Antipermeability and antiproliferative effects of standard and frozen bevacizumab on choroidal endothelial cells. Issue 6 (19th December 2006)
- Record Type:
- Journal Article
- Title:
- Antipermeability and antiproliferative effects of standard and frozen bevacizumab on choroidal endothelial cells. Issue 6 (19th December 2006)
- Main Title:
- Antipermeability and antiproliferative effects of standard and frozen bevacizumab on choroidal endothelial cells
- Authors:
- Peters, Swaantje
Julien, Sylvie
Heiduschka, Peter
Grisanti, Salvatore
Ziemssen, Focke
Adler, Martin
Schraermeyer, Ulrich
Bartz-Schmidt, Karl-Ulrich - Other Names:
- group-author.
- Abstract:
- Abstract : Background: Bevacizumab is an antiangiogenic compound developed to target tumour vessels. Its off-label use in ophthalmology requires in vitro testing on ocular cells. Aim: To quantify the antipermeability and antiproliferative effects of bevacizumab on cultured choroidal endothelial cells (CECs). It was examined whether deep-freezing of bevacizumab attenuates its antiangiogenic activity. Methods: Porcine CECs were cultured in permeable insert systems. Permeability of the cell monolayers was quantified by a fluorescent isothiocyanate-dextran assay after treatment with vascular endothelial growth factor (VEGF; 20–100 ng/ml) alone and in combination with bevacizumab (0.1–1 mg/ml). Proliferation of the CECs was tested using a "wound scratch" assay. The experiments were repeated with bevacizumab after freezing at −20°C for 5 days. Results: Bevacizumab significantly reduced VEGF-induced permeability in a dose-dependant manner. A molar ratio of 2.6:1 of bevacizumab to VEGF was required for complete blocking of VEGF-induced rise in permeability. CEC proliferation was significantly blocked by bevacizumab (0.5 mg/ml). Thawed bevacizumab after deep freezing showed a moderate, but not statistically significant loss in activity. Conclusion: Bevacizumab significantly reduces VEGF-induced permeability and proliferation of CECs. Freezing and thawing of bevacizumab will affect its biological activity.
- Is Part Of:
- British journal of ophthalmology. Volume 91:Issue 6(2007)
- Journal:
- British journal of ophthalmology
- Issue:
- Volume 91:Issue 6(2007)
- Issue Display:
- Volume 91, Issue 6 (2007)
- Year:
- 2007
- Volume:
- 91
- Issue:
- 6
- Issue Sort Value:
- 2007-0091-0006-0000
- Page Start:
- 827
- Page End:
- 831
- Publication Date:
- 2006-12-19
- Subjects:
- ARMD, age-related macular degeneration -- CEC, choroidal endothelial cell -- CFA, cell-free area -- FDA, Food and Drug Administration -- FITC, fluorescent isothiocyanate -- VEGF, vascular endothelial growth factor
Ophthalmology -- Periodicals
617.7 - Journal URLs:
- http://bjo.bmj.com/ ↗
http://bjo.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/bjo.2006.109702 ↗
- Languages:
- English
- ISSNs:
- 0007-1161
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 19694.xml