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Mannosylated enzyme-driven nanomotors actively target cancer cells. Surface modification enhances their speed and specificity for improved cancer therapy applications.

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Area of Science:

  • Biomedical Engineering
  • Nanotechnology
  • Cancer Therapeutics

Background:

  • Motile nanoparticles offer a promising strategy for active cancer cell targeting in therapy.
  • Developing nanomotors with enhanced specificity and autonomous motion is crucial for effective cancer treatment.

Purpose of the Study:

  • To design and evaluate mannosylated compartmentalized cross-linked enzyme-driven nanomotors (c-CLEnM) for targeted cancer therapy.
  • To investigate the effect of mannose functionalization on nanomotor targeting efficiency and motility.

Main Methods:

  • Biodegradable stomatocytes were fabricated and loaded with glucose oxidase (GOx) and catalase (CAT) enzymes.
  • Enzyme crosslinking ensured nanomotor stability, followed by surface modification with a mannose-functional glycopolymer.
  • Targeting specificity and motility of mannosylated c-CLEnM were assessed against Hep G2 cells in varying ionic environments.

Main Results:

  • Mannosylated c-CLEnM demonstrated specific and efficient targeting of Hep G2 cells.
  • Enhanced autonomous motion and increased motility were observed in mannosylated nanomotors compared to non-mannosylated counterparts.
  • Glycopolymer surface modification increased zeta potential and provided shielding, accelerating nanomotor speed in ionic solutions.

Conclusions:

  • Functional glycopolymer modification synergistically enhances cellular uptake and nanomotor performance.
  • Mannosylated c-CLEnM represent a novel nanomotor design with improved targeting and motility for cancer therapy.
  • This approach offers enhanced control over nanomotors for advanced applications in cancer treatment.