Диссертация (1154377), страница 43
Текст из файла (страница 43)
‒ №1. ‒С. 143-138.376. Titorovich, O.V. Influence of deuterium depleted water on biologicalactivity/toxicity components of pharmaceuticals / O.V. Titorovich, M.A. Morozova,T. V. Maksimova, T. V. Pleteneva // 3rd International Congress on DeuteriumDepletion. − Budapest, 2015.
– P. 8.377. Goncharuk, V.V. Physicochemical Properties and biological activity ofthe water depleted of heavy isotopes / V.V. Goncharuk, V.B. Lapshin, T.N.Burdeinaya, T.V. Pleteneva, A.S. hernopyatko, I.D. Atamanenko, A.S. Ul’yantsev,E.V. spenskaya, A.O.
Sаmsoni-Todorov, V.V. Taranov, G.M. Nikolaev, A.A.Kavitskaya,I.Yu.Romanyukina,R.V.Prikhod’ko,E.A.Orekhova,V.A.Yaremenko, A.S.Kotel’chuk, A.V. Syroeshkin // Chemistry and Technology ofWater.− 2011. − 33(1) − Р.15−25.378. Avila, D.S. Antiaging effects of deuterium depletion on Mn-inducedtoxicity in a C.elegans model / D.S.Avila, G.
Somlyai, I. Somlyai, M. Aschner //Toxicology Letters. – 2012. – 211. – Р. 319−324.379. Doina, P.M. The effect of deuterium depleted water on some hepaticenzimes’ activity in rats intoxicated with chromium (VI) / P.M. Doina, V. Olariu,311M. Scurtu, C. Tulcan, I. Brudiu, D. Muntean, F. Petcu, I. Pădeanu, M. Ostan, A.U.din Oradea // Ecotoxicologie, Zootehnieşi Tehnologii de Industrie Alimentară. –2012. − XI/B (11).
− 521−526.380. Burdeinaya, T.N. Combined toxicity of Na2EDTA and D2O / T.N.Burdeinaya, O.Y. Zrelov, G.I. Mtei, T.V. Maksimova, М.А. Мorozova, E.V.Uspenskaya, T.V. Pleteneva, A.V. Syroeshkin // Vestnik RUDN, Medicine. – 2013.– 2 Р. 5–9.381. Титорович, О.В. Биологическая активность фармацевтических ивспомогательных субстанций в водах разного изотопного состава/ О.В.Титорович, О.Ю. Зрелов, Т.В. Плетенева и др. // «Здоровье и образование вXXI веке», серия «Медицина».
– 2015. -№2, Т.17− С.91-93.382. Зрелов, О.Ю. Влияние изотопного состава воды на кинетикумутаротации галактозы / О.Ю. Зрелов, А.В. Сыроешкин, Е.В. Успенская и др.// Химико-фармацевтический журнал. – 2015. − Т. 49, № 6. – С. 51-54.383. Morozova, M.A. Physico-chemical properties of DDW as its qualityindicators for pharmaceutical analysis practice / M.A. Morozova, A. V. Syroeshkin,E.
V. Uspenskaya et al. // 3rd International Congress on Deuterium Depletion. −Budapest, 2015. – P. 7.384. Goncharuk, V.V. Determination of Biological Activity of Water Having aDifferent Isotope Ratio of Protium and Deuterium/ V.V. Goncharuk, T. V.Pleteneva, T. V. Grebennikova, A. V. Syroeshkin, E. V. Uspenskaya, N. V.Antipova, V. F. Kovalenko, M. N. Saprykina, M.
D. Skil’skaya, I. A. Zlatskiy//Journal of Water Chemistry and Technology. ‒ 2018. ‒ V. 40. ‒ I.1. ‒ Р. 27–34.385. Гончарук, В.В. О возможности существования в воде хиральныхструктурно-плотностныхсубмиллиметровыхнеоднородностей/В.В.Гончарук, А.В. Сыроешкин, Т.В. Плетенева, Е.В. Успенская, О.В. Левицкая,В.А. Твердислов//Химия и технология воды. ‒ 2017. ‒ Т.39. ‒ №6. ‒ С.573-584.386. Tsisanova, E.S. Study of biological activity and D/H ratio of water withthe aid of cellular biosensor spirostomum ambiguum / E.S. Tsisanova,312E.V.Uspenskaya, T.V.Pleteneva, A.V. Syroeshkin // Trace elements in medicine.−2010. −Т.−11.− № 2. −С. 8.5387.
Fasoli, E. Hydrogen/Deuterium Exchange Study of Subtilisin CarlsbergDuring Prolonged Exposure to Organic Solvents / E. Fasoli, A. Ferrer, L. Gabriel //Barletta Biotechnol Bioeng. − 2009. – V. 102(4) – Р. 1025–1032.388. Vladlen, V. Radiative cooling of H3O+ and its deuterated isotopologues /V. V. Melnikov, А S.
Yurchenko , P. Jensenc // Phys Chem Chem Phys. – 2016. –V. 18(37). –Р. 26268–26274.389. Wu, T. Measurement of the D/H, 18O/16O, and 17O/16O Isotope Ratios inWater by Laser Absorption Spectroscopy at 2.73 μm / W. Tao, C. Weidong, F. Eric,P. Masselin, X. Gao, W. Zhang, Y. Wang , J. Koeth, D. Brückner, X. He //. ensors(Basel). – 2014. −№ 14(5). – Р.
9027–9045.390. Beczek, M. The differences in crown formation during the splash on thethin water layers formed on the saturated soil surface and model surface / M.Beczek, M. Ryżak, A. Sochan, R. Mazur, C. Polakowski, A. Bieganowski // PLoSOne. −2017. – V. 12(7). – Р.0181-974.391.
Ферронский, В. И. Изотопия гидросферы / В.И.Ферронский, В.А.Поляков – М.: Наука. −1983.–217 c.392. Goncharuk, V.V. Controlled chaos: Heterogeneous catalysis/ V.V.Goncharuk, T. V. Pleteneva, E. V. Uspenskaya, A. V. Syroeshkin //Journal of WaterChemistry and Technology. ‒ 2017. ‒ V. 39. ‒ № 6. ‒ Р. 325–330.393. Duboué-Dijon, E. Characterization of the Local Structure in Liquid Waterby Various Order Parameters / E. Duboué-Dijon, D.
Laage // J Phys Chem B.−2015. − V. 119(26). − Р. 8406–8418.394. Goncharuk, V.V. On the possibility of chiral structure-densitysubmillimeter inhomogeneities existing in water / V.V. Goncharuk, A.V.Syroeshkin, T.V. Pleteneva, E. V. Uspenskaya, O. V. Levitskaya, V. A. Tverdislov /Journal of Water Chemistry and Technology.
− 2017. −V.39. – № 6. ‒ Р. 319–324.395. Craven, C.J. A model to explain specific cellular communications andcellular harmony: - a hypothesis of coupled cells and interactive coupling313molecules/ C.J. Craven // Theor Biol Med Model. ‒ 2014. ‒ V.11. ‒ Р.
40-47. doi:10.1186/1742-4682-11-40.396.Казанчева, О.Д.Методология поиска новых биологически активныхфармакологических веществ с рецепторной активностью / О.Д. Казанчева,А.С. Герасименко // International journal of applied and fundamental research.−2016. ‒ № 8. − Р. 522–525.397. Miller, E.J. Discovery of Tetrahydroisoquinoline-Containing CXCR4Antagonists with Improved in Vitro ADMET Properties / E.J. Miller, E. Jecs, V.M.Truax, B.M.
Katzman, Y.A. Tahirovic, R.J. Wilson, K.M. Kuo, M.B. Kim, H.H.Nguyen, M.T. Saindane, H. Zhao, T. Wang, C.S. Sum, M.E. Cvijic, G.M.Schroeder, L.J. Wilson, D.C. Liotta. // J Med Chem. ‒ 2018. ‒V.61. ‒№(3). ‒ Р.946-979.398. Бригас, Е.Р. Изучение сравнительной кинетики растворенияантигипертензивных лекарственных средств II класса биофармацевтическойклассификационной системы в соответствии с процедурой «биовейвер»/ Е.Р.Бригас,Е.В.Успенская,В.В.Писарев//Разработкаирегистрациялекарственных средств. – 2016.‒ №4.‒ Т.17. – С.152 –158.399. Dorozhkin, S.V. Dissolution mechanism of calcium apatites in acids: Areview of literature / S.
V. Dorozhkin // World J Methodol. −2012. – V. 2(1). −Р. 1–17.400. Perlovich, G.L. Influence of Position and Size of Substituents on theMechanism of Partitioning: A Thermodynamic Study on Acetaminophens,Hydroxybenzoic Acids, and Parabens / G.L. Perlovich, T.V. Volkova, A. N.
Manin,A. Bauer-Brandl // AAPS PharmSciTech.− 2008. V.−1.− Р. 205–216.401. Liu, C. Oral bioavailability enhancement of β-lapachone, a poorly solublefast crystallizer, by cocrystal, amorphous solid dispersion, and crystalline soliddispersion / C. Liu, Z. Liu, Y. Chen, Z. Chen, H. Chen, Y. Pui, F. Qian // Eur JPharm Biopharm. − 2018. – V. 124− Р.
73–81.314402. Avdeef, A. Cocrystal Solubility Product Prediction Using an in comboModel and Simulations to Improve Design of Experiments/A. Avdeef // PharmRes. ‒ 2018. ‒V.35. ‒ № 2. ‒Р.40.403. Nazemiyeh, E. Formulation and Physicochemical Characterization ofLycopene-Loaded Solid Lipid Nanoparticles / E. Nazemiyeh, M.
Eskandani, H.Sheikhloie, H. Nazemiyeh // Adv Pharm Bull. − 2016.− V. 2. – Р. 235–241.404. Ghani, S. The preparation, characterization and in vitro applicationevaluation of soluble soybean polysaccharide films incorporated with cinnamonessential oil nanoemulsions /S. Ghani, H. Barzegar, M. Noshad, M Hojjati / Int JBiol Macromol. − 2018.−V. 112.
− Р. 197-202.405. Hagedorn, M. Dual centrifugation - A new technique for nanomilling ofpoorly soluble drugs and formulation screening by an DoE-approach/ M. Hagedorn,A. Bögershausen, M. Rischer, R. Schubert, U. Massing// Int J Pharm. – 2017. –V.530. – Р. 79–88.406. Sun, J. Effect of particle size on solubility, dissolution rate, and oralbioavailability: evaluation using coenzyme Q10 as naked nanocrystals / J. Sun, F.Wang, Y. Sui, Z.
She, W. Zhai, C. Wang, Y. Deng. // Int J Nanomedicine . – 2012. –V.7. –Р. 5733-5744.407. Lipinski, C. Poor Aqueous Solubility – an Industry wide Problem in DrugDiscovery / C. Lipinski // Am. Pharm. Rev. − 2002. −V. 5. – Р. 82-85.408. Ibrahim, S. Curcumin marinosomes as promising nano-drug deliverysystem for lung cancer / S.
Ibrahim, T. Tagami, T. Kishi, T. Ozeki // Int J Pharm. –2018. ‒ V. 540. ‒ I. 1-2. ‒ P. 40-49.409. Jawahar, N. Enhanced oral bioavailability of an antipsychotic drugthrough nanostructured lipid carriers/ N. Jawahar, P.K. Hingarh, R. Arun, J.Selvaraj, A. Anbarasan, S. Sathianarayanan, G. Nagaraju // Int J Biol Macromol.−2018. V. 110. ‒ P. 269-275.410. Abuhelwa, A.Y. Population in vitro-in vivo pharmacokinetic model offirst-pass metabolism: itraconazole and hydroxy-itraconazole/ A.Y. Abuhelwa, S.315Mudge, R.N.
Upton, DJ.R. Foster / J Pharmacokinet Pharmacodyn. −2017.− Р. 117.411.Анфимова,Е.В.Исследованиекинетикирастворимостилекарственных субстанций методом лазерной дифракции в водных растворах сразличным изотопным составом по водороду/ Анфимова Е.В., Успенская Е.В.,Плетенева Т.В. Сыроешкин А.В.// Разработка и регистрация лекарственныхсредств. – 2017.‒ №1. ‒Т. 18. – С.150 – 155.412. Huang, S.
olubility Advantage (and Disadvantage) of PharmaceuticalAmorphous Solid Dispersion s/ S. Huang, C. Mao, R.O. Williams, C.Y. Yang//JPharm Sci.‒2016. ‒ V. ‒ 105. ‒ №12. ‒ Р. 3549-3561.413. Henry, N. С. Diffraction before destruction / N.C. Henry, C. Caleman //B Biol Sci. − 2014. − № 17. − Р. 369-1647.414. Уварова, Н. Исследование растворимости субстанции бендазолагидрохлорида методом лазерной дифракции / Н.
Уварова, У. Борисова // НПЖ«Фармация». − 2015. – С.510-513.415. Borisova, U. Study of solubility kinetics for pharmaceutical substancesby laser diffraction method / U. Borisova, N. Uvarova / VI International ScientificConference SCIENCE4HEALTH 2015. – Р.32-33.416. Anfimova, E.V. Active pharmaceutical ingredient solubility studies inwater with different isotope content by LALLS method / E.V.
Anfimova, E.V.Uspenskaya, A.V. Syroeshkin // VII International Scientific ConferenceSCIENCE4HEALTH 2016. – Мaterials of the conference : PFUR, Moscow− 2016.C.68.417. Huang, Z. Interactions between a poorly soluble cationic drug and sodiumdodecyl sulfate in dissolution medium and their impact on in vitro dissolutionbehavior r/ Z. Huang, S. Parikh, W.P. Fish // Int J Pharm.– 2018. ‒V. 535.
−I.1-2. ‒Р. 350-359.418. Zhao, S. Immobilization of phenanthrene onto gemini surfactant modifiedsepiolite at solid/aqueous interface: Equilibrium, thermodynamic and kinetic studies/ S. Zhao, G. Huang, S. Mu, C. An, X. Chen. −2017. – V. 598. ‒ Р. 619-627.316419. Yeşilbas, M. Particle Size Controls on Water Adsorption andCondensation Regimes at Mineral Surfaces / M. Yeşilbaş, J.F. Boily // Sci Rep.−2016.− Р. 6420. Baird, J.K. Theory of First Order Chemical Kinetics at the Critical Pointof Solution/ J.K. Baird, J.R. Lang.
// J Phys Chem A. – 2017. ‒ V.121. ‒ I. 42. ‒P.8048-8052. doi: 10.1021/acs.jpca.7b07635.421. Laidler, K.J. The development of Transition-State Theory / K.J. Laidler,M.C. King //J. Phys. Chem. − 1983.− № 87(15). – Р. 2657–2664.422. H. Е. Citation The Activated Complex in Chemical Reactions/ HenryEyring Citation // J.
![](https://s.studizba.com/z.php?f=/templates/si/i/noavatar.png&w=100&h=100&t=1"){kind=avatar}
