Gelatin Nanocarrier Enables Efficient Delivery and Phototoxicity of Hypocrellin B Against a Mice Tumour Model

被引:40
作者
Babu, Anish [1 ]
Jeyasubramanian, Kadarkaraithangam [2 ]
Gunasekaran, Paramasamy [1 ]
Murugesan, Ramachandran [1 ]
机构
[1] Madurai Kamaraj Univ, Sch Biol Sci, Madurai 625021, TN, India
[2] Mepco Schlenk Engn Coll, Dept Nanosci & Nanotechnol, Sivakasi 626005, TN, India
关键词
Gelatin Nanoparticles; Hypocrellin B; Photodynamic Therapy; Nanocarrier; PDT Agent; Tumour Regression; PHOTODYNAMIC THERAPY; 2-STEP DESOLVATION; CANCER-CELLS; BEARING MICE; NANOPARTICLES; PHOTOSENSITIZER; LIPOSOMES; EFFICACY; AGENTS; BIODISTRIBUTION;
D O I
10.1166/jbn.2012.1354
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Nanoparticles formulated from biodegradable and natural polymer gelatin, were investigated for their potential to enable efficient delivery and enhanced efficacy of a well-known photodynamic agent, Hypocrellin B (HB). The HB-loaded poly(ethylene glycol) modified gelatin nanoparticles (HB-PEG-GNP) possessed near-spherical shape, with particle size in the range of 292 +/- 42 nm, and demonstrated characteristic optical properties for photodynamic therapy (PDT). Photophysical studies of the HB-PEG-GNP demonstrated photogeneration of reactive oxygen species (ROS). The nanoparticles were tested for cellular uptake in vitro, on Daltons' Lymphoma Ascites (DLA) cells and demonstrated dose dependent phototoxicity upon visible light treatment. HB-PEG-GNP induced mitochondrial damage, as investigated by JC-1 staining, leading to apoptotic cell death. Biodistribution measurements revealed that nanoformulation reduces liver uptake of HB-PEG-GNP and increases tumour uptake with time. In vivo PDT studies in solid tumour bearing mice showed markedly significant regression (38.5 +/- 2.2%, p < 0.05) for HB-PEG-GNP treated mice in contrast to those treated with free HB (29.36 +/- 1.62%). The present study reveals gelatin nanocarrier to be an effective drug delivery system for enhancement of therapeutic efficacy of the PDT agent, HB.
引用
收藏
页码:43 / 56
页数:14
相关论文
共 42 条
  • [1] Azarmi S, 2006, J PHARM PHARM SCI, V9, P124
  • [2] Nanoparticles as vehicles for delivery of photodynamic therapy agents
    Bechet, Denise
    Couleaud, Pierre
    Frochot, Celine
    Viriot, Marie-Laure
    Guillemin, Francois
    Barberi-Heyob, Muriel
    [J]. TRENDS IN BIOTECHNOLOGY, 2008, 26 (11) : 612 - 621
  • [3] Efficiency of Liposomes in the Delivery of a Photosensitizer Controlled by the Stereochemistry of a Gemini Surfactant Component
    Bombelli, Cecilia
    Stringaro, Annarita
    Borocci, Stefano
    Bozzuto, Giuseppina
    Colone, Marisa
    Giansanti, Luisa
    Sgambato, Rosa
    Toccaceli, Laura
    Mancini, Giovanna
    Molinari, Agnese
    [J]. MOLECULAR PHARMACEUTICS, 2010, 7 (01) : 130 - 137
  • [4] Nanoparticles in photodynamic therapy: An emerging paradigm
    Chatterjee, Dev Kumar
    Fong, Li Shan
    Zhang, Yong
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2008, 60 (15) : 1627 - 1637
  • [5] In vitro uptake of gelatin nanoparticles by murine dendritic cells and their intracellular localisation
    Coester, C
    Nayyar, P
    Samuel, J
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2006, 62 (03) : 306 - 314
  • [6] Coester CJ, 2000, J MICROENCAPSUL, V17, P187
  • [7] Photodynamic therapy
    Dougherty, TJ
    Gomer, CJ
    Henderson, BW
    Jori, G
    Kessel, D
    Korbelik, M
    Moan, J
    Peng, Q
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (12): : 889 - 905
  • [8] Drummond DC, 1999, PHARMACOL REV, V51, P691
  • [9] Biodistribution of charged 17.1A photoimmunoconjugates in a murine model of hepatic metastasis of colorectal cancer
    Hamblin, MR
    Del Governatore, M
    Rizvi, I
    Hasan, T
    [J]. BRITISH JOURNAL OF CANCER, 2000, 83 (11) : 1544 - 1551
  • [10] PHARMACOKINETICS AND BODY DISTRIBUTION OF LIPOSOMAL ZINC PHTHALOCYANINE IN TUMOR-BEARING MICE - INFLUENCE OF AGGREGATION STATE, PARTICLE-SIZE, AND COMPOSITION
    ISELE, U
    SCHIEWECK, K
    KESSLER, R
    VANHOOGEVEST, P
    CAPRARO, HG
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 84 (02) : 166 - 173