Objective To develop the enteric-coated Budesonide pellets.
目的研制布地奈德肠溶微丸。
Objective:To improved the dissolution of Oxiprozin Enteric-coated Tablets.
前言： 目的：提高奥沙普秦肠溶片的释放度。
The pellet preparation can be prepared into slow release or enteric-coated preparation.
上述微丸制剂可以按照要求制备成缓释或肠溶制剂。
The invention discloses a glutathione enteric-coated pellet and preparation method thereof.
本发明公开了一种谷胱甘肽肠溶微丸胶囊及其制备方法。
OBJECTIVES: To prepare indomethacin enteric-coated pellets and investigate their release properties.
目的：制备吲哚美辛肠溶包衣徽丸，考察其释放特性。
The pellet preparation can be prepared into a slow-release or enteric-coated preparation as required.
上述微丸制剂可以按照要求制备成缓释或肠溶制剂。
Objective: to optimize the formulation and preparation of Pantoprazole Sodium Enteric-Coated Capsules.
前言：目的：研究泮托拉唑钠肠溶胶囊工艺处方。
OBJECTIVE To develop naproxen enteric-coated pellets and evaluate its release characteristics in vitro.
目的：研制萘普生肠溶微丸，评价其体外释药特性。
Objective:To study the pharmacokinetics of tinidazole colon-specific enteric-coated tablets in healthy volunteers.
目的：研究替硝唑结肠定位肠溶片在健康受试者中的药动学特征。
The glutathione enteric-coated pellet comprises a core including glutathione and a enteric-coated layer from the inside out.
所述谷胱甘肽肠溶微丸由内至外包括含谷胱甘肽的核芯和肠溶层。
Objective To study the relative bioavailability and bioequivalence of omeprazole Enteric-coated capsules in healthy volunteers.
目的研究奥美拉唑肠溶胶囊的人体相对生物利用度和生物等效性。
AIM: To study the bioequivalence and pharmacokinetics of doxycycline enteric-coated microsomes capsules and doxycycline tablets.
目的：研究多西环素肠溶微粒胶囊和多西环素片的人体生物等效性与药动学。
Objective: Alkaloids of sophora flavescens enteric-coated tablets was developed, and the method of drug release was established.
目的：制备苦参总碱肠溶片，并建立体外释放度分析方法。
Because Super Fisol is enteric-coated and better absorbed by the body, its required dose is less than taking non-coated fish oil.
由于超级Fisol肠溶和更好地被人体吸收，其所需的剂量小于非涂布鱼油。
Methods The (-) -pantoprazole sodium enteric-coated pellets were prepared by centrifugal granulation and fluid-bed coating method.
方法采用离心造粒法及流化床包衣法制备左旋泮托拉唑钠肠溶微丸。
RESULTS the concentrations were incomplete for enteric-coated Metformin Hydrochloride tablets after the same doses were administrated.
结果在测定方法与给药量相同的情况下，肠溶片的血药浓度数据不完整。
Conclusions the preparation of (-) -pantoprazole sodium enteric-coated pellets is feasible and the quality of the pellets is reliable.
结论离心造粒法制备左旋泮托拉唑钠肠溶微丸的工艺可行、质量可靠。
The invention discloses a biguanide anti-diabetes medicine, in particular to a metformin hydrochloride enteric-coated medicine compound.
本发明公开了一种双胍类抗糖尿病药物，特别是盐酸二甲双胍的肠溶药物组合物。
In the other part, the improvement of dissolubility of sulfadiazine and aspirin enteric-coated tablet is studied with surfactant as modifier.
然后以磺胺嘧啶片和阿司匹林肠溶片的溶出为例，就表面活性剂的增溶作用进行了考察。
METHODS: A prospective multi-center, randomized , double blind, controlled clinical trial of serrapeptase enteric-coated tablets was conducted.
方法：用前瞻性随机双盲双模拟对照多中心试验设计，以进口舍雷肽酶肠溶片为阳性对照药。
Buffered esomeprazole (BE) is an oral preparation consisting of an inner core of non-enteric-coated esomeprazole with a shell of sodium bicarbonate.
埃索美拉唑缓释剂(BE)是由碳酸氢钠包被非肠溶性埃索美拉唑组成的口服制剂。
The dissolution of 27(?) lots of aspirin enteric-coated tablet and SMZ Co. Tabletmade by 9 factories was determined with ultraviolet spectrophotometry.
本文用紫外分光光度法对9个厂家27个批号的阿斯匹林肠溶衣片和复方新诺明片进行了体外溶出度测定。
OBJECTIVE To compare the influence of different pore-forming agents and their amount on the release of budesonide enteric-coated sustained-release pellets.
目的比较不同致孔剂及其用量对水难溶性药物布地奈德肠溶缓释微丸释药行为的影响。
However, they found no link between the use of enteric-coated aspirin and resistance to the drug; past studies, they note, have had "conflicting" findings on this point.
但是，他们发现服用肠溶阿司匹林和阿司匹林抵抗之间没有关系，而以前有些研究却认为两者存在相关性。
OBJECTIVES: To prepare indomethacin enteric coated pellets and investigate their release properties.
目的：制备吲哚美辛肠溶包衣微丸，考察其释放特性。
Objective To design a stable formulation for enteric coated lansoprazole tablets.
目的制备性质稳定的兰索拉唑肠溶片并考察其稳定性。
These tablets are enteric coated and blister packed to prevent breakdown and inactivation of the ingredients.
这些药片是肠溶和吸塑包装，以防止故障和失活的成分。
The technology of orally disintegrating tablets prepared with drug-loading enteric coated particles or sustained-release particles and appropriate excipients is introduced.
介绍了将药物制成肠溶或缓释的微粒后再与适宜的辅料压制得到微粒型口腔崩解片的技术。
The technology of orally disintegrating tablets prepared with drug-loading enteric coated particles or sustained-release particles and appropriate excipients is introduced.
介绍了将药物制成肠溶或缓释的微粒后再与适宜的辅料压制得到微粒型口腔崩解片的技术。
应用推荐