头孢唑烷-他唑巴坦与肠外营养的理化兼容性

Pharmaceuticals Pub Date : 2024-07-05 DOI:10.3390/ph17070896
J. T. De Pourcq, Adria Riera, Laura Gras, N. Garin, M. Antònia Busquets, J. Cardenete, Daniel Cardona, P. Riera
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引用次数: 0

摘要

头孢唑烷-他唑巴坦(CT)用于治疗复杂性感染以及铜绿假单胞菌和产广谱β-内酰胺酶肠杆菌的多重耐药菌株。在某些情况下,可能需要同时给予 CT 和肠外营养(PN),但 Y 位联合给药的兼容性尚不清楚。本研究旨在分析 CT Y 位点与肠外营养(PN)给药的理化兼容性。我们对本中心危重病人的 PN 方案进行了评估。我们研究了栓剂输注(2 克头孢妥赞/1 克他唑巴坦,1 小时内)和持续输注 (CI)(6 克头孢妥赞/3 克他唑巴坦)两种策略。对样品进行肉眼逆光观察和显微镜检查,并使用 pH 计分析 pH 值。通过动态光散射测定平均脂滴直径(MDD)。使用 HPLC-HRMS 对 CT 浓度进行量化。肉眼或显微镜检查均未发现任何变化。pH 值变化小于 0.2,渗透压变化小于 5%。MDD 保持在 500 nm 以下(栓剂 CT 为 284.5 ± 2.1,CI CT 为 286.8 ± 7.5)。在两种输注策略中,t = 0 小时和 t = 24 小时的 CT 浓度均保持在预设参数范围内。在模拟 Y 位点给药过程中,CT 在测试浓度和输注速度下与 PN 的生理生化相容。
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Physicochemical Compatibility of Ceftolozane-Tazobactam with Parenteral Nutrition
Ceftolozane-tazobactam (CT) is used for the treatment of complicated infections and for multidrug-resistant strains of Pseudomonas aeruginosa and extended-spectrum beta-lactamase-producing enterobacteria. In certain cases, simultaneous administration of CT and parenteral nutrition (PN) may be required, but compatibility of Y-site co-administration is unknown. The aim of this study was to analyse the physicochemical compatibility of CT Y-site administered with PN. We evaluated a protocolized PN approach for critical patients in our center. We studied both bolus infusion (2 g ceftolozane/1 g tazobactam in 1 h) and continuous infusion (CI) (6 g ceftolozane/3 g tazobactam) strategies. Samples were visually observed against light, microscopically inspected, and pH was analysed using a pH meter. The mean lipid droplet diameter (MDD) was determined via dynamic light scattering. CT concentration was quantified using HPLC–HRMS. No alterations were observed through visual or microscopic inspection. Changes in pH were ≤0.2, and changes in osmolarity were less than 5%. MDD remained below 500 nm (284.5 ± 2.1 for bolus CT and 286.8 ± 7.5 for CI CT). CT concentrations at t = 0 h and t = 24 h remained within prespecified parameters in both infusion strategies. CT is physiochemically compatible with PN during simulated Y-site administration at the tested concentration and infusion rates.
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