Saokham Phennapha, Loftsson Thorsteinn
Faculty of Pharmaceutical Sciences, University of Iceland, Hofsvallagata 53, IS-107 Reykjavik, Iceland.
Faculty of Pharmaceutical Sciences, University of Iceland, Hofsvallagata 53, IS-107 Reykjavik, Iceland.
Int J Pharm. 2017 Jan 10;516(1-2):278-292. doi: 10.1016/j.ijpharm.2016.10.062. Epub 2016 Oct 29.
γ-Cyclodextrin (γCD) is a cyclic oligosaccharide formed by bacterial digestion of starch and used as solubilizing agent and stabilizer in a variety of pharmaceutical and food products. γCD is a large (molecular weight 1297Da) hydrophilic molecule that does not readily permeate biological membranes and is rapidly digested by bacteria in the gastrointestinal tract. In humans γCD is metabolized by α-amylase that is found in, for example, saliva, bile fluid and tears. Thus, bioavailability of γCD is negligible. Also, γCD is readily excreted unchanged in the urine after parenteral administration. Like other cyclodextrins, γCD can form water-soluble inclusion complexes with many poorly-soluble compounds. In comparison with the natural αCD and βCD, γCD has the largest hydrophobic cavity, highest water solubility and the most favorable toxicological profile. The focus of this review is production, physiochemical properties, pharmacokinetics, toxicity and applications of γCD and its derivatives. Also, the aggregation behavior of γCD in aqueous media is discussed.
γ-环糊精(γCD)是由细菌消化淀粉形成的环状寡糖,在多种药品和食品中用作增溶剂和稳定剂。γCD是一种大分子(分子量1297Da)亲水分子,不易透过生物膜,且在胃肠道中会被细菌迅速消化。在人类体内,γCD由例如唾液、胆汁和眼泪中存在的α-淀粉酶代谢。因此,γCD的生物利用度可忽略不计。此外,γCD经肠胃外给药后很容易原样从尿液中排出。与其他环糊精一样,γCD可与许多难溶性化合物形成水溶性包合物。与天然αCD和βCD相比,γCD具有最大的疏水腔、最高的水溶性和最有利的毒理学特性。本综述的重点是γCD及其衍生物的生产、理化性质、药代动力学、毒性和应用。此外,还讨论了γCD在水性介质中的聚集行为。