Influence of the antiseptic agents polyhexanide and octenidine on FL cells and on healing of experimental superficial aseptic wounds in piglets -: A double-blind, randomised, stratified, controlled, parallel-group study

被引:104
作者
Kramer, A
Roth, B
Müller, G
Rudolph, P
Klöcker, N
机构
[1] Univ Greifswald, Inst Hyg & Environm Med, DE-17489 Greifswald, Germany
[2] Audit Inst Med Serv & Qual Assurance, Taunusstein, Germany
[3] Dist Hosp, Dept Surg, Wattenwil, Switzerland
关键词
polyhexanide; octenidine; wound healing; superficial aseptic wounds; cytotoxicity;
D O I
10.1159/000077241
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 [皮肤病与性病学];
摘要
The main target of the combination of octenidine with phenoxyethanol (Octenisept(R)) is the antisepsis of acute wounds, whereas polyhexanide combined with polyethylene glycol in Ringer solution (Lavasept(R)) is the agent of choice for antisepsis of chronic wounds and burns. Because comparative data for both agents on the effects on wound healing are lacking, we investigated the influence of preparations based on polyhexanide and octenidine versus placebo (Ringer solution) in experimental superficial aseptic skin wounds (n = 108) of 20 mm diameter, using a double-blind, randomised, stratified, controlled, parallel-group design in piglets. Computerised planimetry and histopathological methods were used for the assessment of wound healing. Histologically, no significant differences could be verified at any time between the 3 groups. However, in the early phase (day 9 after wounding), the octenidine-based product retarded wound contraction to a significantly greater extent than placebo and polyhexanide, whereas in the later phase (days 18 and 28), polyhexanide promoted contraction significantly more than did placebo and octenidine. The consequence is complete wound closure after 22.9 days using polyhexanide, in comparison to the placebo after 24.1 days (p < 0.05) and octenidine after 28.3 days (no statistical difference to placebo). This may be explained by the better tolerance of polyhexanide in vitro, which was demonstrated with dose and time dependence in cytotoxicity tests on human amnion cells. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:141 / 146
页数:6
相关论文
共 18 条
[1]
ALAM R, 1994, J IMMUNOL, V152, P1298
[2]
BABICH H, 1990, ATLA-ALTERN LAB ANIM, V18, P129
[3]
Babich H, 1992, IN VITRO METHODS TOX, V17, P237
[4]
COMPARATIVE-STUDY OF 4 WOUND DRESSINGS ON EPITHELIZATION OF PARTIAL-THICKNESS WOUNDS IN PIGS [J].
CHVAPIL, M ;
CHVAPIL, TA ;
OWEN, JA .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 1987, 27 (03) :278-282
[5]
Gokoo C, 1993, Decubitus, V6, P42
[6]
Harke H., 1989, HYG MED, V14, P372
[7]
INTERACTION OF BIOLOGICALLY-ACTIVE MOLECULES WITH PHOSPHOLIPID-MEMBRANES .1. FLUORESCENCE DEPOLARIZATION STUDIES ON THE EFFECT OF POLYMERIC BIOCIDE BEARING BIGUANIDE GROUPS IN THE MAIN CHAIN [J].
IKEDA, T ;
TAZUKE, S ;
WATANABE, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 735 (03) :380-386
[8]
Kramer A, 1998, CHIRURG, V69, P840, DOI 10.1007/s001040050498
[9]
Kramer A, 2002, DEV OPHTHALMOL, V33, P117
[10]
KRAMER A, IN PRESS J WOUND CAR