Green nanocomposites: synthesis and characterization.

A series of intercalated and exfoliated nanocomposites montmorillonite-ulvan was prepared. Ulvan, extracted from the green algae, is a water-soluble polysaccharide biopolymer. Depending on the drying process, air or freeze drying, ulvan were inserted in the interlayer space or adsorbed on the both sides of inorganic layers. The crystallization of water molecules bounded to the ulvan induced the delamination of the layers during the lyophilization. Thermogravimetric experiments show a high percentage (approximately 51%) of organic matter for the freeze dried samples and a lowest one (approximately 17%) for the air dried solids. X-Ray Diffraction patterns exhibit a d(001) varying with the content of organic matter. When the delamination occurs, the (001) reflection disappears. Transmission electron microscopy micrographs show individual layers for the highest amount of ulvan.

Synthesis and cytotoxic and antitumor activity of benzo[b]pyrano[3, 2-h]acridin-7-one analogues of acronycine.

Benzo¿bacronycine (6-methoxy-3,3,14-trimethyl-3, 14-dihydro-7H-benzo¿bpyrano¿3,2-hacridin-7-one, 4), an acronycine analogue with an additional aromatic ring linearly fused on the natural alkaloid basic skeleton, was synthesized in three steps, starting from 3-amino-2-naphthalenecarboxylic acid (5). Eight 1, 2-dihydroxy-1,2-dihydrobenzo¿bacronycine esters and diesters (17-24) were obtained by catalytic osmic oxidation, followed by acylation. All these compounds were significantly more cytotoxic than acronycine, when tested against L1210 leukemia cells in vitro. The potency of the cyclic carbonate 24 was in the range of the most active drugs currently used in cancer chemotherapy. Two selected diesters (17 and 24) were evaluated in vivo against P388 leukemia and colon 38 adenocarcinoma implanted in mice. Both compounds were markedly active at doses 16-fold lower than the dose of acronycine itself. Against colon 38 adenocarcinoma, compounds 17 and 24 were highly efficient, inhibiting tumor growth by more than 80%. Diacetate 17 was the most active, inhibiting tumor growth by 96% at 6.25 mg/kg, with two of seven mice being tumor-free on day 43.