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1.079  Articles
1 of 109 pages  |  10  records  |  more records»
This study aims to analyze and identify the arrangements related to the merger and dissolution of foundations based on Law no. 16 of 2001 jo. UU no. 28 of 2004 concerning Foundations and regarding the classification and mechanism for the merger and dissol... see more

Cocrystallization of mefenamic acid (AM) with para-aminobenzoic acid (PABA) as a coformer has been carried out using the liquid-assisted grinding method. This study aims to determine whether mefenamic acid can be increased its dissolution rate through the... see more

This research formulates several problems, namely: 1) why do reasons and applicants for the dissolution of political party in Indonesia need to be extended in the request?, 2) how is the ius constituendum of the stage of the application for the dissolutio... see more

Since there are conflicting reports in the literature on solubility and dissolution advantages of cocrystals over free forms, we systematically studied solubility and intrinsic dissolution rates of a weakly basic drug, ketoconazole, and its cocrystals wit... see more

In vitro dissolution/release tests are an indispensable tool in the drug product development, its quality control and the regulatory approval process. Mucosal drug delivery systems are designed to provide both local and systemic drug action following ocul... see more

The choice of an appropriate medium for dissolution tests is an essential step during a dosage form development. The adequate design of dissolution testing enables forecasting in vivo behavior of drug formulation. Biorelevant media were developed for this... see more

Diclofenac sodium is included in the class II category based on the biopharmaceutics classification system (BCS), sodium diclofenac has low solubility and high permeability. Low solubility will affect the absorption of drugs in the body because the rate o... see more

A mathematical model to predict the dissolution of salt particles suspended in a brine flow is provided. The model consists of a system of three partial differential equations (PDE) based on mass conservation of salt dissolved in the fluid phase, on mass ... see more

In drug release kinetics, the drug-matrix interaction is one of the important mechanisms to be dictated. Unfortunately, there is still minimum information discussing the effect of interaction between a drug and its matrix to the release profile of the dru... see more

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