Preclinical Investigation of Methylene Blue-mediated Antimicrobial Photodynamic Therapy on Leishmania Parasites Using Real-Time Bioluminescence

被引:22
作者
Cabral, Fernanda V. [1 ]
Sabino, Caetano P. [2 ,3 ]
Dimmer, Jesica A. [4 ,5 ]
Sauter, Ismael P. [1 ]
Cortez, Mauro J. [6 ]
Ribeiro, Martha S. [1 ]
机构
[1] Nucl & Energy Res Inst IPEN CNEN SP, Ctr Lasers & Applicat, Sao Paulo, SP, Brazil
[2] Univ Sao Paulo, Sch Pharmaceut Sci, Sao Paulo, SP, Brazil
[3] Biolambda, Translat Biophoton LTD, Sao Paulo, SP, Brazil
[4] Univ Nacl Cordoba, Sch Chem Sci, Pharmaceut Sci Dept, Cordoba, Argentina
[5] Consejo Nacl Invest Cient & Tecn, Multidisciplinary Inst Plant Biol IMBIV, Cordoba, Argentina
[6] Univ Sao Paulo ICB USP, Inst Biosci, Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
CUTANEOUS LEISHMANIASIS; VISCERAL LEISHMANIASIS; BALB/C MICE; AMAZONENSIS; INFECTION; INACTIVATION; HYPERALGESIA; EFFICACY; LIGHT;
D O I
10.1111/php.13188
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
Cutaneous leishmaniasis (CL) is a neglected disease that promotes destructive lesions. Difficulties in treatment are related to accessibility of drugs, resistance and toxicity. Antimicrobial photodynamic therapy (APDT) has been emerging as a promising treatment for CL. In this work, we evaluated methylene blue (MB)-mediated APDT (MB-APDT) on Leishmania amazonensis in vitro and in vivo by bioluminescence technique. In vitro, MB-APDT was performed using a red LED (lambda = 660 +/- 11 nm, 100 mW cm(-2)) and MB (100 mu m) at different light doses. In vivo, mice were infected and 4 weeks later, randomly divided into three groups: control, APDT 1 (single session) and APDT 2 (two sessions of MB-APDT). MB was used at 100 mu m and energy dose was established at 150 J cm(-2). Parasite burden, lesion size and pain were evaluated weekly for 4 weeks. In vitro, lethal dose for 90% parasite inactivation was achieved at 48.8 J cm(-2). In vivo, although APDT 1 and APDT 2 groups have showed similar parasite burden after 4 weeks, two sessions were clinically better, especially considering the inflammatory process associated to CL. Our findings reinforce MB-APDT as a cost-effective treatment to combat CL.
引用
收藏
页码:604 / 610
页数:7
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