Objective: To prepare the compound ornidazole gargle and determine its contents.
目的：制备复方奥硝唑含漱液并建立其含量测定方法。
Objective: to prepare ornidazole cream and to determine the content of ornidazole.
目的：制备奥硝唑乳膏并对其进行含量测定。
Aim To study the preparation and quality control method for ornidazole Aphthae liquor.
目的研究奥硝唑口腔溃疡液的制备并对其质量进行控制。
Conclusion Ornidazole showed obvious therapeutic effect on maxillofacial space infection.
结论奥硝唑治疗颌面部间隙感染疗效显著。
OBJECTIVE: to study the in vitro antibiotic activity of compound ornidazole suppositories.
目的：研究复方奥硝唑栓的体外抗菌活性。
CONCLUSION Gatifloxacin for injection can be mixed in ornidazole sodium chloride injection.
结论：加替沙星与奥硝唑氯化钠注射液可以配伍使用。
OBJECTIVE To prepare and establish the method for measuring the content of ornidazole gargle.
目的制备奥硝唑含漱液并建立其含量测定方法。
Method: use Carbomer as a base to prepare Ornidazole gel and use HPLC to determine its content.
方法：以卡波姆为基质制备奥硝唑凝胶剂，采用HPLC法测定含量。
Results: Ornidazole and Sodium Chloride Injection has no interference to the bacterial endotoxin.
结果：奥硝唑氯化钠注射液对细菌内毒素检查法无干扰。
Objective For patients with severe periodontal disease oral anaerobic bacteria ornidazole sensitivity.
目的探讨重度牙周炎患者口腔厌氧菌对奥硝唑的敏感性。
Objective: To prepare the compound ornidazole tincture and study the quality control of this preparation.
前言：目的：研制复方奥硝唑酊剂并对制剂进行质量控制。
OBJECTIVE To establish a method for determining the concentration of ornidazole in breast milk by RP-HPLC.
目的：建立测定母乳中奥硝唑浓度的反相高效液相色谱法。
Objective To evaluate the clinical effect of ornidazole on the treatment of maxillofacial space infection.
目的观察奥硝唑治疗颌面部间隙感染的疗效。
Result: The method has a high stability and repetitiveness. Ornidazole gel is relatively stable to heat and light.
结果：奥硝唑含量测定方法稳定，重复性好，奥硝唑凝胶剂对热和光较稳定。
OBJECTIVE:To develop the preparation technic of compound ornidazole suppository and establish the quality standard.
目的：建立复方奥硝唑栓剂的制备方法及质量控制标准。
Conclusion Using ornidazole can effectively improve the clinical symptoms, effectively kill anaerobic bacteria strains.
结论应用奥硝唑能有效改善临床症状，有效杀灭厌氧菌株。
Objective To study the compatible stability of lomefloxacin hydrochloride with ornidazole and sodium chloride injection.
目的研究盐酸洛美沙星与奥硝唑氯化钠注射液的配伍稳定性。
OBJECTIVE: To evaluate the therapeutic effect of Ornidazole on the anaerobic infections after maxillofacial plastic surgery.
目的：评价奥硝唑氯化钠注射液治疗口腔颌面部整形术后厌氧菌感染的疗效。
Results: Various doses of compound ornidazole-rhubarb buccal film significantly shrank the ulcer areas at different degrees.
结果：各剂量复方奥硝唑大黄口腔膜均能不同程度减小溃疡面直径。
Objective To investigate the stability of the mixture of cefotaxime sodium injection and ornidazole sodium chloride injection.
目的观察注射用头孢噻肟钠与奥硝唑氯化钠注射液配伍后的稳定性。
Objective To evaluate the compatible stability of cefpiramide sodium for injection with ornidazole and sodium chloride injection.
目的考察注射用头孢匹胺钠与奥硝唑氯化钠注射液配伍的稳定性。
Conclusion The sustained-release periodontal suppository of ornidazole and pefloxacin have sustained-release effect of long time.
结论复方奥硝唑甲磺酸培氟沙星缓释牙栓具有较长时间的缓释效果。
CONCLUSIONS: This method is simple, accurate and reproducible, and suitable for the quality control of ornidazole hollow suppository.
结论：本方法简便、准确、重现性好，可用于奥硝唑中空栓的质量控制。
To introduce the preparation and quality control methods of the ornidazole slow-release membranes which take CM-chitosan as carriers.
研制以羧甲基壳聚糖为载体的奥硝唑缓释膜（药膜，下同）并建立质量控制方法。
Results After ornidazole treatment of patients of each index and anaerobic bacteria periodontitis were significantly lower proportion.
结果奥硝唑治疗后患者的牙周炎各项指标及厌氧菌的比例均明显降低。
CONCLUSION: Compound Ornidazole suppositories are characterized by broad spectrum, high performance, low toxicity etc for gynecological inflammation.
结论：复方奥硝唑栓对妇科炎症具有广谱、高效、低毒的特点。
Methods Divide them into two groups at random: the treatment group using Ornidazole calcium hydroxide; and the comparative group using Camphor phenol.
方法通过随机分为两组，治疗组奥硝唑氢氧化钙糊剂组，对照组樟脑酚组。
Conclusion: The method can be used for separating the enantiomers of Ornidazole and controlling of the impurity of dextroisomer in S-Ornidazole substances.
结论：本方法可以实现奥硝唑的手性分离，并能应用于左旋奥硝唑原料药中的右旋体杂质的控制。
Conclusion: The method can be used for separating the enantiomers of Ornidazole and controlling of the impurity of dextroisomer in S-Ornidazole substances.
结论：本方法可以实现奥硝唑的手性分离，并能应用于左旋奥硝唑原料药中的右旋体杂质的控制。
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