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Том 52, № 3 (2018) Analgesic Activity of a Polypeptide Modulator of TRPV1 Receptors PDF
(Eng)
D’yachenko I., Belous G., Skobtsova L., Zharmukhamedova T., Palikov V., Palikova Y., D’yachenko E., Kalabina E., Rudenko V., Andreev Y., Logashina Y., Kozlov S., Yavorskii A., Murashev A.
Том 52, № 3 (2018) Glucokinase Activators Based on N-Aryl-N′-Pyridin-2-Ylurea Derivatives PDF
(Eng)
Semenov A., Tarasova I., Khramov V., Semenova E., Inchina V., Vakaeva S.
Том 52, № 3 (2018) Synthesis and Antioxidant and Cytotoxic Activity of New Dihydroquercetin Derivatives PDF
(Eng)
Knyazev V., Rogovskii V., Sveshnikova E., Semeikin A., Matyushin A., Fedotcheva T., Shimanovskii N., Pozdeev A., Koroteev A., Koroteev M.
Том 52, № 3 (2018) Possible Ways of Studying Pharmacokinetic Parameters of Calcium Preparations PDF
(Eng)
Eremenko N., Shikh E., Serebrova S., Goryachev D.
Том 52, № 3 (2018) Estimated Heavy-Metal and Arsenic Contents in Medicinal Plant Raw Materials of the Voronezh Region PDF
(Eng)
D’yakova N., Samylina I., Slivkin A., Gaponov S., Myndra A.
Том 52, № 3 (2018) Solubility and Stability of Proroxan at Various PH Values PDF
(Eng)
Krechetov S., Nifontova G., Dolotova O., Veselov M.
Том 52, № 3 (2018) Optimization of Culture Conditions for the Production of Lovastatin by Aspergillus Terreus in Submerged Fermentation PDF
(Eng)
Azeem M., Saleem Y., Hussain Z., Zahoor S., Javed M.
Том 52, № 3 (2018) Method Development and Stress Degradation Profile of 5-Benzyl-1,3,4-Oxadiazole-2-Thiol Studied by UV Spectroscopy PDF
(Eng)
Qamar S., Hussain K., Bukhari N., Shehzadi N., Islam M., Siddique S., Aziz-ur-Rehman .
Том 52, № 3 (2018) Stability-Indicating UV-Spectrophotometric Assay of Diethylcarbamazine Citrate in Pharmaceuticals PDF
(Eng)
Basavaiah K., Swamy N.
Том 52, № 3 (2018) Reversed-Phase HPLC Method for Determination of Temozolomide in Rat Plasma and Brain: Simple, Sensitive and Robust Method PDF
(Eng)
Attari Z., Kumar L., Mallikarjuna Rao C., Koteshwara K.
Том 52, № 3 (2018) Release Testing of Selected Drugs from Surface Magnetic Nanoparticles and Their Diffusion Through a Membrane PDF
(Eng)
Gronczewska E., Worobiec W., Defort A., Jurkowski A., Kozioł J.
Том 52, № 3 (2018) Approaches to Pharmaceutical Analysis of an Innovative Liposomal Preparation for Treating Hepatitis C PDF
(Eng)
Smirnov V., Krasnykh L., Shilovskii I., Ryzhenkova A., Khaitov M., Drozdov V.
Том 52, № 3 (2018) Development and Validation of a Quantitative Determination Method for the Antitubercular Drug PBTZ169 in Biological Media PDF
(Eng)
Stepanova E., Barsegyan S., Makarenkova L., Chistyakov V.
Том 52, № 3 (2018) Effect of Solid Dispersions with Polyethylene Glycol 1500 on the Solubility of Indomethacin PDF
(Eng)
Krasnyuk I., Kosheleva T., Belyatskaya A., Krasnyuk I., Stepanova O., Skovpen Y., Grikh V., Ovsyannikova L.
Том 52, № 2 (2018) Hydrogel Nanoparticles of Chitosan—Folic-Acid Conjugate with Imatinib Methanesulfonate PDF
(Eng)
Lozovskaya M., Kulikovskaya V., Ignatovich Z., Koroleva E., Agabekov V.
Том 52, № 2 (2018) Ag – ZnO Nanocomposites Cause Cytotoxicity and Induce Cell Cycle Arrest in Human Gastric and Melanoma Cancer Cells PDF
(Eng)
Rad M., Najafzadeh N., Tata N., Jafari A.
Том 52, № 2 (2018) Synthesis and Neurotropic Activity of New 7-Cyclohexyl-6,7,8,9-Tetrahydro-3H-Pyrazolo[3,4-c]-2,7-Naphthyridine-1,5-Diamines PDF
(Eng)
Sirakanyan S., Hakobyan E., Nikoghosyan A., Paronikyan R., Dzhagatspanyan I., Nazaryan I., Akopyan A., Hovakimyan A.
Том 52, № 2 (2018) Simple Extraction Cum RP-HPLC Method for Estimation of Nanotized Quercetin in Serum and Tissues of Mice PDF
(Eng)
Gupta K., Sharma A., Gupta R., Dixit S., Singh S., Das M., Dwivedi P.
Том 52, № 2 (2018) Technology Development and Antiulcer Activity of Gastroretentive Tablets with Aspen Bark Dry Extract PDF
(Eng)
Krylova S., Turetskova V., Makarova O., Zueva E.
Том 52, № 2 (2018) Preparation of Gallic Acid – Anhydride Conjugate and Evaluation of Prodrug Release Through Pva-Based Hydrogel PDF
(Eng)
Mahire R., Agrawal D., Patil D., More D.
Том 52, № 2 (2018) Development of a Sample-Preparation Procedure for Quantitative Determination of Lead in Sugars by Inductively Coupled-Plasma—Atomic-Emission Spectrometry (ICP-AES) PDF
(Eng)
Olefir Y., Sakanyan E., Ladygina L., Shchukin V.
Том 52, № 2 (2018) Development and Validation of an HPLC-UV Method for Anilocaine Determination in Blood Plasma PDF
(Eng)
Ryzhikova V., Kursakov S., Belov V., Sevast’yanov V.
Том 52, № 2 (2018) Validation of an NMR-Spectroscopic Method for Authenticity Confirmation of Buserelin Acetate Pharmaceutical Substance PDF
(Eng)
Kuz’mina N., Moiseev S., Krylov V., Deryabin A., Yashkir V., Merkulov V.
Том 52, № 2 (2018) Comparison of Spectrophotometric and Chromatographic (HPLC) Procedures for Determining 3-Phenethylrhodanine Drug Substance with Anticancer Activity PDF
(Eng)
Novozhilova N., Kutina N., Kharitonov Y.
Том 52, № 2 (2018) Development of an HPLC-UV Method for Quantitative Determination of Acetylsalicylic Acid and Its Main Metabolite PDF
(Eng)
Belov V., Kursakov S., Sevast’yanov V., Antonov E., Bogorodskii S., Popov V.
Том 52, № 2 (2018) Resonance Light-Scattering Enhancement Effect of the Y(III)–PUFX–Eosin System and its Fluorescence Study PDF
(Eng)
Bano S., Mohd A., Khan A., Asiri A., Siddiqui J., Hussain S.
Том 52, № 1 (2018) Sustained-Release Tablets of Hydrochlorothiazide, a Slightly Water-Soluble Molecule Using Glyceryl Behenate PDF
(Eng)
Chemsa S., Maïza A., Arnaud P.
Том 52, № 1 (2018) Multidrug Resistance Reversal Activity of Some New Dihydropyridines Studied by IN SITU Single-Pass Intestinal Perfusion (SPIP) Method in Rat PDF
(Eng)
Sirisha K., Achaiah G., Prasad N., Bhasker S., Umachander L., Malla Reddy V.
Том 52, № 1 (2018) Encapsulation and Controlled Release of Vitamin B2 Using Peracetyl-β-Cyclodextrin Polymer-Based Electrospun Nanofiber Scaffold PDF
(Eng)
Heydari A., Mehrabi F., Shamspur T., Sheibani H., Mostafavi A.
Том 52, № 1 (2018) Acetoxybenzoylglycylglycines as Potential Cerebroprotective Compounds PDF
(Eng)
Brel’ A., Tyurenkov I., Lisina S., Popov S., Verkholyak D., Budaeva Y., Volotova E., Atapina N., Kurkin D.
Том 52, № 1 (2018) Synthesis and Anticonvulsive Activity of 3- and 4-Benzoylpyridine Oxime Derivatives PDF
(Eng)
Zhmurenko L., Voronina T., Litvinova S., Nerobkova L., Gaidukov I., Mokrov G., Gudasheva T.
Том 52, № 1 (2018) Synthesis and Antiaggregant Activity of 2-[3-Methyl-1-Ethylxanthinyl-8-Thio]Acetic Acid Salts Containing a Thietane Ring PDF
(Eng)
Khaliullin F., Shabalina Y., Samorodov A., Kamilov F., Timirkhanova G., Murataev D.
Том 52, № 1 (2018) Development of an Industrial Reference Sample for the Specific Activity of Erythropoietin PDF
(Eng)
Yakovlev A., Volkova R., Simutenko L., Postnova E., Batuashvili T., Voropaev A., Alpatova N., Tomilin V., Mytsa E., Bondarev V., Merkulov V.
Том 52, № 1 (2018) Controlled-Release Matrixes for Drugs Based on Polyamide-Polyhydroxybutyrate Compositions PDF
(Eng)
Ol’khov A., Pankova Y., Kosenko R., Gol’dshtrakh M., Markin V., Iordanskii A.
Том 52, № 1 (2018) A Study on Essential Oil Chemical Compositions, Antioxidant, and Antimicrobial Activities of Native and Endemic Satureja Species Growing in Iran PDF
(Eng)
Jafari F., Farmani F., Zomorodian K., Moein M., Faridi P., Zarshenas M.
Том 51, № 12 (2018) Coumarinyl Thiosemicarbazides as Antimicrobial Agents PDF
(Eng)
Molnar M., Tomić M., Pavić V.
Том 51, № 12 (2018) Benzimidazole Ring System as a Privileged Template for Anticancer Agents PDF
(Eng)
Kanwal A., Saddique F., Aslam S., Ahmad M., Zahoor A., Mohsin N.
Том 51, № 12 (2018) Anti-Candida Activity of 4-Morpholino-5-Nitro- and 4,5-Dinitro-Imidazole Derivatives PDF
(Eng)
Olender D., Zaprutko L., Mertas A., Szliszka E., Wyrozumski D., Król W.
Том 51, № 12 (2018) Synthesis and Biological Activity of 2-Mercapto-7,10-Dimethyl-3H-Spiro[Benzo[H]Quinazoline-5,1′-Cyclopentane]-4(6H)-One from Ethyl 4′-Amino-5′,8′-Dimethyl-1′H-Spiro[Cyclopentane-1,2′-Naphthalene]-3′-Carboxylate PDF
(Eng)
Grigoryan N., Markosyan A., Grigoryan A., Stepanyan G., Sukasyan R., Paronikyan R.
Том 51, № 12 (2018) HPLC-MS/MS Method for Determining Dabigatran in Human Blood Serum PDF
(Eng)
Rodina T., Mel’nikov E., Aksenov A., Belkov S., Sokolov A., Prokof’ev A., Ramenskaya G.
Том 51, № 12 (2018) Hemostasis Parameters and Toxic Effects of 3-Substituted and Condensed Chromen-2-Ones (Coumarins) PDF
(Eng)
Ibragimova D., Fedotova O., Ozerova A., Koftin O., Borodulin V., Samokhvalov V.
Том 51, № 12 (2018) Hydrophobic Constituents Extracted from Chaga by Ethylacetate PDF
(Eng)
Kyyamova G., Khabibrakhmanova V., Sysoeva M.
Том 51, № 12 (2018) Evaluation of Polyphenol and Flavonoid Profiles and the Antioxidant Effect of Carduus Acanthoides Hydroalcoholic Extract Compared with Vaccinium Myrtillus in an Animal Model of Diabetes Mellitus PDF
(Eng)
Varut R., Gîrd C., Rotaru L., Varut M., Pisoschi C.
Том 51, № 12 (2018) Novel Free-Radical Scavengers Based on Ferrofluid/Polyaniline Nanocomposites PDF
(Eng)
Pur F., Arsalani N., Safa K.
Том 51, № 12 (2018) Flupirtine Determination in Human Blood Plasma by HPLC with Mass-Spectrometric Detection and its Application to Pharmacokinetic Studies PDF
(Eng)
Krasnykh L., Rodina T., Mel’nikov E., Vasilenko G., Smirnov V., Sokolov A., Arkhipov V.
Том 51, № 12 (2018) Determination of Bacterial Endotoxins in Drugs: False-Negative Results PDF
(Eng)
Shapovalova O., Neugodova N., Sapozhnikova G., Simutenko L., Agashirinova A.
Том 51, № 12 (2018) Simultaneous Determination of Metoprolol and Bisoprolol in Human Serum by HPLC-MS/MS for Clinical Drug Monitoring PDF
(Eng)
Rodina T., Mel’nikov E., Dmitriev A., Belkov S., Sokolov A., Arkhipov V., Prokof’ev A.
Том 51, № 12 (2018) Development of a Procedure for Identification of Biperiden Hydrochloride with Specificity for Triperiden Hydrochloride PDF
(Eng)
Kuz’mina N., Moiseev S., Krylov V., Kutin A., Yashkir V., Merkulov V.
Том 51, № 11 (2018) Experimental Antioxidant Activity of a β-Cyclodextrin – Histochrome Complex PDF
(Eng)
Bikbov M., Nikitin N., Surkova V., Farkhutdinov R., Khalilov L., Tulyabaev A., Nikitina A., Fedoreev S., Mishchenko N.
Том 51, № 11 (2018) Synthesis, Docking, and Anticoagulant Activity of New Factor-Xa Inhibitors in a Series of Pyrrolo[3,2,1-ij]Quinoline-1,2-Diones PDF
(Eng)
Medvedeva S., Potapov A., Gribkova I., Katkova E., Sulimov V., Shikhaliev K.
Том 51, № 11 (2018) The Effects of Cimetidine, N-Acetylcysteine, and Taurine on Thioridazine Metabolic Activation and Induction of Oxidative Stress in Isolated Rat Hepatocytes PDF
(Eng)
Eftekhari A., Ahmadian E., Azarmi Y., Parvizpur A., Fard J., Eghbal M.
Том 51, № 11 (2018) Inhibitory Effect of Excoecaria Agallocha L. Extracts on Elastase and Collagenase and Identification of Metabolites Using HPLC-UV-MS Techniques PDF
(Eng)
Satyavani K., Gurudeeban S., Ramanathan T.
Том 51, № 11 (2018) Comparison of Pharmacokinetics, Bioequivalence, and Safety of Femorix® (Valenta Pharm Company, Russia) and Aubagio® (Sanofi Winthrop Industrie, France) Film-Coated Tablets (14 mg) PDF
(Eng)
Reikhart D., Arnautov V., Belostotskii A., Globenko A., Lopukhov I., Torshina E.
Том 51, № 11 (2018) Hampered Binding to Blood Serum Proteins and the Biological Activity of Antimicrobial Peptide Containing N3-(4-Methoxyfumaroyl)-L-2,3-Diaminopropanoic Acid Immobilized on Magnetic Nanoparticles PDF
(Eng)
Nowak-Jary J., Gronczewska E., Worobiec W.
Том 51, № 11 (2018) Synthesis of Analogs of Trans-Fagaramide and Their Cytotoxic Activity PDF
(Eng)
Tomas M., Shiao T., Nguyen P., Bourgault S., Roy R.
Том 51, № 11 (2018) Synthesis, Characterization, Pharmacokinetics and Evaluation of Cytotoxicity for Docetaxel-Oleate Conjugate Targeting MCF-7 Breast Cancer Cells PDF
(Eng)
Bhatia N., Kulkarni P., Ashtekar S., Mahuli D., Bhatia M.
Том 51, № 11 (2018) Applicability of an Alternative Method for Sterility Testing of Medicinal Preparations PDF
(Eng)
Roshchina M., Gunar O., Sakhno N.
Том 51, № 11 (2018) Standardization of the Method for Determining Hemagglutinin Content in Human Immunoglobulin Preparations in Russia PDF
(Eng)
Kornilova O., Nechaev A., Borisevich I., Kudasheva É.
Том 51, № 11 (2018) Validation of a Quantitative Determination Method for Ormustine in a Lyophilized Dosage Form PDF
(Eng)
Bunyatyan N., Nikolaeva L., Olefir Y., Sanarova E., Oborotova N., Prokof’ev A., Ignat’eva E., Yartseva I., Gulyakin I.
Том 51, № 10 (2018) QSAR Modelling of Thymidylate Synthase Inhibitors in a Series of Quinazoline Derivatives PDF
(Eng)
Khairullina V., Gerchikov A., Lagunin A., Zarudii F.
Том 51, № 10 (2018) Antioxidant Properties of Fullerene C60/Dihydroquercetin Composites PDF
(Eng)
Dumpis M., Prokopenko V., Litasova E., Arutyunyan A., Piotrovskii L.
Том 51, № 10 (2018) Synthesis and Biological Activity of (Z)-Dialkylaminoalkylamides of N-Benzoyl-α,β-Dehydroamino Acids and Their Iodomethylates PDF
(Eng)
Topuzyan V., Tosunyan S., Chshmarityan S., Paronikyan R.
Том 51, № 10 (2018) Synthesis and Biological Activity of β-Aroylacrylate Salts PDF
(Eng)
Khachikyan R., Ovakimyan Z., Mikaelyan A., Paronikyan R., Stepanyan G.
Том 51, № 10 (2018) Synthesis and Antiproliferative Activity Evaluation of Aryl(Hetaryl)Cyclopentenone Analogs of Combretastatin A-4 PDF
(Eng)
Shirinyan V., Markosyan A., Baryshnikova M., Yaminova L., L’vov A., Gabrielyan S.
Том 51, № 10 (2018) Captopril-Loaded Superparamagnetic Nanoparticles as a New Dual-Mode Contrast Agent for Simultaneous In Vitro/In Vivo MR Imaging and Drug Delivery System PDF
(Eng)
Pour S., Shaterian H.
Том 51, № 10 (2018) Synthesis, X-Ray Structure and In Vitro Cytotoxic Activity of a New Dinuclear Cobalt(III) Complex with Diazine Ligands PDF
(Eng)
Li F., Chen H., Jin Y., Zhao Q., Xie M.
Том 51, № 10 (2018) In Vitro Antitumor Activity of Newly Synthesized Pyridazin-3(2H)-One Derivatives via Apoptosis Induction PDF
(Eng)
Bouchmaa N., Tilaoui M., Boukharsa Y., Jaâfari A., Mouse H., Ali Oukerrou M., Taoufik J., Ansar M., Zyad A.
Том 51, № 10 (2018) Method Development for Quantitative Determination of Ascorbic Acid by High-Performance Thin-Layer Chromatography PDF
(Eng)
Trineeva O., Safonova E., Slivkin A.
Том 51, № 10 (2018) Design, Synthesis and Evaluation of Antitubercular Activity of Novel 1,2,4-Triazoles Against MDR Strain of Mycobacterium tuberculosis PDF
(Eng)
Gautham Shenoy G., Kar S., Shenoy V., Bairy I., Ganesh Kumar T.
Том 51, № 10 (2018) β-Ionone-Derived Curcumin Analogs as Potent Anti-Inflammatory Agents PDF
(Eng)
Hu W., Cai M., Qi D., Ying X., Huang C., Xing C.
Том 51, № 9 (2017) Seasonal Oscillations in Statistical Mean Measures of Blood Composition and Blood Cell Morphology in Healthy White Rats PDF
(Eng)
Pushkin A., Drugova E., Kamshilin S., Obraztsov N., Polekhina O., Dvoretskaya S., Churyumova A.
Том 51, № 9 (2017) Preparation and Activity of a Complex of Oligohexamethyleneguanine with P-Aminosalicylic Acid Derivatives PDF
(Eng)
Kedik S., Shatalov D., Isaikina P., Askretkov A., Sedishev I., Panov A., Evseeva A.
Том 51, № 9 (2017) Tuberculostatic Activity of 2-Amino-6-Chloropurine Derivatives PDF
(Eng)
Kravchenko M., Skornyakov S., Bekker O., Maslov D., Danilenko V., Charushin V., Krasnov V., Vigorov A., Gruzdev D., Levit G.
Том 51, № 9 (2017) Synthesis and Antimicrobial Properties of Ammonium Salts Containing a Substituted Butyn-2-yl Group PDF
(Eng)
Manukyan M., Barsegyan K., Gyulnazaryan A., Paronikyan R., Stepanyan G., Minasyan N., Babakhanyan A.
Том 51, № 9 (2017) Synthesis and Antitumor Activity of 2-N-,3-S-Substituted 5-(4-Benzyloxyphenyl)-1,2,4-Triazoles PDF
(Eng)
Kaldrikyan M., Melik-Ohanjanyan R., Arsenyan F.
Том 51, № 9 (2017) Effects of Cilostazol on the Pharmacokinetics of Nifedipine After Oral and Intravenous Administration in Rats PDF
(Eng)
Lee C., Choi J., Choi D.
Том 51, № 9 (2017) Comparison of the Antitumor Efficacy of Bismuth and Gadolinium as Dose-Enhancing Agents in Formulations for Photon Capture Therapy PDF
(Eng)
Lipengol’ts A., Cherepanov A., Kulakov V., Grigor’eva E., Merkulova I., Sheino I.
Том 51, № 9 (2017) Anticonvulsant Activity of 3-imidazolylflavanones and Their Flexible Analogs: 1-[(2-benzyloxy)phenyl]-2-(azol-1-yl)ethanones as New Lead Compounds PDF
(Eng)
Ahangar N., Hafezi S., Irannejad H., Emami S.
Том 51, № 9 (2017) Evaluation of Anti-Hyperglycemic Effect of Synthetic Schiff Base Vanadium(IV) Complexes PDF
(Eng)
El-Saied F., Salem T., Aly S., Shakdofa M.
Том 51, № 9 (2017) Validation of a Method of Measuring Mean Molecular Weight of Dextrans by Diffusion-Ordered Spectroscopy PDF
(Eng)
Moiseev S., Kuz’mina N., Krylov V., Yashkir V., Merkulov V.
Том 51, № 9 (2017) Green Approach to Synthesis of Silver Nanoparticles Using Ficus Palmata Leaf Extract and Their Antibacterial Profile PDF
(Eng)
Nasar S., Murtaza G., Mehmood A., Bhatti T.
Том 51, № 9 (2017) Extraction of Mangiferin from the Leaves of the Mango Tree Mangifera indica and Evaluation of its Biological Activity in Terms of Blockade of α-glucosidase PDF
(Eng)
Vo T., Nguyen T., Nguyen Q., Ushakova N.
Том 51, № 9 (2017) Synthesis, Spectral Characterization, In Vitro Antibacterial Evaluation and POM Analyses of Palladium(II) Thiocyanate Complexes of Thioamides PDF
(Eng)
Nadeem S., Sirajuddin M., Ahmad S., Yaqub S., Ali M., Tirmizi S., Ali S., Hameed A.
Том 51, № 8 (2017) An Environmentally Benign Lemon Juice Mediated Synthesis of Novel Furan Conjugated Pyrazole Derivatives and Their Biological Evaluation PDF
(Eng)
Mahadevaswamy L., Kariyappa A.
Том 51, № 8 (2017) An Accessible Route for the Synthesis of Novel Lignan Derivatives and Their Biological Evaluation PDF
(Eng)
Raghavendra K., Renuka N., Kumar K., Shashikanth S.
Том 51, № 8 (2017) Synthesis, in vitro Antibacterial and in vivo Anti-Inflammatory Activity of Some New Pyridines PDF
(Eng)
Ghattas A., Khodairy A., Moustafa H., Hussein B., Farghaly M., Aboelez M.
Том 51, № 8 (2017) Search for Anti-Inflammatory Agents in the Tetrahydropyrido[2,1-B ][1,3,5]-Thiadiazine Series PDF
(Eng)
Bibik E., Yaroshevskaya O., Devdera A., Demenko A., Zakharov V., Frolov K., Dotsenko V., Krivokolysko S.
Том 51, № 8 (2017) Synthesis and Antimicrobial Activity of 4-Hydroxy-2-[5-Nitrofuran(Thien)-2-Yl]-6h-1,3-Oxazin-6-Ones PDF
(Eng)
Chernov N., Koshevenko A., Yakovlev I., Anan’eva E., Ksenofontova G., Shchegolev A.
Том 51, № 8 (2017) Synthesis and Anti-Arrhythmic Activity of the Chloride and Salicylate Salts of Morpholinoacetic Acid Ortho-Toluidide PDF
(Eng)
Gashkova O., Rudakova I., Syropyatov B.
Том 51, № 8 (2017) Angio-Suppressive Effect of Sterols from Ardisia Pyramidalis (Cav.) Pers. PDF
(Eng)
Raga D., Herrera A., Alimboyoguen A., Shen C., Ragasa C.
Том 51, № 8 (2017) Optimization of Drug Administration Dosage Regimen Considering Chronorhythms and Desynchronosis of Gastrointestinal-Tract Organs PDF
(Eng)
Bunyatyan N., Drogovoz S., Kononenko A., Olefir Y., Prokof’ev A.
Том 51, № 8 (2017) Determination and Degradation Study of Enalapril Maleate by High Performance Liquid Chromatography PDF
(Eng)
Bouabdallah S., Trabelsi H., Driss M., Touil S.
Том 51, № 8 (2017) Pharmacopoeial Quality Requirements for Compounded Pharmaceuticals: Present and Future PDF
(Eng)
Shishova L., Sakanyan E., Shemeryankina T., Gubareva O.
Том 51, № 8 (2017) Colorimetric and Indirect X-Ray Fluorescence Determination of Drug Substances Using Chemically Modified Polyurethane-Foam Absorbents PDF
(Eng)
Chaplenko A., Monogarova O., Oskolok K., Chaplenko S.
Том 51, № 8 (2017) Interchangeability Problems of Drugs with Narrow Therapeutic Indices PDF
(Eng)
Zatolochina K., Pasternak E., Alyautdin R., Snegireva I., Romanov B., Polivanov V., Olefir Y.
Том 51, № 8 (2017) Cellulose Orodispersible Films of Donepezil: Film Characterization and Drug Release PDF
(Eng)
Reddy K., Karpagam S.
Том 51, № 8 (2017) Physical, Chemical, and Kinetic Properties of Trypsin-Based Heterogeneous Biocatalysts Immobilized on Ion-Exchange Fiber Matrices PDF
(Eng)
Holyavka M., Artyukhov V., Sazykina S., Nakvasina M.
Том 51, № 7 (2017) Synthesis and Anti-Inflammatory Activity of 2-{[5-(2-Chlorophenyl)-4H-1,2,4-Triazol- 3-YL]Sulfanyl}-1-(Substituted Phenyl)Ethanones PDF
(Eng)
Karande N., Rathi L.
Том 51, № 7 (2017) Synthesis and Biological Properties of {[(4-Hydroxy-1-Methyl-2,2-Dioxido-1H-2,1-Benzothiazin-3-YL)Carbonyl]Amino}-Benzoic Acids and Their Derivatives PDF
(Eng)
Ukrainets I., Petrushova L., Dzyubenko S., Grinevich L., Sim G.
Том 51, № 7 (2017) Antimicrobial Activity of 1,2,5-Trimethylpiperidin-4-Ol Derivatives PDF
(Eng)
Dyusebaeva M., Elibaeva N., Kalugin S.
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Согласие на обработку персональных данных с помощью сервиса «Яндекс.Метрика»

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2. Категории обрабатываемых данных: файлы «cookies» (куки-файлы). Файлы «cookie» – это небольшой текстовый файл, который веб-сервер может хранить в браузере Пользователя. Данные файлы веб-сервер загружает на устройство Пользователя при посещении им Сайта. При каждом следующем посещении Пользователем Сайта «cookie» файлы отправляются на Сайт Оператора. Данные файлы позволяют Сайту распознавать устройство Пользователя. Содержимое такого файла может как относиться, так и не относиться к персональным данным, в зависимости от того, содержит ли такой файл персональные данные или содержит обезличенные технические данные.

3. Цель обработки персональных данных: анализ пользовательской активности с помощью сервиса «Яндекс.Метрика».

4. Категории субъектов персональных данных: все Пользователи Сайта, которые дали согласие на обработку файлов «cookie».

5. Способы обработки: сбор, запись, систематизация, накопление, хранение, уточнение (обновление, изменение), извлечение, использование, передача (доступ, предоставление), блокирование, удаление, уничтожение персональных данных.

6. Срок обработки и хранения: до получения от Субъекта персональных данных требования о прекращении обработки/отзыва согласия.

7. Способ отзыва: заявление об отзыве в письменном виде путём его направления на адрес электронной почты Оператора: info@rcsi.science или путем письменного обращения по юридическому адресу: 119991, г. Москва, Ленинский просп., д.32А

8. Субъект персональных данных вправе запретить своему оборудованию прием этих данных или ограничить прием этих данных. При отказе от получения таких данных или при ограничении приема данных некоторые функции Сайта могут работать некорректно. Субъект персональных данных обязуется сам настроить свое оборудование таким способом, чтобы оно обеспечивало адекватный его желаниям режим работы и уровень защиты данных файлов «cookie», Оператор не предоставляет технологических и правовых консультаций на темы подобного характера.

9. Порядок уничтожения персональных данных при достижении цели их обработки или при наступлении иных законных оснований определяется Оператором в соответствии с законодательством Российской Федерации.

10. Я согласен/согласна квалифицировать в качестве своей простой электронной подписи под настоящим Согласием и под Политикой обработки персональных данных выполнение мною следующего действия на сайте: https://journals.rcsi.science/ нажатие мною на интерфейсе с текстом: «Сайт использует сервис «Яндекс.Метрика» (который использует файлы «cookie») на элемент с текстом «Принять и продолжить».