1)Enteric-coated tablet肠溶片
1.Relative bioavailability of metformin hydrochloride enteric-coated tablets in human;盐酸二甲双胍肠溶片的人体相对生物利用度
2.Investigation on in vitro release of diclofenac sodium enteric-coated tablets;双氯芬酸钠肠溶片体外释放度比较
3.Determination of dissolution among 6 kinds of commercialized enteric-coated tablets of aspirin;6种市售阿司匹林肠溶片释放度的测定
英文短句/例句
1.Clinical observation of tribendimidine enteric-coated tablets in the treatment of patients with intestinal nematodiasis三苯双脒肠溶片治疗肠道线虫感染的临床观察
2.Study on Enteric-Coated Tablets of Compound Alendronate Sodium and Vitamin D_3;复方阿仑膦酸钠VitD_3肠溶片的研制
3.Bioequiavailability Investigation of Omeprazole Enteric Coated Tablet in Human;奥美拉唑肠溶片人体生物等效性研究
4.Determination of Related Substances in Bisacodyl Enteric-coated Tablets by HPLCHPLC法测定比沙可啶肠溶片的有关物质
5.Bioequivalence of Azithromycin Enteric-coated Tablets in healthy volunteers阿奇霉素肠溶片人体生物等效性研究
6.Preparation and Quality Control of Gongling Enteric-coated Tablets中药宫灵肠溶片的制备及其质量控制
7.Content determination of Aspirin Enteric-Coated Tablets by HPLCHPLC测定阿司匹林肠溶片的含量
8.Determination of Pantoprazole Sodium Enteric-Coated Tablets by HPLCHPLC法测定泮托拉唑钠肠溶片的含量
9.Preparation and stability study of enteric coated lansoprazole tablets兰索拉唑肠溶片的制备及稳定性考察
10.Preparation and Quality Control of Rosiglitazone Sodium Enteric-coated Tablets罗格列酮钠肠溶片的制备及质量控制
11.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
12.Related substances and conents of protionamide determined by HPLCHPLC法测定丙硫异烟胺肠溶片的有关物质及含量
13.Pharmacokinetics of duloxetine hydrochloride enteric-coated tablets in healthy volunteers盐酸度洛西汀肠溶片在健康人体内的药动学
14.Comparative Study on the Release Rate of Rabeprazole Sodium Enteric-coated Tablets雷贝拉唑钠肠溶片体外释放度比较研究
15.Clinical Effects of Serrapeptase Enteric-coated Tablets in Treatment of Chronic Sinusitis舍雷肽酶肠溶片对慢性鼻窦炎的疗效观察
16.Determination of the Conent of Salicylic Acid in Aspirin Enteric-coated Tablets by Spectrophotometry分光光度法测定阿司匹林肠溶片中水杨酸含量
17.Pharmacokinetics of Omeprazole Enteric-coated Tablets in Healthy Volunteers奥美拉唑肠溶片在汉族健康人体的药动学研究
18.RP-HPLC determination of lansoprazole enterosoluble tablets in human plasmaRP-HPLC法测定人血浆中兰索拉唑肠溶片血药浓度
相关短句/例句
Enteric-coated tablets肠溶片
1.Study on the prescription and method for coating of erythromycin enteric-coated tablets;红霉素肠溶片包衣处方工艺
2.Determination of dirithromycin in its enteric-coated tablets by HPLC;高效液相色谱法测定地红霉素肠溶片中地红霉素的含量
3.The release of pancreatic kininogenase enteric-coated tablets was determined by UV method at the detection wavelength of 253nm, according to the second method of appendix ⅩD in ChP 2000 under the stirring rate of 100r/min.建立了UV法测定胰激肽原酶肠溶片的释放度。
3)Enteric tablets肠溶片
1.Preparation and stability study of (l) -pantoprazole sodium enteric tablets;左旋泮托拉唑钠肠溶片的制备及其稳定性考察
2.Pharmacokinetics of oxaprozin enteric tablets in healthy volunteers;奥沙普秦肠溶片在健康人体内的药动学
4)enteric tablet肠溶药片
5)enteric dispersible tablets肠溶分散片
1.Indomethacin enteric dispersible tablets were prepared, and factors affected disintegration time and dissolution rate were studied.制备了吲哚美辛肠溶分散片 ,考察辅料对其崩解时限及溶出速度的影响。
6)garlicinenteric-coated tablets大蒜肠溶片
1.Objective:To establish HPLC method for determination of alliin in garlicinenteric-coated tablets.目的:测定大蒜肠溶片中蒜氨酸的含量。
延伸阅读
阿司匹林肠溶片【通用名称】阿司匹林肠溶片 【其他名称】阿司匹林肠溶片 阿司匹林肠溶片 拼音名:Asipilin Changrong Pian 英文名:Aspirin Enteric-coated Tablets 书页号:2000年版二部-329 本品含阿司匹林(C9H8O4)应为标示量的95.0%~105.0 %。 【性状】 本品为肠溶包衣片,除去包衣后显白色。 【鉴别】 取本品的细粉适量(约相当于阿司匹林0.1g),加水10ml,煮沸,放冷, 加三氯化铁试液1 滴,即显紫堇色。 【检查】 游离水杨酸 取本品5 片,研细,用乙醇30ml分次研磨,并移入 100ml 量瓶中,充分振摇,用水稀释至刻度,摇匀,立即滤过,精密量取滤液2ml ,置50ml纳 氏比色管中,用水稀释至50ml,立即加新制的稀硫酸铁铵溶液(取1mol/L盐酸溶液1ml, 加硫酸铁铵指示液2ml 后再加水适量使成100ml)3ml ,摇匀,30秒钟内如显色,与对 照液(精密量取0.01%水杨酸溶液4.5ml ,加乙醇3ml ,0.05%酒石酸溶液1ml ,用水 稀释至50ml,再加上述新制的稀硫酸铁铵溶液3ml ,摇匀)比较,不得更深(1.5%) 。 释放度 取本品1 片,照释放度测定法[附录Ⅹ D 第二法 (1)],采用溶出度测定法 第一法装置,以0.1mol/L盐酸溶液750ml 为溶剂,转速为每分钟100 转,依法操作, 经120分钟时,取溶液10ml滤过,作为供试品溶液(1)。然后加入37℃的0.2mol/L磷酸钠溶 液250ml,混匀,用2mol/L盐酸溶液或2mol/L氢氧化钠溶液调节溶液的pH值为6.8±0.05,继 续溶出45分钟,取溶液10ml滤过,作为供试品溶液(2)。取供试品溶液(1),以0.1mol/L盐酸 溶液为空白,在280nm 波长处测定吸收度,吸收值不得大于0.25。另取阿司匹林对照品 21mg,置100ml 量瓶中,加磷酸钠缓冲液(0.05mol/L)(量取0.2mol/L磷酸钠溶液250ml与 0.1mol/L盐酸溶液750ml,混合,pH值为6.8±0.05)适量使溶解,并稀释至刻度,作为对照 品溶液。取供试品溶液(2)和对照品溶液,以磷酸钠缓冲液(0.05mol/L)为空白,在265nm ±2nm波长处测定吸收度,计算出每片的释放量。限度为标示量的70%,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10片,研细,用中性乙醇70ml,分数次研磨,并移入100ml 量瓶中,充分振摇,再用水适量洗涤研钵数次,洗液合并于100ml 量瓶中,再用水稀释 至刻度,摇匀,滤过,精密量取滤液10ml(相当于阿司匹林0.3g),置锥形瓶中,加中 性乙醇(对酚酞指示液显中性)20ml,振摇,使阿司匹林溶解,加酚酞指示液3 滴,滴 加氢氧化钠滴定液(0.1mol/L)至溶液显粉红色,再精密加氢氧化钠滴定液(0.1mol/L)40 ml,置水浴上加热15分钟并时时振摇,迅速放冷至室温,用硫酸滴定液(0.05mol/L) 滴 定,并将滴定的结果用空白试验校正。每1ml 氢氧化钠滴定液(0.1mol/L)相当于18.02mg C9H8O10 。 【类别】 同阿司匹林。 【规格】 0.3g 【贮藏】 遮光,密封,在干燥处保存。