Bioresponsive micro-to-nano albumin-based systems for targeted drug delivery against complex fungal


The bioresponsive micro-to-nano albumin-based system was accumulated in the lungs and responds to the upregulated MMP-3, then targeted the lung tissue, brain, and infected macrophages, reaching multiple targets and efficient treatment. Credit: Acta Pharmaceutica Sinica B
The bioresponsive micro-to-nano albumin-based system was accumulated in the lungs and responds to the upregulated MMP-3, then targeted the lung tissue, brain, and infected macrophages, reaching multiple targets and efficient treatment. Credit: Acta Pharmaceutica Sinica B

As a typical human pathogenic fungus, Cryptococcus neoformansis a life-threatening invasive fungal pathogen with a worldwide distribution causing ∼700,000 deaths annually. Cryptococcosis is not just an infection with multi-organ involvement, intracellular survival and extracellular multiplication of the fungus also play important roles in the pathogenesis of C. neoformansinfections. Because adequate accumulation of drugs at target organs and cells is still difficult to achieve, and effective delivery strategy is desperately required to treat these infections.


The authors report a bioresponsive micro-to-nano (MTN) system that effectively clears the C. neoformans in vivo. This strategy is based on the author's in-depth study of the overexpression of matrix metalloproteinase 3 (MMP-3) in infectious microenvironments (IMEs) and secreted protein acidic and rich in cysteine (SPARC) in several associated target cells. In this MTN system, bovine serum albumin (BSA, a natural ligand of SPARC) was used for the preparation of nanoparticles (NPs), and then microspheres were constructed by conjugation with a special linker, which mainly consisted of a BSA-binding peptide and an MMP-3-responsive peptide. This MTN system was mechanically captured by the smallest capillaries of the lungs after intravenous injection and then hydrolyzed into BSA NPs by MMP-3 in the IMEs. The NPs further targeted the lung tissue, brain, and infected macrophages based on the overexpression of SPARC, reaching multiple targets and achieving efficient treatment.


The authors have developed a size-tunable strategy where microspheres shrink to NPs in IMEs, which effectively combines active and passive targeting and maybe especially powerful in the fight against complex fungal infections.


Journal Information:  Liting Cheng et al, Bioresponsive micro-to-nano albumin-based systems for targeted drug delivery against complex fungal infections, Acta Pharmaceutica Sinica B (2021). DOI: 10.1016/j.apsb.2021.04.020

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