3.8 Article

Transmucosal Delivery of Self-Assembling Photosensitizer-Nitazoxanide Nanocomplexes with Fluorinated Chitosan for Instillation-Based Photodynamic Therapy of Orthotopic Bladder Tumors

Journal

ACS BIOMATERIALS SCIENCE & ENGINEERING
Volume 7, Issue 4, Pages 1485-1495

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsbiomaterials.0c01786

Keywords

instillation-based photodynamic therapy; fluorinated chitosan; transmucosal delivery; nitazoxanide; bladder cancer

Funding

  1. Youth Program of the National Natural Science Foundation of China [81903090]
  2. Shenzhen Key Laboratory Program [ZDSYS20190902092857146]
  3. Special Funds for Strategic Emerging Industries Development in Shenzhen [20180309163446298]
  4. Shenzhen Municipal Science and Technology Innovation Commission [JSGG20180712090411521]

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The combination of nitazoxanide and photosensitizer to form nanoparticles, along with fluorinated chitosan as a transmucosal carrier, can improve the delivery efficiency of intravesical drugs. Meanwhile, the metabolic regulation of tumor cells by nitazoxanide can help ameliorate tumor hypoxia, enhancing the effectiveness of photodynamic therapy.
Theoretically, on account of improved local bioavailability of photosensitizers and attenuated systemic phototoxicity, intravesical instillation-based photodynamic therapy (PDT) for bladder cancer (BCa) would demonstrate significant advantages in comparison with the intravenous route. Actually, the low transmucosal efficiency, hypoxia regulation deficiency, as well as the biosafety risks of intravesical drug agents all have greatly limited the clinical development of instillation-based PDT for BCa. Herein, based on our recent findings on bladder intravesical vectors and photodynamic treatment, we explore and find that the conventional antiparasitic agent nitazoxanide (NTZ) by mixing with chlorine e6 (Ce6) conjugated human serum albumin (HSA), HSA-Ce6, is capable of forming self-assembled HSA-Ce6/NTZ nanoparticles (NPs). Then, the HSA-Ce6/NTZ complexes further fabricate with fluorinated chitosan (FCS), the synthesized transmucosal carrier, to form a biocompatible nanoscale system HSA-Ce6/NTZ/FCS NPs, which exhibit remarkably improved transmucosal delivery and uptake capacities compared with HSA-Ce6/NTZ alone or non-fluorinated HSA-Ce6/ NTZ/CS NPs. Meanwhile, due to the metabolic regulation of tumor cells by NTZ, the tumor hypoxia could be efficaciously ameliorated to further favor PDT. This work represents a new photosensitizer nanomedicine formulation for the perfection of PDT performance through the modulation of tumor hypoxia by clinically approved agents. Thus, intravesical instillation of HSA-Ce6/ NTZ/FCS NPs with favorable biocompatibility, followed by cystoscope-mediated PDT, could achieve a dramatically improved therapeutic effect to ablate orthotopic bladder tumors.

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