Long-Term Stability of Anti-Vascular Endothelial Growth Factor (a-VEGF) Biologics Under Physiologically Relevant Conditions and Its Impact on the Development of Long-Acting Delivery Systems

J Pharm Sci. 2021 Feb;110(2):860-870. doi: 10.1016/j.xphs.2020.09.043. Epub 2020 Oct 5.

Abstract

The port delivery system with ranibizumab (PDS) is an investigational long-acting drug delivery system for the continuous release of ranibizumab, an anti-VEGF biologic, in the vitreous humor. The efficacy of the PDS implant relies on the maintenance of long-term drug stability under physiological conditions. Herein, the long-term stability of three anti-VEGF biologics - ranibizumab, bevacizumab and aflibercept - was investigated in phosphate buffered saline (PBS) at 37 °C for several months. Comparison of stability profiles shows that bevacizumab and aflibercept are increasingly prone to aggregation whereas ranibizumab undergoes minimal aggregation. Ranibizumab also shows the smallest loss in antigen binding capacity after long-term incubation in PBS. Even though the aggregated forms of bevacizumab and aflibercept bind to VEGF, the consequences of aggregation on immunogenicity, implant function and efficacy are unknown. These results highlight the importance of maintaining long-term drug stability under physiologically relevant conditions which is necessary for achieving efficacy with an in vivo continuous drug delivery device such as the PDS implant.

Keywords: Aflibercept; Bevacizumab; Long-acting delivery; Ranibizumab; Stability; nAMD.

MeSH terms

  • Angiogenesis Inhibitors
  • Bevacizumab
  • Biological Products*
  • Intravitreal Injections
  • Ranibizumab
  • Recombinant Fusion Proteins
  • Vascular Endothelial Growth Factor A*

Substances

  • Angiogenesis Inhibitors
  • Biological Products
  • Recombinant Fusion Proteins
  • Vascular Endothelial Growth Factor A
  • Bevacizumab
  • Ranibizumab