Table 1.
Encapsulation technique | Capsule size | Advantages | Disadvantages | References |
---|---|---|---|---|
Emulsification | 0.2 um−8 mm | • Higher survival rates of bacteria • Control release of capsules with desired size |
• Variation in shape of capsules • Addition of extra polymer layer to protect encapsulated cells |
(9) (28) |
Spray drying | 10–120 um | • Easy scale- up with mass production • Inexpensive • Economic process with minimum energy utilization |
• Higher temperatures results in loss of viability of cells • Incorporation of additional cooling devices |
(29) (30) |
Lyophilisation | - | • Provides larger surface areas of microcapsules • Most widely used method for sensitive materials |
• Formation of ice crystals damage probiotic cells • Need of additional cryo- protectants |
(31) (32) |
Extrusion | 1,000–5,000 um | • Easy scale- up with mass production • Inexpensive • Continuous process |
• Large size capsules formation • Complex setting of physico- chemical parameters |
(33) (34) |
Electrospraying | 5 um- 1,000 um | • High voltage and speed reduces chances of toxicity due to solvents • Inexpensive • Control release of capsules with desired size |
• Shear forces affect the viability of encapsulated probiotics | (35) |