OBJECTIVE: To Produce gentamycin sulfate sustained-release tablets.
目的：制备硫酸庆大霉素缓释片。
Objective: To prepare Paeonol Sustained-release Tablets of zero order release.
目的：制备具零级释药特征的丹皮酚缓释片。
Aim To study the preparation method of ferrous sulfate sustained-release tablets.
目地研究复方硫酸亚铁缓释片的制备方法。
Objective To obtain an average safe dose of Fuzi Lizhong sustained-release tablets.
目的确定附子理中缓释片的安全剂量。
Aim To prepare compound hyoscyamine sustained-release tablets and investigate its quality.
目的制备复方莨菪碱缓释片。
Objective To prepare the allopurinol sustained-release tablets and study the release mechanism.
目的制备别嘌醇缓释片并探讨其释药机理。
OBJECTIVE To prepare vitamin C sustained-release tablets and determine their in vitro release rate.
目的：研制维生素c微囊并制成缓释片剂，评价其体外释放特性。
Objective to explore the methods that how to prepared salbutamol sulfate pulse sustained-release tablets.
目的探讨制备硫酸沙丁胺醇脉冲缓释片的方法。
The control group was treated with Nifedipine Sustained-release Tablets, Benaaepril Hydrochleride Tablets.
对照组给予硝苯地平缓释片、盐酸贝那普利片等治疗。
Objective To obtain effective materials from the total alkaloids of Fuzi Lizhong sustained-release tablets.
目的分析附子理中缓释片中总生物碱的药效物质。
Objective to study on the factors involved in the release rate of metformin hydrochloride in vitro sustained-release tablets.
目的对盐酸二甲双胍缓释片体外释放度相关因素进行研究。
The quality standard of Panax notoginseng sustained-release tablets and Paris Polyphylla saponin dispersible tablets were different established.
分别建立了三七总皂苷缓释片、重楼皂苷分散片的质量标准。
Conclusion This method is reliable and simple which could be used for the quality control of compound ferrous sulfate sustained-release tablets.
结论方法可靠，简单可行，可用于复方硫酸亚铁缓释片的质量控制。
Objective to establish a UV method to determine the release degree of rotundine sustained-release tablets and to evaluate its in-vitro release behavior.
目的建立罗通定缓释片体外释放度测定方法，评价其体外释药行为。
Methods Ultraviolet spectrophotometry was applied to determine the release degree of rotundine sustained-release tablets with different release mediums.
方法用紫外分光光度法和体外释放度试验，考察罗通定缓释片在不同释放介质中和不同释放时间的累积释放度。
OBJECTIVE A reversed phase HPLC method was developed to determine the contents of metoprolol tartrate and felodipine in compound felodipine sustained-release tablets.
目的对复方非洛地平缓释片中酒石酸美托洛尔和非洛地平的含量测定方法进行研究。
The results indicated that the sustained-release tablets had an expected sustained-release quality, and drug release pattern was in accorded with the first order kinetics.
结果表明，制得的酒石酸美托洛尔缓释片具有明显的缓释作用，体外释放符合一级释药动力学规律。
Conclusions the determination method is simple and swift, and can be applied in the determination of in vitro release rate of metformin hydrochloride sustained-release tablets.
结论本释放度方法简单，快速，可用于盐酸二甲双胍缓释片体外释放度测定。
Conclusion: Both captopril sustained-release tablets and valsartan are effective, and the combining use of the two drugs is effective on refractory hypertension in uremia patients.
结论：缬沙坦、卡托普利缓释片是治疗高血压的有效药物，二者联合应用是治疗尿毒症顽固性高血压的较好方法。
OBJECTIVE Breviscapine sustained-release tablets(BST)were formulated with hydroxypropyl-methylcellulose as the matrix material and the release mechanism of the tablets was studied.
目的以羟丙甲基纤维素为骨架材料制得灯盏花素缓释片，并对释药机制进行探讨。
Methods Ultraviolet spectrophotometry and release test were applied to determine the release of cefixime in cefixime sustained-release tablets under different media and time points.
方法用紫外分光光度法和释放度试验，考察头孢克肟缓释片在不同释放介质中不同释放时间的累积释放度。
Method: GBE sustained-release tablets were prepared by direct compression method using sodium carboxymethylcellulose CMC-Na and hydroxypropyl methylcellulose HPMC as matrix excipients.
方法：以溶胀性材料羧甲基纤维素钠和羟丙甲基纤维素为骨架材料，直接粉末压片制备银杏提取物缓释片。
Objective: to develop the methods to determine the in vitro release of multi-target ingredients in Compound Danshen Sustained-release Tablets and to evaluate its release behavior in vitro.
目的：建立复方丹参缓释片多指标成分的体外释放度测定方法，评价其体外释药行为。
METHODS Use solvent-non-methods to prepare vitamin C sustained-release tablets, UV method was used to determine its content and the in vitro release rate was determined by rotate basket method.
方法：采用溶剂-非溶剂法制备维生素C微囊，制成缓释片剂，采用紫外分光光度法测定其载药量，采用转篮法测定体外释放特性。
OBJECTIVE: To prepare sustained release tablets and evaluate its drug release property.
目的：制备美沙拉嗪缓释片剂，并评价其体外释放特性。
Objective To use ANN to quantitatively predict the influence of the amount of HPMC and its internal viscosity on allopurinol release from HPMC sustained release tablets.
目的用人工神经网络模型定量的预测HPMC的量和其固有黏度对药物释放的影响。
Objective to manufacture Amoxicillin into gastric floating sustained release tablets, which can extend their stay time in stomach to make Amoxicillin release slowly and to increase bioavailability.
目的将阿莫西林制成胃漂浮缓释片，延长在胃中的停留时间，逐渐释放，提高生物利用度。
OBJECTIVE: to prepare the sustained release tablets of salbutamol sulfate, and to establish the method of quality control.
目的：制备硫酸沙丁胺醇延迟释药片，并建立其质量控制方法。
OBJECTIVE To observe the effect of low doses of theophylline sustained release tablets for children with cough variant asthma and compare with the effect of normal recommended doses.
目的观察以小剂量茶碱缓释片治疗小儿咳嗽变异性哮喘的临床疗效，并与常规推荐剂量的用药疗效相比较。
Objective to establish HPLC method to determine the content of indapamide sustained release tablets.
目的建立高效液相色谱法测定吲达帕胺缓释片含量。
应用推荐