Evidence map›Paper›PMID 29520719›Full record

ArticleEuropean journal of drug metabolism and pharmacokinetics2018

Determination of Puquitinib in Human Plasma by HPLC-ESI MS/MS: Application to Pharmacokinetic Study.

Jing Zhan, Ya Ding, Benyan Zou, Hai Liao, Wenqi Jiang, Su Li

Open access · hybridAbstract readValidation Study
In one paragraph

Article in European journal of drug metabolism and pharmacokinetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 99% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Jing ZhanState Key Laboratory of Oncology in Southern China, Sun Yat-sen University, Room 601, Building 1, No.651, Dongfengdong Road, Guangzhou, 510060, Guangdong, People's Republic of China.
Ya DingState Key Laboratory of Oncology in Southern China, Sun Yat-sen University, Room 601, Building 1, No.651, Dongfengdong Road, Guangzhou, 510060, Guangdong, People's Republic of China.
Benyan ZouState Key Laboratory of Oncology in Southern China, Sun Yat-sen University, Room 601, Building 1, No.651, Dongfengdong Road, Guangzhou, 510060, Guangdong, People's Republic of China.
Hai LiaoState Key Laboratory of Oncology in Southern China, Sun Yat-sen University, Room 601, Building 1, No.651, Dongfengdong Road, Guangzhou, 510060, Guangdong, People's Republic of China.
Wenqi JiangState Key Laboratory of Oncology in Southern China, Sun Yat-sen University, Room 601, Building 1, No.651, Dongfengdong Road, Guangzhou, 510060, Guangdong, People's Republic of China.
Su LiState Key Laboratory of Oncology in Southern China, Sun Yat-sen University, Room 601, Building 1, No.651, Dongfengdong Road, Guangzhou, 510060, Guangdong, People's Republic of China. suli201706@sina.com.
Sun Yat-sen University · CNSun Yat-sen University Cancer Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivePuquitinib mesylate (XC-302) is a new multiple-target anticancer inhibitor, which directly suppresses the activity of phosphatidylinositol 3-kinase (PI3K). This study was aimed to develop a sensitive and specific liquid chromatography electrospray ionization tandem mass spectrometry (HPLC-ESI MS/MS) method for the quantification and pharmacokinetic investigation of plasma puquitinib in cancer patients.

methodsThe analytes of human plasma were prepared by liquid-liquid extraction using methyl-t-butyl ether (MTBE). The plasma analytes were separated by HPLC on Thermo ODS Hypersil column (2.1 × 150 mm; 3 μm) at 25 °C with 5 mmol/L ammonium acetate (A)-acetonitrile (B) (30:70, v/v) as the mobile phase.

resultsThe total run time was 3.5 min and the elution of puquitinib was at 1.38 min. The detection were analyzed by multiple reaction monitoring (MRM) mode with positive-ion electrospray ionization (ESI) interface using the respective [M + H]

conclusionsThe optimized method was successfully applied to the pharmacokinetic profile study in human cancer patient plasma after the oral administration of puquitinib.

Indexed as

Chromatography, High Pressure LiquidSpectrometry, Mass, Electrospray IonizationTandem Mass SpectrometryAdenineAdministration, OralAgedAminoquinolinesAntineoplastic AgentsDrug MonitoringFemaleHumansMaleMiddle AgedNeoplasmsPredictive Value of TestsProtein Kinase InhibitorsAdenineAminoquinolinesAntineoplastic AgentsProtein Kinase Inhibitorspuquitinib

Identifiers

PMID29520719
PMCPMC6133078
OpenAlexW2790417844

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.