Диссертация (1154377), страница 38
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doi: 10.1208/s12249-017-0759-4.185. Liem-Nguyen, V. Thermodynamic Modeling of the Solubility andChemical Speciation of Mercury and Methylmercury Driven by Organic Thiols andMicromolar Sulfide Concentrations in Borea Wetland Soils / L.-N.V. Liem-Nguyen,S.U. Björn // Environ Sci Technol. ‒ 2017. ‒ V. 51(7). ‒ P. 3678-3686. doi:10.1021/acs.est.6b04622.187. Shakeel, F. Solubility and thermodynamics of apremilast in differentmono solvents: Determination, correlation and molecular interactions / F.
Shakeel,N. Haq, F.K. Alanazi, I.A. Alsarra // Int J Pharm. ‒ 2017. ‒ V. 523(1) ‒ P. 410-417.188. Bharate, S.S. Thermodynamic equilibrium solubility measurements insimulated fluids by 96-well plate method in early drug discovery / S.S. Bharate,R.A. Vishwakarma // Bioorg Med Chem Lett.
‒ 2015.‒V. 25(7). P. 1561-7. doi:10.1016/j.bmcl.2015.02. 013.189. Wenlock, M.C. A highly automated assay for determining the aqueousequilibrium solubility of drug discovery compounds / M.C.Wenlock, R.P. Austin, T.Potter, P. Barton // J Lab Autom. ‒ 2011. ‒ V.‒ 16(4). P. 276-284.
doi:10.1016/j.jala.2010.10.002.190. Heikkilä, T. Equilibrium drug solubility measurements in 96-well platesreveal similar drug solubilities in phosphate buffer pH 6.8 and human intestinal fluid/ T. Heikkilä, M. Karjalainen, K. Ojala, K. Partola, F. Lammert, P. Augustijns, A.Urtti, M. Yliperttula, L .Peltonen, Т. Hirvonen // J.Int J Pharm.‒ 2011. ‒V. 405. ‒ P.2-6. doi: 10.1016/j.ijpharm.2010.12.007.191. Baka, E. Study of equilibrium solubility measurement by saturationshake-flask method using hydrochlorothiazide as model compound / E. Baka, J.E.Comer, K. Takács-Novák // Acta Pharm Hung.
‒ 2011. ‒ V.81(1).‒ Р. 18-28.288192. Zhou, L. Development of a high throughput equilibrium solubility assayusing miniaturized shake-flask method in early drug discovery / L. Zhou, L. Yang,S. Tilton, J.Wang // J Pharm Sci. ‒ 2007. ‒ V. 96(11). ‒ P.3052-3071.193. Völgyi, G.
Study of pH-dependent solubility of organic bases. Revisit ofHenderson-Hasselbalch relationship / G. Völgyi, E. Baka, K.J. Box, J.E. Comer, K.Takács-Novák // Anal Chim Acta. ‒ 2010. ‒ V. 673(1). ‒ Р.40-46. doi:10.1016/j.aca.2010.05.022.194. Avdeef, A. pH-metric solubility. Dissolution titration template method forsolubility determination / A. Avdeef, C.M . Berger // Eur J Pharm Sci. ‒ 2001. ‒ V.14(4).‒ P.281-291.195. Avdeef, A. pH-metric solubility. 2: correlation between the acid-basetitration and the saturation shake-flask solubility-pH methods / A.
Avdeef, C.M.Berger, C. Brownell. // Pharm Res.‒ 2000. ‒ V. 17(1). ‒ P. ‒ 85-89.196. Takács-Novák, K. Equilibrium solubility measurement of compoundswith low dissolution rate by Higuchi's Facilitated Dissolution Method. A validationstudy / K. Takács-Novák, M. Urac, P. Horváth, G. Völgyi, B.D. Anderson, A.Avdeef // Eur J Pharm Sci.
‒ 2017. ‒ V. 106. P. 133-141. doi:10.1016/j.ejps.2017.05.064.197. Varelas, C.G. Zero-order release from biphasic polymer hydrogels /C.G.Varelas, D.G. Dixon, C. Steiner // J. Control. Release. – 1995. – Vol. 34. – P.185-192.198. Bevan, C.D. A high-throughput screening method for the determination ofaqueous drug solubility using laser nephelometry in microtiter plates / C.D. Bevan,R.S. Lloyd // Anal.
Chem. – 2000. – Vol. 72. – № 8. – P. 1781-1787.199. Comparison of Nephelometric, UV-Spectroscopic, and HPLC Methodsfor High-Throughput Determination of Aqueous Drug Solubility in Microtiter Plates/ B. Hoelke, S.Gieringer, M. Arlt, C.Saal // Anal. Chem. – 2009. – Vol. 81. – № 8.– P. 3165-3172.200. Mannhold, R. Molecular Drug Properties. Measurements and prediction/R. Mannhold, H. Kubiniy, G. Folkers // Edited by R. Mannhold. – 2008. – 502 p.289201. Dokoumetzidis, A.
A century of dissolution research: From Noyes andWhitney to the Biopharmaceutics Classification System / A. Dokoumetzidis, P.Macheras // Int. J. Pharm. – 2006. – Vol. 321. – P. 1–11.202. Bruner, L. Über die Auflösungsgeschwindigkeit fester Körper / L. Bruner,S. Tolloczko // Zeitschrift für anorganische und allgemeine Chemie. – 1901. – Vol.28. – I. 1 ‒P. 283–290.203. Mayock, S.P. In Vitro Drug Release After Crushing: Evaluation ofXtampza® ER and Other ER Opioid Formulations / S.P.
Mayock, S. Saim, A.B.Fleming // Clin Drug Investig. – 2017.− V. 37. ‒ I. 12. ‒ P. 1117-1124.204. Singhvi, G. Review: in-vitro drug release characterization models / G.Singhvi, M. Singh // Int J Pharm Studies and Research. – 2011. – V. 2. – № 1. – Р.77-84.205. Wang, Y.Comparison and Analysis of Theoretical Models for DiffusionControlled Dissolution / Y.Wang, B. Abrahamsson, L. Lindfors, J.
G. Brasseur //Mol Pharmaceutics. – 2012. – V. 9. – P. 1052-1066.206. Faruk, Md. A. Basic Biopharmaceutics / Md. Al- Faruk // DaffodilInternational University. – 2013. –197. P.207. Miyamoto, S. A theory of the rate of solution of solid into liquid / S.Miyamoto // Trans. Faraday Soc.
– 1933. – Vol. 29. – P. 789-794.208. Khan, W. An extension of Danckwerts theoretical surface renewal modelto mass transfer at contaminated turbulent interfaces / W. Khan // Math.Comput.Modelling. – 1990. – V. 14. – P. 750-754.209. Singhvi, G. Review: in-vitro drug release characterization models / G.Singhvi, M. Singh // Int J Pharm Studies and Research.
– 2011. – Vol. 2. – № 1. – Р.77-84.210. Kumar, A. Self Emulsifying Drug Delivery System (SEDDS): FutureAspects / A. Kumar, S. Sharma, R. Kamble // International Journal of Pharmacyand Pharmaceutical Sciences. – 2010. – Vol. 2. – № 4. – Р. 7–13.211. Халиков, С.С. Способы увеличения растворимости лекарственныхвеществ: принципы, технологии, свойства / С.С. Халиков, Архипов И.А. //290Теория и практика борьбы с паразитарными болезнями.
– 2017. –№ 18. – С.513-516.212. Краснюк, И.И. Повышение биодоступности лекарственных форм сприменением твёрдых дисперсий: автореф. дисс. д. фарм. н.: 14.04.01, 14.04.02/ Краснюк Иван Иванович. – М.-2010. – 48 с.213. Sinn, A.M. Non-eroding drug-releasing implants with ordered nanoporousand nanotubular structures: concepts for controlling drug release / A.M. Sinn, M.Kurian, D.Losic // Biomater. Sci. – 2014.Vol. 2.– № 10. – Р. 10-34.214. Zhu, Y. In Vitro Release and Bioavailability of Silybin from MicelleTemplated Porous Calcium Phosphate Microparticles / Y.
Zhu, M. Wang, Y. Zhang,J. Zeng, E. Omari-Siaw, J.Yu, X. Xu // AAPS PharmSciTech. – 2016. – Vol. 17. –№ 5. – Р. 1232-1239.215. Savjani, K.T. Drug Solubility: Importance and Enhancement Techniques /K.T. Savjani, A.K. Gajjar, J.K. Savjani // ISRN Pharm. – 2012. –Vol.− 2012.− 10 p.216. Yang C., Use of the co-grinding method to enhance the dissolutionbehavior of a poorly water-soluble drug: generation of solvent-free drug-polymersolid dispersions / C.
Yang, X. Xu, J. Wang, Z. An // Chem Pharm Bull. – 2012. –Vol. 60. – № 7. – Р. 837-845.217. Ye. F. Effect of micronization on the physicochemical properties ofinsoluble dietary fiber from citrus (Citrus junos Sieb. ex Tanaka) pomace / F. Ye, B.Tao, J. Liu, Y. Zou, G.
Zhao // Food Sci Technol Int. – 2016. – Vol. 22. – № 3. – Р.246-255.218. Shcherbachenko, L.A. Аccumulation of free electret charges in smallsizedelectrically active systems / L.A. Shcherbachenko, Sh. B. Tsydypov, Ya. V.Bezrukova, V. A. Karnakov, L. I. Arskaya, S. D. Marchuk, D. O. Chernykh, V. A.Zhovnitskii // Russian Physics Journal. – 2017. –Vol. 60. – №1.– Р.109–114.219.Перлович,Г.Л.Улучшениерастворимостилекарственныхсоединений с использованием сокристальной технологии / Г.Л. Перлович //Сборник материалов IV всероссийской научно-практической конференции смеждународным участием «инновации в здоровье нации .
– 2016. – С. 476-479.291220. Leleux, J. Recent advancements in mechanical reduction methods:particulate systems / J. Leleux // Drug Dev Ind Pharm. – 2014.− V. − 40(3). – Р.289-300.221. Sowunmi, A. Bioavailability of sulphate and dihydrochloride salts ofquinine / A. Sowunmi, L.A. Salako, F.A. Ogunbona // Afr J Med Med Sci. ‒ 1994. ‒V. 23. ‒№3. ‒ Р. 275-278.222. Болдырев, В.В. Механохимия и механическая активации твердыхвеществ / В.В. Болдырев // Успехи химии. ‒ 2006. ‒ Т. 75. ‒ №3.
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