OBJECTIVE To study the formulation, preparation and dissolution of amoxicillin and clavulanate potassium tablets.
目的：研究阿莫西林克拉维酸钾片处方及工艺，并考察其溶出度。
Objective: To determine the bioequivalence of amoxicillin-clavulanate potassium (14 : 1) granules in healthy volunteers.
目的：测定阿莫西-林克拉维酸钾（14：1）颗粒剂生物等效性。
Objective: To explore the best method was determined for the sterile test of Amoxicilin sodium and Clavulanate potassium for injection.
目的：选择注射用阿莫西林钠克拉维酸钾的最佳无菌检查方法，保证检验结果的准确和可靠性。
Result: the best washing condition and operation method for the sterile test of Amoxicilin sodium and Clavulanate potassium for injection were determined.
结果：确定了注射用阿莫西林钠克拉维酸钾无菌检查法的最佳冲洗条件及操作方法。
Objective: to establish a high performance liquid chromatography method for simultaneous determination of amoxicillin and clavulanate potassium in amoxicillin and clavulanate potassium granules.
目的：建立高效液相色谱法同时测定阿莫西林克拉维酸钾颗粒中阿莫西林和克拉维酸钾的含量。
METHODS The impurity profiling changes of amoxicillin plus potassium clavulanate were compared with both amoxicillin and potassium clavulanate alone by HPLC.
方法采用HPLC，比较阿莫西林和克拉维酸钾单独存在及复方后杂质谱的变化。
OBJECTIVE: to investigate the affecting factors to the stability of the suspension for oral administration containing potassium clavulanate and amoxicillin.
目的：对影响克拉维酸钾阿莫西林干混悬剂稳定性的各种因素进行考察。
OBJECTIVE: to investigate the affecting factors to the stability of the suspension for oral administration containing potassium clavulanate and amoxicillin.
目的：对影响克拉维酸钾阿莫西林干混悬剂稳定性的各种因素进行考察。
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