Table 2.
Various studies employing albumin-based nanoparticles for intranasal delivery.
| Sr. No | Albumin Type | Preparation Method | Research Purposes |
API | Results | Ref. |
|---|---|---|---|---|---|---|
| 1 | Bovine serum albumin | Coacervation method | Plasma profile evaluation —bioavailability | Silybin (SLB) | Intranasal administration of BSA-Nanoparticles (NPs)/SLB in rats improved SLB bioavailability by fourfold compared to free SLB | [87] |
| 2 | Bovine serum albumin | Desolvation method | Local nasal therapy—ABR | Amoxicillin trihydrate (AMT) | AMT-loaded BSA NPs with in situ thermosensitive polymer inhibited the growth of ABR pathogens | [88] |
| 3 | Bovine serum albumin | Desolvation method | Local nasal therapy—ABR | Amoxicillin trihydrate (AMT) | AMT-loaded BSA NPs with in situ ionic-sensitive polymer inhibited the growth of ABR pathogens | [89] |
| 4 | Bovine serum albumin | Desolvation method | Nose-to-brain—Alzheimer disease | Tacrine hydrochloride | Albumin-based NPs with hydrophilic derivatives of betacyclodextrin showed an interesting drug permeation profile | [90] |
| 5 | Human serum albumin | Desolvation method | Nose-to-brain | Sulforhodamine B sodium salt | The formulation was able to influence the tight junction, allowing permeation of the molecules | [91] |
| 6 | Human serum albumin | Coacervation method | Nose-to-brain—Neuroinflammation | Meloxicam (MEL) | Enhanced permeation of MEL was detected through specific BBB-lipid fraction | [7] |
| 7 | Human serum albumin | Coacervation method | Nose-to-brain—Neuroinflammation | Meloxicam (MEL) | Higher cerebral concentration of MEL was observed | [8] |
| 8 | Human serum albumin (Albutein 20%) | Simple mixture with water | Nose-to-brain—Alzheimer disease | R-Flurbiprofen (R-FP) | In vivo brain concentration albumin-based nanoparticles of R-FP was higher compared to intranasal and oral R-FP solution | [85] |