Solubilization of hydrophobic drugs in 6-O-octanoyl-ascorbic acid micellar dispersions

SANTIAGO PALMA,; DANIEL ALBERTO ALLEMANDI; RUBEN MANZO,; LAURA FRATONI,; LO NOSTRO, PIERANDREA

JOURNAL OF PHARMACEUTICAL SCIENCES

Wiley-Liss, Inc. and the American Pharmaceutical Association

Año: 2002 vol. 91 p. 1810 - 1810

0022-3549

span lang="en" style="FONT-SIZE: 8pt; COLOR: black; FONT-FAMILY: Arial; mso-bidi-font-size: 10.0pt; mso-fareast-font-family: "Times New Roman"; mso-bidi-font-family: "Times New Roman"; mso-ansi-language: EN-US; mso-fareast-language: ES; mso-bidi-language: AR-SA">Alkanoyl-6-O-ascorbic acid esters are easily obtained from vitamin C, and produce self-assembled aggregates in water solutions, with an inner hydrophobic pool surrounded by an external hydrophilic shell. Compared to ascorbic acid, their solubility in oils and fats is greatly enhanced, while the peculiar antioxidant activity is retained in the polar head groups of such surfactants. In virtue of their amphiphilic nature, ascorbic acid-based supramolecular systems can dissolve relevant amounts of hydrophobic, poorly water soluble chemicals such as drugs, vitamins, and so on, and at the same time they provide a suitable shield against oxidative deterioration of valuable materials. In this article we report