Gemcitabine-incorporated polyurethane films for controlled release of an anticancer drug.

Biomater Res

3Department of Biomedical Engineering, College of Health Science, Eulji University, 553 Sanseongdae-ro, Sujeong-gu, Seongnam-si, Gyeonggi-do 13135 Republic of Korea.

Published: November 2019

AI Article Synopsis

  • Local delivery of anti-cancer drugs through stents shows promise for treating gastrointestinal obstructions caused by tumors, but current drug release methods, like those using gemcitabine, are too rapid.
  • Researchers developed a method to slow down drug release by enveloping a gemcitabine-loaded polyurethane film with different barrier films, with the pure polyurethane film proving effective in reducing the initial drug burst from 90% to 26%.
  • The silicone barrier film was ineffective due to separation and defects, indicating that optimizing the barrier properties is essential for improving drug release behavior in stent applications.

Article Abstract

Background: Local delivery of anti-cancer drugs through a stent is a very promising and anticipated treatment modality for patients who have obstructions in their gastrointestinal tract with malignant tumors. Anticancer drug release via stents, however, needs to be optimized with respect to drug delivery behavior for the stents to be effective for prolonged containment of tumor proliferation and stent re-obstruction. Local stent-based drug delivery has been tested using an effective anti-cancer drug, gemcitabine, but the release from the stent-coated polyurethane films is often too fast and the drug is depleted from the coated film virtually in a day.

Methods: To moderate the drug release from a polyurethane film, a gemcitabine-incorporated polyurethane film was enveloped with a pure polyurethane film, with no drug loading, and with a silicone film by solution casting after activation of the silicone film surface with plasma treatment.

Results: The pure polyurethane barrier film was effective; the interface of the two were indistinguishable on scanning electron microscopy, and the initial burst, i.e., the cumulative release in a day, decreased from 90 to 26%. The silicone film barrier, on the other hand, was defective as voids were seen using a scanning electron microscope, and micro-separation of the two layers was observed after the film was immersed in phosphate-buffered saline for 1 day during the in vitro drug release study.

Conclusions: Enveloping a gemcitabine-releasing polyurethane film with a homo-polymer barrier film was quite effective for moderating the initial burst of gemcitabine, thus, prolonging the release time of the drug. Enveloping the polyurethane film with a silicone film was also possible after plasma treatment of the silicone film surface, but the two films eventually separated in the aqueous environment. More studies are needed to tune the drug release behavior of gemcitabine from the stent covering film before attempting a clinical application of an anti-cancer drug releasing stent.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6865006PMC
http://dx.doi.org/10.1186/s40824-019-0169-7DOI Listing

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