AI Article Synopsis

  • I-PDT is a technique using optical fibers to target and treat deeply seated tumors effectively by enhancing the light delivery for photosensitizer activation.
  • The study introduces a biocompatible polymer optical fiber (POF) featuring a strongly scattering spherical end (SSSE) that improves the excitation area, leading to better therapeutic results both in lab settings and live subjects.
  • The POF exhibits advantageous optical qualities such as low transmission loss, excellent biocompatibility, and a broad excitation domain, making it a promising candidate for clinical use in I-PDT.

Article Abstract

Interstitial photodynamic therapy (I-PDT), which utilizes optical fibers to deliver light for photosensitizer excitation and the elimination of penetration depth limitation, is a promising modality in the treatment of deeply seated tumors or thick tumors. Currently, the excitation domain of the optical fiber is extremely limited, restricting PDT performance. Here, we designed and fabricated a biocompatible polymer optical fiber (POF) with a strongly scattering spherical end (SSSE) for I-PDT applications, achieving an increased excitation domain and consequently excellent in vitro and in vivo therapeutical outcomes. The POF, which was drawn using a simple thermal drawing method, was made of polylactic acid, ensuring its superior biocompatibility. The excitation domains of POFs with different ends, including flat, spherical, conical, and strongly scattering spherical ends, were analyzed and compared. The SSSE was achieved by introducing nanopores into a spherical end, and was further optimized to achieve a large excitation domain with an even intensity distribution. The optimized POF enabled outstanding therapeutic performance of I-PDT in in vitro cancer cell ablation and in vivo anticancer therapy. All of its notable optical features, including low transmission/bending loss, superior biocompatibility, and a large excitation domain with an even intensity distribution, endow the POF with great potential for clinical I-PDT applications.

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Source
http://dx.doi.org/10.1364/OL.497596DOI Listing

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