Overall, while casein-based nanomaterials represent a promising platform for drug delivery, the current evidence remains fragmented and further standardised in vivo and clinically oriented investigations are required to establish their translational potential.
Abstract
Casein, a common milk phosphoprotein, has been increasingly investigated as a potential
biopolymer for drug delivery due to its amphiphilicity, biocompatibility, and capacity to selfassemble
into micellar nanostructures. These features enable the encapsulation of both hydrophilic
and hydrophobic drugs and have prompted increasing research interest in their application as a
nanocarrier system. This review critically assesses the current state of research on casein-based nanomaterials,
focusing on physicochemical features, formulation techniques, and application across
oral, Ocular and parenteral drug delivery systems. Available studies suggest that casein-based nanoparticles
may improve drug solubility, encapsulation efficiency, and controlled release. However, the
majority of the evidence is derived from in vitro experiments and limited in vivo models, with relatively
few studies addressing pharmacokinetic behaviour or clinical relevance. In addition, substantial
variability in formulation methods, including differences in preparation techniques and particle
characteristics, complicates reproducibility and cross-study comparison. Key challenges such as
long-term stability, scalability, and potential immunogenicity remain insufficiently addressed. Furthermore,
claims of enhanced targeting or therapeutic efficacy are often based on indirect or preliminary
data rather than validated in vivo outcomes. Overall, while casein-based nanomaterials represent
a promising platform for drug delivery, the current evidence remains fragmented and further standardised
in vivo and clinically oriented investigations are required to establish their translational potential.
Lipid nanocarriers demonstrate significant advantages, including enhanced stability, improved drug loading, controlled and targeted drug release, and adaptability to various formulation requirements, which makes them suitable for applications in pharmaceuticals, vaccines, nutraceuticals, and diagnostic systems.
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