It will be possible to extend this strategy to incorporate other inorganic PSs with NIR wavelength, such as osmium analogs.[28] The four biotin‐binding pockets are still accessible after modification to incorporate multiple copies of targeting ligands for enhanced internalization into TNBC in a more controlled fashion compared to other platforms such as human serum albumin.[20] The in situ assembly of the RuAvi platform with functional b‐FK peptides, which targets FPR‐1‐expressing cancer cells, allows rapid screening through this approach. This evidence concerns the gene FPR1 and cancer.