A novel excipient, 1-perfluorohexyloctane shows limited utility for the oral delivery of poorly water-soluble drugs

被引:15
作者
Holm, Rene [1 ]
Jorgensen, Erling Bonne [1 ]
Harborg, Michael [1 ]
Larsen, Rune [1 ]
Holm, Per [3 ]
Mullertz, Anette [2 ]
Jacobsen, Jette
机构
[1] H Lundbeck & Co AS, Preformulat, DK-2500 Valby, Denmark
[2] Univ Copenhagen, Fac Pharmaceut Sci, Dept Pharmaceut & Analyt Chem, Danish Drug Dev Ctr,Bioneer FARMA, DK-2100 Copenhagen, Denmark
[3] H Lundbeck & Co AS, Prod Dev & Lifecycle, DK-2500 Valby, Denmark
关键词
Lipid based formulation; Semi fluorinated alkane; Bioavailability; 1-Perfluorohexyloctane; Poorly water soluble drugs; IN-VITRO LIPOLYSIS; INTESTINAL LYMPHATIC TRANSPORT; LIPID-BASED FORMULATIONS; FLUOROCARBON EMULSIONS; BLOOD SUBSTITUTES; CYCLOSPORINE-A; CONSCIOUS RAT; MEDIUM-CHAIN; BIOAVAILABILITY; HALOFANTRINE;
D O I
10.1016/j.ejps.2011.01.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The applicability of the semi-fluorinated alkane 1-perfluorohexyloctane (F6H8) as a novel excipient in lipid based drug delivery systems was studied. Solubility studies of 11 poorly water soluble drugs (cinnarizine, danazol, estradiol, fenofibrate, griseofulvin, halofantrine, lidocaine, prednisolone, probucol, rolipram and siramesine) showed significantly lower equilibrium solubility in F6H8 compared to soy bean oil (long chain triglyceride). F6H8 was miscible with medium chain triglycerides (MCT) but not miscible with long chain triglycerides, neither was pure F6H8 nor the mixture F6H8:MCT (1:1) miscible with 7 commonly used surfactants (Cremophor EL, Span 20, Span 80, Labrasol, Softigen 767 and Gelucite 44/14, polysorbate 80). In vitro lipolysis studies confirmed that F6H8 was non-digestible. F6H8:MCT (1:1) showed initially faster lipolysis compared to pure MCT. Thus, final phase lipolysis was lower indicating that F6H8 may affect the lipolysis of MCT. However, in vivo bioavailability studies in rats showed the same plasma concentration-time profiles when dosing 10 mg/kg halofantrine at two dose levels of F6H8, MCT or F6H8:MCT (1:1) (AUC ranged from 3058 to 3447 h ng/ml. T-max similar to 6.0 h. C-max ranged from 168 to 265 mg/ml). Generally, the addition of polysorbate 80 shortened the time to reach C-max (T-max ranged 1.3-4.5 h), but had limited effect on the bioavailability from F6H8 or MCT in combination with polysorbate 80(4:1) (AUC ranged from 3807 to 4403 (h ng/ml)). Although a synergistic effect was obtained with halofantrine in F6H8:MCT:polysorbate 80(2:2:1) (AUC 5574 +/- 675 h ng/ml; mean +/- SEM), it was not superior to dosing halofantrine in pure polysorbarte 80 (AUC 7370 579 h ng/ml; mean +/- SEM). The applicability of F6H8 as an excipient for future use in lipid based formulations for poorly water soluble drugs is therefore considered to be very limited. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:416 / 422
页数:7
相关论文
共 58 条
[1]  
Araya Hiroshi, 2005, Drug Metab Pharmacokinet, V20, P244, DOI 10.2133/dmpk.20.244
[2]  
BalandraudPieri N, 1997, DRUG METAB DISPOS, V25, P912
[3]   VAN DER WAALS VOLUMES + RADII [J].
BONDI, A .
JOURNAL OF PHYSICAL CHEMISTRY, 1964, 68 (03) :441-+
[4]   Semifluorinated alkanes - Primitive surfactants of fascinating properties [J].
Broniatowski, Marcin ;
Dynarowicz-Latka, Patrycja .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 2008, 138 (02) :63-83
[5]  
Caliph SM, 2000, J PHARM SCI, V89, P1073, DOI 10.1002/1520-6017(200008)89:8<1073::AID-JPS12>3.0.CO
[6]  
2-V
[7]   A NEW FORMULATION FOR BLOOD SUBSTITUTES [J].
CECUTTI, C ;
NOVELLI, A ;
RICO, I ;
LATTES, A .
JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY, 1990, 11 (02) :115-123
[8]   Solubilisation of poorly water-soluble drugs during in vitro lipolysis of medium- and long-chain triacylglycerols [J].
Christensen, JO ;
Schultz, K ;
Mollgaard, B ;
Kristensen, HG ;
Mullertz, A .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 23 (03) :287-296
[9]   Biomaterials used in the posterior segment of the eye [J].
Colthurst, MJ ;
Williams, RL ;
Hiscott, PS ;
Grierson, I .
BIOMATERIALS, 2000, 21 (07) :649-665
[10]   TOXICOLOGY OF FLUORO-OLEFINS [J].
COOK, EW ;
PIERCE, JS .
NATURE, 1973, 242 (5396) :337-338