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Artem O. Surov

Researcher at Russian Academy of Sciences

Publications -  61
Citations -  1119

Artem O. Surov is an academic researcher from Russian Academy of Sciences. The author has contributed to research in topics: Solubility & Cocrystal. The author has an hindex of 17, co-authored 52 publications receiving 766 citations. Previous affiliations of Artem O. Surov include University of Southern Denmark & Ivanovo State University.

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Pharmaceutical Cocrystals of Diflunisal and Diclofenac with Theophylline

TL;DR: Crystal lattice energy calculations showed that the packing energy gain of the [DIC + THP] cocrystal is derived mainly from the dispersion energy, which dominates the structures of the cocrystals.
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Pharmaceutical salts of ciprofloxacin with dicarboxylic acids

TL;DR: New salts of antibiotic drug ciprofloxacin with pharmaceutically acceptable maleic (Mlt), fumaric (Fum) and adipic (Adp) acids were obtained and their crystal structures were determined.
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Crystallization and Polymorphism of Felodipine

TL;DR: Two previously known polymorphs (forms I and II) and two new polymorphs(forms III and IV) of the calcium-channel blocker felodipine were obtained during attempts to cocrystallize the compound with a variety of potential cocrystal formers as mentioned in this paper.
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Thermodynamic and Structural Aspects of Some Fenamate Molecular Crystals

TL;DR: In this article, the properties of the crystal lattices and the hydrogen bond networks of nonsteroidal anti-inflammatory drugs (Diclofenac, niflumic, flufenamic, tolfenamic and mefenamic acid) and structural relative compounds (N-phenylanthranilic acid and diphenylamine) were compared.
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γ-Cyclodextrin-metal organic frameworks as efficient microcontainers for encapsulation of leflunomide and acceleration of its transformation into teriflunomide

TL;DR: It was demonstrated that teriflunomide released from γCD-MOF has improved pharmacologically relevant properties such as solubility, dissolution rate and membrane permeability and it can be proposed that γ CD- MOF can be considered as novel strategy for delivery of leflunomid.