sustained-release tablet
- 网络缓释片
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Nifedipine sustained-release tablet , combined treatment , Essentia hypertension in old age ;
硝苯地平缓释片;联合治疗;老年原发性高血压;
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The HPLC method developed for the stability study of mizolastine sustained-release tablet
咪唑斯汀缓释片稳定性分析法&HPLC法
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Objective : To study the quality specification of Gliclazide Sustained-release Tablet .
目的:对格列齐特缓释片进行质量标准研究。
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Study on releasing characteristic of sodium valproate sustained-release tablet in vitro
丙戊酸钠缓释片体外释放特性
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Preparation of Matrine Sustained-release Tablet and Study on Characteristics of the Release Trial in Vitro
苦参碱缓释片的研制及体外释放特性研究
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Preparation of Zhitong sustained-release tablet and its release property in vitro
止痛缓释片的制备工艺及其体外释放度研究
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Conclusion : This standard was capable to effectively control the quality of Gliclazide Sustained-release Tablet .
紫外分光光度法测定格列齐特缓释片含量结论:格列齐特缓释片的质量得到有效控制。
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This review includes the application and research direction of hydrophilic matrix materials in orally sustained-release tablet .
作为研究方向之一,几何骨架片有着广阔的发展前景。
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Calcium antagonizing effect of Compound Danshen Sustained-release Tablet and comprehensive evaluation of sustained-release effect in vitro
复方丹参缓释片钙拮抗作用及体外缓释作用的综合评价
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Treatment for type 2 diabetic mellitus with Glipizide sustained-release tablet or Glimepiride
格列吡嗪控释片和格列美脲治疗2型糖尿病的对比研究
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Preparation and Study of Glipizide Gastrointestinal Tract Bioadhesion Sustained-release Tablet
格列吡嗪胃肠道生物粘附缓释片的研制
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Pharmacokinetics study of Diclofenac lysine sustained-release tablet in dogs
双氯芬酸赖氨酸盐缓释片家犬体内药物动力学研究
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Studies on the bioavailability of compound theophylline-ketofen sustained-release tablet in dogs
犬口服复方茶酮缓释片的生物利用度试验
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The pharmacokinetics study and bioequivalence evaluation of the VPA sustained-release tablet in dogs were made .
进行了家犬体内VPA缓释片药物动力学研究和生物等效性评价。
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Methods The preparation formulation of the sustained-release tablet was optimized by orthogonal design which took the released rate as the index .
方法以大蒜油中成分大蒜素的释放度为指标,采用正交设计法优化缓释片的制剂处方工艺。
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Aim To prepare matrine sustained-release tablet for prolong effective time and study on characteristics of the release trial in vitro .
目的为延长苦参碱的作用时间,将其制成缓释片,并对该缓释片的体外释放特性进行研究。
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Conclusion Cyclovirobuxinum D sustained-release tablet has apparently protective effects on myocardium in canine experimental myocardial infarction models .
结论:黄杨宁缓释片对实验性心肌梗塞犬的心肌具有明显的保护作用。
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Evaluation of release similarity of multicomponents in Zuojin Sustained-Release Tablet by the total quantum statistical moment similarity
总量统计矩相似度法对左金缓释片多成分释放相似度的评价研究
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Conclusions The morphine hydrochloride sustained-release tablet is a kind of safe and effective analgesic to advanced aged cancer patients with pain .
结论高龄癌痛患者应用美菲康进行镇痛治疗是安全有效的。
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Conclusion The method is simple , rapid , accurate and selective , so this method is suitable for the determination of gliclazide sustained-release tablet .
结论该法比药典上规定的滴定法操作简便、快速、准确、专属性强,适用于格列齐特缓释片的含量测定。
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Domestic and Original Sodium Valproate Sustained-release Tablet in Releasing Rate in Vitro Studies on the Factors Influencing Oleanolic Acid Release from Matrix Tablets
国产与原研丙戊酸钠缓释片的体外释放度考察齐墩果酸骨架缓释片释药影响因素的考察
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Study on the PNS Bio-adhesive Sustained-release Tablet
三七总皂苷生物粘附型缓释片的研究
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We calculate the concentration of acemetacin by standard curve , and then get the accumulative release percentage of the sustained-release tablet .
根据标准曲线计算药物浓度,求得阿西美辛速释缓释双层片的累计释放百分率。制备三批阿西美辛速释缓释双层片,考察批与批之间体外药物释放度的重现性。
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OBJECTIVE : To study the application of the spherical symmetric design in the optimization of the roxatidine sustained-release tablet and to study its releasability .
目的研究球面对称设计法在缓释片处方优化中的应用并考察其释放度。
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OBJECTIVE To study the drug release mechanism of helicid ( HD ) bioadhesive sustained-release tablet and to determine the adhesive force in vitro .
目的研究生物黏附性神衰果素缓释片的体外释放度及释药规律,并测定其体外黏附力。
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Preparation and Study of m-Nisoldipine Intragastric Floating Sustained-release Tablet ; Prescription screening of Nicardipine hydrochloride sustained-release tablet and determination of release rate
间尼索地平胃内漂浮型缓释片的研制盐酸尼卡地平缓释片的制备及释放度测定
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The paper discussed the consideration and method to produce the sustained-release tablet using traditional Chinese medicine - Helicid ( HD ) as the model drug under the principles of biopharmaceutics and pharmacokinetics .
本课题以中药单体成分神衰果素(HD)为模型药物探讨在生物药剂学和药物动力学理论指导下进行生物粘附缓释片研制的思路和方法。
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The paper discussed the factors which influence the release of VPA sustained-release tablet including viscosity of HPMC , quantity of HPMC , optimize the VPA sustained-release tablet prescription .
以释放度为指标,考察了VPA缓释片释放的影响因素,包括HPMC粘度的影响、HPMC用量的影响,优化了VPA缓释片的处方。
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The Preparation of Bioadhesive Sustained-release Tablet of Total Puerariae Flavones and Its Evalution in Vivo and in Vitro ; The Effect on Adhesion of Schwann Cells with Different Biological Substance
葛根总黄酮及其生物粘附性缓释片的研制与体内外评价不同生物活性物质修饰对雪旺细胞的粘附影响
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The results of the bioavailability study in the human indicate that the Ketoprofen sustained-release tablet retention time prolongs , the release decreases and the purpose of once daily designed by the research was achieved .
人体内生物利用度试验结果表明,本课题所研制的酮洛芬缓释片体内滞留时间延长,药物释放减慢,达到了课题设计的一日给药一次的目的。