DSpace university logo mark
Advanced Search
Japanese | English 

NAOSITE : Nagasaki University's Academic Output SITE > School of Pharmaceutical Sciences > Articles in academic journal >

Transport of Timolol and Tilisolol in Rabbit Corneal Epithelium

File Description SizeFormat
BPBul29_2143.pdf124.07 kBAdobe PDFView/Open

Title: Transport of Timolol and Tilisolol in Rabbit Corneal Epithelium
Authors: Sakanaka, Koji / Kawazu, Kouichi / Nishida, Koyo / Nakamura, Junzo / Nakashima, Mikiro / Nakamura, Tadahiro / Oshita, Akemi / Ichikawa, Nobuhiro / Sasaki, Hitoshi
Issue Date: Dec-2006
Publisher: Pharmaceutical Society of Japan
Citation: Biological & Pharmaceutical Bulletin v.29(10) p.2143-2147, 2006
Abstract: The purpose of this study is to characterize the transport of tilisolol and timolol through the corneal epithelium, which is believed to be a tight barrier of ocular drug absorption. Cultured normal rabbit corneal epithelial cells (RCEC) were used to investigate drug transport. Primary RCEC were seeded on a filter membrane of Transwell-COL? insert coated with fibronectin and grown in Dulbecco's modified Eagle's medium/nutrient mixture F-12 with various supplements. Beta-blocker permeability through the RCEC layer was measured to assess the transcellular permeability coefficient (Ptranscell) in the absence or presence of inhibitors. The transcellular permeability of tilisolol was dependent on drug concentration although timolol showed no concentration dependency. Tilisolol flux from the apical to the basal side was larger than in the opposite direction although timolol showed no direction dependency. The transcellular permeability of tilisolol from the apical to the basal side was inhibited by sodium azide, tetraethylammonium, quinidine, taurocholic acid, guanidine and carnitine. Tilisolol had an active mechanism in uptake to the corneal epithelium, probably by the organic cation transporter family, although timolol predominantly permeated via passive diffusion. This RCEC system was useful to characterize the ocular permeation mechanism of drugs.
Keywords: cultured rabbit cornea / drug delivery system / transporter / beta-blocker / tilisolol / timolol
URI: http://hdl.handle.net/10069/8395
ISSN: 09186158
DOI: 10.1248/bpb.29.2143
PubMed ID: 17015968
Relational Links: http://dx.doi.org/10.1248/bpb.29.2143
Type: Journal Article
Text Version: publisher
Appears in Collections:Articles in academic journal

Citable URI : http://hdl.handle.net/10069/8395

All items in NAOSITE are protected by copyright, with all rights reserved.


Valid XHTML 1.0! Copyright © 2006-2015 Nagasaki University Library - Feedback Powerd by DSpace