Release characteristics and antibacterial activity of solid state eugenol/β-cyclodextrin inclusion complex

2011 ◽  
Vol 71 (1-2) ◽  
pp. 207-213 ◽  
Author(s):  
Ting Wang ◽  
Bin Li ◽  
Hongyan Si ◽  
Li Lin ◽  
Li Chen
2015 ◽  
Vol 107 ◽  
pp. 265-272 ◽  
Author(s):  
Noriko Ogawa ◽  
Takuro Hashimoto ◽  
Takayuki Furuishi ◽  
Hiromasa Nagase ◽  
Tomohiro Endo ◽  
...  

Pharmaceutics ◽  
2018 ◽  
Vol 10 (4) ◽  
pp. 189 ◽  
Author(s):  
Mario Jug ◽  
Paola Mura

Among the different techniques proposed for preparing cyclodextrin inclusion complex in the solid state, mechanochemical activation by grinding appears as a fast, highly efficient, convenient, versatile, sustainable, and eco-friendly solvent-free method. This review is intended to give a systematic overview of the currently available data in this field, highlighting both the advantages as well as the shortcomings of such an approach. The possible mechanisms involved in the inclusion complex formation in the solid state, by grinding, have been illustrated. For each type of applied milling device, the respective process variables have been examined and discussed, together with the characteristics of the obtained products, also in relation with the physicochemical characteristics of both the drug and cyclodextrin subjected to grinding. The critical process parameters were evidenced in order to provide a useful guide for a rational selection of the most suitable conditions for an efficient inclusion complex preparation by grinding, with the final purpose of promoting a wider use of this effective solvent-free cyclodextrin inclusion complex preparation method in the solid state.


2001 ◽  
Vol 79 (11) ◽  
pp. 1806-1811
Author(s):  
Manfred T Reetz ◽  
Joachim Rudolph ◽  
Richard Goddard

The phenomenon of diastereotopic group recognition has been structurally documented for the first time. A diphenylphosphine-modified β-cyclodextrin having two diastereotopic phenyl groups in close vicinity to the inner cavity of this host was prepared. The crystal structure analysis reveals selective intramolecular complexation of one of the two diastereotopic phenyl groups.Key words: supramolecular chemistry, stereotopic group recognition, cyclodextrins, intramolecular complexation.


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