Validation of a UV-spectrophotometric analytical method for determination of LPSF/AC04 from inclusion complex and liposomes

Authors

  • Rafaela Siqueira Ferraz Universidade Federal de Pernambuco; Laboratório de Imunopatologia Keizo-Asami, LIKA; Universidade Federal de Pernambuco
  • Elisângela Afonso Moura Mendonça Universidade Estadual da Paraíba; Laboratório de Síntese e Vetorização de Moléculas; Universidade Estadual da Paraíba
  • Jéssica Priscila Avelino Silva Universidade Federal de Pernambuco; Laboratório de Imunopatologia Keizo-Asami, LIKA; Universidade Federal de Pernambuco
  • Isabella Macário Ferro Cavalcanti Centro Acadêmico de Vitória
  • Mariane Cajubá Britto Lira-Nogueira Centro Acadêmico de Vitória
  • Suely Lins Galdino Universidade Federal de Pernambuco; Laboratório de Planejamento e Síntese de Fármacos; Departamento de Antibióticos; Universidade Federal de Pernambuco
  • Ivan Rocha Pitta Universidade Federal de Pernambuco; Laboratório de Planejamento e Síntese de Fármacos; Departamento de Antibióticos; Universidade Federal de Pernambuco
  • Maria do Carmo Alves Lima Universidade Federal de Pernambuco; Laboratório de Planejamento e Síntese de Fármacos; Departamento de Antibióticos; Universidade Federal de Pernambuco
  • Nereide Stela Santos-Magalhães Universidade Federal de Pernambuco; Laboratório de Imunopatologia Keizo-Asami, LIKA; Universidade Federal de Pernambuco

DOI:

https://doi.org/10.1590/S1984-82502015000100018

Abstract

The aim of this study was to develop and validate a UV spectrophotometric method for determination of LPSF/AC04 from inclusion complex and encapsulated into liposomes. The validation parameters were determined according to the International Conference on Harmonisation (ICH) and National Health Surveillance Agency (ANVISA) guidelines. LPSF/AC04 was determined at 250 nm in methanol by a UV spectrophotometric method, exhibiting linearity in the range from 0.3 to 2 µg.mL−1 (Absorbance=0.18068 x [LPSF/AC04 µg.mL-1] + 0.00348), (r2=0.9995). The limits of detection and quantification were 0.047µg.mL−1 and 0.143µg.mL−1, respectively. The method was accurate, precise, reproducible and robust since all the samples analyzed had coefficient of variation of less than 5% and no statistically significant difference between theoretical and practical concentrations was detected. Thus, a rapid, simple, low cost and sensitive spectrophotometric method was developed and validated for determining the content of inclusion complex and liposomes containing LPSF/AC04.

Downloads

Download data is not yet available.

Downloads

Published

2015-03-01

Issue

Section

Articles

How to Cite

Validation of a UV-spectrophotometric analytical method for determination of LPSF/AC04 from inclusion complex and liposomes . (2015). Brazilian Journal of Pharmaceutical Sciences, 51(1), 183-191. https://doi.org/10.1590/S1984-82502015000100018