Table 2.
Categories | Liposomes | Emulsion | ISCOMs | Natural polymers | Synthetic polymers |
---|---|---|---|---|---|
Application | DNA, peptides, proteins | Whole-cell killed, proteins, peptides | Proteins, peptides | Proteins, peptides, conjugates | Proteins, peptides, conjugates |
Pros |
-Intrinsic adjuvant characteristics -Can accommodate both hydrophilic and lipophilic antigens -Modified liposomes have optimal stability across the intestine -Controlled release |
-Tailored immunomodulation, for example, Th1 (water-in-oil) and Th 2 (oil-in-water) -High loading efficiency of both hydrophilic (water in oil) and hydrophobic (oil-in-water) -Slow or controlled release |
-Easy modification -High antigen loading efficiency -Potent built-in adjuvant (Quil A) |
-Controlled release -Easy modification -Highly stable and adaptable |
-Controlled release -Controlled size -Engineered surface chemistry |
Cons |
-Weak loading efficiency of hydrophilic antigens -Nonspecific interactions -Cationic liposomes could be toxic |
-Poor stability under the harsh environment in the GI system |
-Poor loading of hydrophilic antigens -Rapid clearance |
-Low antigen loading -Poor aqueous solubility |
-May have poor solubility -Insufficient antigen protection -Exposed to proteolysis in mucus |