A Review on Cyclodextrins/Estrogens Inclusion Complexes

被引:9
|
作者
Araj, Szymon Kamil [1 ]
Szeleszczuk, Lukasz [1 ]
机构
[1] Univ Warsaw, Fac Pharm Med, Dept Organ & Phys Chem, Banacha 1 Str, PL-02093 Warsaw, Poland
关键词
cyclodextrin; inclusion complex; estrogen; CD; host-guest complexes; ENDOCRINE-DISRUPTING CHEMICALS; BETA-CYCLODEXTRIN; STEROID-HORMONES; GAMMA-CYCLODEXTRIN; ESTROGEN-RECEPTOR; ETHINYL ESTRADIOL; ALPHA-CYCLODEXTRIN; DRIVING FORCES; SEPARATION; TEMPERATURE;
D O I
10.3390/ijms24108780
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This review focuses on the methods of preparation and biological, physiochemical, and theoretical analysis of the inclusion complexes formed between estrogens and cyclodextrins (CDs). Because estrogens have a low polarity, they can interact with some cyclodextrins' hydrophobic cavities to create inclusion complexes, if their geometric properties are compatible. For the last forty years, estrogen-CD complexes have been widely applied in several fields for various objectives. For example, CDs have been used as estrogen solubilizers and absorption boosters in pharmaceutical formulations, as well as in chromatographic and electrophoretic procedures for their separation and quantification. Other applications include the removal of the endocrine disruptors from environmental materials, the preparation of the samples for mass spectrometric analysis, or solid-phase extractions based on complex formation with CDs. The aim of this review is to gather the most important outcomes from the works related to this topic, presenting the results of synthesis, in silico, in vitro, and in vivo analysis.
引用
收藏
页数:30
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