Kremer D, Bujía J
HNO-Klinik, Ludwig-Maximilians-Universität München.
Laryngorhinootologie. 1995 Feb;74(2):76-80. doi: 10.1055/s-2007-997693.
The use of autologous cartilage grafts is one of the most common procedures in plastic surgery. Commonly used chemical preservation procedures of the cartilage for a second operation usually lead to the loss of vitality of the graft. In the past few years cryopreservation methods were used in the maintenance of the vitality of the autologous grafts, although these efforts yielded a low vitality of the grafts. It seems that the matrix of the grafts is mainly responsible for the unsuccessful cryopreservation of cartilage. In this work we tried to degrade the matrix of the cartilage grafts by partial enzymatic digestion with collagenase type II and hyaluronidase to facilitate the penetration of dimethylsulfoxide (DMSO). Cell vitality was assessed by trypan dye exclusion. We could demonstrate that it is possible to raise the permeability of the matrix by enzymatic digestion. Cryopreservation of the digested cartilage yielded a vitality of nearly 20%. Our results suggest that pretreatment of cartilage grafts with specific enzymes before preservation enable more successful vital cryopreservation.
自体软骨移植的应用是整形手术中最常见的手术之一。用于二次手术的软骨常用化学保存方法通常会导致移植组织活力丧失。在过去几年中,冷冻保存方法被用于维持自体移植组织的活力,尽管这些努力使移植组织的活力较低。似乎移植组织的基质是软骨冷冻保存失败的主要原因。在这项工作中,我们试图用II型胶原酶和透明质酸酶进行部分酶消化来降解软骨移植组织的基质,以促进二甲基亚砜(DMSO)的渗透。通过台盼蓝拒染法评估细胞活力。我们可以证明通过酶消化提高基质的通透性是可能的。消化后的软骨冷冻保存产生了近20%的活力。我们的结果表明,在保存前用特定酶对软骨移植组织进行预处理能使重要的冷冻保存更成功。