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Moxifloxacin hydrochloride eardrops Preparation and Quality Control
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Moxifloxacin hydrochloride eardrops Preparation and Quality Control
Author: Du Xi-Chi Xi-Kui Rui-Min Li Hongyan Li Jinwei Dr Tan Yi \
【Abstract】 Objective: Preparation of Moxifloxacin hydrochloride eardrops to establish its quality control methods. Methods: The main high-performance liquid chromatography Moxifloxacin hydrochloride content, and examine its stability. Results: Moxifloxacin hydrochloride linear range of 0.4μg ~ 3μg, the average recovery was 97 67%, RSD = 1.75% (n = 6), Ear Drops good stability. Conclusion: The design is reasonable, accurate and reliable method of quality control, preparation and good stability.
Keywords: Moxifloxacin hydrochloride; Ear Drops; preparation; Quality Control
In recent years, chronic ear inflammation diffuse upward trend in the incidence of clinical bacterial culture results showed that the inflammation caused by bacterial infection [1]. Moxifloxacin (moxifolxacin) for Bayer’s newly developed 4th generation of new, ultra-broad-spectrum quinolone antibacterial agents [2], it is good to keep the traditional quinolone resistant Gram-negative bacteria based on the in vitro activity of anti-Ge the activity of Gram-positive bacteria has been enhanced [3], of this product-resistant Gram-positive bacteria resistant produce little or very slow. Pairs of aerobic Gram-positive cocci in vitro antibacterial activity of ciprofloxacin stronger than the 4 to 8 times. Currently on the market already tablets, injections, we prepared the basis of clinical need Moxifloxacin hydrochloride eardrops and the establishment of quality control methods.
An instrument and reagent
Shimadzu LC 10AD-based high-performance liquid chromatography (including the SPD 10A UV detector, SC1 10A controller, C RTA-based chromatographic data processor); 7312 1 Electric mixer (Beijing Poor Analysis of General Instrument Co., Ltd.); PHB 1 Portable pH meter (TriTrust companies). Mo
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