In vitro release studies of furosemide reference tablets: influence of agitation rate, USP apparatus and dissolution media [PDF]
, 2020 Furosemide is a diuretic drug widely used in chronic renal failure. The drug has low solubility and permeability, which cause clinical problems. Studying the in vitro release performance elucidates the rate and extent of drug dissolved from dosage forms ...
Marcela Hurtado +2 more
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Биопрепараты: Профилактика, диагностика, лечениеINTRODUCTION. The advancement of manufacturing technologies and the expanding range of biological medicinal products (BMPs) and indications for their use necessitate the development of a unified approach to BMP standardisation at both national and ...
O. G. Kornilova, V. L. Bagirova
doaj +1 more source
Future Journal of Pharmaceutical Sciences, 2023 Background Microbes’ resistance to orthodox drugs and continued emergence of new infections call for search of new drugs that can mitigate such resistance and cure newly emerging infections.
Mubo A. Sonibare +2 more
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Valacyclovir: A Comparative Analysis of Pharmacopoeial Quality Requirements
Регуляторные исследования и экспертиза лекарственных средствINTRODUCTION. Lack of national requirements regulating the quality of valacyclovir hydrochloride active pharmaceutical ingredient (API) in hydrated form and valacyclovir medicinal products may be challenging not only for manufacturers, but also for ...
K. S. Arhipova +3 more
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Modern approaches to drafting general and individual monographs on human blood products
Регуляторные исследования и экспертиза лекарственных средств, 2018 Blood products were first represented in the State Pharmacopoeia of the USSR IX and X editions (1961 and 1968) by a single monograph "Gamma globulin for the prevention of measles".
A. V. Karyakin +5 more
doaj
Oxcarbazepine: validation and application of an analytical method
Brazilian Journal of Pharmaceutical Sciences, 2010 Oxcarbazepine (OXC) is an important anticonvulsant and mood stabilizing drug. A pharmacopoeial monograph for OXC is not yet available and therefore the development and validation of a new analytical method for quantification of this drug is essential. In
Paula Cristina Rezende Enéas +2 more
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A VALIDATED STABILITY INDICATING RP-HPLC METHOD FOR ESTIMATION OF TOLFENAMIC ACID IN PRESENCE OF ITS PHARMACOPOEIAL IMPURITIES [PDF]
, 2019 Objective: The proposed research work was conducted to develop a single reverse-phase high-performance chromatography (RP-HPLC) method capable of separating two Pharmacopoeial related impurities as well as degradation product of Tolfenamic acid (TA). The
FERNANDES, ADISON, P. N., SANJAY PAI
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Анатомо-морфологическое исследование корневищ и корней родиолы розовой [PDF]
, 2015 родиола розоваяРОДИОЛАзолотой кореньRhodiola rosea L.ЛЕКАРСТВЕННЫЕ РАСТЕНИЯРАСТЕНИЯ ...
Куркин, В. А. +1 more
core
Comprehensive HPTLC fingerprinting as a tool for a simplified analysis of purity of ginkgo products [PDF]
, 2019 Ethnopharmacological relevance: Herbal medicinal products based on ginkgo leaf refined dry extract (GBE) are an European development from the Eastern Asia traditionally used species Ginkgo biloba L.
Booker, A. +11 more
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VALIDATION OF THE SPECTROPHOTOMETRIC PROCEDURE FOR DESLORATADINE ASSAY IN TABLETS APPLYING THE UNCERTAINTY CONCEPT OF THE STATE PHARMACOPOEIA OF UKRAINE [PDF]
, 2020 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 ...
Gryzodub, Oleksandr +3 more
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