Evidence map›Paper›PMID 42430209›Full record

ArticleBiomedical chromatography : BMC2026

A Simple and Sensitive LC-MS/MS Method for Simultaneous Quantification of Dasatinib and Erythromycin in Mice Plasma: Application to Preclinical Pharmacokinetic Study.

Avinash Kumar, Nirbhay Kumar Tiwari, Sanjeev Giri, Ramesh Patnam, Rameshwar Ameta

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Article in Biomedical chromatography : BMC, 2026. 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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1 · What the graph read from it

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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

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Avinash KumarDepartment of Chemistry, Pacific Academy of Higher Education and Research University (PAHER), Udaipur, Rajasthan, India.
Nirbhay Kumar TiwariDrug Metabolism and Pharmacokinetic Department, Aurigene Oncology Limited, Bengaluru, Karnataka, India.
Sanjeev GiriDrug Metabolism and Pharmacokinetic Department, Aurigene Oncology Limited, Bengaluru, Karnataka, India.
Ramesh PatnamProchem Organics Private Limited, Telangana, India.
Rameshwar AmetaDepartment of Chemistry, Pacific Academy of Higher Education and Research University (PAHER), Udaipur, Rajasthan, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dasatinib (DAS) is a tyrosine kinase inhibitor used in the treatment of chronic myeloid leukemia (CML) and erythromycin (ERY) is macrolide antibiotic used to treat a range of inflammatory conditions are often co-administered in clinical practice. The simultaneous estimation of DAS and ERY helps in understanding the pharmacokinetics and drug-drug interactions. In this respect, we presented novel, sensitive, and validated bio-analytical LC-ESI-MS/MS method for simultaneous estimation of DAS and ERY in CD-1 mice plasma. The LLOQ was 2.0 ng/mL with an S/N ratio of 15. This validated method was used to study the PK of DAS and ERY in mice following intravenous and oral administration. The DAS was administered at 5 mg/kg via both oral and intraveneous route, whereas ERY was administered at 50 mg/kg orally and 5 mg/kg intraveneousaly. Following intravenous dosing, DAS showed high clearance and distribution, while ERY exhibited high clearance and distribution. The oral bioavailability was 64% for DAS and 21% for ERY. When co-administered orally at 5 mg/kg for DAS and 50 mg/kg of ERY, the AUC and C

Indexed as

DasatinibErythromycinLiquid Chromatography-Mass SpectrometryTandem Mass SpectrometryAdministration, OralAnimalsChromatography, LiquidLimit of DetectionLinear ModelsMaleMiceReproducibility of ResultsSensitivity and SpecificityDasatinibErythromycindasatiniberythromycinLC–MS/MSmethod validationmice plasmapharmacokinetics

Identifiers

PMID42430209
PMCPMC13353865

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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.