Table 1.
Method | Advantages | Disadvantages | Interactions/Example | References |
---|---|---|---|---|
Physical adsorption | The most simple. Less aggressive. Reagent-free. |
Less stable. Less reproducible. |
Van der Waals. Hydrogen bonding. Hydrophobic interactions. Electrostatic interactions. |
[56,77] |
Entrapment | 3D-conformational structure of ligands and drug biomolecules remain almost unaltered, keeping the biological activity. | Poor retention. Diffusional barrier. Limited molecules transport & longer response time. |
Gel (polyacrylamide) Silicone, Jelly Chitosan hydrogel |
[80] |
Cross-linking | Simple Additional stability by intermolecular linking. |
Alter the 3D conformation of biomolecules and active center of enzymes. Induce restriction in molecules diffusion. |
Glutaraldehyde, Hexamethylene diisocyanate, |
[56,77,83] |
Biocomposite | Improved properties. | Stability of bioreceptors in solvents and matrix | Embedded active principle in a complex matrix | [56] |
Covalent linking | Better stability (pH, ionic strength and temperature). Longer lifetime. |
Longer protocols. Lower bioactivity. |
Through functional groups (NH2, COOH, OH, SH, Ph-OH). | [86,93] |