Determination of the antibacterial efficacy of a new porphyrin-based photosensitizer against MRSA ex vivo

被引:61
作者
Maisch, T.
Bosl, C.
Szeimies, R.-M.
Love, B.
Abels, C.
机构
[1] Univ Regensburg, Dept Dermatol, Dermatol Klin & Poliklin, D-93053 Regensburg, Germany
[2] Destiny Pharma Ltd, Sussex Innovat Ctr, Brighton, E Sussex, England
关键词
D O I
10.1039/b614770d
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Following extensive in vitro screening of new photosensitizers the purpose of the present study was to examine penetration as well as antibacterial efficacy of a lead photosensitizer against MRSA using an ex vivo porcine skin model. Two different applications were performed: ( i) preincubation of bacteria in solution with a porphyrin-based photosensitizer XF73 and subsequent application on the ex vivo porcine skin; ( ii) application of pure bacteria on the explants followed by an incubation with XF73 in a water-ethanol formulation for up to 60 min under occlusion. The localisation of XF73 was restricted to the stratum corneum. Different concentrations ( 0-10 mu M) of XF73 and different incubation times ( 5-60 min) were used to determine phototoxicity against methicillin-resistant and methicillin-sensitive S. aureus, which was applied on the explants. Preincubation of S. aureus with 0.1 mu M XF73 in solution prior to the application of these XF73-incubated bacteria on the skin demonstrates a higher efficacy (> 3 log(10)) after irradiation. Antibacterial photodynamic inactivation resulted in a similar to 1 log(10) ( 0.1 mu M) 3.64 +/- 0.035 ( 10 mu M) log(10) growth reduction independently of the antibiotic resistance pattern of used S. aureus strains. Irradiation of applied bacteria without photosensitizer incubation did not show any marked decrease (< 1 log(10)) of bacteria cell number, indicating a significant phototoxicity of the XF73. Histological evaluations of untreated and treated skin areas upon irradiation within 24 h showed no significant degree of necrosis or apoptosis determined by TUNEL-assay indicating that the porcine skin is still vital. This study demonstrates that this XF73 porphyrin-based photosensitizer had concentration-dependent differences in killing efficacy of MRSA in comparison to skin cells using an ex vivo porcine skin model. The results described here imply that topical delivery of XF73 may be considered as a possible treatment in patients with superficial infections of the skin.
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收藏
页码:545 / 551
页数:7
相关论文
共 49 条
[1]   ANTIMICROBIAL RESISTANCE AND GENE-TRANSFER IN STAPHYLOCOCCUS-AUREUS [J].
ALMASAUDI, SB ;
DAY, MJ ;
RUSSELL, AD .
JOURNAL OF APPLIED BACTERIOLOGY, 1991, 70 (04) :279-290
[2]  
[Anonymous], 2002, MMWR MORB MORTAL WKL, V51, P565
[3]   MRSA: status and prospects for therapy? An evaluation of key papers on the topic of MRSA and antibiotic resistance [J].
Barrett, JF .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2004, 8 (06) :515-519
[4]   Synthesis and biological studies of 5-aminolevulinic acid-containing dendrimers for photodynamic therapy [J].
Battah, SH ;
Chee, CE ;
Nakanishi, H ;
Gerscher, S ;
MacRobert, AJ ;
Edwards, C .
BIOCONJUGATE CHEMISTRY, 2001, 12 (06) :980-988
[5]   Photo-oxidative killing of human colonic cancer cells using indocyanine green and infrared light [J].
Bäumler, W ;
Abels, C ;
Karrer, S ;
Weiss, T ;
Messmann, H ;
Landthaler, M ;
Szeimies, RM .
BRITISH JOURNAL OF CANCER, 1999, 80 (3-4) :360-363
[6]  
Boehncke W.H., 2001, PHOTODYNAMIC THERAPY, P259
[7]   The 500 Dalton rule for the skin penetration of chemical compounds and drugs [J].
Bos, JD ;
Meinardi, MMHM .
EXPERIMENTAL DERMATOLOGY, 2000, 9 (03) :165-169
[8]   PIG SKIN AS TEST SUBSTRATE FOR EVALUATING TOPICAL ANTIMICROBIAL ACTIVITY [J].
BUSH, LW ;
BENSON, LM ;
WHITE, JH .
JOURNAL OF CLINICAL MICROBIOLOGY, 1986, 24 (03) :343-348
[9]   Photodynamic inactivation of Escherichia coli by novel meso-substituted porphyrins by 4-(3-N,N,N-trimethylammoniumpropoxy)phenyl and 4-(trifluoromethyl)phenyl groups [J].
Caminos, DA ;
Spesia, MB ;
Durantini, EN .
PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES, 2006, 5 (01) :56-65
[10]   Costs of treating infections caused by methicillin-resistant staphylococci and vancomycin-resistant enterococci [J].
Carbon, C .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1999, 44 :31-36