Drug delivery strategies for photodynamic antimicrobial chemotherapy: From benchtop to clinical practice

被引:76
作者
Cassidy, Corona M. [1 ]
Tunney, Michael M. [1 ]
McCarron, Paul A. [2 ]
Donnelly, Ryan F. [1 ]
机构
[1] Queens Univ Belfast, Sch Pharm, Ctr Med Biol, Belfast BT9 7BL, Antrim, North Ireland
[2] Univ Ulster, Dept Pharm & Pharmaceut Sci, Coleraine BT52 1SA, Londonderry, North Ireland
关键词
Photodynamic antimicrobial chemotherapy; Drug delivery; Targeting; TOPICAL 5-AMINOLEVULINIC ACID; FRESH-FROZEN PLASMA; TOLUIDINE-BLUE; STAPHYLOCOCCUS-AUREUS; ACNE-VULGARIS; IN-VITRO; PORPHYROMONAS-GINGIVALIS; PATHOGEN INACTIVATION; AMINOLEVULINIC-ACID; WOUND INFECTIONS;
D O I
10.1016/j.jphotobiol.2009.01.005
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
Light and photosensitizer-mediated killing of many pathogens, termed photodynamic antimicrobial chemotherapy (PACT), has been extensively investigated in vitro. A wide range of organisms from the Gram-positive Staphylococcus aureus to the Gram-negative Pseudomonas aeruginosa have been proven to be susceptible to PACT. Multidrug-resistant strains are just as susceptible to this treatment as their naive counterparts. Both enveloped and non-enveloped viruses have demonstrated susceptibility in vitro, in addition to fungi and protozoa. Significantly, however, no clinical treatments based on PACT are currently licensed. This paper provides a comprehensive review of work carried out to date on delivery of photosensitizers for use in PACT, including topical, intranasal and oral/buccal delivery, as well as targeted delivery. We have also reviewed photo-antimicrobial surfaces. It is hoped that, through a rational approach to formulation design and subsequent success in small-scale clinical trials, more widespread use will be made of PACT in the clinic, to the benefit of patients worldwide. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:71 / 80
页数:10
相关论文
共 85 条
[1]  
Andersen Roger, 2007, J Clin Dent, V18, P34
[2]  
[Anonymous], 2008, PROD INF LEV KER TOP
[4]   Bacteriophage therapy and prophylaxis: Rediscovery and renewed assessment of potential [J].
Barrow, PA ;
Soothill, JS .
TRENDS IN MICROBIOLOGY, 1997, 5 (07) :268-271
[5]   Lipid cubic phases for improved topical drug delivery in photodynamic therapy [J].
Bender, J ;
Ericson, MB ;
Merclin, N ;
Iani, V ;
Rosén, A ;
Engström, S ;
Moan, J .
JOURNAL OF CONTROLLED RELEASE, 2005, 106 (03) :350-360
[6]   ANTIBODY-TARGETED PHOTOLYSIS OF BACTERIA IN-VIVO [J].
BERTHIAUME, F ;
REIKEN, SR ;
TONER, M ;
TOMPKINS, RG ;
YARMUSH, ML .
BIO-TECHNOLOGY, 1994, 12 (07) :703-706
[7]   PHOTODYNAMIC INACTIVATION OF ESCHERICHIA-COLI BY ROSE-BENGAL IMMOBILIZED ON POLYSTYRENE BEADS [J].
BEZMAN, SA ;
BURTIS, PA ;
IZOD, TPJ ;
THAYER, MA .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1978, 28 (03) :325-329
[8]   Effect of dosimetric and physiological factors on the lethal photosensitization of Porphyromonas gingivalis in vitro [J].
Bhatti, M ;
MacRobert, A ;
Meghji, S ;
Henderson, B ;
Wilson, M .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1997, 65 (06) :1026-1031
[9]   Water disinfection using photosensitizers immobilized on chitosan [J].
Bonnett, R ;
Krysteva, MA ;
Lalov, IG ;
Artarsky, SV .
WATER RESEARCH, 2006, 40 (06) :1269-1275
[10]   PHOTOBACTERICIDAL MATERIALS BASED ON PORPHYRINS AND PHTHALOCYANINES [J].
BONNETT, R ;
BUCKLEY, DG ;
BURROW, T ;
GALIA, ABB ;
SAVILLE, B ;
SONGCA, SP .
JOURNAL OF MATERIALS CHEMISTRY, 1993, 3 (03) :323-324