All-trans-retinoic acid nanodisks

被引:55
作者
Redmond, Katherine A. [1 ]
Nguyen, Thanh-Son [1 ]
Ryan, Robert O. [1 ]
机构
[1] Childrens Hosp Oakland, Res Inst, Ctr Prevent Obes Cardiovasc Dis & Diabet, Oakland, CA 94609 USA
关键词
all-trans-retinoic acid; apolipoprotein; nanodisk; phospholipid; cell culture; drug delivery;
D O I
10.1016/j.ijpharm.2007.02.033
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Nanodisks are nanoscale, disk-shaped phospholipid bilayers whose edge is stabilized by association of apolipoprotein molecules. Self-assembled ND particles enriched with all-trans-retinoic acid (ATRA) (phospholipid:ATRA molar ratio = 5.5:1) were generated wherein all reaction components were solubilized. ATRA-ND migrated as a single band (Stokes' diameter similar to 20 nm) on native gradient polyacrylamide gel electrophoresis. ATRA, phospholipid and apolipoprotein co-eluted from a Sepharose 6B gel filtration column, consistent with stable integration of ATRA into the ND particle milieu. Spectroscopic analysis of ATRA-ND in buffer yielded an absorbance spectrum characteristic of ATRA. ATRA-ND mediated time-dependent inhibition of cultured HepG2 cell growth more effectively than free ATRA. The nanoscale size of the formulation particles and the stable integration of biologically active ATRA suggest ND represent a potentially useful vehicle for solubilization and in vivo delivery of ATRA. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:246 / 250
页数:5
相关论文
共 27 条
[1]   Apoptotic events induced by naturally occurring retinoids ATRA and 13-cis retinoic acid on human hepatoma cell lines Hep3B and HepG2 [J].
Arce, F ;
Gätjens-Boniche, O ;
Vargas, E ;
Valverde, B ;
Díaz, C .
CANCER LETTERS, 2005, 229 (02) :271-281
[2]   Properties of retinoids - Structure, handling, and preparation [J].
Barua, AB ;
Furr, HC .
MOLECULAR BIOTECHNOLOGY, 1998, 10 (02) :167-182
[3]   A NEW RETINOIC ACID RECEPTOR IDENTIFIED FROM A HEPATOCELLULAR-CARCINOMA [J].
BENBROOK, D ;
LERNHARDT, E ;
PFAHL, M .
NATURE, 1988, 333 (6174) :669-672
[4]   C/EBPβ:: a major PML-RARA-responsive gene in retinoic acid-induced differentiation of APL cells [J].
Duprez, E ;
Wagner, K ;
Koch, H ;
Tenen, DG .
EMBO JOURNAL, 2003, 22 (21) :5806-5816
[5]   Potential curability of newly diagnosed acute promyelocytic leukemia without use of chemotherapy:: the example of liposomal all-trans retinoic acid [J].
Estey, E ;
Koller, C ;
Tsimberidou, AM ;
O'Brien, S ;
Beran, M ;
Cortes, J ;
Tirado-Gomez, M ;
Lopez-Berestein, G ;
Kantarjian, H .
BLOOD, 2005, 105 (03) :1366-1367
[6]   Bacterial overexpression, isotope enrichment, and NMR analysis of the N-terminal domain of human apolipoprotein E [J].
Fisher, CA ;
Wang, JJ ;
Francis, GA ;
Sykes, BD ;
Kay, CM ;
Ryan, RO .
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 1997, 75 (01) :45-53
[7]   Increasing the complexity of coactivation in nuclear receptor signaling [J].
Freedman, LP .
CELL, 1999, 97 (01) :5-8
[8]   Retinoids in cancer therapy and chemoprevention: promise meets resistance [J].
Freemantle, SJ ;
Spinella, MJ ;
Dmitrovsky, E .
ONCOGENE, 2003, 22 (47) :7305-7315
[9]   Retinoid-dependent growth inhibition, differentiation and apoptosis in acute promyelocytic leukemia cells. Expression and activation of caspases [J].
Gianni, M ;
Ponzanelli, I ;
Mologni, L ;
Reichert, U ;
Rambaldi, A ;
Terao, M ;
Garattini, E .
CELL DEATH AND DIFFERENTIATION, 2000, 7 (05) :447-460
[10]   Spectroscopic studies of amphotericin B solubilized in nanoscale bilayer membranes [J].
Hargreaves, PL ;
Nguyen, TS ;
Ryan, RO .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2006, 1758 (01) :38-44