1) CIPROFLOXACIN HCL
环丙沙星盐酸
2) 1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7(1-piperazinyl)-3-quinolinecarboxylic acid, hydrochloride monohydrate
环丙沙星盐酸盐
3) ciprofloxacin hydrochloride tablet
盐酸环丙沙星片
1.
Objective To screen the optimum prescription and preparing techniques of ciprofloxacin hydrochloride tablets.
目的筛选盐酸环丙沙星片的最佳处方和制备工艺。
2.
Low dissolved speed of ciprofloxacin hydrochloride and great difference between determining value and theoretical value in ciprofloxacin hydrochloride tablets and capsules.
用高效液相色谱法测定盐酸环丙沙星片及盐酸环丙沙星胶囊的含量时,如果以水作溶刺,测定值明显偏低,宜改用0。
4) Ciprofloxacin hydrochloride
盐酸环丙沙星
1.
In situ preparation of ciprofloxacin hydrochloride/silica composites and their sustained release properties;
盐酸环丙沙星/二氧化硅复合粒子的原位制备及其缓释性能
2.
Green synthesis of Piperazine condensation in the preparation of Ciprofloxacin hydrochloride;
盐酸环丙沙星制备中哌嗪缩合的绿色合成
3.
Determination of amoxicillin and ciprofloxacin hydrochloride inamoxicillin & ciprofloxacin hydrochloride soluble powder by RP-HPLC;
RP-HPLC法测定阿莫西林—盐酸环丙沙星可溶性粉的含量
5) ciprofloxacin
盐酸环丙沙星
1.
Toxic effects of trichloroisocyanuric acid and ciprofloxacin hydrochloride on a freshwater alga,chlorella pyrenoidosa;
三氯异氰尿酸与盐酸环丙沙星对蛋白核小球藻的毒性效应
2.
Influencing factors in preparation of ciprofloxacin liposomes by ammonium sulfate transmembrane gradients;
硫酸铵梯度法制备盐酸环丙沙星脂质体的影响因素
3.
Determination of the efficiency of ciprofloxacin liposomes by cation exchange resin-first order derivative spectrophotometry;
阳离子交换树脂一阶导数分光光度法测定盐酸环丙沙星脂质体包封率
6) Ciporfloxacin hydrochloride
盐酸环丙沙星
1.
Determination of Ciporfloxacin Hydrochloride by Charge-Transferred Spectrophotometry with ρ-Nitropheno;
对硝基苯酚荷移分光光度法测定盐酸环丙沙星
2.
8), an excessed sodium tetraphenylborat (Na-TPB) reacted with ciporfloxacin hydrochloride and then precipitate occurred.
本法操作简便，终点直观、敏锐，已用于盐酸环丙沙星片剂的测定。
3.
A new spectrophoto method has been developed for the determinatio of ciporfloxacin hydrochloride.
5～7的水溶液中,盐酸环丙沙星与茜素红能发生荷移反应,形成2∶1的荷移络合物,最大吸收波长λmax=526 nm,表观吸收系数为1。
补充资料：环丙沙星盐酸盐
分子式：C17H19ClFN3O3
分子量：385.82
CAS号：86393-32-0
性质：白色或微黄色结晶粉末。易溶于水，微溶于甲醇，难溶于乙醇。
制备方法：暂无
用途：该品为广谱抗生素。通过抑制细菌DNA旋转酶，使DNA合成和复制受阻而导致细菌死亡。对大肠杆菌、克雷白杆菌和其他肠杆菌属有较强抗菌活性；对绿脓杆菌、金黄色葡萄球菌和肺炎链球菌的抗菌作用优于诺氟沙星和培氟沙星。用于敏感菌所致的中耳炎、外耳道炎和鼓膜炎等。偶有中耳痛及瘙痒感。
分子量：385.82
CAS号：86393-32-0
性质：白色或微黄色结晶粉末。易溶于水，微溶于甲醇，难溶于乙醇。
制备方法：暂无
用途：该品为广谱抗生素。通过抑制细菌DNA旋转酶，使DNA合成和复制受阻而导致细菌死亡。对大肠杆菌、克雷白杆菌和其他肠杆菌属有较强抗菌活性；对绿脓杆菌、金黄色葡萄球菌和肺炎链球菌的抗菌作用优于诺氟沙星和培氟沙星。用于敏感菌所致的中耳炎、外耳道炎和鼓膜炎等。偶有中耳痛及瘙痒感。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条