Am J Vet Res. 2021 May;82(5):358-366. doi: 10.2460/ajvr.82.5.358.
To evaluate physical compatibility of small animal (SAE) and large animal (LAE) injectable formulations of enrofloxacin with select IV fluids and drugs.
162 admixtures containing SAE or LAE with saline (0.9% NaCl) solution, lactated Ringer solution (LRS), Plasma-Lyte A (PLA), 6% hydroxyethylstarch 130/0.4 (HES), metoclopramide, or ampicillin-sulbactam.
In the first of 2 simultaneously conducted experiments, admixtures containing enrofloxacin (10 mg/kg) and a volume of IV fluid that would be administered over a 20-minute period when dosed at the maintenance infusion rate (40 mL/kg/d for saline solution, LRS, and PLA and 20 mL/kg/d for HES) were created. In the second experiment, enrofloxacin (10 mg/kg) was admixed with saline solution (40 mL/kg/d) and metoclopramide (2 mg/kg/d) or ampicillin-sulbactam (30 mg/kg). In both experiments, admixture components were infused into a flask over 20 minutes assuming patient weights of 5, 10, and 20 kg. Admixtures were created by use of undiluted SAE and SAE diluted 1:1 with saline solution and undiluted LAE and LAE diluted 1:1 and 1:10 with saline solution. Admixtures were assessed for physical incompatibility at 0, 15, 30, and 60 minutes after completion of mixing. Physical incompatibility was defined as gross precipitation, cloudiness, Tyndall effect, or change in turbidity.
Admixtures containing undiluted SAE or LAE were physically incompatible with saline solution, PLA, LRS, and HES. Because saline solution was used to dilute SAE and LAE, all admixtures containing diluted SAE or LAE were also physically incompatible. Physical compatibility of enrofloxacin with metoclopramide or ampicillin-sulbactam could not be assessed because those admixtures also contained saline solution.
Enrofloxacin was physically incompatible with all tested solutions.
评估小(SAE)大和(LAE)动物可注射恩诺沙星制剂与特定静脉输液和药物的物理相容性。
162 种混合物,含有 SAE 或 LAE 与生理盐水(0.9% NaCl)溶液、乳酸林格溶液(LRS)、Plasma-Lyte A(PLA)、6%羟乙基淀粉 130/0.4(HES)、甲氧氯普胺或氨苄西林-舒巴坦。
在同时进行的 2 项实验中的第 1 项实验中,创建了含有恩诺沙星(10 mg/kg)和在维持输注率(生理盐水溶液、LRS 和 PLA 为 40 mL/kg/d,HES 为 20 mL/kg/d)下给药时在 20 分钟内给予的静脉输液体积的混合物。在第 2 项实验中,将恩诺沙星(10 mg/kg)与生理盐水溶液(40 mL/kg/d)和甲氧氯普胺(2 mg/kg/d)或氨苄西林-舒巴坦(30 mg/kg)混合。在这两项实验中,假设患者体重为 5、10 和 20 kg,将混合物成分通过输液器在 20 分钟内输注到一个烧瓶中。通过使用未稀释的 SAE 和 1:1 稀释的 SAE 与生理盐水溶液以及未稀释的 LAE 和 1:1 和 1:10 稀释的 LAE 与生理盐水溶液来制备混合物。混合完成后 0、15、30 和 60 分钟评估混合物的物理不相容性。物理不相容性定义为明显沉淀、混浊、Tyndall 效应或浊度变化。
含有未稀释的 SAE 或 LAE 的混合物与生理盐水溶液、PLA、LRS 和 HES 物理不相容。由于生理盐水溶液用于稀释 SAE 和 LAE,因此所有含有稀释 SAE 或 LAE 的混合物也物理不相容。由于这些混合物还含有生理盐水溶液,因此无法评估恩诺沙星与甲氧氯普胺或氨苄西林-舒巴坦的物理相容性。
恩诺沙星与所有测试溶液均物理不相容。