Safety assessment of oral photodynamic therapy in rats

被引:15
作者
Fontana, Carla R. [1 ]
Lerman, Mark A. [2 ]
Patel, Niraj [3 ,6 ]
Grecco, Clovis [4 ]
de Souza Costa, Carlos A. [5 ]
Amiji, Mansoor M. [6 ]
Bagnato, Vanderlei S. [4 ]
Soukos, Nikolaos S. [3 ]
机构
[1] Univ Sao Paulo State UNESP, Sch Pharmaceut Sci, Dept Clin Anal, BR-14801960 Araraquara, Sau Paulo, Brazil
[2] Harvard Univ, Sch Dent Med, Dept Oral Med Infect & Immun, Boston, MA 02115 USA
[3] Forsyth Inst, Appl Mol Photomed Lab, Boston, MA 02115 USA
[4] Univ Sao Paulo, Inst Phys Sao Carlos, BR-15980900 Sao Carlos, Sau Paulo, Brazil
[5] Univ Sao Paulo State UNESP, Dent Sch Araraquara, BR-14801960 Araraquara, Sau Paulo, Brazil
[6] Northeastern Univ, Bouve Coll Hlth Sci, Sch Pharm, Dept Pharmaceut Sci, Boston, MA 02115 USA
基金
巴西圣保罗研究基金会;
关键词
Photodynamic therapy; Photosensitizers; Histological analysis; Fluorescence; STAPHYLOCOCCUS-AUREUS; CANDIDA-ALBICANS; NANOPARTICLES; INACTIVATION; LIGHT; PHOTOFRIN; MODEL;
D O I
10.1007/s10103-012-1091-6
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Photodynamic therapy (PDT) is based on the synergism of a photosensitive drug (a photosensitizer) and visible light to destroy target cells (e.g., malignant, premalignant, or bacterial cells). The aim of this study was to investigate the response of normal rat tongue mucosa to PDT following the topical application of hematoporphyrin derivative (PhotogemA (R)), PhotodithazineA (R), methylene blue (MB), and poly(lactic-co-glycolic acid) (PLGA) nanoparticles loaded with MB. One hundred and thirty three rats were randomly divided in various groups: the PDT groups were treated with the photosensitizers for 10 min followed by exposure to red light. Those in control groups received neither photosensitizer nor light, and they were subjected to light exposure alone or to photosensitizer alone. Fluorescent signals were obtained from tongue tissue immediately after the topical application of photosensitizers and 24 h following PDT. Histological changes were evaluated at baseline and at 1, 3, 7, and 15 days post-PDT treatment. Fluorescence was detected immediately after the application of the photosensitizers, but not 24 h following PDT. Histology revealed intact mucosa in all experimental groups at all evaluation time points. The results suggest that there is a therapeutic window where PDT with PhotogemA (R), PhotodithazineA (R), MB, and MB-loaded PLGA nanoparticles could safely target oral pathogenic bacteria without damaging normal oral tissue.
引用
收藏
页码:479 / 486
页数:8
相关论文
共 38 条
[21]   Nanoparticle-based Endodontic Antimicrobial Photodynamic Therapy [J].
Pagonis, Tom C. ;
Chen, Judy ;
Fontana, Carla Raquel ;
Devalapally, Harikrishna ;
Ruggiero, Karriann ;
Song, Xiaoqing ;
Foschi, Federico ;
Dunham, Joshua ;
Skobe, Ziedonis ;
Yamazaki, Hajime ;
Kent, Ralph ;
Tanner, Anne C. R. ;
Amiji, Mansoor M. ;
Soukos, Nikolaos S. .
JOURNAL OF ENDODONTICS, 2010, 36 (02) :322-328
[22]   Rapid endo-lysosomal escape of poly(DL-lactide-co-glycolide) nanoparticles:: implications for drug and gene delivery [J].
Panyam, J ;
Zhou, WZ ;
Prabha, S ;
Sahoo, SK ;
Labhasetwar, V .
FASEB JOURNAL, 2002, 16 (10) :1217-1226
[23]   Photodynamic inactivation of microorganisms present on complete dentures. A clinical investigation [J].
Ribeiro, Daniela Garcia ;
Pavarina, Ana Claudia ;
Dovigo, Livia Nordi ;
de Oliveira Mima, Ewerton Garcia ;
Machado, Ana Lucia ;
Bagnato, Vanderlei Salvador ;
Vergani, Carlos Eduardo .
LASERS IN MEDICAL SCIENCE, 2012, 27 (01) :161-168
[24]   Effect of photodynamic therapy with photodithazine on morphofunctional parameters of M-1 sarcoma [J].
Romanko, YS ;
Tsyb, AF ;
Kaplan, MA ;
Popuchiev, VV .
BULLETIN OF EXPERIMENTAL BIOLOGY AND MEDICINE, 2004, 138 (06) :584-589
[25]   Poly(ethylene oxide)-modified poly(β-amino ester) nanoparticles as a pH-sensitive system for tumor-targeted delivery of hydrophobic drugs.: 1.: In vitro evaluations [J].
Shenoy, Dinesh ;
Little, Steven ;
Langer, Robert ;
Amiji, Mansoor .
MOLECULAR PHARMACEUTICS, 2005, 2 (05) :357-366
[26]   Application of an active attachment model as a high-throughput demineralization biofilm model [J].
Silva, Thiago C. ;
Pereira, Agnes Fatima F. ;
Exterkate, Rob A. M. ;
Bagnato, Vanderlei S. ;
Buzalaf, Marilia A. R. ;
Machado, Maria Aparecida de A. M. ;
ten Cate, Jacob M. ;
Crielaard, Wim ;
Deng, Dong Mei .
JOURNAL OF DENTISTRY, 2012, 40 (01) :41-47
[27]   Photodynamic therapy in the control of oral biofilms [J].
Soukos, Nikolaos S. ;
Goodson, J. Max .
PERIODONTOLOGY 2000, 2011, 55 :143-166
[28]  
Strakhovskaya M. G., 2002, Mikrobiologiya, V71, P349
[29]   Photodynamic therapy in oncology [J].
Triesscheijn, Martijn ;
Baas, Paul ;
Schellens, Jan H. M. ;
Stewart, Fiona A. .
ONCOLOGIST, 2006, 11 (09) :1034-1044
[30]   Photodynamic therapy of virus-associated precancer and early stages cancer of cervix uteri [J].
Trushina, O. I. ;
Novikova, E. G. ;
Sokolov, V. V. ;
Filonenko, E. V. ;
Chissov, V. I. ;
Vorozhtsov, G. N. .
PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY, 2008, 5 (04) :256-259