| Literature DB >> 18619585 |
Jian Shen1, Aiyou Hao, Guangyan Du, Huacheng Zhang, Hongyuan Sun.
Abstract
6-Oligo(lactic acid)cyclomaltoheptaose (6-OLA-betaCD) with an average substitution of about 7.0 lactic acid units was prepared as a new water-soluble cyclomaltoheptaose (betaCD) derivative (solubility of about 70.7-fold that of betaCD), based on the ring-opening polymerization of 3,6-dimethyl-1,4-dioxane-2,5-dione (lactide). The product was characterized by (1)H NMR, (13)C NMR, IR, and MS spectroscopy. The complexation of amoxicillin with 6-OLA-betaCD was found to be much stronger than that with betaCD at first, and then 6-OLA-betaCD was shown to decompose moderately into betaCD and lactic acid. 6-OLA-betaCD might be greatly valuable in a controlled release system for Amoxicillin (AMX).Entities:
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Year: 2008 PMID: 18619585 DOI: 10.1016/j.carres.2008.06.010
Source DB: PubMed Journal: Carbohydr Res ISSN: 0008-6215 Impact factor: 2.104