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Validation and clinical application of a method to quantify efavirenz in cervicovaginal secretions from flocked swabs using liquid chromatography tandem mass spectrometry.
Olagunju, Adeniyi; Nwogu, Jacinta; Eniayewu, Oluwasegun; Atoyebi, Shakir; Amara, Alieu; Kpamor, John; Bolaji, Oluseye; Adejuyigbe, Ebunoluwa; Owen, Andrew; Khoo, Saye.
Afiliación
  • Olagunju A; Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.
  • Nwogu J; Department of Pharmaceutical Chemistry, Obafemi Awolowo University, Ile-Ife, Nigeria.
  • Eniayewu O; Department of Pharmaceutical Chemistry, University of Ibadan, Ibadan, Nigeria.
  • Atoyebi S; Department of Pharmaceutical Chemistry, Obafemi Awolowo University, Ile-Ife, Nigeria.
  • Amara A; Department of Pharmaceutical and Medicinal Chemistry, University of Ilorin, Ilorin, Nigeria.
  • Kpamor J; Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.
  • Bolaji O; Department of Pharmaceutical Chemistry, Obafemi Awolowo University, Ile-Ife, Nigeria.
  • Adejuyigbe E; Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.
  • Owen A; Federal Medical Centre, Makurdi, Nigeria.
  • Khoo S; Department of Pharmaceutical Chemistry, Obafemi Awolowo University, Ile-Ife, Nigeria.
Wellcome Open Res ; 6: 246, 2021.
Article en En | MEDLINE | ID: mdl-36034058
Background: A liquid chromatography tandem mass spectrometry method to quantify drugs in dried cervicovaginal secretions from flocked swabs was developed and validated using the antiretroviral efavirenz as an example. Methods: Cervicovaginal swabs (CVS) were prepared by submerging flocked swabs in efavirenz-spiked matrix. Time to full saturation, weight uniformity, recovery and room temperature stability were evaluated. Chromatographic separation was on a reverse-phase C18 column by gradient elution using 1mM ammonium acetate in water/acetonitrile at 400 µL/min. Detection and quantification were on a TSQ Quantum Access triple quadrupole mass spectrometer operated in negative ionisation mode. The method was used to quantify efavirenz in CVS samples from human immunodeficiency virus (HIV)-positive women in the VADICT study (NCT03284645). A total of 98 samples (35 paired intensive CVS and DBS samples, 14 paired sparse CVS and DBS samples) from 19 participants were available for this analysis. Results: Swabs were fully saturated within 15 seconds, absorbing 128 µL of matrix with coefficient of variation (%CV) below 1.3%. The method was linear with a weighting factor (1/X) in the range of 25-10000 ng/mL with inter- and intra-day precision (% CV) of 7.69-14.9%, and accuracy (% bias) of 99.1-105.3%. Mean recovery of efavirenz from CVS was 83.8% (%CV, 11.2) with no significant matrix effect. Efavirenz remained stable in swabs for at least 35 days after drying and storage at room temperature. Median (range) CVS efavirenz AUC 0-24h was 16370 ng*h/mL (5803-22088), C max was 1618 ng/mL (610-2438) at a T max of 8.0 h (8.0-12), and C min was 399 ng/mL (110-981). Efavirenz CVS:plasma AUC 0-24 ratio was 0.41 (0.20-0.59). Conclusions: Further application of this method will improve our understanding of the pharmacology of other therapeutics in the female genital tract, including in low- and middle-income countries.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Wellcome Open Res Año: 2021 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Wellcome Open Res Año: 2021 Tipo del documento: Article Pais de publicación: Reino Unido