recovery of 2-mercaptobenzothiazole and triphenyl phosphine oxide from dregs generated in cefotaxime sodium production

1、

objective: to improve the determination experimental condition of cefotaxime sodium in chp.

目的：对中国药典收载的头孢噻肟钠聚合物测定条件进行改进。

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2、

stability after compatibility of cefotaxime sodium and cimetidine in different kinds of intravenous infusions

注射用头孢噻肟钠与西咪替丁注射液在4种输液中配伍后的稳定性

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3、

objective study on the stability of cefotaxime sodium tazobactam sodium for injection.

目的：观察注射用头孢噻肟钠、他唑巴坦钠稳定性。

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4、

objective to determine sodium cefotaxime in renal dialysate from burn injured patients.

目的测定肾替代治疗的烧伤患者肾脏透析排出液中头孢噻肟钠的含量。

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5、

determination of cefotaxime sodium injection by hplc and in vitro antibacterial activity assay

注射用头孢噻肟钠的含量测定及体外抗菌活性检查

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6、

ethanol or ethanol plus cefotaxime sodium was injected into the simple cysts;

卵巢单纯性囊肿注入无水乙醇或无水乙醇+头孢噻肟钠；

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7、

resource the reuse of dregs generated in cefotaxime sodium

头孢噻肟钠生产废渣资源化

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8、

chymotrypsin and cefotaxime sodium were injected into the encapsulated pelvic effusion.

包裹性积液注入糜蛋白酶或头孢噻肟钠。

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9、

in vitro antibacterial activities of different ratios from matching cefotaxime/ tazobactam

不同配比头孢噻肟钠/他唑巴坦钠的体外抗菌作用

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10、

quantitative test of bacterial endotoxins in cefotaxime sodium for injection

注射用头孢噻肟钠的细菌内毒素定量检测

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11、

biological transport of cefotaxime sodium by human periodontal ligament fibroblasts

人牙周膜成纤维细胞对头孢噻肟钠的跨膜转运

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12、

study on the effect of metronidazole on protein-binding of cefotaxime

甲硝唑对头孢噻肟钠蛋白结合影响的研究

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13、

clinical observation for the curative effect compound cefotaxime sodium for injection

注射用复方头孢噻肟钠的临床疗效观察

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14、

clinical analysis of cefotaxime sodium treating 86 cases of neonatal septicemia

头孢噻肟钠治疗新生儿败血症86例临床分析

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15、

measurement and correlation of liquid-solid equilibrium of cefotaxime sodium in water-isopropanol

头孢噻肟钠在水-异丙醇中的液固平衡测量与关联

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16、

results: no significant change was noted in the detection results of all the items of cefotaxime sodium for injection in 4 kinds of infusion packages and under different temperatures;

结果注射用头孢噻肟钠在各温度条件下于4种包装输液中各检测项目均无明显变化，4组间比较无显著性差异（P0.1）。

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17、

the cumulative urinary excretion rates of cefotaxime sodium and tazobactam sodium were ( 49.6 ± 0.58)% and ( 80.0 ± 7.0)% after intravenous drip of a single 2.4 g dose, respectively.

单次给药中剂量组10h头孢噻肟钠和他唑巴坦钠累计尿排率为49.6±0.58%和80.0±7.0%。

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18、

conclusion: the mixture of ornidazole injection and cefotaxime sodium for injection can be used after ( storing) at 4 ℃ for 8 h, 25 ℃ for 4 h and 37 ℃ for 1 h.

结论：奥硝唑注射液与注射用头孢噻肟钠的配伍液在配伍后4℃8h内、25℃4h内、37℃1h内可使用。

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19、

objective: to evaluate the stability of tinidazole and cefotaxime sodium mixed in infusion fluid at 4 ℃, 25 ℃ and 37 ℃ for 24 hours.

目的：考察4℃、25℃、37℃下24h内替硝唑葡萄糖注射液与注射用头孢噻肟钠的配伍稳定性。

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20、

objective: to observe the stability of cefotaxime sodium for injection in pvc infusion bags, pp plastic infusion bottle, non-pvc multilayer polymer infusion bags and glass bottles.

目的考察注射用头孢噻肟钠在聚氯乙烯（PVC）输液袋、聚丙烯（PP）塑料输液瓶、非聚氯乙烯（NPVC）多层共挤膜输液袋及玻璃瓶包装输液中的稳定性差异。

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