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一种用于研究抗生素在椎间盘内渗透情况的新型体外模型。

A new in-vitro model to investigate antibiotic penetration of the intervertebral disc.

作者信息

Thomas R de W, Batten J J, Want S, McCarthy I D, Brown M, Hughes S P

机构信息

Department of Orthopaedics, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK.

出版信息

J Bone Joint Surg Br. 1995 Nov;77(6):967-70.

PMID:7593116
Abstract

We have studied the ability of a range of antibiotics to penetrate intervertebral disc tissue in vitro, using a mouse disc model. Equilibrium concentrations of antibiotics incorporated into the entire disc were determined by bioassay using a microbial growth-inhibition method. Uptake was significantly higher with positively-charged aminoglycosides compared with negatively-charged penicillins and cephalosporins. Uncharged ciprofloxacin showed an intermediate degree of uptake. Our results support the hypothesis that electrostatic interaction between charged antibiotics and negatively-charged glycosaminoglycans in the disc is an important factor in antibiotic penetration, and may explain their differential uptake.

摘要

我们使用小鼠椎间盘模型,在体外研究了一系列抗生素穿透椎间盘组织的能力。通过微生物生长抑制法进行生物测定,确定了掺入整个椎间盘中的抗生素的平衡浓度。与带负电荷的青霉素和头孢菌素相比,带正电荷的氨基糖苷类抗生素的摄取量显著更高。不带电荷的环丙沙星显示出中等程度的摄取。我们的结果支持这样的假设,即带电荷的抗生素与椎间盘中带负电荷的糖胺聚糖之间的静电相互作用是抗生素渗透的一个重要因素,并且可以解释它们摄取的差异。

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