Post-irradiation recovery time strongly influences fractional laser-facilitated skin absorption

Int J Pharm. 2019 Jun 10:564:48-58. doi: 10.1016/j.ijpharm.2019.04.043. Epub 2019 Apr 15.

Abstract

Fractional CO2 laser treatment has been used in some clinical trials to promote topical drug delivery. Currently, there is no standard for laser settings to achieve a feasible therapy. The cutaneous recovery following laser treatment and its influence on drug absorption have not been well explored. This study evaluated the kinetics of laser-treated skin-barrier restoration and drug permeation in nude mice. The skin recovery and observation of the process were characterized by transdermal water loss (TEWL), erythema measurement, gross appearance, optical microscopy, and scanning electron microscopy (SEM). The skin absorption of a lipophilic small permeant (tretinoin), a hydrophilic small permeant (acyclovir), and a large molecule (fluorescein isothiocyanate dextran 4 kDa, FD4) was examined in vitro using Franz cell. TEWL suggested that the laser-treated skin restored its barrier function at 16 h after irradiation. The fractional laser produced microchannels of about 150 μm in diameter and 25 μm in depth that were surrounded with thermal coagulation. The bright-field imaging indicated that the micropores were progressively closed during the recovery period but had not completely closed even after a 16-h recovery. The laser treatment led to a rapid tretinoin penetration across the skin immediately after irradiation, with a 5-fold enhancement compared to intact skin. This enhancement was gradually reduced following the increase of recovery time. Conversely, the acyclovir and FD4 permeation peaked at 1-2 h post-irradiation. The FD4 flux was even elevated as the recovery time increased. The reasons for this could have been the subsequent inflammation after laser exposure and the deficient tight junction (TJ) barrier. The confocal imaging demonstrated the perpendicular diffusion of rhodamine B and FD4 through microchannels immediately after laser exposure. The lateral diffusion from the microchannels was observed at 2 h post-irradiation. Our results revealed a time-dependent recovery of skin permeation. The time frame for applying the drugs after laser irradiation was dependent upon the permeants and their various physicochemical properties.

Keywords: Fractional laser; Laser-facilitated drug delivery; Recovery time; Stratum corneum; Tight junction.

MeSH terms

  • Acyclovir / administration & dosage
  • Acyclovir / pharmacokinetics
  • Administration, Cutaneous
  • Animals
  • Dextrans / administration & dosage
  • Dextrans / pharmacokinetics
  • Drug Delivery Systems*
  • Female
  • Fluorescein-5-isothiocyanate / administration & dosage
  • Fluorescein-5-isothiocyanate / analogs & derivatives
  • Fluorescein-5-isothiocyanate / pharmacokinetics
  • Lasers*
  • Mice, Nude
  • Rhodamines / administration & dosage
  • Rhodamines / pharmacokinetics
  • Skin / drug effects
  • Skin / metabolism
  • Skin / radiation effects
  • Skin / ultrastructure
  • Skin Absorption / drug effects
  • Skin Absorption / radiation effects*
  • Tight Junction Proteins / metabolism
  • Tretinoin / administration & dosage
  • Tretinoin / pharmacokinetics

Substances

  • Dextrans
  • Rhodamines
  • Tight Junction Proteins
  • fluorescein isothiocyanate dextran
  • Tretinoin
  • Fluorescein-5-isothiocyanate
  • rhodamine B
  • Acyclovir