Sterilization of Mycobacterium tuberculosis infected samples using methanol preserves anti-tuberculosis drugs for subsequent pharmacological testing studies.


Journal

Tuberculosis (Edinburgh, Scotland)
ISSN: 1873-281X
Titre abrégé: Tuberculosis (Edinb)
Pays: Scotland
ID NLM: 100971555

Informations de publication

Date de publication:
07 2019
Historique:
received: 14 03 2019
revised: 01 06 2019
accepted: 05 06 2019
entrez: 6 8 2019
pubmed: 6 8 2019
medline: 18 2 2020
Statut: ppublish

Résumé

Pharmacokinetic/pharmacodynamic studies of anti-tuberculosis agents in animal models of tuberculosis are hampered by the frequent necessity to perform sample bioanalysis outside the biosafety level-3 environment. Thus, each specimen has to undergo tedious and time-consuming sample sterilization procedures that may also affect drug stability. Here, we tested treatment of Mycobacterium tuberculosis (Mtb) infected samples with methanol to sterilize samples while preserving drug integrity for further pharmacokinetic/pharmacodynamic evaluations. Tissue samples harvested from Mtb infected mice were homogenized, incubated in methanol, and tested for sterility. Once sterility was confirmed, the samples were used to determine concentrations of the anti-tuberculosis drug spectinamide-1599 in lung homogenates using liquid chromatography coupled with mass spectrometry. The results demonstrate that methanol sterilizes tissue samples harvested from Mtb infected mice without altering the integrity of the drug in the tissue.

Identifiants

pubmed: 31378268
pii: S1472-9792(19)30085-X
doi: 10.1016/j.tube.2019.06.002
pmc: PMC10226109
mid: NIHMS1896088
pii:
doi:

Substances chimiques

Antitubercular Agents 0
spectinamide 1599 0
Spectinomycin 93AKI1U6QF
Methanol Y4S76JWI15

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

52-55

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI120670
Pays : United States
Organisme : NIH HHS
ID : S10 OD016226
Pays : United States

Informations de copyright

Copyright © 2019. Published by Elsevier Ltd.

Références

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pubmed: 30711150
Nat Med. 2014 Feb;20(2):152-158
pubmed: 24464186
Eur J Pharm Sci. 2019 Jan 15;127:233-239
pubmed: 30419293
ACS Infect Dis. 2017 Jan 13;3(1):72-88
pubmed: 28081607
Science. 2008 Nov 28;322(5906):1392-5
pubmed: 19039139
Am J Respir Crit Care Med. 2003 Jun 1;167(11):1472-7
pubmed: 12569078
ACS Chem Biol. 2007 Aug 17;2(8):545-552
pubmed: 17696316
Lancet Respir Med. 2015 Mar;3(3):220-34
pubmed: 25773212

Auteurs

Amanda Walz (A)

Mycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, 80523, USA.

Pradeep B Lukka (PB)

Department of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN, USA.

Camron Pearce (C)

Mycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, 80523, USA.

Elizabeth Creissen (E)

Mycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, 80523, USA.

Miriam Braunstein (M)

Department of Microbiology and Immunology, University of North Carolina-Chapel Hill, Chapel Hill, NC, USA.

Anthony J Hickey (AJ)

Engineering Sciences, RTI International, RTP, Durham, NC, 27709, USA.

Bernd Meibohm (B)

Department of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN, USA.

Mercedes Gonzalez-Juarrero (M)

Mycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, 80523, USA. Electronic address: mercedes.gonzalez-juarrero@colostate.edu.

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Classifications MeSH