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Cited by in F6Publishing
For: Manin A, Surov A, Churakov A, Perlovich G. Crystal Structures, Thermal Analysis, and Dissolution Behavior of New Solid Forms of the Antiviral Drug Arbidol with Dicarboxylic Acids. Crystals 2015;5:650-69. [DOI: 10.3390/cryst5040650] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 1.1] [Reference Citation Analysis]
Number Citing Articles
1 Li X, Wang X, Jiang Q, Chi F, Liu Q, Zhang T. The delivery of arbidol by salt engineering: synthesis, physicochemical properties and pharmacokinetics. Drug Dev Ind Pharm 2017;43:151-9. [PMID: 27533023 DOI: 10.1080/03639045.2016.1225755] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
2 Przybyłek M, Jeliński T, Słabuszewska J, Ziółkowska D, Mroczyńska K, Cysewski P. Application of Multivariate Adaptive Regression Splines (MARSplines) Methodology for Screening of Dicarboxylic Acid Cocrystal Using 1D and 2D Molecular Descriptors. Crystal Growth & Design 2019;19:3876-87. [DOI: 10.1021/acs.cgd.9b00318] [Cited by in Crossref: 12] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
3 Drozd KV, Manin AN, Voronin AP, Boycov DE, Churakov AV, Perlovich GL. A combined experimental and theoretical study of miconazole salts and cocrystals: crystal structures, DFT computations, formation thermodynamics and solubility improvement. Phys Chem Chem Phys 2021;23:12456-70. [PMID: 34037030 DOI: 10.1039/d1cp00956g] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Manin AN, Voronin AP, Drozd KV, Churakov AV, Perlovich GL. Pharmaceutical salts of emoxypine with dicarboxylic acids. Acta Crystallogr C Struct Chem 2018;74:797-806. [PMID: 29973419 DOI: 10.1107/S2053229618007386] [Cited by in Crossref: 6] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
5 Lu JZ, Ye D, Chen L, Ma BL. Pharmacokinetic comparison of four arbidol hydrochloride preparations in beagle dogs. Biomed Chromatogr 2022;36:e5245. [PMID: 34532879 DOI: 10.1002/bmc.5245] [Reference Citation Analysis]
6 Zhang C, Wen T, Jiang M, Xu Y, Wang H, Ouyang J, Xu J. Solid-liquid phase equilibrium, Hansen solubility parameters and thermodynamic behavior of Arbidol hydrochloride monohydrate in eleven mono-solvents. Journal of Molecular Liquids 2022;346:118300. [DOI: 10.1016/j.molliq.2021.118300] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
7 Wen T, Wang H, Li C, Xu J, Zhang C. Insight into the role of hydrochloric acid in the thermodynamics and nucleation kinetics behavior of Arbidol hydrochloride monohydrate from metastable zone widths. CrystEngComm 2022;24:389-403. [DOI: 10.1039/d1ce01426a] [Reference Citation Analysis]
8 Cysewski P, Przybyłek M. Selection of effective cocrystals former for dissolution rate improvement of active pharmaceutical ingredients based on lipoaffinity index. Eur J Pharm Sci 2017;107:87-96. [PMID: 28687528 DOI: 10.1016/j.ejps.2017.07.004] [Cited by in Crossref: 20] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]