Ficarra R, Tommasini S, Raneri D, Calabrò M L, Di Bella M R, Rustichelli C, Gamberini M C, Ficarra P
Facoltà di Farmacia, Università di Catanzaro, compl. Barbieri, 88021 Roccelletta di Borgia, Catanzaro, Italy.
J Pharm Biomed Anal. 2002 Aug 1;29(6):1005-14. doi: 10.1016/s0731-7085(02)00141-3.
Flavonoids are natural substances with a lot of biological activities, including the antioxidant one. Their use in pharmaceutical field is, however, limited by their aqueous insolubility. As the formation of the inclusion complexes can improve their solubility in water, the flavonoids hesperetin, hesperidin, naringenin and naringin have been complexed with beta-cyclodextrin (beta-CD) by the coprecipitation method and studied in solution and in solid state by NMR, FT-IR, differential scanning calorimetry and X-ray techniques. The effects of complexation on the chemical shifts of the internal and external protons of beta-CD in the presence of each flavonoid were observed.
黄酮类化合物是具有多种生物活性的天然物质,包括抗氧化活性。然而,它们在制药领域的应用受到其水不溶性的限制。由于包合物的形成可以提高它们在水中的溶解度,因此通过共沉淀法将橙皮素、橙皮苷、柚皮素和柚皮苷等黄酮类化合物与β-环糊精(β-CD)复合,并通过核磁共振(NMR)、傅里叶变换红外光谱(FT-IR)、差示扫描量热法和X射线技术对其在溶液和固态下进行了研究。观察到在每种黄酮类化合物存在下,复合对β-CD内部和外部质子化学位移的影响。