A head-to-head multi-parametric high content analysis of a series of medium chain fatty acid intestinal permeation enhancers in Caco-2 cells

被引:78
作者
Brayden, David J. [1 ]
Gleeson, John
Walsh, Edwin G.
机构
[1] Univ Coll Dublin, Sch Vet Med, Dublin 4, Ireland
基金
爱尔兰科学基金会;
关键词
High content analysis; Oral peptide delivery; Medium chain fatty acids; Sodium caprate; Caco-2; monolayers; Cytotoxicity assays; DRUG ABSORPTION; TIGHT JUNCTIONS; SODIUM CAPRATE; IN-VITRO; PERMEABILITY; MONOLAYERS; PHARMACOKINETICS; TOXICITY; GROWTH; PK(A);
D O I
10.1016/j.ejpb.2014.10.008
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
There is debate over the narrow safety margin of many oral permeation enhancers. The sodium salts of medium chain fatty acids (MCFAs) are components of selected oral peptide formulations being assessed in advanced clinical studies. The aim of the study was to examine the effects of the C-8-C-12 series on filter-grown Caco-2 monolayers and cells grown on 96 well plates in order to dissect the relationship between paracellular permeability enhancement (Papp of [C-14]mannitol, reduction in TEER), critical micellar concentration (CMC), and sub-lethal cytotoxicity (high content analysis (HCA). There was a high degree of correlation between the EC50 for increasing the Papp with reduction in transepithelial electrical resistance (TEER), and with CMC values. C-8 had the highest EC50 and highest CMC value and was the least cytotoxic, while C-12 had the reverse, suggesting a close association between increases in chain length with increases in permeability, hydrophobicity and cytotoxicity. HCA revealed further association between MCFA-induced intracellular calcium increases and plasma membrane permeability reductions in Caco-2 cells with the EC50 to increase the Papp across monolayers. HCA identified sub-lethal cytotoxicity in a series of MCFA and related cell parameters to physicochemical properties and efficacy as intestinal permeation enhancers. These mild surfactants therefore non-specifically partition into the plasma membrane causing membrane fluidization, which is associated with concentration-dependent increases in permeability. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:830 / 839
页数:10
相关论文
共 36 条
[1]
SODIUM CAPRATE ELICITS DILATATIONS IN HUMAN INTESTINAL TIGHT JUNCTIONS AND ENHANCES DRUG ABSORPTION BY THE PARACELLULAR ROUTE [J].
ANDERBERG, EK ;
LINDMARK, T ;
ARTURSSON, P .
PHARMACEUTICAL RESEARCH, 1993, 10 (06) :857-864
[2]
Absorption Enhancers: Applications and Advances [J].
Aungst, Bruce J. .
AAPS JOURNAL, 2012, 14 (01) :10-18
[3]
Efficacious Intestinal Permeation Enhancement Induced by the Sodium Salt of 10-undecylenic Acid, A Medium Chain Fatty Acid Derivative [J].
Brayden, David J. ;
Walsh, Edwin .
AAPS JOURNAL, 2014, 16 (05) :1064-1076
[4]
Cerella C., 2010, INT J CELL BIOL, V10
[5]
Dittmann I., 2014, PHARM RES
[6]
Myosin light chain kinase inhibition:: Correction of increased intestinal epithelial permeability in vitro [J].
Feighery, Linda M. ;
Cochrane, Sean W. ;
Quinn, Teresa ;
Baird, Alan W. ;
O'Toole, Daniel ;
Owens, Sian-Eleri ;
O'Donoghue, Diarmuid ;
Mrsny, Randall J. ;
Brayden, David J. .
PHARMACEUTICAL RESEARCH, 2008, 25 (06) :1377-1386
[7]
Florence A.T., 2012, FASTRACK PHYS PHARM
[8]
Analysis of phase diagram and microstructural transitions in an ethyl oleate/water/Tween 80/Span 20 microemulsion system using high-resolution ultrasonic spectroscopy [J].
Hickey, Sinead ;
Hagan, Sue A. ;
Kudryashov, Evgeny ;
Buckin, Vitaly .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2010, 388 (1-2) :213-222
[9]
Determination of drug permeability and prediction of drug absorption in Caco-2 monolayers [J].
Hubatsch, Ina ;
Ragnarsson, Eva G. E. ;
Artursson, Per .
NATURE PROTOCOLS, 2007, 2 (09) :2111-2119
[10]
Effect of premicellar aggregation on the pKa of fatty acid soap solutions [J].
Kanicky, JR ;
Shah, DO .
LANGMUIR, 2003, 19 (06) :2034-2038