Pharmaceutical development of a parenteral formulation of conivaptan hydrochloride

Analysis of particulate matter in liquid-finished dosage forms

J Duchek, B Havasi - PDA Journal of Pharmaceutical Science and …, 2018 - journal.pda.org
Pharmacopeias recognize particulate matter as a common phenomenon. The current
regulatory requirements relating to particulate matter in parenterals state that solutions for …
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Estimation and Correlation of Solubility of Practically Insoluble Drug Itraconazole in 1, 4-Butanediol+ Water Mixtures Using Extended Hildebrand Solubility Approach

SK Jagdale, RB Nawale - Journal of Pharmaceutical Innovation, 2020 - Springer
Abstract Purpose Extended Hildebrand solubility approach (EHSA) was applied to estimate
and correlate the solubilities of itraconazole in 1, 4-butanediol+ water mixtures at 298.15 K …
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Combination of the double log–log model with Abraham solvation parameters to predict solubility of drugs in ethanol+ water mixtures

M Barzegar-Jalali, A Shayanfar, S Yaqoubi… - Journal of Solution …, 2016 - Springer
Mathematical modeling of physicochemical properties such as solubility is an interesting
issue for drug discovery and development. Modeling and prediction of solubility in …
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13.20 PHARMACEUTICAL INDUSTRY

M Bauer, C Barthélémy - … of Solvents, Volume 2: Volume 2: Use …, 2019 - books.google.com
The manufacturing of a pharmaceutical drug is almost totally the responsibility of:• the
chemical industry for the preparation of the drug substance (active principle) and the …
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[CITATION][C] پیش بینی محلولیت داروها در مخلوط آب و کمک حلال با استفاده از مدل لگاریتمی مضاعف_ لگاریتمی و پارامترهای ساختمانی حل شونده‎

محمودلو, سودا‎ - دانشگاه علوم پزشکی تبریز، دانشکده …‎
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