目的：改善环扁桃酯胶囊的装量差异及崩解时限。
OBJECTIVE:To improve the gross deviation and disintegration of cyclandelate capsules.
目的：提高其崩解时限及脆碎度，确保产品质量。
Objective: To improve its disintegration time limited and friability and make sure the quality of the production.
方法采用正交设计法，以片剂的硬度、崩解时限为指标优选辅料配方。
Methods the combined excipients were optimized by using orthogonal design, and taking the hardness and the disintegrating time of tablet as indices.
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。
Indomethacin enteric dispersible tablets were prepared, and factors affected disintegration time and dissolution rate were studied.
在稳定性研究中，尤应注意反映制剂特点的指标，如外观性状、崩解时限等。
Characteristic indexes such as appearance and disintegration time should be especially paid attention to in stability tests.
方法用均匀设计法，以片剂的硬度、脆碎度、崩解时限为指标，优选辅料配比。
Methods the ratio of excipients was optimized by using uniform design, and taking the hardness and the disintegrating time of tablet as indices.
方法以崩解时限为指标，采用正交设计试验，对灯盏花素分散片处方进行筛选。
METHODS The formulae of Breviscarpin dispersed tablet were optimized in terms of disintegrating time by orthogonal design test.
为保持方法的标准化和一致性，FDA推荐采用US P中崩解时限的测定方法。
To assure the standardization and consistency of the methods, FDA recommends using the USP method.
方法：采用均匀设计试验法，以片剂崩解时限为指标，筛选灯盏花素口腔崩解片的最佳处方。
METHODS: to adopt the multifactor and multilevel uniform design to optimize the preparation prescription, disintegrating time as the assessment index.
目的比较保健食品软胶囊的破裂试验结果与崩解时限检查结果，了解两者的相关性和差异性。
Objective To compare the rupture test of soft capsules of dietary supplements with the disintegration test, and to find the correlations and differences.
方法：筛选处方制备拉西地平软胶囊，并参照中国药典进行崩解时限，含量测定、均匀度检测。
Method sieving the prescription of preparation lacidipine soft capsule, and disintegration time, assaying, uniformity detection in accordance with Chinese Pharmacopeia.
方法筛选富硒茶多糖泡腾片的最佳处方和制备工艺，并对其崩解时限、含量、稳定性等进行了考察。
METHODS the optimal prescription and technology of effervescent tablets were screened and the disintegration time, content stability were tested.
对制得的茶多酚片进行质量标准研究，该片剂外观完整光洁、色泽均匀，硬度、片重差异、崩解时限都符合标准。
The quality standard of TP tablet was investigated. The tablet had smooth faces, uniform colour, appropriate rigidity, low smash ratio, little fluctuate of tablet weight, short breakdown time.
硬脂酸镁能减少低聚合度纤维素I片的崩解时限，但是对低、高聚合度纤维素ii和高聚合度纤维素I片没有影响。
Magnesium stearate decreased the disintegration times of low DP cellulose I compacts but had no effect on the low and high DP cellulose II and high DP cellulose I compacts.
方法将羧甲基淀粉钠、微晶纤微素按一定比例混合，作为片剂基本处方，以分散片的外观、崩解时限、体外溶出度及混悬性为指标进行处方筛选。
METHOD s Mixing the CMSNa and MCC in certain proportion as the basic formulation of the tablets, the appearance, disintegration, dissolution and the suspensibility were investigated.
方法采用L9(34)正交试验法，以崩解时限为指标，以微晶纤维素、低取代羟丙基纤维素、交联乙烯吡咯烷酮、甘露醇等为辅料，筛选最佳处方和制备工艺。
Methods the L9 (34) orthogonal was designed with disintegrating time as the assessment index, and MCC, LHPC, PVPP, Mannitol et al were used in the formulation and preparation.
方法采用L9(34)正交试验法，以崩解时限为指标，以微晶纤维素、低取代羟丙基纤维素、交联乙烯吡咯烷酮、甘露醇等为辅料，筛选最佳处方和制备工艺。
Methods the L9 (34) orthogonal was designed with disintegrating time as the assessment index, and MCC, LHPC, PVPP, Mannitol et al were used in the formulation and preparation.
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