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Relevant bibliographies by topics / Desloratadine tablets

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Journal articles

Academic literature on the topic 'Desloratadine tablets'

Author: Grafiati

Published: 4 June 2025

Last updated: 15 July 2025

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Journal articles on the topic "Desloratadine tablets"

1

Tamader, Elghnimi1* Wadiaa Benamer2 Rehab Walli3 Mawadda Benshaban1 Marwa Benashour1. "Comparative in-vitro Evaluation of Some Desloratadine Tablets Marketed in Tripoli Libya." Alq J Med App Sci 5, no. 2 (2022): 556–64. https://doi.org/10.5281/zenodo.7391018.

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<strong>Background and aims.</strong> Desloratadine is a tricyclic, potent, rapidly effective, long acting, non-sedative antihistamine, which has a selective and peripheral H1 receptor antagonist action, used to treat the allergies. The availability of several brands of Desloratadine tablets in Libyan pharmacies today places health practitioners and a pharmacist in a problem of drug substitution in case of a particular brand is not available. The aim of the present study was the evaluation and comparison of pharmaceutical equivalence of five different Desloratadine tablets 5 mg, which are comm

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2

Rummana Amin, Sabana,, Brishti, Shadia Afrin, Hossain Nazmul, and Rahman, Mohammed Shafikur. "In-Vitro Evaluation of Different Brands of Desloratadine Tablets Available in Bangladeshi market." DIU Journal of Health and Life Sciences 3, no. 1 & 2 (2016): 05–11. http://dx.doi.org/10.36481/diuhls.v03i1-2.9zdn3e56.

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Desloratadine, a long acting antihistamine with high selectivity for peripheral histamine H1- receptors has a rapid onset of action and a duration of action of 24-hours. Due to difference in the formulation process for different brands different physicochemical properties may vary which ultimately leads to change in the efficacy and duration of action of the drug when given orally. The aim of this study was to analyze the quality and stability of desloratadine 5mg tablet by evaluating various in-vitro parameters. For this purpose, five different brands from different pharmaceutical companies o

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3

Sabana, Rummana Amin, Shadia Afrin Brishti, Nazmul Hossain, and Mohammed Shafikur Rahman. "In-Vitro Evaluation of Different Brands of Desloratadine Tablets Available in Bangladeshi market." DIU Journal of Allied Health Sciences 3, no. 1 & 2 (2016): 05–11. https://doi.org/10.36481/diujahs.v03i1-2.9zdn3e56.

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Desloratadine, a long acting antihistamine with high selectivity for peripheral histamine H1- receptors has a rapid onset of action and a duration of action of 24-hours. Due to difference in the formulation process for different brands different physicochemical properties may vary which ultimately leads to change in the efficacy and duration of action of the drug when given orally. The aim of this study was to analyze the quality and stability of desloratadine 5mg tablet by evaluating various in-vitro parameters. For this purpose, five different brands from different pharmaceutical companies o

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4

Rummana, Amin Sabana, Afrin Brishti Shadia, Hossain Nazmul, and Shafikur Rahman Mohammed. "In-Vitro Evaluation of Different Brands of Desloratadine Tablets Available in Bangladeshi Market." Journal of Allied Health and Life Sciences 3, no. 1&2 (2016): 5–11. https://doi.org/10.5281/zenodo.11001391.

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Abstract: Desloratadine, a long acting antihistamine with high selectivity for peripheral histamine H1- receptors has a rapid onset of action and a duration of action of 24-hours. Due to difference in the formulation process for different brands different physicochemical properties may vary which ultimately leads to change in the efficacy and duration of action of the drug when given orally. The aim of this study was to analyze the quality and stability of desloratadine 5mg tablet by evaluating various in-vitro parameters. For this purpose, five different brands from different pharmaceutical c

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5

Berginc, Katja, Nadica Sibinovska, Simon Žakelj, Jurij Trontelj, and Igor Legen. "Biopharmaceutical classification of desloratadine – not all drugs are classified the easy way." Acta Pharmaceutica 70, no. 2 (2020): 131–44. http://dx.doi.org/10.2478/acph-2020-0006.

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AbstractThe biopharmaceutical classification of drugs was designed as a basis for bio-waivers – a mechanism with the double ethical benefit of delivering new drug formulations to the market with less human testing and lower cost. However, many drugs defy simple classification because in vitro permeability and stability assessment can be challenging as shown in this study for desloratadine. Literature shows that desloratadine is highly soluble, while data on luminal stability and permeability are circumstantial. Combined with borderline bioavailability and not really known fraction of absorbed

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6

Abbas, Muhammad, Musharraf Abbas, Fatima Tariq, Rabiya Yasin, and Muhammad Nabeel. "Formulation and evaluation of chewable tablets of Desloratadine prepared by aqueous and non-aqueous techniques." Journal of Drug Delivery and Therapeutics 10, no. 1 (2020): 5–10. http://dx.doi.org/10.22270/jddt.v10i1.3796.

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In the modern era, chewable tablets are preferred over conventional dosage forms by pediatric, geriatric and bedridden patients due to difficulty in swallowing, lesser amount of water for swallowing medications as well as unable to tolerate the bitter taste of certain drugs. Chewable tablets of Desloratadine (DS) were formulated by aqueous and non-aqueous granulation method using water paste and Isopropyl alcohol (IPA) as a wetting agents respectively. Desloratadine is used to treat the symptoms of allergy such as sneezing, watery eyes. In the recent research, we have formulated eight trials b

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7

Leontiev, Dmytro, Vasyl Petrus, Natalia Volovyk, and Oleksandr Gryzodub. "VALIDATION OF THE SPECTROPHOTOMETRIC PROCEDURE FOR DESLORATADINE ASSAY IN TABLETS APPLYING THE UNCERTAINTY CONCEPT OF THE STATE PHARMACOPOEIA OF UKRAINE." EUREKA: Health Sciences, no. 6 (November 29, 2020): 74–87. http://dx.doi.org/10.21303/2504-5679.2020.001527.

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Aim. This work aimed to validate an assay procedure for desloratadine tablets by direct spectrophotometric method. Materials and methods. A pilot-scale batch of the pharmaceutical preparation Alerdez, film-coated tablets containing 5 mg of desloratadine, manufactured by PJSC SIC “Borshchahivskiy CPP”, Ukraine, was used as an object of the study. A UV-Vis spectrophotometer Lambda 25 (Perkin Elmer), analytical balance Mettler Toledo XP 205DR, and class A volumetric apparatus were used in the study. Validation of the procedure was performed following the metrological approach of the State P

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8

Çğalar, Sena, and Aysel Öztun. "A Sensitive Spectrophotometric Method for the Determination of Desloratadine in Tablets." Journal of AOAC INTERNATIONAL 90, no. 2 (2007): 372–75. http://dx.doi.org/10.1093/jaoac/90.2.372.

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Abstract A simple, rapid, and sensitive visible spectrophotometric method was developed, for the first time, for analysis of desloratadine (DE) in tablets. The method is based on the deep-blue colored TCNQ- radical anion formed by interaction of the drug (n-donor) with 7,7,8,8-tetracyanoquinodimethane (TCNQ, π-acceptor) in acetonitrile at ambient temperature. Optimum conditions for the reaction were investigated, absorbances were read at 843 nm, and the linearity range for concentrations of DE was found to be 1.5-13 μg/mL. The reaction product remains stable up to 8 h when kept at room tempera

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9

Dmytro, Leontiev, Petrus Vasyl, Volovyk Natalia, and Gryzodub Oleksandr. "VALIDATION OF THE SPECTROPHOTOMETRIC PROCEDURE FOR DESLORATADINE ASSAY IN TABLETS APPLYING THE UNCERTAINTY CONCEPT OF THE STATE PHARMACOPOEIA OF UKRAINE." EUREKA: Health Sciences, no. 6 (November 30, 2020): 74–87. https://doi.org/10.21303/2504-5679.2020.001527.

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<strong>Aim</strong>. This work aimed to validate an assay procedure for desloratadine tablets by direct spectrophotometric method. <strong>Materials and methods</strong>. A pilot-scale batch of the pharmaceutical preparation <em>Alerdez</em>, film-coated tablets containing 5 mg of desloratadine, manufactured by PJSC SIC “Borshchahivskiy CPP”, Ukraine, was used as an object of the study. A UV-Vis spectrophotometer Lambda 25 (Perkin Elmer), analytical balance Mettler Toledo XP 205DR, and class A volumetric apparatus were used in the study. Validation of the procedure was perfor

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10

Dmytro, Leontiev, Petrus Vasyl, Volovyk Natalia, and Gryzodub Oleksandr. "A study of the influence of the test sample inhomogeneity on variability in assay results of desloratadine in film-coated tablets." ScienceRise: Pharmaceutical Science, no. 5(27) (October 30, 2020): 43–51. https://doi.org/10.15587/2519-4852.2020.215287.

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<strong>Aim</strong>. The work aimed at metrological evaluation and management of the risk of inconsistency in the results of desloratadine assay in film-coated tablets. <strong>Materials and methods</strong>. A pilot-scale batch of the pharmaceutical preparation Alerdez served as a study object. Spectrophotometric readings were performed on a UV-Vis spectrophotometer Lambda 25 at 282 nm. An analytical balance Mettler Toledo, pH-meter Metrohm, Class A volumetric pipettes and flasks were used for analysis. The test sample was prepared by manual tablet grinding. <strong>Results and discussion</s

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