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Preparation and characterization of injectable Mitoxantrone poly (lactic acid)/fullerene implants for in vivo chemo-photodynamic therapy. | LitMetric

Preparation and characterization of injectable Mitoxantrone poly (lactic acid)/fullerene implants for in vivo chemo-photodynamic therapy.

J Photochem Photobiol B

School of Pharmaceutical Sciences, Zhengzhou University, 100 Kexue Avenue, Zhengzhou 450001, PR China. Electronic address:

Published: August 2015

AI Article Synopsis

  • Researchers created a new drug delivery method using fullerene (C60) and L-phenylalanine attached to poly(lactic acid) to make injectable implants for the cancer drug Mitoxantrone (MTX).
  • These self-assembled microspheres can slowly release MTX for nearly 15 days and primarily target tumors while minimizing exposure to healthy organs.
  • The study found that the C60-phe-PLA microspheres effectively fight tumors with fewer side effects, making them a promising option for treating solid tumors in the future.

Article Abstract

Fullerene (C60) L-phenylalanine derivative attached with poly (lactic acid) (C60-phe-PLA) was developed to prepare injectable Mitoxantrone (MTX) multifunctional implants. C60-phe-PLA was self-assembled to form microspheres consisting of a hydrophilic antitumor drug (MTX) and a hydrophobic block (C60) by dispersion-solvent diffusion method. The self-assembled microspheres showed sustained release pattern almost 15days in vitro release experiments. According to the tissue distribution of C57BL mice after intratumoral administration of the microspheres, the MTX mainly distributed in tumors, and rarely in heart, liver, spleen, lung, and kidney. Photodynamic antitumor efficacy of blank microsphere was realized. Microspheres afforded high antitumor efficacy without obvious toxic effects to normal organs, owing to its significantly increased MTX tumor retention time, low MTX levels in normal organs and strong photodynamic activity of PLA-phe-C60. These C60-phe-PLA microspheres may be promising for the efficacy with minimal side effects in future treatment of solid tumors.

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Source
http://dx.doi.org/10.1016/j.jphotobiol.2015.05.018DOI Listing

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