | Low yield; long time-consuming. |
| 8 | Preparative zone electrophoresis | Good separation effect. | Long time-consuming; small purification capacity; only used for semi-micro preparation. |