复方乙酰水杨酸片,compound aspirin tablets
1)compound aspirin tablets复方乙酰水杨酸片
1.The application of PLS (partial least squares) and near infrared spectroscopy forcompound aspirin tablets non destructive quantitative analysis was investigated and the best mathematic calibration models were built.将偏最小二乘法 (PLS)与近红外漫反射光谱法相结合 ,对复方乙酰水杨酸片进行无损非破坏定量分析 ,建立了最佳的数学校正模型 ,比较了样品中 3种有效成分 (乙酰水杨酸、非那西丁和咖啡因 )同时测定和单独测定时的主成分数对PLS定量预测能力的影响 ,预测了未知样品。
2.To estapblish a TLC method for identifcation of three components in compound paracetamol tablets andcompound aspirin tablets.方法:样品溶液直接点于硅胶GF_(254)薄层板上,复方对乙酰氨基酚片以醋酸乙酯—无水—乙醇—冰醋酸(50:1:1)为展开剂;复方乙酰水杨酸片以氯仿—乙醚—丙酮—冰醋酸(27:18:1:2)为展开剂,在紫外灯(254nm)下检视。
3.Aim To establish a method for the determination of free salicylic acid incompound aspirin tablets by HPLC.目的采用高效液相色谱法测定复方乙酰水杨酸片中游离水杨酸的含量。
英文短句/例句
1.STUDIES OF THE ANTIDIARREIC CONSTITUENTS OF BURNED SUBSTANCES OF COMPOUND ACETYLSALICYLIC ACID TABLES复方乙酰水杨酸片灼烧物中止泻成分研究
2.Determination of Three Components in Compound Aspirin Tablets by HPLCHPLC测定复方乙酰水杨酸片中3组分的含量
3.Determination of Free Salicylic Acid in Compound Aspirin Tablets by HPLC高效液相色谱法测定复方乙酰水杨酸片中游离水杨酸含量
4.Objective To establish a method for the determination of content of paractamol in Compound Aspirin tablet.目的7建立复方乙酰水杨酸片中扑热息痛含量的测定方法。
5.Determination of Chlorogenic Acid and Acetylsalicylic Acid in Compound Cold Capsule by HPLC高效液相色谱法测定复方感冒胶囊中绿原酸和乙酰水杨酸的含量
6.Amfetamine acetylsalicylate苯丙胺乙酰水杨酸盐
7.antipyrine salicylacetate乙酰水杨酸安替比林
8.pregnenolone acetylsalicylate乙酰水杨酸孕烯醇酮
9.Determination of Acetylsalicylic acid and Salicylic Acid in Julan Anti-influenza Tablets by HPLCHPLC法测定菊蓝抗流感片中乙酰水杨酸和游离水杨酸的含量
10.Effect of Dextrin on Determination for Acetylsalicylic Acid Enteric-coated Tablets糊精对乙酰水杨酸肠溶片含量测定的影响
11.Process for Preparing Binuclear Manganese(Ⅳ) Complex via Acetylsalicylic Acid乙酰水杨酸制备双核水杨酸锰(Ⅳ)配合物
12.Studies on synthesis of acetylsalicylic acid catalyzed by acid bentonite酸性膨润土催化合成乙酰水杨酸研究
13.Study on Synthesis of Acetylsalicylic Acid Catalyzed by Amidosulphonic Acid;氨基磺酸催化合成乙酰水杨酸的研究
14.Study on the synthesis of acetyl salicylic acid with potassium bisulfate as catalyst;硫酸氢钾催化合成乙酰水杨酸的研究
15.Determination of Salicylic Acid and Benzoic Acid in Compound Benzoic Acid Ointment by HPLCHPLC法测定复方水杨酸冰片软膏中水杨酸和苯甲酸的含量
16.para-acetylaminophenyl salicy late对位乙酰胺基苯基水杨酸盐
17.SYNTHESIS OF 5-ACETYLSALICYLAMIDE THROUGH ACETYLATION USING TRIETHYLAMMONIUM CHLOROALUMINATE IONIC LIQUID AS CATALYST盐酸三乙胺-三氯化铝离子液体催化酰基化合成乙酰水杨酰胺
18.A Research on Synthesis of Acetylsalicylic Acid Catalyzed over Aminosulfonic Acid under Ultrasound Irradiation超声辐射氨基磺酸催化合成乙酰水杨酸的研究
相关短句/例句
Compound Asprin复方乙酰水杨酸片,复方阿司匹林片
3)Buffered Acetylsalicylic Acid Tablets(Buffaspirin R)乙酰水杨酸缓冲片
4)acetylsalicylic acid乙酰水杨酸
1.Studies on synthesis ofacetylsalicylic acid catalyzed by acid bentonite;酸性膨润土催化合成乙酰水杨酸研究
2.Fluorescence study on the Interaction of Acetylsalicylic Acid and Bovine Serum Albumin;荧光光谱法研究乙酰水杨酸和牛血清蛋白的相互作用
3.Synthesis ofacetylsalicylic acid by microwave irradiation under the assistance of sodium bicarbonate catalyst;微波辐射催化合成乙酰水杨酸
5)Acetyl salicylic acid乙酰水杨酸
1.Synthesis of acetyl salicylic acid with sodium benzoate as catalytic;苯甲酸钠催化合成乙酰水杨酸的研究
2.And it is determined the release of such model medicines as acetyl salicylic acid and rifampin in the ways of dynamic release.讨论了药物丝素膜采用动态或静态释放法对膜中药物释放的差异性 ,并采用动态释放法测定了复层丝素膜对模型药物乙酰水杨酸及利福平的释放 ,实验结果表明 ,复层药物丝素膜比单层药物丝素膜在释放液中初始释放浓度稍大 ,释放时间延长 ,更符合药物缓释制剂的要求。
3.It has proved that acetyl salicylic acid can be synthesized in high yield with the catalysis of NiSO4.首次用路易斯酸作为催化剂,以水杨酸和乙酸酐为原料合成乙酰水杨酸。
6)aspirin[英]["?spr?n][美]["?spr?n]乙酰水杨酸
1.Simultaneous determination of paracetamol andaspirin in Xiaoertuishaopian by dual wavelength ultraviolet spectrophotometry;双波长紫外分光光度法同时测定小儿退烧片中对乙酰氨基酚和乙酰水杨酸的含量(英文)
2.Design and Practice of Aspirin on Synthesis of Microscale;乙酰水杨酸合成的微型化设计与实践
3.Simultaneous determination ofaspirin and paracetamol in Xiaoer Tuishao tablet by HPLC;HPLC法同时测定小儿退烧片中乙酰水杨酸和对乙酰氨基酚的含量(英文)
延伸阅读
水杨酸镁片【通用名称】水杨酸镁片【其他名称】水杨酸镁片 水杨酸镁片 拼音名：Shuiyangsuanmei Pian 英文名：Magnesium Salicylate Tablets 书页号：2000年版二部－82 本品含无水水杨酸镁(C14H10MgO6)应为标示量的95.0％～105.0 ％。 【性状】 本品为白色片。 【鉴别】 (1)取含量测定项下的溶液，照分光光度法（附录Ⅳ A）测定，在296 nm的波长处有最大吸收。 (2) 取本品1片，研细，加水使水杨酸镁溶解，滤过，滤液显镁盐与水杨酸盐的鉴 别反应（附录Ⅲ）。 【检查】 溶出度 取本品，照溶出度测定法（附录Ⅹ C第二法），以水900ml为 溶剂，转速为每分钟50转，依法操作，经45分钟时，取溶液10ml，滤过，精密量取续滤 液适量，用水定量稀释成每1ml中约含无水水杨酸镁20μg 的溶液，照水杨酸镁含量测定 项下的方法，自“另取水杨酸镁对照品”起，依法测定，计算出每片的溶出量。限度为标 示量的80％，应符合规定。 其他 应符合片剂项下有关的各项规定（附录Ⅰ A）。 【含量测定】 取本品20片，精密称定，研细，精密称取适量（约相当于无水水杨 酸镁0.5g）置250ml量瓶中，加水适量，振摇使水杨酸镁溶解并稀释至刻度，摇匀，滤 过，精密量取续滤液2ml， 置200ml量瓶中，加水稀释至刻度，摇匀。照水杨酸镁含量测定 项下的方法，自“另取水杨酸镁对照品”起，依法测定，即得。 【类别】 同水杨酸镁。 【规格】 0.25g(按C14H10MgO6计算) 【贮藏】 密封保存。
