Method for tissue fixation

Prosthesis (i.e. – artificial body members) – parts thereof – or ai – Implantable prosthesis – Tissue

Reexamination Certificate

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C008S094110

Reexamination Certificate

active

06231614

ABSTRACT:

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates generally to tissue fixation, and in particular, to an epoxy compound and method for use in tissue fixation.
2. Description of the Prior Art
Biological tissues such as autologous pericardium and homologous aortic valves have been used in various surgical applications because of their good mechanical properties and biocompatibility. Biological tissue-derived, chemically-modified heterologous tissues have been provided as conduits for peripheral or coronary revascularization, patches, ligament substitutes, and prosthetic heart valves. It is well-known that collagen fibers constitute the fundamental structural framework of biological tissues.
The physiochemical and biomechanical properties of collagen matrices are directly related to the structure of the collagen fibrils. The collagen molecules are stabilized in the fibrils by covalent intermolecular crosslinks, which provide the fibrillate matrices with an adequate degree of tensile strength and biostability.
After a prosthesis having heterologous tissue has been implanted in a living host environment, the biological tissue will be subject to a host response, which includes both cellular and enzymatic attack. Previous studies have shown that implanted heterologous collagenous tissues provoke a cellular response which leads to physical invasion of the implanted prosthesis by phacocytes (polymorphonuclear leukocytes, macrophages) and fibroblasts. Phagocytes are known to be able to secrete collagenase and other proteases and oxygen free radicals. Heterologous biological tissues can be readily degraded by such proteolytic enzymes, and/or through an oxidation process, significantly reducing the strength and life span of the collagen fibrils. To achieve long-term stability, bioprostheses derived from heterologous tissues have to be chemically modified to increase their resistance to enzymatic degradation before they can be implanted into a human being for long term use. These chemical modifications include:
(1) Crosslinking to stabilize the collagen matrix, such as enhancing the molecular interaction between collagen fibrils, elastin and other proteins; increasing tissue fatigue limit under stress; and maintaining the tissue integrity and preventing inflammatory cell infiltration;
(2) Modification of collagenous tissue to minimize the immunogenicity: heterologous tissue needs to be modified to reduce the immunogenicity so that systemic and local adverse effects (e.g., chronic inflammation or rejection) will be minimized;
(3) Modification to minimize enzymatic attack: chemically modified tissue might be less recognizable by proteolytic enzymes; and
The crosslinking and modification are preferably stable to achieve optimum long-term results.
The extent of enzymatically catalyzed breakdown of fibrous collagen may be influenced by two factors: the availability to the enzyme of recognizable cleavage sites, and the extent of the helical integrity of the collagen. Previous works have suggested that tissue subjected to fixation and having greater crosslinking density will have a greater resistance to degradation.
Fixation refers to the deactivation of the amino acid of a collagen by reaction with a chemical to minimize the antigenicity of the heterologous biological material and the possibility of enzymatic degradation by collagenase and other proteases. Thus, fixation would enhance the durability of the collagen.
Two types of fixation treatment can be differentiated. The first type is crosslinking, in which one molecule of a fixation agent having multiple functional groups reacts with two or more groups in a collagen. After crosslinking, the mechanical properties of the tissue change. The second type of fixation treatment can be referred to as branching, in which the fixative reacts with a single group only, resulting in a branch produced by the reacted amino acid. In branching, the mechanical properties (e.g., flexibility) of the tissue will normally experience little change.
Both cross-linking and branching will alter the antigenicity of the collagenous tissue if there is modification of a sufficient amount of amino acids, and if the grafting structure (i.e., branching) is large enough to change the local molecular conformation (i.e., both sequential and conformatial antigen determination sites/epitopes). A higher degree of fixation of the fixed biomaterial (tissue) will generally result in lower antigenicity.
Since the host cellular and enzymatic activity is highly associated with inflammation, and the toxicity of the residual fixative may contribute to the local chronic inflamation, a minimal residual toxicity of the prosthesis is desirable.
Collagenous tissue for blood-contacting applications, such as for heart valves and conduits, should also have excellent hemocompatibility. Hydrophilicity, charge, surface texture and other surface characteristics on the blood-contacting surface can significantly impact the performance and durability of the tissue when used in these applications. Some trends can be observed in relation to surface tension and hemocompatibility/bioadhesion. R. R. Baier and V. A. DePalma, “The Relation of the Internal Surface of Grafts to Thrombosis”,
Management of Arterial Occlusive Disease
, Year Book Medical Publisher, Chicago, Ill., 147-163 (1971) has accumulated an extensive amount of data over many years on the observed trend of biological reactivity of materials as a function of their relative critical surface tensions. An empirically derived graph from their work is divided into three zones: (1) A first zone, coincident to a minimum in biological interaction, is the “hypothetical zone of biocompatability:, which surface tension ranges from 20 to 30 dynes/cm (hydrophobic surface). This zone is the range of surface tensions that most natural arteries possess and is descriptive of relatively nonthrombogenic surfaces. (2) A second zone which ranges from 33 to 38 dynes/cm and comprises the surface tensions of most commonly available polymers, which surprisingly, excludes the most commonly used polymers for vascular grafts (i.e., ePTFE and Dacron). (3) A third zone which ranges from 40 to 72 dynes/cm and known as the zone of “good bioadhesion”. This “good bioadhesion” zone would be favored by prostheses in which good ingrowth is required, such as orthopedic and dental implants.
Critical surface tensions in the range of 20 to 30 dynes/cm, which correlate to surfaces dominant with methyl (CH
3
) groups, do indicate inherent thromboresistance for implanted specimens.
Biological tissues can be chemically modified or fixed with formaldehyde (FA) or glutaraldehyde (GA). Heterologous and homologous tissues have been fixed and implanted as prostheses for over the past thirty years. Clinically, GA has been the most common fixative. GA modifies most lysyl &egr;-amino groups, forms cross-linkage between nearby structures, and it polymerizes and gains stability through Schiff base interaction. GA provides adequate modification to minimize the antigenicity of the prosthesis while making the prosthesis hydrophobic and negatively-charged on the surface for good blood interaction. However, the tendencies of GA to markedly alter tissue stiffness and promote tissue calcification are well-known drawbacks of this fixative. For these reasons, GA has been linked to a number of prosthesis failures.
Attempts have been made to reduce the potential for calcification in prostheses that have been fixed with GA. For example, U.S. Pat. No. 5,080,670 to Imamura et al. discloses a number of polyglycidl ethers (sold under the trademark DENACOL by Nagasi Chemicals, Osaka, Japan) for cross-linking tissue heart valves. Imamura et al. believe that the existence of the ether linkage (C—O) in the backbone of the fixative will allow the oxygen arm to work as a flexible joint in the cross-linking bridge, so that the cross-linked tissue can be more flexible and hydrophilic. Biological tissues cross-linked with polyglycidl ethers have shown great flexibility (pliability) and r

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