Premium
2‐[1‐hexyloxyethyl]‐2‐devinyl pyropheophorbide‐ a (HPPH) in a nude rat glioma model: Implications for photodynamic therapy
Author(s) -
Lobel Jeffrey,
MacDonald Ian J.,
Ciesielski Michael J.,
Barone Tara,
Potter William R.,
Pollina John,
Plunkett Robert J.,
Fenstermaker Robert A.,
Dougherty Thomas J.
Publication year - 2001
Publication title -
lasers in surgery and medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.888
H-Index - 112
eISSN - 1096-9101
pISSN - 0196-8092
DOI - 10.1002/lsm.10001
Subject(s) - photodynamic therapy , photosensitizer , glioma , in vivo , pharmacokinetics , brain tumor , pathology , medicine , brain tissue , chemistry , animal model , cancer research , biology , microbiology and biotechnology , organic chemistry
Background and Objective In this study, we evaluated 2‐[1‐hexyloxyethyl]‐2‐devinyl pyropheophorbide‐α (HPPH or Photochlor) as a photosensitizer for the treatment of malignant gliomas by photodynamic therapy (PDT). Study Design/Materials and Methods We performed in vivo reflection spectroscopy in athymic rats to measure the attenuation of light in normal brain tissue. We also studied HPPH pharmacokinetics and PDT effects in nude rats with brain tumors derived from stereotactically implanted U87 human glioma cells. Rats implanted with tumors were sacrificed at designated time points to determine the pharmacokinetics of HPPH in serum, tumor, normal brain, and brain adjacent to tumor (BAT). HPPH concentrations in normal brain, BAT and tumor were determined using fluorescence spectroscopy. Twenty‐four hours after intravenous injection of HPPH, we administered interstitial PDT treatment at a wavelength of 665 nm. Light was given in doses of 3.5, 7.5 or 15 J/cm at the tumor site and at a rate of 50 mW/cm. Results In vivo spectroscopy of normal brain tissue showed that the attenuation depth of 665 nm light is ∼30% greater than that of 630 nm light used to activate Photofrin, which is currently being evaluated for PDT as an adjuvant to surgery for malignant gliomas. The t½ of disappearance of drug from serum and tumor was 25 and 30 hours, respectively. Conclusion Twenty‐four hours after injection of 0.5 mg/kg HPPH, tumor‐to‐brain drug ratios ranged from 5:1 to 15:1. Enhanced survival was observed in each of the HPPH/PDT‐treated animal groups. These data suggest that HPPH may be a useful adjuvant for the treatment of malignant gliomas. Lasers Surg. Med. 29:397–405, 2001. © 2001 Wiley‐Liss, Inc.