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高静压技术是制备 PVA-肝素杂化凝胶的有效方法。

High-hydrostatic pressure technique is an effective method for the preparation of PVA-heparin hybrid gel.

机构信息

Division of Biofunctional Molecules, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan.

出版信息

Eur J Pharm Sci. 2010 Dec 23;41(5):617-22. doi: 10.1016/j.ejps.2010.09.001. Epub 2010 Sep 15.

Abstract

To develop an antithrombotic material for preparation of small-diameter vascular graft, we describe a novel method to prepare a poly(vinyl alcohol) (PVA)-heparin hydrogels prepared by high-hydrostatic pressure (HHP, 980 MPa), which is designed for sustained release of heparin. Antithrombogenic test revealed that HHP method would not affect the antithrombin III (ATIII) activity of the released heparin. The distribution of heparin in the polymer matrix was homogeneous than freeze-thawing gel, due to the fast gelling affect of PVA which takes approximately 10 min for gel formation. The formation of intra- and intermolecular hydrogen bonds between PVA chains has trapped the heparin inside, suppressing the phase separation between PVA and heparin. Furthermore, evenly distribution of heparin induced the formation of heparin and PVA molecular complex, which brought the sustained release of heparin from the PVA despite the high swelling ratio. Our results show that it is possible to prepare a PVA-heparin hybrid gel which can be applied as an effective material for an antithrombotic system without using any chemical agent.

摘要

为了开发用于制备小直径血管移植物的抗血栓材料,我们描述了一种通过高静压(HHP,980 MPa)制备聚(乙烯醇)(PVA)-肝素水凝胶的新方法,该方法旨在持续释放肝素。抗血栓形成试验表明,HHP 方法不会影响释放的肝素的抗凝血酶 III(ATIII)活性。肝素在聚合物基质中的分布比冻融凝胶更均匀,因为 PVA 的快速胶凝作用大约需要 10 分钟才能形成凝胶。PVA 链之间的分子内和分子间氢键的形成将肝素困在内部,抑制了 PVA 和肝素之间的相分离。此外,肝素的均匀分布诱导了肝素和 PVA 分子复合物的形成,尽管具有高溶胀比,但肝素仍能从 PVA 中持续释放。我们的结果表明,可以制备一种 PVA-肝素杂化凝胶,可作为无需使用任何化学试剂的抗血栓系统的有效材料。

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