A novel type of biodegradable/biocompatible amphiphilic hyperbranched copolymer (H40‐PLA‐b‐MPEG) was synthesized. Its micellar properties were studied by DLS, fluorescence spectroscopy and TEM. The drug release profile showed that the H40‐PLA‐b‐MPEG micelles provide an initial burst release, followed by a sustained release of the entrapped hydrophobic model drug over a period of 4 to 58 h. The copolymer degraded hydrolytically within 6 weeks under physiological conditions. The MTT assay showed no obvious cytotoxicity against a human endothelial cell line at a concentration range of 0–400 µg · mL−1. These results indicate that the H40‐PLA‐b‐MPEG micelles have great potential as hydrophobic drug delivery carriers.
Azepino[3,4,5-cd]indole derivatives represent the core scaffold of important natural products and biologically relevant compounds. Therefore, the establishment of step- and atom-economic strategies to access this class of compounds is of paramount importance. To this end, complexity-to-diversity (CtD) strategy has become one of the most important tools that transforms complex molecules into diverse skeleta. However, many of the reactions that could be employed in CtD are restricted by the functional handles exist in these molecules. This limits the achievement of the desired skeletal diversity. Herein, an efficient and step-economic strategy to access a diverse collection of azepino-[3,4,5-cd]indole architectures through a cascade that combines Pictet-Spengler with Michael addition, is described. This was achieved by reacting cyclohexadienone acetaldehydes 2 a – 2 d with indolyl-4-ethyl amine 1 . Employing a CtD strategy on the developed azepino-[3,4,5-cd]indoles, a rapid rearrangement reaction that provided a modular, chemo- and diastereoselective access to diverse collection of spiro azepinocarbazole nature-inspired frameworks, was encountered. 相似文献
