AI Article Synopsis

  • Oral delivery systems for medicines face challenges due to biological barriers in the gastrointestinal tract, making it difficult for single-type carriers to function effectively.
  • Researchers developed a biomimetic spore nanoplatform (SC@DS NPs) using spore capsids to create multifunctional nanoparticles that can efficiently deliver drugs like doxorubicin (DOX) and sorafenib (SOR).
  • The SC@DS NPs successfully navigate the harsh stomach environment and enhance therapeutic effects by improving mucus penetration and transepithelial transport thanks to the unique properties of spore capsids.

Article Abstract

The biological barriers have seriously restricted the efficacious responses of oral delivery system in diseases treatment. Utilizing a carrier based on the single construction means is hard to overcome these obstacles simultaneously because the complex gastrointestinal tract environment requires carrier to have different or even contradictory properties. Interestingly, spore capsid (SC) integrates many unique biological characteristics, such as high resistance, good stability etc. This fact offers a boundless source of inspiration for the construction of multi-functional oral nanoplatform based on SC without further modification. Herein, we develop a type of biomimetic spore nanoplatform (SC@DS NPs) to successively overcome oral biological barriers. Firstly, doxorubicin (DOX) and sorafenib (SOR) are self-assembled to form carrier-free nanoparticles (DS NPs). Subsequently, SC is effectively separated from probiotic spores and served as a functional vehicle for delivering DS NPs. As expect, SC@DS NPs can efficaciously pass through the rugged stomach environment after oral administration and further be transported to the intestine. Surprisingly, we find that SC@DS NPs exhibit a significant improvement in the aspects of mucus penetration and transepithelial transport, which is related to the protein species of SC. This study demonstrates that SC@DS NPs can efficiently overcome multiple biological barriers and improve the therapeutic effect.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463901PMC
http://dx.doi.org/10.1186/s12951-023-01995-zDOI Listing

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