Статті в журналах з теми "Pharmaceutical cocrystal systems"
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Mnguni, Malitsatsi J., Joseph P. Michael, and Andreas Lemmerer. "Binary polymorphic cocrystals: an update on the available literature in the Cambridge Structural Database, including a new polymorph of the pharmaceutical 1:1 cocrystal theophylline–3,4-dihydroxybenzoic acid." Acta Crystallographica Section C Structural Chemistry 74, no. 6 (May 23, 2018): 715–20. http://dx.doi.org/10.1107/s2053229618006861.
Повний текст джерелаLeng, Fucheng, Koen Robeyns, and Tom Leyssens. "Urea as a Cocrystal Former—Study of 3 Urea Based Pharmaceutical Cocrystals." Pharmaceutics 13, no. 5 (May 7, 2021): 671. http://dx.doi.org/10.3390/pharmaceutics13050671.
Повний текст джерелаBrittain, Harry G. "Cocrystal Systems of Pharmaceutical Interest: 2010." Crystal Growth & Design 12, no. 2 (January 5, 2012): 1046–54. http://dx.doi.org/10.1021/cg201510n.
Повний текст джерелаBrittain, Harry G. "Cocrystal Systems of Pharmaceutical Interest: 2011." Crystal Growth & Design 12, no. 11 (October 8, 2012): 5823–32. http://dx.doi.org/10.1021/cg301114f.
Повний текст джерелаRajput, Lalit, Manas Banik, Jayasubba Reddy Yarava, Sumy Joseph, Manoj Kumar Pandey, Yusuke Nishiyama, and Gautam R. Desiraju. "Exploring the salt–cocrystal continuum with solid-state NMR using natural-abundance samples: implications for crystal engineering." IUCrJ 4, no. 4 (June 5, 2017): 466–75. http://dx.doi.org/10.1107/s205225251700687x.
Повний текст джерелаWong, Si Nga, Susan Wing Sze Chan, Xuexin Peng, Bianfei Xuan, Hok Wai Lee, Henry H. Y. Tong, and Shing Fung Chow. "Effects of the Glass-Forming Ability and Annealing Conditions on Cocrystallization Behaviors via Rapid Solvent Removal: A Case Study of Voriconazole." Pharmaceutics 12, no. 12 (December 14, 2020): 1209. http://dx.doi.org/10.3390/pharmaceutics12121209.
Повний текст джерелаKaur, Navpreet, Naga Kiran Duggirala, Seema Thakral, and Raj Suryanarayanan. "Role of Lattice Disorder in Water-Mediated Dissociation of Pharmaceutical Cocrystal Systems." Molecular Pharmaceutics 16, no. 7 (May 22, 2019): 3167–77. http://dx.doi.org/10.1021/acs.molpharmaceut.9b00386.
Повний текст джерелаBordignon, Simone, Paolo Cerreia Vioglio, Elena Amadio, Federica Rossi, Emanuele Priola, Dario Voinovich, Roberto Gobetto, and Michele R. Chierotti. "Molecular Crystal Forms of Antitubercular Ethionamide with Dicarboxylic Acids: Solid-State Properties and a Combined Structural and Spectroscopic Study." Pharmaceutics 12, no. 9 (August 28, 2020): 818. http://dx.doi.org/10.3390/pharmaceutics12090818.
Повний текст джерелаBirolo, Rebecca, Federica Bravetti, Simone Bordignon, Ilenia D’Abbrunzo, Paolo P. Mazzeo, Beatrice Perissutti, Alessia Bacchi, Michele R. Chierotti, and Roberto Gobetto. "Overcoming the Drawbacks of Sulpiride by Means of New Crystal Forms." Pharmaceutics 14, no. 9 (August 23, 2022): 1754. http://dx.doi.org/10.3390/pharmaceutics14091754.
Повний текст джерелаPerlovich, German L. "Thermodynamic characteristics of cocrystal formation and melting points for rational design of pharmaceutical two-component systems." CrystEngComm 17, no. 37 (2015): 7019–28. http://dx.doi.org/10.1039/c5ce00992h.
Повний текст джерелаBaykov, Sergey V., Alexander S. Mikherdov, Alexander S. Novikov, Kirill K. Geyl, Marina V. Tarasenko, Maxim A. Gureev та Vadim P. Boyarskiy. "π–π Noncovalent Interaction Involving 1,2,4- and 1,3,4-Oxadiazole Systems: The Combined Experimental, Theoretical, and Database Study". Molecules 26, № 18 (18 вересня 2021): 5672. http://dx.doi.org/10.3390/molecules26185672.
Повний текст джерелаGerhardt, Valeska, and Michael Bolte. "6-Chloroisocytosine and 5-bromo-6-methylisocytosine: again, one or two tautomers present in the same crystal?" Acta Crystallographica Section C Structural Chemistry 72, no. 1 (January 1, 2016): 84–93. http://dx.doi.org/10.1107/s2053229615024080.
Повний текст джерелаKumari, Nimmy, and Animesh Ghosh. "Cocrystallization: Cutting Edge Tool for Physicochemical Modulation of Active Pharmaceutical Ingredients." Current Pharmaceutical Design 26, no. 38 (October 27, 2020): 4858–82. http://dx.doi.org/10.2174/1381612826666200720114638.
Повний текст джерелаTimofeeva, Tatiana, Sofia Antal, Sergiu Draguta, Karla Ordonez, Raul Castaneda, and Evgeniya Leonova. "Cocrystallization of acetaminophen and glutaric acid with different coformers." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C1028. http://dx.doi.org/10.1107/s2053273314089712.
Повний текст джерелаMikhailovskaya, Anastasiya Vital'yevna, Svetlana Anatol'yevna Myz, Konstantin Borisovich Gerasimov, Svetlana Alekseyevna Kuznetsova, and Tat'yana Petrovna Shakhtshneider. "SYNTHESIS OF COCRYSTALS OF BETULIN WITH SUBERIC ACID AND STUDY OF THEIR PROPERTIES." chemistry of plant raw material, no. 4 (December 14, 2021): 183–92. http://dx.doi.org/10.14258/jcprm.2021049736.
Повний текст джерелаPalanisamy, Vasanthi, Palash Sanphui, Muthuramalingam Prakash, and Vladimir Chernyshev. "Multicomponent solid forms of the uric acid reabsorption inhibitor lesinurad and cocrystal polymorphs with urea: DFT simulation and solubility study." Acta Crystallographica Section C Structural Chemistry 75, no. 8 (July 9, 2019): 1102–17. http://dx.doi.org/10.1107/s2053229619008829.
Повний текст джерелаLloyd, Hayleigh, Colin Pulham, Paul Coster, Craig Henderson, David Williamson, and Andy Jardine. "Energetic Cocrystals – Structural Studies of Nitrotriazolone Salts & Cocrystals." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C1012. http://dx.doi.org/10.1107/s2053273314089876.
Повний текст джерелаBerry, David J., and Jonathan W. Steed. "Pharmaceutical cocrystals, salts and multicomponent systems; intermolecular interactions and property based design." Advanced Drug Delivery Reviews 117 (August 2017): 3–24. http://dx.doi.org/10.1016/j.addr.2017.03.003.
Повний текст джерелаSanphui, Palash, Lalit Rajput, Shanmukha Prasad Gopi, and Gautam R. Desiraju. "New multi-component solid forms of anti-cancer drug Erlotinib: role of auxiliary interactions in determining a preferred conformation." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 72, no. 3 (May 13, 2016): 291–300. http://dx.doi.org/10.1107/s2052520616003607.
Повний текст джерелаDutt, Braham, Manjusha Choudhary, and Vikas Budhwar. "A Comparative Study of Selected Drug Delivery Systems: Key Emphasis on Cocrystallization." Drug Delivery Letters 11, no. 2 (June 28, 2021): 136–55. http://dx.doi.org/10.2174/2210303111666210111142458.
Повний текст джерелаAljohani, Marwah, Pól MacFhionnghaile, Patrick McArdle, and Andrea Erxleben. "Investigation of the formation of drug-drug cocrystals and coamorphous systems of the antidiabetic drug gliclazide." International Journal of Pharmaceutics 561 (April 2019): 35–42. http://dx.doi.org/10.1016/j.ijpharm.2019.02.024.
Повний текст джерелаLopez-Toledano, Miguel A., Vaibhav Saxena, Jason D. Legassie, Haiyang Liu, Ajay Ghanta, Stephen Riseman, Courtney Cocilova, et al. "Advanced Lipid Technologies® (ALT®): A Proven Formulation Platform to Enhance the Bioavailability of Lipophilic Compounds." Journal of Drug Delivery 2019 (July 8, 2019): 1–10. http://dx.doi.org/10.1155/2019/1957360.
Повний текст джерелаSutar, Yogesh, Tejabhiram Yadavalli, Sagar Kumar Paul, Sudipta Mallick, Raghuram Koganti, Harsh Chauhan, Abhijit A. Date, and Deepak Shukla. "BX795-Organic Acid Coevaporates: Evaluation of Solid-State Characteristics, In Vitro Cytocompatibility and In Vitro Activity against HSV-1 and HSV-2." Pharmaceutics 13, no. 11 (November 12, 2021): 1920. http://dx.doi.org/10.3390/pharmaceutics13111920.
Повний текст джерелаVener, Mikhail V., Denis E. Makhrov, Alexander P. Voronin, and Daria R. Shalafan. "Molecular Dynamics Simulation of Association Processes in Aqueous Solutions of Maleate Salts of Drug-Like Compounds: The Role of Counterion." International Journal of Molecular Sciences 23, no. 11 (June 4, 2022): 6302. http://dx.doi.org/10.3390/ijms23116302.
Повний текст джерелаVaghela, Sohansinh, Sunita Chaudhary, and Ankit Chaudhary. "A Systemic Review on the Self Micro Emulsifying Drug Delivery System." International Journal of Pharmaceutical Sciences Review and Research 69, no. 1 (July 15, 2021). http://dx.doi.org/10.47583/ijpsrr.2021.v69i01.027.
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