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环丙沙星在骨组织中的渗透:一种新型可生物吸收植入物。

Penetration of ciprofloxacin into bone: a new bioabsorbable implant.

作者信息

Overbeck J P, Winckler S T, Meffert R, Törmälä P, Spiegel H U, Brug E

机构信息

Department of Trauma and Hand Surgery, Westfaelische Wilhelms University, Muenster, Germany.

出版信息

J Invest Surg. 1995 May-Jun;8(3):155-62. doi: 10.3109/08941939509023138.

DOI:10.3109/08941939509023138
PMID:7547723
Abstract

The implantation of antibiotic-containing cement beads became standard adjuvant local antibiotic therapy of chronic osteomyelitis. The new developed bioabsorbable drug carrier system of polyglycolic acid with the antibiotic Ciprofloxacin was tested in vitro and in vivo. The goal of this study was to determinate the penetration depth of Ciprofloxacin into bone cortex and marrow. Two monofil, PGA cylinders, 3.2 x 5 mm in size, containing 3 mg of Ciprofloxacin each, were implanted into the proximal part of both femora of 18 rabbits (New Zealand white). After sacrifice, the concentration of Ciprofloxacin in micrograms/g cortex and marrow was measured with high-performance liquid chromatography in relation to the distance from the test material at day 2, as well as at 1, 2, 3, 4, and 6 weeks postimplantation. For a distance up to 5 mm, marrow levels of the drug exceeded cortical levels at day 2 (5000 to 240 micrograms/g). At a distance of 5-10 mm, cortex levels were similar to marrow levels after 2 weeks and were higher than marrow levels at week 3. This observation could be made at a distance between 10 and 15 mm only after 2 days. Later, marrow concentrations again exceeded that in cortex. At a distance of more than 15 mm, antibiotic levels were low and approximated. After 6 weeks, at 5 mm distance, a bactericidal drug concentration of about 2 micrograms/g in bone marrow could be measured. Drug penetration into cortical bone in bactericidal concentrations of about 2 micrograms/g was achieved at up to 30 mm in the first few days.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

含抗生素的骨水泥珠植入术已成为慢性骨髓炎的标准辅助局部抗生素治疗方法。一种新开发的聚乙醇酸与抗生素环丙沙星的生物可吸收药物载体系统在体外和体内进行了测试。本研究的目的是确定环丙沙星在骨皮质和骨髓中的渗透深度。将两个尺寸为3.2×5mm、各含3mg环丙沙星的单丝聚乙醇酸圆柱体植入18只新西兰白兔双股骨近端。处死后,在植入后第2天以及第1、2、3、4和6周,用高效液相色谱法测量距测试材料不同距离处骨皮质和骨髓中环丙沙星的浓度(微克/克)。在2天时,距测试材料5mm范围内,骨髓中的药物水平超过骨皮质水平(5000至240微克/克)。在5-10mm距离处,2周后骨皮质水平与骨髓水平相似,第3周时高于骨髓水平。仅在2天后,在10至15mm距离处才能观察到这种情况。之后,骨髓浓度再次超过骨皮质。在超过15mm的距离处,抗生素水平较低且接近。6周后,在5mm距离处,骨髓中可测得约2微克/克的杀菌药物浓度。在最初几天,在高达30mm的骨皮质中可实现约2微克/克杀菌浓度的药物渗透。(摘要截断于250字)

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