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首页> 外文期刊>Canadian Journal of Veterinary Research >Pharmacokinetics of a combination of amikacin sulfate and penicillin G sodium for intravenous regional limb perfusion in adult horses
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Pharmacokinetics of a combination of amikacin sulfate and penicillin G sodium for intravenous regional limb perfusion in adult horses

机译:Amikacin硫酸盐和青霉素G钠组合的药代动力学在成人马中静脉内区域肢体灌注

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摘要

The aim of this study was to determine the pharmacokinetics of amikacin and penicillin G sodium when administered in combination as an intravenous regional limb perfusion (IVRLP) to horses. Seven healthy adult horses underwent an IVRLP in the cephalic vein with 2 g of amikacin sulfate and 10 mill IU of penicillin G sodium diluted to 60 mL in 0.9% saline. A pneumatic tourniquet set at 450 mmHg was left in place for 30 min. Synovial fluid was collected from the metacarpophalangeal joint 35 min and 2, 6, 12, and 24 h after infusion of the antimicrobials. Concentrations of amikacin and penicillin in synovial fluid were quantitated by liquid chromatography tandem-mass spectrometry analysis. Therapeutic concentrations of amikacin and penicillin for equine-susceptible pathogens were achieved in the synovial fluid. Maximum synovial concentrations (C-max) (mean 6 SE) for amikacin and penicillin were 132 +/- 33 mu g/mL and 8474 +/- 5710 ng/mL, respectively. Only 3 horses had detectable levels of penicillin at 6 h and 1 at the 12 h sample. The combination of amikacin with penicillin G sodium via IVDLP resulted in reported therapeutic concentrations of both antibiotics in the synovial fluid. The C-max : MIC (minimum inhibitory concentration) ratio for amikacin was 8: 1 and Time. MIC for penicillin was 6 h. At 24 h, the mean concentration of amikacin was still above 4 mg/mL. Terminal elimination rate constants (T-1/2lambdaz) were 13.6 h and 2.8 h for amikacin and penicillin, respectively. The use of IVDLP with penicillin may therefore not be practical as rapid clearance of penicillin from the synovial fluid requires frequent perfusions to maintain acceptable therapeutic concentrations.
机译:该研究的目的是在组合给予静脉内区域肢体灌注(IVRLP)时,确定Amikacin和青霉素G钠的药代动力学。七个健康成年马在头部静脉中接受了IVRLP,用2g Amikacin硫酸盐和10毫米的青霉素G钠稀释至60ml的0.9%盐水。设置在450 mmHg的气动止血带70分钟。在输注抗微生物后,从Metacarpalangeal关节35分钟和2,6,12和24小时收集滑液。通过液相色谱串联光谱分析定量了氨基辛和青霉素在滑液中的浓度。在滑液中,在滑液中实现了Amikacin和青霉素的治疗浓度,在滑膜中实现了易感病原体。 Amikacin和青霉素的最大滑膜浓度(C-MAX)(平均6E)分别为132 +/-33μg/ ml和8474 +/- 5710ng / ml。只有3匹马在12小时样品下在6小时和1处具有可检测到的青霉素水平。 Amikacin与青霉素G钠通过IVDLP的组合导致了在滑液中报道的两种抗生素的治疗浓度。 Amikacin的C-MAX:MIC(最小抑制浓度)比为8:1和时间。青霉素的MIC为6小时。在24小时,Amikacin的平均浓度仍高于4mg / ml。 Amikacin和青霉素分别为13.6小时,分别为13.6小时和2.8小时。因此,使用IVDLP与青霉素可能是不实际的,因为青霉素来自滑膜液需要频繁的灌注以维持可接受的治疗浓度。

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