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W/O/W型复乳剂软膏基质的研究 被引量:1
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作者 蒋竞 吕育齐 +2 位作者 李津明 张秀娟 郭春梅 《中草药》 CAS CSCD 北大核心 1996年第1期19-21,共3页
用正交试验法,选用L9(34)和L8(27)正交表安排实验,对影响复乳剂的因素及生产工艺条件进行了考察及优选。
关键词 软膏 基质 复乳剂 稳定性
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醋酸氯己定缓释复乳剂作用的初步研究 被引量:1
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作者 李涢 杨圣辉 刘颖 《北京口腔医学》 CAS 2010年第4期212-214,共3页
目的探讨W/O/W型醋酸氯己定缓释复乳剂的体外缓释作用和抑菌效果,为牙周炎和根尖周炎的治疗提供新药使用依据。方法采用高效液相色谱法测定醋酸氯已定复乳剂中醋酸氯己定含量和1~13d该复乳剂中药物成分醋酸氯已定的体外释放情况;并采... 目的探讨W/O/W型醋酸氯己定缓释复乳剂的体外缓释作用和抑菌效果,为牙周炎和根尖周炎的治疗提供新药使用依据。方法采用高效液相色谱法测定醋酸氯已定复乳剂中醋酸氯己定含量和1~13d该复乳剂中药物成分醋酸氯已定的体外释放情况;并采用钢管法观察该复乳剂倍比稀释后对牙龈卟啉单胞菌的体外抑菌作用。结果醋酸氯已定浓度与色谱峰面积在0.005~0.10mg/ml范围内呈良好的线性关系,相关系数R为0.9999,回归方程为Y=6×107X-56851。体外释放实验表明,该复乳剂主要成分醋酸氯己定的释放稳定,在13天内能保持有效的释药浓度。体外抑菌实验显示:该复乳剂连续稀释15倍仍对牙龈卟啉单胞菌具有明显的抑菌作用。结论该醋酸氯已定复乳剂在体外具有明显的药物缓释效果、对所选细菌有良好的抑菌作用,值得进一步研发。 展开更多
关键词 醋酸氯己定 复乳剂 缓释
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5种杀虫剂不同处理对小菜蛾的防效试验
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作者 付祖科 邓士元 金雪晴 《当代蔬菜》 2004年第7期32-32,共1页
关键词 杀虫剂 小菜蛾 药效试验 虫清二号乳剂 阿维乳剂 蔬菜害虫
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Effect of Huzikang-duannaibao on piglets' ablactation stress
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作者 ZhouShenglin JiangZhengyun 《Hunan Agricultural Science & Technology Newsletter》 2003年第4期18-20,共3页
Piglets’ alactation stress with diarrhea as a main symptom is a serious problem in pig farming. The experiment indicates that the complex premix additive Huzikang duannaibao can be used to control ablactation stress ... Piglets’ alactation stress with diarrhea as a main symptom is a serious problem in pig farming. The experiment indicates that the complex premix additive Huzikang duannaibao can be used to control ablactation stress syndromes and its effects are better than that of the common antibiotic ligomycin. 展开更多
关键词 PIGLET complex premix additive Huzikang duannaibao ablactation stress DIARRHEA
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Characterization of amphiphilic dendrimer modified PEG-PLA nanoparticles prepared by a double emulsion-solvent evaporation method
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作者 李欣 庞宁 +1 位作者 李骥 齐宪荣 《Journal of Chinese Pharmaceutical Sciences》 CAS CSCD 2017年第7期521-527,共7页
Drug delivery by nanocarriers requires characterizations of suitable particle size, high drug loading and safety. In this work, we prepared an amphiphilic dendrimer modified PEG-PLA mixed nanoparticles(NPs) by a dou... Drug delivery by nanocarriers requires characterizations of suitable particle size, high drug loading and safety. In this work, we prepared an amphiphilic dendrimer modified PEG-PLA mixed nanoparticles(NPs) by a double emulsion-solvent evaporation(DESE) method. The particle size and drug encapsulation efficacy(EE) were compared to evaluate and optimize the preparation parameters. The mixed NPs had average size ranging from(102±1) nm to(137±5) nm, and the zeta potential turned to positive with incorporation of the amphiphilic dendrimer. The NPs showed different EE of docetaxel(DTX) and paclitaxel(PTX) with higher affinity to more lipophilic PTX. The blank mixed NPs showed little cytotoxicity, and the DTX-loaded NPs could effectively facilitate the antiproliferation activity on PC-3 cells. The NPs could be used as an effective drug delivery system, and its anti-tumor effect is worthy of further study. 展开更多
关键词 PEG-PLA nanoparticles DOCETAXEL PACLITAXEL Double emulsion-solvent evaporation method Amphiphilic dendrimer
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