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“Objective: Despite the efficacy of collagen in femoral artery

pseudoaneurysm treatment, as reported in one patient study, its use has not yet gained wide acceptance in clinical practice. In this particular study, the collagen was not described in detail. To further investigate the potential of collagen preparations, we prepared and characterized highly purified injectable fibrillar type I collagen Paclitaxel and evaluated its use for femoral artery pseudoaneurysm (PSA) treatment in vivo using a pig model.

Methods: Purified fibrillar type I collagen was characterized using electron microscopy. The effect of three different sterilization procedures, ie, hydrogen peroxide gas plasma (H(2)O(2)), ethylene oxide gas (EtO), and gamma irradiation, was studied on both SDS-PAGE and platelet aggregation. Different collagen injectables were prepared (3%, 4%, and 5%) and tested using an injection force test applying a 21-gauge needle. To evaluate the network characteristics of the injectable collagen, the collagen was suspended in phosphate buffered saline (PBS) at 37 degrees C and studied both macroscopically and electron microscopically. To determine whether the collagen induced hemostasis in vivo, a pig PSA model was used applying a 4% EtO sterilized collagen injectable, and evaluation by angiography and routine histology.

Results: Electron microscopy of the purified

type I collagen revealed R788 intact fibrils with a distinct striated pattern and a length <300 gm. Both SDS-PAGE and platelet aggregation analysis of the sterilized collagen indicated no major differences between EtO and H(2)O(2) sterilization, although gamma-irradiated collagen showed degradation products. Both 3% and 4% (w/v) collagen suspensions were acceptable with respect to the force used (<50 N). The 4% suspension was selected as the preferred injectable collagen, which formed a dense network under physiologic conditions. Testing the collagen in vivo (n Dapagliflozin = 5), the angiograms revealed that the PSA partly or completely coagulated. Histology

confirmed the network formation, which was surrounded by thrombus.

Conclusions: Collagen injectables were prepared and EtO sterilized without major loss of structural integrity and platelet activity. In vivo, the injectable collagen formed a dense network and triggered (partial) local hemostasis. Although optimization is needed, an injectable collagen may be used as a therapeutic agent for femoral PSA treatment. (J Vase Surg 2010;52:1330-8.)

Clinical Relevance: This study explores the use of collagen for femoral artery pseudoaneurysm (PSA) treatment. The efficacy of collagen has been reported in one patient study, but it has not gained acceptance for PSA treatment. The current study combines the characterization of a collagen preparation with its evaluation using a porcine model for PSA.