Development and optimization of apigenin-loaded transfersomal system for skin cancer delivery: in vitro evaluation

Artif Cells Nanomed Biotechnol. 2017 Nov;45(7):1452-1462. doi: 10.1080/21691401.2016.1247850. Epub 2017 Jan 4.

Abstract

The aim of this work is to apply Box-Behnken design to optimize the transfersomes were formulated by modified rotary evaporation sonication technique using surfactant Tween 80. The response surface methodology was used having three-factored with three levels. The prepared formulations were characterized for vesicle shape, size, entrapment efficiency (%), stability, and in vitro permeation. The result showed that drug entrapment of 84.24% with average vesicle size of 35.41 nm and drug loading of 8.042%. Thus, optimized formulation was found good stability and is a promising approach to improve the permeability of apigenin in sustained release for prolonged period of time.

Keywords: Box-Behnken design; Optimization; apigenin; phospholipids; sustained release; transfersomes.

MeSH terms

  • Apigenin / chemistry*
  • Apigenin / metabolism
  • Apigenin / therapeutic use
  • Delayed-Action Preparations
  • Drug Carriers / chemistry*
  • Drug Liberation
  • Particle Size
  • Permeability
  • Phospholipids / chemistry
  • Polysorbates / chemistry
  • Skin Neoplasms / drug therapy
  • Skin Neoplasms / metabolism*
  • Surface-Active Agents / chemistry

Substances

  • Delayed-Action Preparations
  • Drug Carriers
  • Phospholipids
  • Polysorbates
  • Surface-Active Agents
  • Apigenin