Formation of liposomal antivirus drug butaminophrn

  • И. М. Бушмакина State Scientific Institution "Institute of Biophysics and Cell Engineering of the National Academy of Sciences of Belarus"
  • Н. И. Дроздова State Scientific Institution "Institute of Biophysics and Cell Engineering of the National Academy of Sciences of Belarus"
  • Н. С. Голенко State Scientific Institution "Institute of Biophysics and Cell Engineering of the National Academy of Sciences of Belarus"
  • М. А. Мартынова State Scientific Institution "Institute of Biophysics and Cell Engineering of the National Academy of Sciences of Belarus"
Keywords: herpetic infection, polylayered liposomes, monolayered liposomes, butaminophen, vortexing techniques, US- dispersion techniques

Abstract

The physicochemical condition of butaminophen incorporation into poly- and monolayered liposomes were determined. These liposomal substances can be used to peroral gelatinous drug designing (polylayered liposomes) and to the designing of injection drug which can be sterilization by membrane filtration (monolayered liposomes).
Published
2018-05-31
How to Cite
Бушмакина, И., Дроздова, Н., Голенко, Н., & Мартынова, М. (2018). Formation of liposomal antivirus drug butaminophrn. Bulletin of the International Scientific Surgical Association, 2(1), 15-16. Retrieved from http://surgjournal.ru/index.php/BISSA/article/view/132
Section
Original Articles