Carbon-encapsulated Co3O4-doped Co/CoFe bifunctional catalysts prepared by annealing LDHs act as a highly efficient air cathode in rechargeable Zn–air batteries.
As a highly oxygen-dependent
process, the effect of photodynamic
therapy is often obstructed by the premature leakage of photosensitizers
and the lack of oxygen in hypoxic cancer cells. To overcome these
limitations, this study designs bovine serum albumin protein (BSA)-encapsulated
Pt nanoclusters (PtBSA) as O2-supplied biocoats and further
incorporates them with mesoporous silica nanospheres to develop intelligent
nanoaggregates for achieving improved therapeutic outcomes against
hypoxic tumors. The large number of amino groups on BSA can provide
sufficient functional groups to anchor tumor targeting agents and
thus enhance the selective cellular uptake efficiency. Owing to the
outstanding biocompatibility features of BSA and the state-of-the-art
catalytic activity of Pt nanoclusters, the nanocomposites have lower
dark cytotoxicity, and O2 continuously evolves via the
decomposition of H2O2 in a tumor microenvironment.
Both in vivo and in vitro experiments indicate that the resulting
nanocomposites can effectively relieve hypoxic conditions, specifically
induce necrotic cell apoptosis, and remarkably hinder tumor growth.
Our results illuminate the great potential of BSA-encapsulated Pt
nanoclusters as versatile biocoats in designing intelligent nanocarriers
for hypoxic-resistant photodynamic therapy.
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