In vitro and in vivo photosensitizing capabilities of 5-ALA versus Photofrin® in vascular endothelial cells

Cheng Jen Chang, Chung Ho Sun, Lih Huei L. Liaw, Michael W. Berns, J. Stuart Nelson

Research output: Contribution to journalArticle

32 Citations (Scopus)

Abstract

Background and Objective: The objective of the present study was to evaluate the feasibility of photodynamic therapy (PDT) for complicated hemangiomas. The photosensitizing activities of 5-aminolevulinic acid (5- ALA) and Photofrin® were evaluated in vitro with human dermal microvascular endothelial cells (MEC) and in vivo with the chicken cox comb. Study Design/Materials and Methods: The in vitro absorption and photosensitizing activities of 5-ALA and Photofrin® were examined in a MEC culture system. The percentages of MEC killed by different drug concentrations at a wavelength of 630 nm were measured by either live/dead or lactate dehydrogenase-released assays. Similarly, the in vivo biological activities of 5-ALA and Photofrin® exposed to different total light dosages at 630 nm were studied by determining the amount of necrosis produced in chicken combs. Results: MEC incubated with 5-ALA at a concentration of 35 μg/ml and exposed to laser light at 630 nm at a power density of 100 mW/cm2 showed a 50% cell kill. MEC incubated with Photofrin® at a concentration of 3.5 μg/ml and exposed to laser light at 630 nm at a power density of 100 mW/cm2 showed a 50% cell kill. Chicken combs that received 200 mg/kg of 5-ALA exposed to laser light at 630 nm at a power density of 100 mW/cm2 had an injury depth of 362.5 ± 27.6 μm at histologic examination. Combs exposed to a power density of 100 or 120 mW/cm2 showed injury depths of 732.5 ± 29.1 and 792.5 ± 36.0 μm, respectively. Chicken combs that received 2.5 mg/kg of Photofrin® exposed to laser light at 630 nm at a power density of 80 mW/cm2 had an injury depth of 535.6 ± 22.3 μm at histologic examination. Combs exposed to a power density of 100 or 120 mW/cm2 showed injury depths of 795.8 ± 32.5 and 805.2 ± 49.1 μm, respectively. Conclusion: Both 5-ALA and Photofrin® have the capability to destroy MEC in vitro and vasculature in vivo. However, Photo 5-ALA and Photofrin® in Vascular Endothelial Cells frin® achieved a higher degree of cell kill and tissue destruction at lower drug concentrations and at lower power densities.

Original languageEnglish
Pages (from-to)178-186
Number of pages9
JournalLasers in Surgery and Medicine
Volume24
Issue number3
DOIs
Publication statusPublished - Apr 21 1999
Externally publishedYes

Fingerprint

Dihematoporphyrin Ether
Comb and Wattles
Endothelial Cells
Chickens
Light
Lasers
Wounds and Injuries
Aminolevulinic Acid
Photochemotherapy
Hemangioma
In Vitro Techniques
L-Lactate Dehydrogenase
Pharmaceutical Preparations
Necrosis
Cell Culture Techniques
Skin

Keywords

  • 5-ALA
  • Microvascular endothelial cells (MEC)
  • PDT
  • Photofrin®

ASJC Scopus subject areas

  • Surgery
  • Dermatology

Cite this

In vitro and in vivo photosensitizing capabilities of 5-ALA versus Photofrin® in vascular endothelial cells. / Chang, Cheng Jen; Sun, Chung Ho; Liaw, Lih Huei L.; Berns, Michael W.; Nelson, J. Stuart.

In: Lasers in Surgery and Medicine, Vol. 24, No. 3, 21.04.1999, p. 178-186.

Research output: Contribution to journalArticle

Chang, Cheng Jen ; Sun, Chung Ho ; Liaw, Lih Huei L. ; Berns, Michael W. ; Nelson, J. Stuart. / In vitro and in vivo photosensitizing capabilities of 5-ALA versus Photofrin® in vascular endothelial cells. In: Lasers in Surgery and Medicine. 1999 ; Vol. 24, No. 3. pp. 178-186.
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