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首页> 外文期刊>Journal of plastic, reconstructive & aesthetic surgery: JPRAS >A prospective randomised controlled trial to investigate the effect of local anaesthetic in vivo on cell culture.
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A prospective randomised controlled trial to investigate the effect of local anaesthetic in vivo on cell culture.

机译:前瞻性随机对照试验,研究体内局部麻醉对细胞培养的影响。

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Cell culture is an important adjunct in the management of major burns in that it enables keratinocytes derived from the patient to be grown and used to attain cover when there is little autologous skin available. The purpose of this prospective randomised trial was to determine if the type of local anaesthetic used to harvest the skin biopsy in vivo affected the subsequent culture of keratinocytes. Lignocaine 1% was compared with a eutectic mixture of local anaesthetic (EMLA) and a control. The subjects recruited were patients undergoing abdominoplasty. Sixteen patients were recruited but two were excluded from final analysis due to infection of the culture medium in one and poor yield from biopsies in all groups in the other. The tissue to be removed from the abdomen was divided into three areas. EMLA was applied to a 5x5 cm randomised area 2 h prior to surgery. Lignocaine 1% was injected into a 5x5 cm randomised area of abdominal skin immediately after anaesthesia. The third 5x5 cm randomised area was used as a control. Three 4-mm punch biopsies were harvested from each site of local anaesthetic application as well as the control area. The Rheinwald & Green method was used to culture these cells [Rheinwald JG, Green H. Serial cultivation of strains of human epidermal keratinocytes: the formation of keratinizing colonies from single cells. Cell 1975;6:331-5.] Cell counts were performed after harvesting keratinocytes from the biopsy and after 10 days of culture. Statistical analysis was undertaken. In conclusion, in contrast to in vitro studies when lignocaine 1% or EMLA is applied in vivo, there is no inhibition of cell culture. In vivo EMLA was also found to significantly increase cell multiplication.
机译:细胞培养是处理严重烧伤的重要辅助手段,因为它可使自患者产生的角质形成细胞生长,并在自体皮肤很少的情况下用于覆盖。这项前瞻性随机试验的目的是确定用于体内收集皮肤活检的局部麻醉剂的类型是否影响随后的角质形成细胞培养。将1%的利多卡因与局部麻醉剂(EMLA)和对照的低共熔混合物进行了比较。招募的对象是接受腹部成形术的患者。招募了16例患者,但由于其中一种感染了培养基,而另一组的所有活检结果均较差,因此有2例被排除在最终分析之外。将要从腹部去除的组织分为三个区域。在手术前2小时,将EMLA应用于5x5 cm的随机区域。麻醉后立即将1%的利多卡因注射到5x5 cm的腹部皮肤随机区域中。第三个5x5 cm随机区域用作对照。从局部麻醉应用的每个部位以及对照区域收获了3个4毫米打孔活检标本。用Rheinwald&Green方法培养这些细胞[Rheinwald JG,GreenH。人表皮角质形成细胞菌株的系列培养:由单个细胞形成角化集落。 [Cell 1975; 6:331-5。]细胞计数是在从活检组织中收集角质形成细胞之后以及培养10天后进行的。进行了统计分析。总之,与在体内应用1%木质素卡因或EMLA的体外研究相反,对细胞培养没有抑制作用。还发现体内EMLA显着增加细胞增殖。

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