Evidence map›Paper›PMID 38948504›Full record

ArticleF1000Research2023

A stability indicating method development and validation of a rapid and sensitive RP-HPLC method for Nintedanib and its application in quantification of nanostructured lipid carriers.

Varalakshmi Velagacherla, Yogendra Nayak, K Vijaya Bhaskar, Usha Yogendra Nayak

Abstract readValidation Study
In one paragraph

Article in F1000Research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Varalakshmi VelagacherlaDepartment of Pharmaceutics, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.
Yogendra NayakDepartment of Pharmacology, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.ORCID https://orcid.org/0000-0002-0508-1394
K Vijaya BhaskarDepartment of Pharmaceutical Chemistry, Manipal College of Pharmaceutical Science, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.
Usha Yogendra NayakDepartment of Pharmaceutics, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.ORCID https://orcid.org/0000-0002-1995-3114

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Nintedanib (NTB) is a multiple tyrosine kinase inhibitor, been investigated for many disease conditions like idiopathic pulmonary fibrosis (IPF), systemic sclerosis interstitial lung disease (SSc-ILD) and non-small cell lung cancer (NSCLC). NTB is available as oral capsule formulation, but its ability to detect degradants formed through oxidative, photolytic and hydrolytic processes makes it difficult to quantify. In the current work, a novel reversed-phase high-performance liquid chromatography (RP-HPLC) method was developed and validated. Methods: The developed method is simple, precise, reproducible, stable and accurate. The inherent stability of NTB was evaluated using the proposed analytical method approach and force degradation studies were carried out. NTB was separated chromatographically on the Shimadzu C Results: NTB was eluted at 6.77±0.00 min of retention time (t Conclusion: The formulation excipients didn't interfere with the determination of NTB, demonstrating the specificity of the developed method. The proposed approach of the analytical method developed can be used to quantify the amount of NTB present in bulk drugs and pharmaceutical formulations.

Indexed as

Chromatography, Reverse-PhaseIndolesLipidsChromatography, High Pressure LiquidDrug CarriersDrug StabilityNanostructuresReproducibility of ResultsDrug CarriersIndolesLipidsnintedanibEntrapment efficiencyNanostructured lipid carriersNintedanibRP-HPLCStress degradationValidation

Identifiers

PMID38948504
PMCPMC11214665

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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.