Results 181 to 190 of about 1,538 (221)
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Biowaiver Monograph for Immediate-Release Solid Oral Dosage Forms: Bisoprolol Fumarate
Journal of Pharmaceutical Sciences, 2014Literature data relevant to the decision to allow a waiver of in vivo bioequivalence (BE) testing for the approval of immediate-release (IR) solid oral dosage forms containing bisoprolol as the sole active pharmaceutical ingredient (API) are reviewed.
Charoo, NA +10 more
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Incompatibility of Bisoprolol Fumarate with Some Super-disintegrating Agents
British Journal of Pharmaceutical Research, 2015Aims: Bisoprolol fumarate, a selective β1adrenoreceptor blocker, is usually formulated as immediate release tablet dosage form. While developing the immediate release tablet formula in laboratory, the assay and dissolution results were found below acceptance limit in some formulation. The formulations differed only in disintegrating agents. Therefore a
Abu Shakar +4 more
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SIMULTANEOUS ESTIMATION OF IVABRADINE HCl AND BISOPROLOL FUMARATE BY UV-SPECTROSCOPIC METHOD
GLOBAL JOURNAL FOR RESEARCH ANALYSIS, 2022A simple UV spectrophotometric analytical method has been developed for simultaneous estimation of Ivabradine HCl and Bisoprolol used in the treatment of angina pectoris. Modied simultaneous equation method was developed with double beam UV-Visible spectrophotometer using water as a solvent.
Pushpak Pandit +5 more
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Monitoring of bisoprolol fumarate stability under different stress conditions
2017Stability studies of drugs by stress study is a very important process which is done by treating the study drug with different stress agents, with the aim to define the critical factors affecting the stability of the drug, to accurately define the storage conditions of the drug, as well as to identify the resulting degradation products.
Kasagić-Vujanović, Irena +2 more
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Degradation of Bisoprolol Fumarate in Tablets Formulated with Dicalcium Phosphate
Drug Development and Industrial Pharmacy, 1995Degradation of Bisoprolol Fumarate in tablet dosage forms was accelerated when granular Dicalcium Phosphate Anhydrous USP was substituted for milled Dicalcium Phosphate Anhydrous USP.
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Spectrophotometric method for estimation of bisoprolol fumarate in tablets.
Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi, 2014Bisoprolol fumarate is prescribed for the treatment of hypertension and angina pectoris.The purpose of this study was to develop a simple, sensitive, accurate, and reproducible method for estimation of bisoprolol fumarate in tablets.The proposed method was based on a yellow colored complex formed with tropaeolin 00, extractable in dichloromethane with ...
Alina Diana, Panainte +5 more
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Development and Evaluation of Bilayer Tablets of Bimodal release of Bisoprolol Fumarate
Research Journal of Pharmaceutical Dosage Forms and TechnologyBisoprolol is a type of antihypertensive drug (β-blocker). It is a poorly water-soluble and highly permeable drug that belongs to class II biopharmaceutical classification. This investigation represents the formulation development of bisoprolol to immediate and sustained the drug release.
Vinay R. Kothawade +2 more
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Preparation of bisoprolol fumarate nasal spray and its nasal delivery in rats.
Pakistan journal of pharmaceutical sciences, 2016The aim of the present work was to prepare a nasal spray of bisoprolol fumarate (BF). The Pharmacokinetics and relative bioavailability of the BF nasal formulation were evaluated in Wistar rats. The BF nasal spray after administration exhibited very fast absorption and higher plasma drug concentration.
Gu, Fugen +4 more
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Pakistan journal of pharmaceutical sciences, 2008
Two analytical methods have been developed for simultaneous quantification of bisoprolol fumarate and hydrochlorothiazide in combined pharmaceutical dosage form using spectrophotometer. Excellent simplicity, accuracy, precision and economy were achieved by the assay.
Shirkhedkar Atul, A +2 more
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Two analytical methods have been developed for simultaneous quantification of bisoprolol fumarate and hydrochlorothiazide in combined pharmaceutical dosage form using spectrophotometer. Excellent simplicity, accuracy, precision and economy were achieved by the assay.
Shirkhedkar Atul, A +2 more
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Current Computer-Aided Drug Design
Background: An important characteristic of the quality-by-design approach is defining risk, which is a combination of the probability of harm and its severity. During risk assessment, it is essential to determine how the formulation, properties of active ingredients and excipients, and process parameters can ...
Nadia Malanchuk +3 more
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Background: An important characteristic of the quality-by-design approach is defining risk, which is a combination of the probability of harm and its severity. During risk assessment, it is essential to determine how the formulation, properties of active ingredients and excipients, and process parameters can ...
Nadia Malanchuk +3 more
openaire +2 more sources