Optimizing the bio-degradability and biocompatibility of a biogenic collagen membrane through cross-linking and zinc-doped hydroxyapatite

You Wu(Sun Yat-sen University), Shoucheng Chen(Sun Yat-sen University), Pu Luo(Sun Yat-sen University), Shudan Deng(Sun Yat-sen University), Zhengjie Shan(Sun Yat-sen University), Jinghan Fang(University of Hong Kong - Shenzhen Hospital), Xingchen Liu(Sun Yat-sen University), Jia-Xin Xie(Sun Yat-sen University), Runheng Liu(Sun Yat-sen University), Shiyu Wu(Sun Yat-sen University), Xiayi Wu(Sun Yat-sen University), Zetao Chen(Sun Yat-sen University), Zetao Chen(Sun Yat-sen University), Kwk Yeung(Sun Yat-sen University), Quan Liu(Sun Yat-sen University), Zhuofan Chen(Sun Yat-sen University), Zhuofan Chen(Sun Yat-sen University)
Acta Biomaterialia
February 8, 2022
Cited by 63Open Access
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Abstract

Biogenic collagen membranes have been widely used as soft tissue barriers in guided bone regeneration (GBR) and guided tissue regeneration (GTR). Nevertheless, their clinical performance remains unsatisfactory because of their low mechanical strength and fast degradation rate in vivo. Although cross-linking with chemical agents is effective and reliable for prolonging the degradation time of collagen membranes, some adverse effects including potential cytotoxicity and undesirable tissue integration have been observed during this process. As a fundamental nutritional trace element, zinc plays an active role in promoting the growth of cells and regulating the degradation of the collagen matrix. Herein, a biogenic collagen membrane was cross-linked with glutaraldehyde-alendronate to prolong its degradation time. The physiochemical and biological properties were enhanced by the incorporation of zinc-doped nanohydroxyapatite (nZnHA), with the native structure of collagen preserved. Specifically, the cross-linking combined with the incorporation of 1% and 2% nZnHA seemed to endow the membrane with the most appropriate biocompatibility and tissue integration capability among the cross-linked membranes, as well as offering a degradation period of six weeks in a rat subcutaneous model. Thus, improving the clinical performance of biogenic collagen membranes by cross-linking together with the incorporation of nZnHA is a promising strategy for the improvement of biogenic collagen membranes. The significance of this research includes: We fabricated a cross-linked collagen membrane with enhanced mechanical properties, prolonged degradation time and uncompromised biocompatibility by GA-alendronate cross-linking and nZnHA doping. Tuning the incorporation concentration of zinc ions can effectively manipulate the biocompatibility and degradation process of the membrane fabricated. We proposed a promising strategy to improve the clinical performance of biogenic collagen membranes by cross-linking together with the incorporation of nZnHA.


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