Development and validation of simple, rapid and sensitive LC-PDA ultraviolet method for quantification of Nebivolol in rat plasma and its application to pharmacokinetic studies
Author:
Publisher
Akademiai Kiado Zrt.
Subject
General Chemistry
Link
https://www.akademiai.com/doi/pdf/10.1556/achrom.27.2015.2.6
Reference25 articles.
1. Pharmacological and Hemodynamic Profile of Nebivolol,* a Chemically Novel, Potent, and Selective β1-Adrenergic Antagonist
2. β-blockers in the management of hypertension: focus on nebivolol
3. Nebivolol in the Management of Essential Hypertension
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1. Simple and Economical Uv-Spectrophotometric Method for Simultaneous Estimation of Chlorthalidone and Nebivolol in Combined Tablet Dosage Form: An Alternative Approach to the HPLC Method;Journal of Applied Spectroscopy;2024-01
2. Nanosized ethosomal dispersions for enhanced transdermal delivery of nebivolol using intradermal/transfollicular sustained reservoir: in vitro evaluation, confocal laser scanning microscopy, and in vivo pharmacokinetic studies;Pharmaceutical Development and Technology;2023-12-11
3. Formulation, characterization and in vivo evaluation of novel edible dosage form containing nebivolol HCl;Brazilian Journal of Pharmaceutical Sciences;2016-03
4. Stability-Indicating RP-UPLC Method Development and Validation for the Process Related Impurities of Nebivolol and Structural Characterization of Its Forced Degradation Products by LC-MS/MS;British Journal of Pharmaceutical Research;2016-01-10
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