AI Article Synopsis

  • A novel hydrogel coating for retrievable vena cava filters (RVCF) was developed, incorporating heparin and a paclitaxel inclusion complex for improved effectiveness.
  • The hydrogel-coated RVCF (HRVCF) showed a sustainable drug release over two weeks and effectively extended blood clotting time, inhibiting cell proliferation in vitro compared to traditional filters.
  • In vivo studies in sheep demonstrated a significantly higher retrieval rate for the HRVCF (67%) compared to the bare RVCF (0%) after four weeks, indicating its potential for enhancing clinical RVCF retrieval rates.

Article Abstract

Aiming to improve the retrieval rate of retrievable vena cava filters (RVCF) and extend its dwelling time in vivo, a novel hydrogel coating loaded with 10 mg/mL heparin and 30 mg/mL cyclodextrin/paclitaxel (PTX) inclusion complex (IC) was prepared. The drug-release behavior in the phosphate buffer solution demonstrated both heparin and PTX could be sustainably released over approximately two weeks. Furthermore, it was shown that the hydrogel-coated RVCF (HRVCF) with 10 mg/mL heparin and 30 mg/mL PTX IC effectively extended the blood clotting time to above the detection limit and inhibited EA.hy926 and CCC-SMC-1 cells' proliferation in vitro compared to the commercially available bare RVCF. Both the HRVCF and the bare RVCF were implanted into the vena cava of sheep and retrieved at at 2nd and 4th week after implantation, revealing that the HRVCF had a significantly higher retrieval rate of 67 % than the bare RVCF (0 %) at 4th week. Comprehensive analyses, including histological, immunohistological, and immunofluorescent assessments of the explanted veins demonstrated the HRVCF exhibited anti-hyperplasia and anticoagulation properties in vivo, attributable to the hydrogel coating, thereby improving the retrieval rate in sheep. Consequently, the as-prepared HRVCF shows promising potential for clinical application to enhance the retrieval rates of RVCFs.

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Source
http://dx.doi.org/10.1016/j.ijbiomac.2024.134509DOI Listing

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