AI Article Synopsis

  • Enterocyte uptake of oral nanocarriers poses challenges due to high binding efficiency and interference, but a new type of nanoparticle (SDPN) has been developed to address these issues by mimicking cell membranes.
  • The SDPN nanoparticles show better stability in the gastrointestinal tract and improved uptake in cells, facilitating the delivery of cancer-fighting compounds like luteolin and silibinin to reduce breast cancer metastasis in mice.
  • This innovative membrane-biomimetic approach not only enhances drug delivery effectiveness but also helps regulate immune responses and reduce cancer-related blood vessel growth, indicating its potential for future cancer therapies.

Article Abstract

Enterocyte uptake with high binding efficiency and minor endogenous interference remains a challenge in oral nanocarrier delivery. Enterocyte membrane-biomimetic lipids may universally cooperate with endogenous phosphatidyl choline via a biorthogonal group. In this study, we developed a sophorolipid-associated membrane-biomimetic choline phosphate-poly(lactic-co-glycolic) acid hybrid nanoparticle (SDPN). Aided by physical stability in the gastrointestinal tract and rapid mucus diffusion provided by association with sophorolipid, these nanoparticles show improved endocytosis, driven by dipalmitoyl choline phosphate-phosphatidyl choline interaction as well as its optimized membrane fluidity and rigidity. Luteolin- and silibinin-co-loaded with SDPN alleviated breast cancer metastasis in 4T1 tumor-bearing mice by regulating the conversion of tumor-associated M2 macrophages into the M1 phenotype and reducing the proportion of the M2-phenotype through co-action on STAT3 and HIF-1α. In addition, SDPN reduces angiogenesis and regulates the matrix barrier in the tumor microenvironment. In conclusion, this membrane-biomimetic strategy is promising for improving the enterocyte uptake of oral SDPN and shows potential to alleviate breast cancer metastasis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318786PMC
http://dx.doi.org/10.1186/s12951-023-01949-5DOI Listing

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