Phenothiazinium derivatives for pathogen inactivation in blood products

被引:113
作者
Wainwright, Mark
Mohr, Harald
Walker, Wolfram H.
机构
[1] Liverpool John Moores Univ, Sch Pharm & Chem, Liverpool L3 3AF, Merseyside, England
[2] Inst Springe, Blood Ctr German Red Cross Chapters NStOB, D-31832 Springe, Germany
[3] MacoPharma Int GmbH, D-63225 Langen, Germany
关键词
benzo[a]phenothiazinium; blood products; pathogen inactivation; phenothiazinium; platelets; plasma; red blood cells;
D O I
10.1016/j.jphotobiol.2006.07.005
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
Phenothiazine-based photosensitisers have been employed in photoantimicrobial research for nearly 80 years, both as lead and novel compounds. However, the main structural variations have mainly involved the auxochromic side chains and little has been reported concerning either peripheral substitution or structures with chromophores other than those of the phenothiazinium or annelated benzo[a]phenothiazinium type. In terms of application, the plienothiazinium series has featured commonly in cytology and cytopathology, as well as in haematological staining. The current work covers the evolution of improved photosensitisers based on the phenothiazine ring system, with particular reference to the field of pathogen inactivation, and the structural alteration of lead compounds such as methyllne blue and Nile blue to yield improved photosensitisers for this important aspect of blood product safety. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:45 / 58
页数:14
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