Cross Linking Essay

1034 Words3 Pages

Cross-linking agents As shown in Table 1, cross-linking can be classified into three types; chemical, biological and physical cross-linking [9, 15]. Chemical Cross-linking There are two types of chemical cross-linkers; synthetic and naturally derived reagents. The most commonly employed cross-linking reagent for collagen-based biomaterials is glutaraldehyde (GA), a five carbon bifunctional aldehyde, bridging ɛ-amino group of lysyl residues present in the protein over a varying range of distances owing to its less expensive and higher efficiency properties [16]. The mechanical properties of glutaraldehyde-treated tissue is quite different from non-cross-linked, showing more stiffness and increased tensile strength. However, GA is associated …show more content…

N-hydroxysulfosuccinimide (NHS), 1-ethyl-3-(3-dimethyl aminopropyl) carbodiimide (EDC) is responsible for mediating “self cross-linking” or “zero-length” between the collagen molecules and plays an important role in improving the mechanical properties of the scaffolds [15, 24]. Generally, NHS is used in order to provide stability to carbodiimides cross-linking [25]. Compared with GA, carbodiimides are less toxic because they are released as urea substitute that can easily be removed by washing [15]. Powell et al. investigated that EDC facilitates the growth of human keratinocytes, smooth muscle cells and fibroblasts …show more content…

Recently, several chemical synthetic cross-linkers have also been developed having superior cross-linking properties [27]. In particular, 4-aminoethanol-N-hydroxyethanyl-1,8- naphthalimide (AHN), a dual-hydroxyl naphthalimide derivative that have been utilized in fluorescent labeling and as the chemical cross-linking agent but with less toxicity [28]. Naturally derived cross-linking reagents are considered superior to chemical cross-linking demonstrating a low toxicity level after implantation [9]. Genipin (GIP), an aglycone of geniposide obtained from Gardenia jasminoides Ellis Plant, was first discovered by Huang et al. in 1998 [29]. GIP is found to be 10,000 times less toxic than GA. GIP-fixed tissues, usually show resistance against enzymatic degradation as compared to GA resulting in the development of biocompatible cross-linked products [30]. In a recent study, Wang et al. reported that GIP alleviated the xenogeneic host response of decellularized porcine liver scaffolds by reducing the proliferation of lymphocytes and their subsets, accompanied by a decreased release of both Th1 and Th2 cytokines. It was reported that cross-linking using GIP promotes the beneficial tissue repair through enhancing angiogenesis and cell migration

More about Cross Linking Essay

Open Document