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Ther Drug Monit. 2021 Dec 01;43(6):789-796. doi: 10.1097/FTD.0000000000000903.

Determination of Free Valproic Acid Concentration in 569 Clinical Samples by LC-MS/MS After Hollow Fiber Centrifugal Ultrafiltration Treatment.

Therapeutic drug monitoring

Xikun Wu, Haoran Li, Weichong Dong, Xiuling Yang, Yiran Jin, Ying Gong, Zhiqing Zhang, Xiujv Liu

Affiliations

  1. Department of Pharmacy, The Second Hospital of Hebei Medical University, Shijiazhuang, China.

PMID: 33990504 DOI: 10.1097/FTD.0000000000000903

Abstract

OBJECTIVE: To perform therapeutic drug monitoring of total and free plasma valproic acid (VPA) concentrations in clinical samples and to analyze the related factors.

METHODS: The total VPA concentration in plasma was determined by ultrahigh-performance liquid chromatography with precolumn derivatization with α-bromoacetophenone, and the free VPA concentration was determined by liquid chromatography-tandem mass spectrometry after the plasma was treated by hollow fiber centrifugal ultrafiltration. Regression analysis was performed to examine the associations between free plasma VPA, total plasma VPA, and the plasma protein binding rate. The impact of individual situations, outpatient or inpatient factors, and drug combinations on VPA concentrations were examined.

RESULTS: Of the 569 clinical samples, 268 were inpatients and 301 were outpatients, and the total VPA concentration in 138 cases (24.2%) was lower than the effective treatment concentration range; the total and free VPA concentrations in outpatient samples were 11.0% and 26.1% higher than those of inpatients, respectively. There was no linear relationship between the free and total VPA concentrations. The relationship equation between the plasma protein binding rate and free VPA concentrations was as follows: Y = 0.0255X2 - 1.1357X + 97.429 (r = 0.8011). The total and free VPA concentrations were significantly decreased after the coadministration of phenobarbital (83.7% and 64.3% of the control group, P < 0.05) or carbapenem antibiotics (32.0% and 32.7% of the control group, P < 0.05).

CONCLUSIONS: The total VPA concentrations in patients with epilepsy at our hospital was lower than the effective treatment concentration range, which was inadequate for epilepsy control; the total VPA concentrations of outpatients were higher than those of inpatients; as phenobarbital affects VPA metabolism, therapeutic drug monitoring is recommended. Carbapenem antibiotic coadministration with VPA should be avoided because carbapenem antibiotics can lead to the failure of VPA antiepileptic treatment.

Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.

Conflict of interest statement

The authors declare that there are no conflicts of interest regarding the publication of this article.

References

  1. Sweetman SC. Martindale: The Complete Drug Reference. 37th ed. London, UK: Pharmaceutical Press; 2011:485–490. - PubMed
  2. Beydoun A, Sackellares J, Shu V. Safety and efficacy of divalproex sodium monotherapy in partial epilepsy a double-blind, concentration-response design clinical trial. Neurology. 1997;48:182–188. - PubMed
  3. Zhang Y, Wang T, Zhang D, et al. Therapeutic drug monitoring coupled with Bayesian forecasting could prevent vancomycin-associated nephrotoxicity in renal insufficiency patients: a prospective study and pharmacoeconomic analysis. Ther Drug Monit. 2020;42:600–609. - PubMed
  4. Goldenberg MM. Overview of drugs used for epilepsy and seizures: etiology, diagnosis, and treatment. Pharm Ther. 2010;35:392–415. - PubMed
  5. Valproic Acid [Package Insert]. Upsher-Smith Laboratories, Inc, Maple Grove, MN. 2016. - PubMed
  6. Brunton L, Hilaldandan R. Goodman and Gilman Manual of Pharmacology and Therapeutics. 2nd Ed. Open University Press, 2016. - PubMed
  7. de Maat MM, van Leeuwen HJ, Edelbroek PM. High unbound fraction of valproic acid in a hypoalbuminemic critically ill patient on renal replacement therapy. Ann Pharmaco Ther. 2011;45:e18. - PubMed
  8. Methaneethorn J. A systematic review of population pharmacokinetics of valproic acid. Br J Clin Pharmacol. 2018;84:816–834. - PubMed
  9. Łuszczyńska P, Pawiński T, Kunicki PK, et al. Pharmacokinetics of free and total mycophenolic acid in adult lupus nephritis patients-implications for therapeutic drug monitoring. Eur J Clin Pharmacol. 2019;75:371–379. - PubMed
  10. Parachalil DR, Commerford D, Bonnier F, et al. Raman spectroscopy as a potential tool for label free therapeutic drug monitoring in human serum: the case of busulfan and methotrexate. Analyst. 2019;144:5207–5214. - PubMed
  11. Brooks E, Tett SE, Isbel NM, et al. Prednisolone concentrations in plasma (total and unbound) and saliva of adult kidney transplant recipients. Ther Drug Monit. 2019;41:755–760. - PubMed
  12. Zhang ZQ, Dong WC, Yang XL, et al. The influence of plasma albumin concentration on the analysis methodology of free valproic acid by ultrafiltration and its application to therapeutic drug monitoring. Ther Drug Monit. 2015;37:776–782. - PubMed
  13. Gandia P, Arellano C, Lafont T, et al. Should therapeutic drug monitoring of the unbound fraction of imatinib and its main active metabolite N-desmethyl-imatinib be developed? Cancer Chemother Pharmacol. 2013;71:531–536. - PubMed
  14. Qian Y, Sun LN, Liu YJ, et al. Genetic polymorphisms and adverse events on unbound imatinib and its active metabolite concentration in patients with gastrointestinal stromal tumors. Front Pharmacol. 2019;10:854. - PubMed
  15. Brake LH, Ruslami R, Later-Nijland H, et al. Exposure to total and protein-unbound rifampin is not affected by malnutrition in Indonesian tuberculosis patients. Antimicrob Agents Chemother. 2015;59:3233–3239. - PubMed
  16. Byrne CG, Roberts JA, McWhinney B, et al. Variability in trough total and unbound teicoplanin concentrations and achievement of therapeutic drug monitoring targets in adult patients with hematological malignancy. Antimicrob Agents Chemother. 2017;61:e02466–16. - PubMed
  17. Sime FB, Byrne CJ, Parker S, et al. Population pharmacokinetics of total and unbound concentrations of intravenous posaconazole in adult critically ill patients. Crit Care. 2019;23:205. - PubMed
  18. Jansen AJ, Hunfeld NG, van Bommel J, et al. Therapeutic drug monitoring of free fraction valproic acid in patients with hypoalbuminaemia. Neth J Med. 2012;70:329. - PubMed
  19. Krasowski MD, Penrod LE. Clinical decision support of therapeutic drug monitoring of phenytoin: measured versus adjusted phenytoin plasma concentrations. BMC Med Inform Decis Mak. 2012;12:7. - PubMed
  20. Kodama Y, Koike Y, Kimoto H, et al. Binding parameters of valproic acid to serum protein in healthy adults at steady state. Ther Drug Monit. 1992;14:55–60. - PubMed
  21. Cramer JA, Mattson RH, Bennett DM, et al. Variable free and total valproic acid concentrations in sole-and multi-drug therapy. Ther Drug Monit. 1986;8:411–415. - PubMed
  22. Bellver M, Sánchez M, Gonzalez A, et al. Plasma protein binding kinetics of valproic acid over a broad dosage range: therapeutic implications. J Clin Pharm Ther. 1993;18:191–197. - PubMed
  23. Patsalos PN, Zugman M, Lake C, et al. Serum protein binding of 25 antiepileptic drugs in a routine clinical setting: a comparison of free non-protein-bound concentrations. Epilepsia. 2017;58:1234–1243. - PubMed
  24. Zhang L, Zhang ZQ, Dong WC, et al. Accuracy assessment on the analysis of unbound drug in plasma by comparing traditional centrifugal ultrafiltration with hollow fiber centrifugal ultrafiltration and application in pharmacokinetic study. J Chromatogr A. 2013;1318:265–269. - PubMed
  25. Zhang JF, Yang XL, Zhang ZQ, et al. Accuracy of the analysis of free vancomycin concentration by ultrafiltration in various disease states. RSC Adv. 2014;4:40214–40222. - PubMed
  26. Dong WC, Zhang ZQ, Jiang XH, et al. Effect of volume ratio of ultrafiltrate to sample solution on the analysis of free drug and measurement of free carbamazepine in clinical drug monitoring. Eur J Pharm Sci. 2013;48:332–338. - PubMed
  27. Ahlers FS, Benros ME, Dreier JW, et al. Infections and risk of epilepsy in children and young adults: a nationwide study. Epilepsia. 2019;60:275–283. - PubMed
  28. Lin CH, Lin WD, Chou IC, et al. Epilepsy and neurodevelopmental outcomes in children with etiologically diagnosed central nervous system infections: a retrospective cohort study. Front Neurol. 2019;10:528. - PubMed
  29. Bartolini L, Theodore WH, Jacobson S, et al. Infection with HHV-6 and its role in epilepsy. Epilepsy Res. 2019;153:34–39. - PubMed
  30. Bartolini L, Piras E, Sullivan K, et al. Detection of HHV-6 and EBV and cytokine levels in saliva from children with seizures: results of a multi-center cross-sectional study. Front Neurol. 2018;9:834. - PubMed
  31. Cha T, Choi YJ, Oh JW, et al. Respiratory syncytial virus-associated seizures in Korean children, 2011-2016. Korean J Pediatr. 2019;62:131–137. - PubMed
  32. Cruz-Cruz MDR, Gallardo-Elías J, Paredes-Solís S, et al. Factors associated with epilepsy in children in Mexico: a case-control study. Bol Med Hosp Infant Mex. 2017;74:334–340. - PubMed
  33. Lam SK, Lu WY, Weng WC, et al. The short-term and long-term outcome of febrile infection-related epilepsy syndrome in children. Epilepsy Behav. 2019;95:117–123. - PubMed
  34. Gu XR, Yu SR, Peng QL, et al. Determination of unbound valproic acid in plasma using centrifugal ultrafiltration and gas chromatography: application in TDM. Anal Biochem. 2020;588:113475. - PubMed
  35. Itoh H, Suzuki Y, Fujisaki K, et al. Correlation between plasma ammonia level and serum trough concentration of free valproic acidin patients with epilepsy. Biol Pharm Bull. 2012;35:971–974. - PubMed
  36. Nasreddine W, Dirani M, Atweh S, et al. Determinants of free serum valproate concentration: a prospective study in patients on divalproex sodium monotherapy. Seizure. 2018;59:24–27. - PubMed
  37. Drisaldi A, Weeda E, Neyens R, et al. Accuracy of valproic acid concentration correction based on serum albumin. Neurocrit Care. 2019;30:301–306. - PubMed
  38. Riker RR, Gagnon DJ, Hatton C, et al. Valproate protein binding is highly variable in ICU patients and not predicted by total serum concentrations: a case series and literature review. Pharmacotherapy. 2017;37:500–508. - PubMed
  39. Potter WZ, Ketter TA. Pharmacological issues in the treatment of bipolar disorder: focus on mood-stabilizing compounds. Can J Psychiatry. 1993;38(3 suppl 2):S51–S56. - PubMed
  40. Schoemaker R, Wade JR, Stockis A. Brivaracetam population pharmacokinetics in children with epilepsy aged 1 month to 16 years. Eur J Clin Pharmacol. 2017;73:727–733. - PubMed
  41. Wu CC, Pai TY, Hsiao FY, et al. The effect of different carbapenem antibiotics (ertapenem, imipenem/cilastatin and meropenem) on serum valproic acid concentrations. Ther Drug Monit. 2016;38:587–592. - PubMed
  42. Šíma M, Hartinger J, Rulíšek J, et al. Meropenem-induced valproic acid elimination: a case report of clinically relevant drug interaction. Prague Med Rep. 2017;118:105–109. - PubMed
  43. Velghe S, Deprez S, Stove CP. Fully automated therapeutic drug monitoring of anti-epileptic drugs making use of dried blood spots. J Chromatogr A. 2019;1601:95–103. - PubMed
  44. Mollerup CB, Rasmussen BS, Johansen SS, et al. Retrospective analysis for valproate screening targets with liquid chromatography-high resolution mass spectrometry with positive electrospray ionization: an omics-based approach. Drug Test Anal. 2019;11:730–738. - PubMed
  45. Linder C, Hansson A, Sadek S, et al. Carbamazepine, lamotrigine, levetiracetam and valproic acid in dried blood spots with liquid chromatography tandem mass spectrometry; method development and validation. J Chromatogr B Analyt Technol Biomed Life Sci. 2018;1072:116–122. - PubMed
  46. Velghe S, Stove CP. Volumetric absorptive microsampling as an alternative tool for therapeutic drug monitoring of first-generation anti-epileptic drugs. Anal Bioanal Chem. 2018;410:2331–2341. - PubMed
  47. Li Y, Jiang Y, Cao H, et al. Therapeutic drug monitoring of valproic acid using a dried plasma spot sampling device. J Mass Spectrom. 2021;56:e4603. - PubMed
  48. Li ZH, Gao WQ, Liu GF, et al. Prediction of serum-free and cerebrospinal fluid valproic acid levels in patients with hypoalbuminemia after craniotomy. Ther Drug Monit. 2020;42:610–616. - PubMed

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