Development of nanoparticles derived from corn as mass producible bionanoparticles with anticancer activity.

Sci Rep

Laboratory of Biopharmaceutics, Faculty of Pharmaceutical Sciences, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba, 278-8510, Japan.

Published: November 2021

AI Article Synopsis

  • Recent research indicates that plant-derived nanoparticles (NPs) can be produced efficiently and have potential uses in therapy and delivering bioactive molecules.
  • In this study, corn was used to create these nanoparticles, which were about 80 nm in size and negatively charged, and they effectively reduced the growth of colon cancer cells while also stimulating immune response in macrophages.
  • When tested in mice, daily injections of these corn-derived nanoparticles significantly hindered the growth of colon tumors without causing notable weight loss.

Article Abstract

Recent studies showed that plant-derived nanoparticles (NPs) can be easily produced in high yields and have potential applications as therapeutic agents or delivery carriers for bioactive molecules. In this study, we selected corn as it is inexpensive to grow and mass-produced globally. Super sweet corn was homogenized in water to obtain corn juice, which was then centrifuged, filtered through a 0.45-μm-pore size syringe filter, and ultracentrifuged to obtain NPs derived from corn, or corn-derived NPs (cNPs). cNPs obtained were approximately 80 nm in diameter and negatively charged (- 17 mV). cNPs were taken up by various types of cells, including colon26 tumor cells and RAW264.7 macrophage-like cells, with selective reduction of the proliferation of colon26 cells. Moreover, cNPs induced tumor necrosis factor-α release from RAW264.7 cells. cNPs and RAW264.7 in combination significantly suppressed the proliferation of colon26/fluc cells. Daily intratumoral injections of cNPs significantly suppressed the growth of subcutaneous colon26 tumors in mice, with no significant body weight loss. These results indicate excellent anti-tumor activity of cNPs.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8613273PMC
http://dx.doi.org/10.1038/s41598-021-02241-yDOI Listing

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