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1·The solid inclusion complex contains 11 water molecules.

固体包结络合物中含有11个水分子。

2·Cyclodextrin inclusion complex es as pharmaceutical carriers.

环糊精包容的络合物作为药物载体。

3·Both micronized glibenclamide and inclusion complex were fairly stable.

微粉化物及包合物均有良好的稳定性。

4·The ultraviolet spectra of RSA is consistent with RSA inclusion complex.

RSA包结物的紫外吸收特征与化合物RSA一致。

5·The dissolution rates of amoxicillin and inclusion complex were compared.

比较了阿莫西林和包合物的体外溶出速率。

6·Conclusion: Preparation of inclusion complex was simple and quick by sealed-control temperature method.

结论：采用密封控温技术制备中药包合物简便易行，迅速有效。

7·The solubility results of inclusion complex in water indicated that the solubility of glibenclamide increased by 15 times.

包结物的水溶性实验结果表明包结后格列本脲的溶解度增加了15倍。

8·Method for preparing S-omeprazole and salt thereof by forming inclusion complex with (s) - (-) -1, 1 '-dinaphthalene-2, 2' -diol.

通过与(S) -(-) - 1,1-联萘- 2,2-二酚形成包合配合物制备s -奥美拉唑及其盐的方法。

9·The stability of inclusion complex was influenced by the strength between cyclodextrins and guest molecule. Hydrophobic bond was main impetus of inclusion process.

在环糊精和客体分子之间的作用力中，疏水键是包合过程的主要作用力。

10·RESULTS:The content of DATS in freeze-drying powders of inclusion complex had a minimum reduction among the three under conditions of illumination and high temperature.

结果：在光照、高温条件下， 包合物冻干粉中DATS含量下降程度为三者中最小。