AI Article Synopsis

  • Interventional embolization therapy is a key method for treating inoperable liver tumors, utilizing blood-vessel-embolic agents.
  • Innovative thermo-sensitive composite hydrogels, specifically PSHI and PSHI-Ca2+, were developed as liquid embolic agents that transition from a flowing sol to a gel at body temperature, exhibiting low cytotoxicity.
  • Research demonstrated that these hydrogels effectively occluded tumors and peripheral vessels in animal models, indicating their potential as promising embolic agents for transarterial embolization therapy.

Article Abstract

Interventional embolization therapy is an effective, most widely used method for inoperable liver tumors. Blood-vessel-embolic agents were essential in transarterial embolization (TAE). In this work, thermo-sensitive composite hydrogels based on poloxamer 407, sodium alginate, hydroxymethyl cellulose and iodixanol (PSHI), together with Ca2+ (PSHI-Ca2+) were prepared as liquid embolic agents for TAE therapy to liver cancer. With increasing temperature, PSHI exhibited two phase states: a flowing sol and a shrunken gel. Rheology tests showed good fluidity and excellent viscoelastic behavior with a gelation temperature (GT) of 26.5°C. The studies of erosion indicated that PSHI had calcium ion-related erosion characteristics and showed a slow erosion rate in an aqueous environment. When incubated with L929 cells, the thermo-sensitive composite hydrogels had low cytotoxicity in vitro. The results of analyzing the digital subtraction angiography and computed tomography images obtained from in vitro and in vivo assays indicated a good embolic effect in the renal arteries of normal rabbits. Angiography and histological studies on VX2 tumor-bearing rabbits indicated that PSHI-Ca2+ successfully occluded the tumors, including the peripheral vessels. In conclusion, PSHI-Ca2+ was a promising embolic agent for transarterial embolization therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341979PMC
http://dx.doi.org/10.18632/oncotarget.11789DOI Listing

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