Evidence map›Paper›PMID 38213152›Full record

ArticleCurrent pharmaceutical biotechnology2024

Simultaneous Determination of Levo-tetrahydropalmatine and Naltrexone in Rat Plasma by LC-MS/MS and its Application in a Pharmacokinetic Study.

Kun Feng, Sherwin K B Sy, Mingming Yu, Zhihua Lv, Meixing Yan

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Article in Current pharmaceutical biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 50% of its field
1 · What the graph read from it

What it found

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3 · Its place in the literature

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0 citing papers in PubMed, 1 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Kun FengWomen and Children Hospital, Qingdao University, Qingdao, 266034, China.
Sherwin K B SyDepartment of Statistics, State University of Maringá, Maringá, Paraná, Brazil.
Mingming YuSchool of Medicine and Pharmacy, Ocean University of China, Qingdao, 266003, PR China.
Zhihua LvSchool of Medicine and Pharmacy, Ocean University of China, Qingdao, 266003, PR China.
Meixing YanWomen and Children Hospital, Qingdao University, Qingdao, 266034, China.
Qingdao University · CNQingdao National Laboratory for Marine Science and Technology · CNUniversidade Estadual de Maringá · BR

Funding

Fundamental Research Funds for the Central Universities
6 · The paper itself

Abstract

backgroundLevo-tetrahydropalmatine and low-dose naltrexone are used in association with reducing cocaine-related cravings, but there are no analytical methods for the quantitative simultaneous analysis of this drug combination.

objectiveA highly selective and sensitive LC-MS/MS assay was developed and validated to simultaneously quantify l-THP and naltrexone. The analytical method for l-THP offers improved sensitivity compared to previously published methods.

methodsThe product ion transitions of l-THP and naltrexone were 357.0→193.0 and 342.2→324.1, respectively. Chromatographic separations were performed using a BEH-C18 column by an isocratic elution mode with acetonitrile and 0.1% formic acid in water containing 3 mM ammonium acetate. L-THP and naltrexone were extracted from rat plasma using a liquidliquid extraction method.

resultsFor l-THP and naltrexone, the assay displayed good linear response over a concentration range of 0.5-1000 ng/mL and 0.25-500 ng/mL, respectively. The intra-day accuracy of the method for l-THP and naltrexone was 93.8-101% with a precision (%CV) of 2.43-8.15% and 93.4-108% with a precision of 3.47-8.22%. The inter-day accuracy for l-THP and naltrexone was 91.2-102% with a CV of 2.46-8.06% and 91.5-97.8% with a CV of 3.29-8.92%, respectively.

conclusionThe assay has been used for pharmacokinetic studies of l-THP and naltrexone in the rat.

Indexed as

Berberine AlkaloidsNaltrexoneRats, Sprague-DawleyTandem Mass SpectrometryAnimalsChromatography, LiquidLiquid Chromatography-Mass SpectrometryMaleNarcotic AntagonistsRatsReproducibility of ResultsBerberine AlkaloidsNaltrexoneNarcotic AntagoniststetrahydropalmatineLC-MS/MSLevo-tetrahydropalmatinenaltrexonepharmacokinetics.rat plasmavalidation

Identifiers

PMID38213152
OpenAlexW4390795885

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.