Table 6.
Characterization, target indications, drug release pattern, and cytotoxicity of albumin and functionalized albumin nanoparticles prepared by self-assembly
| Albumin used | Conjugating or disulfide reducing agent | Drug or antioxidant loaded | Self-assembly strategy | Target indication | Outcome or applications | Reference |
|---|---|---|---|---|---|---|
| HSA | β-Mercaptoethanol (β-ME) | Paclitaxel (PTX) | Disulfide bond breaking | Breast cancer (MCF-7 and A549 cell lines) |
|
[90] |
| HSA | Dithiothreitol (DTT) | Curcumin (CUR) | Disulfide bond breaking | H22 tumor-bearing mice |
|
[91] |
| BSA | Cholesterol | Paclitaxel (PTX) | Covalent conjugate | Breast cancer (B16F10 and MCF-7 cell lines) |
|
[92] |
| BSA | Aptamer AS1411 | Doxorubicin (DOX) | Hydrophobic drug interaction | Breast cancer (MCF-7 cell line) |
|
[93] |
| BSA | – | Curcumin (CUR) | Hydrophobic drug interaction | – |
|
[94] |
| HSA | PEG | Paclitaxel (PTX) | Covalent conjugation (film casting method) | Human breast cancer cell lines (SK-BR-3, MDA-MB-453 and MCF-7), SK-BR-3 tumor-bearing mice |
|
[95] |
Particle diameters are approximate; BSA, bovine serum albumin; DEE, drug entrapment efficiency (approximate); DLC, drug-loading capacity (approximate); HSA, human serum albumin; NPs, nanoparticles; PEG, polyethylene glycol; ZP, zeta potential.