LOGOYDA LILIYA SVATOSLAVIVNA

  • Piponski M., Stoimenova T. B., Stefov S., Balkanov T., Serafimovska G. T., Logoyda L. S. Development of a novel, fast, simple, nonderivative HPLCmethod with direct UV measurment for quantification of memantine hydrochloride in tablets // Journal of Separation Science. – 2020. – Vol. 43. – Р. 3482-3490.

  • Horyn M., Logoyda L. Bioanalytical method development and validation for the determination of metoprolol and meldonium in human plasma // Pharmacia. – 2020. – Vol. 67(2) – Р. 39–48.

  • Logoyda L. Efficient validated method of HPLC to determine amlodipine in combinated dosage form containing amlodipine, enalapril and bisoprolol and in vitro dissolution studies with in vitro/in vivo correlation // Pharmacia. – 2020. – Vol. 67(2) – Р. 55–61.

  • Logoyda L., Herasymiuk M., Popovych D., Pidruchna S., Hlushok V., Herasymiuk N., Zarivna N. HPLC MS/MS method development for the quantitative determination of verapamil hydrochloride from Caco-2 cell monolayers // Pharmacia. – 2020. – Vol. 67(2) – Р. 63–69.

  • Logoyda L. HPLC-MS/MS method development for the quantitative determination of nifedipine for Caco-2 permeability assay // Pharmacia. – 2020. – Vol. 67(2) – Р. 83–88.

  • Logoyda L., Dutchak O., Horlachuk N. In vitro dissolution kinetics of amlodipine tablets under biowaiver conditions // Pharmakeftiki. – 2020. – Vol. 32(2). – Р. 102–108.

  • Zarivna N., Logoyda L. Development of methods of analysis of biological active substances for standardization of dense extract of Creeping Thyme // Letters of Applied NanoBioScience. – 2020. – Vol. 9(4). – Р. 1644–1654.

  • Piponski M., Peleshok K., Logoyda L., Kravchuk L., Piatnochka V., Zakharchuk U. Efficient Validated HPLC/UV method for determination of valsartan and atenolol in dosage form and in vitro dissolution studies // Biointerface research in applied chemistry. – 2020. – Vol. 10(6). – Р. 6669–6675.

  • Logoyda L., Piatnochka V. HPLC method development and in vitro dissolution kinetics of amlodipine tablets under biowaiver conditions. // Biointerface research in applied chemistry. – 2020. – Vol. 10(5). – Р. 6513–6521.

  • Drapak I., Zimenkovsky B., Ivanauskas L., Bezruk I., Perekhoda L., Muzychenko V., Logoyda L., Demchuk I. HPLC method for simultaneous determination of impurities and degradation products in Cardiazol // Pharmacia. – 2020. – Vol. 67(1). – Р. 29–37.

  • Logoyda L. LC-MS/MS method development and validation for the determination of nifedipine in human plasma // Biointerface research in applied chemistry. – 2020. – Vol. 10(5). – Р. 6189–6196.

  • Logoyda L., Kovalenko S., Gaafar M., M. Abdel-Megied A., Fawzy A. Elbarbry. A validated LC-MS/MS method for the quantification of amlodipine, bisoprolol, enalapril and enalaprilat – Application to pharmacokinetic study in healthy volunteers // Microchemical Journal. – 2020. – Vol. 155: – 104700.

  • Зарівна Н. О., Логойда Л. С. Розробка методики ідентифікації флавоноїдів та гідроксикоричних кислот в екстрактах чебрецю повзучого // Медична та клінічна хімія. – 2020. –Т. 22. № 1, – С.107-111.

  • Logoyda L. Youden’s test for chromatographic determination of enalapril in pharmaceuticals // International Journal of Medicine and Medical Research. – 2019. – Vol. 5(2). – Р. 83-87.

  • Drapak I., Zimenkovsky B., Perekhoda L., Kovalenko S., Logoyda L. Development and validation of LC-MS/MS method for estimation of urocarb in human plasma // International Journal of Applied Pharmaceutics. – 2019. – Vol. 11, № 5. – Р. 125–130.

  • Drapak I., Zimenkovsky B., Perekhoda L., Kovalenko S., Logoyda L. LC-MS/MS method development and validation for the determination of cardiazol in human plasma // International Journal of Applied Pharmaceutics. – 2019. – Vol. 11, № 4. – Р. 380–385.

  • Logoyda L. Analysis of approaches to the development and validation of the methods of analysis of some active pharmaceutical ingredients from the group of angiotensin converting enzyme inhibitors in drugs and biological liquids // International Journal of Applied Pharmaceutics. – 2019. – Vol. 11, № 4. – Р. 1–7.

  • Logoyda L. Efficient validated method of HPLC to determine enalapril in combinated dosage form containing enalapril and bisoprolol and in vitro dissolution studies // International Journal of Applied Pharmaceutics.. – 2019. – Vol. 11, № 4. – Р. 19–24.

  • Логойда Л. С. Процедура вивчення валідаційного параметра «стабільність при розведенні» аналітичної методики кількісного визначення деяких антигіпертензивних аналітів у біологічних рідинах для проведення фармакокінетичних досліджень // Медична та клінічна хімія. – 2019. – № 2. – С. 68–72.

  • Logoyda L., Kovalenko S., M. Abdel-Megied A., Zhulkevych I., Drapak I., Demchuk I., Netsyuk O. HPLC method development for the analysis of bisoprolol in combined dosage form containing bisoprolol and enalapril and in vitro dissolution studied // International Journal of Applied Pharmaceutics. – 2019. – Vol. 11, № 3. – Р. 186–194.

  • Logoyda L. Analysis of approaches to the development and validation of the methods of analysis of some active pharmaceutical ingredients from the group of calcium channel blockers in drugs and biological liquids // International Journal of Applied Pharmaceutics. – 2019. – Vol. 11, № 3. – Р. 26–34.

  • Logoyda L., Horlachuk N., Zarivna N., Polyauk O., Soroka Y., Herasymiuk M. In Vitro dissolution kinetics of bisoprolol tablets under biowaiver conditions // Asian Journal of Pharmaceuticals. – 2019. – Vol. 13, № 1. – Р. 54–58.

  • Horlachuk N., Halkevych I., Logoyda L., Mosula L., Zarivna N., Polyauk O. Chromatography–mass spectrometry analysis of tianeptine in urine // International Journal of Green Pharmacy. – 2019. – Vol. 13, № 1. – Р. 87–91.

  • Mykhalkiv M., Logoyda L., Ivanusa I., Soroka Y., Yakubishyna I. High-performance liquid chromatography as assay method for the investigation of conditions of enalapril maleate extraction by organic solvents // International Journal of Green Pharmacy. – 2018. – Vol. 12, № 1. – Р. 62–65.

  • Mykhalkiv M., Logoyda L., Polyauk O., Zarivna N., Soroka Y., Ryabokon S., Riabokon M. HPLC as assay method for the investigation of conditions of bisoprolol extraction by organic solvents // International Journal of Green Pharmacy. – 2018. – Vol. 12, № 1. – Р. S276–279.

  • Logoyda L., Mykhalkiv M., Polyauk O., Zarivna N., Soroka Y., Demydiak O. UHPLC as assay method for the investigation of conditions of captopril extraction by organic solvents // Asian Journal of Pharmaceuticals. – 2018. – Vol. 12, № 1. – Р. 168–171.

  • Logoyda L. Bioanalytical method development and validation from the simultaneous determination of verapamil and enalapril in the present of enalaprilat by HPLC MS/MS // International Journal of Applied Pharmaceutics. – 2018. – Vol. 10, № 3. – Р. 19–27.

  • Logoyda L. A HPLC-MS/MS method development and validation for the simultaneous determination of nifedipine and enalapril in human plasma // International Journal of Applied Pharmaceutics. – 2018. – Vol. 10, № 4. – Р. 35–42.

  • Logoyda L., Korobko D. A HPLC MS/MS method development for the quantitative determination of bisoprolol from Caco-2 cell monolayers // Asian Journal of Pharmaceutical and Clinical Research. – 2018. – Vol. 11, № 4. – Р. 386–389.

  • Logoyda L. Quantitative determination of amlodipine from Caco-2 cell monolayers by HPLC MS/MS // Asian Journal of Pharmaceutical and Clinical Research. – 2018. – Vol. 11, № 6. – Р. 204–207.

  • Logoyda L. A High-performance liquid chromatography-mass spectrometry method development for the quantitative determination of enalapril maleate from Caco-2 cell monolayers // Asian Journal of Pharmaceutical and Clinical Research. – 2018. – Vol. 11, № 7. – Р. 89–92.

  • Логойда Л. С. Процедура визначення валідаційного параметра «лінійність/калібрувальна модель» аналітичної методики кількісного визначення різних антигіпертензивних аналітів у біологічних рідинах для проведення фармакокінетичних досліджень // Медична та клінічна хімія. – 2018. – № 2. – P. 65–71.

  • Korobko D., Hadjipavlou-Litina D.J., Logoyda L. Antioxidant and anti-inflammatory properties of a series of new 7,8-disubstituted theophylline containing a pyrazole ring // Asian Journal of Pharmaceutical and Clinical Research. – 2018. – № 11(6). – Р. 448-450.

  • Yuryeva O., Kondratova Y., Logoyda L. Development of high-performance liquid chromatography method for simultaneous analysis of amlodipine and valsartan in combined dosage form and in vitro disslotution studies // Asian Journal of Pharmaceutical and Clinical Research. – 2018. – Vol. 11, № 5. – Р. 200–204.

  • Logoyda L., Abdel-Megied A., Kondratova Y., Trofimenko O., Korobko D., Dakhym I. Development and validation of HPLC method for the simultaneous determination of enalapril maleate in present of their impurities: application to tablet analysis // International Journal of Applied Pharmaceutics. – 2018. – Vol. 10, № 1. – Р. 98–102.

  • Logoyda L., Korobko D., Oleshchuk O., Proniv T., Dmutriv M. A HPLC-MS/MS method development and validation for the simultaneous determination of bisoprolol and enalapril in the present of enalaprilat in human plasma // International Journal of Applied Pharmaceutics. – 2018. – Vol. 10, № 2. – Р. 31–40.

  • Logoyda L., Korobko D., Ivanusa I., Kovalenko S. Development of the methodology of the chromatographic determination of nifedipine in medicines // Asian Journal of Pharmaceutical and Clinical Research. – 2017. – № 10(3). – Р. 149-152.

  • Polyauk O., Logoyda L. The investigation of conditions of API from group of calcium channel blockers extraction by organic solvents by using high-performance liquid chromatography as assay method // Asian Journal of Pharmaceutical and Clinical Research. – 2017. – № 10(10). – Р. 354–356.

  • Logoyda L. Robustness evaluation of the chromatographic determination of nifedipine in pharmaceuticals // Ukrainian biopharmaceutical journal. – 2017. – № 3 . – P. 48-51.

  • Logoyda L. Development of methodology for of simultaneous determination of amlodipine, captopril and bisoprolol identification in dosage forms // Ukrainian biopharmaceutical journal. – 2017. – № 4 . – P. 52-54.

  • Logoyda L. Robustness evaluation of the chromatographic determination of verapamil hydrochloride // Medical and clinical chemistry. – 2017. – № 1. – P. 60-64.

  • Logoyda L. Development and methodology for the estimation of bisoprolol in pharmaceuticals // Medical and clinical chemistry. – 2017. – № 2. – P. 34-37.

  • Logoyda L., Kondratova Y., Korobko D.. Robustness evaluation of the chromatographic determination of amlodipine in tablet dosage form // Int J Ayu Pharm Chem. – 2017. – № 7 (1). – Р. 222-229.

  • Logoyda L. S., Proniv T. A., Dmutriv M. I. Development of methodology for identification of simultaneous determination of nifedipine, enalapril and bisoprolol // Медична та клінічна хімія. – 2017. – № 4. – P. 57–60.

  • Logoyda L., Kondratova Y., Korobko D.,. Susla O, Soroka Y., Tsytsiura R., Pidruchna S. Youden's test of the chromatographic determination of captopril in pharmaceuticals // International Journal of Green Pharmacy. – 2017. – Vol. 11, № 3. – Р. 188–191.

  • Logoyda L., Korobko D., Saprun S., Zarivna N. Development of methods for the chromatographic identification of active pharmaceutical ingredient from group of angiotensin-converting enzyme inhibitors in pharmaceuticals // International Journal of Green Pharmacy. – 2017. – Vol. 11, № 4. – Р. 737–741.

  • Logoyda L., Korobko D., Saprun S. Development of methods for identification of calcium channel blockers in medicines // Int. J. Res. Ayurveda Pharm. – 2016. – №7(2). – Р. 88-91.

  • Korobko D., Logoyda L., Markiv I., Berdey I. Computer prognosis of biological activity for a number of new 7-R-8-substituted-1,3-dimethylxantine // Asian Journal of Pharmaceutical and Clinical Research. – 2016. – № 9(6). – Р. 1-5.

  • Logoyda L. S., Polyauk O. B, Korobko D. B., Chir M. B. Development and validation of methods of quantitative determination of loratadine in tablets // Asian Journal of Pharmaceutical Research and Health Care. – 2016. – № 8(2). – Р. 62-66.

  • Kondratova Y., Adebayo T., Logoyda L., Korobko D., Berdey I., Kuchmerovska T. Development of the methodology of the chromatographic determination of amlodipine in medicines // Int. J. Res. Ayurveda Pharm. – 2016. – № 7(4). – Р. 32-35.

  • Logoyda L., Korobko D., Samohalska O., Berdey I. Development of methodology for identification of captopril in medicines // Asian Journal of Pharmaceuticals. – 2016. – № 10(3). – Р. 168-171.

  • Korobko D., Logoyda L., Markiv I., Berdey I. Computer prognosis of biological activity for a number of new 7-R-8-substituted-1,3-dimethylxantine //Asian Journal of Pharmaceutical and Clinical Research. – 2016. – № 9(6). – Р. 1-5.

  • Logoyda L. Development of the methodology of the chromatographic determination of verapamil hydrochloride in medicines // Ukrainian biopharmaceutical journal. – 2016. – № 5. – P. 4-8.

  • Logoyda L. S., Korobko D. B. Validation of assay method of amlodipine in tablets by liquid chromatography // Ukrainian biopharmaceutical journal. – 2016. – № 6. – P. 80-84.

  • Logoyda L.S. Validation of assay method of nifedipine in tablets by liquid chromatography // Medical and clinical chemistry. – 2016. – № 4. – P. 77-81.

  • Logoyda L. Development of methods for identification of desloratadine in medicines // Achievements of Clinical and Experimental Medicine. – 2015.- № 2 (22). – P. 83-86.

  • Logoyda L. Development of the methods for the determination sesquiterpenic acids in stressprotective pharmacological agent with extract of valerian, lemon balm and glycine// Ukrainian biopharmaceutical journal. – 2015. – № 2. – P. 16-21.

  • Logoyda L., Korobko D., Zarivna N. evelopment of methodology for the determination ceterizine hydrochloride in medicines // Ukrainian biopharmaceutical journal. – 2015. – № 4. – P. 62-66.

  • Logoyda L.S., Zarivna N.A., Korobko D.B., Polyak O.B. Development and validation of methods of identification of loratadine tablets // Actual problems of pharmaceutical and medical science and practice. – 2014. – № 1. – P. 55-58.

  • Logoyda L. S.,. Zarivna N. A, Ivanusa I. B. Development of methods of identification phenibut of medicines // The achievements of Clinical and Experimental Medicine. – 2014. – № 1 (20). – P.63-69.

  • Logoyda L. S., Vronska L. V. Assay rosmaric acid in tablets containing dry extracts of valerian and lemon balm and glycine // Medicinal chemistry. – 2011. – № 3. – P. 67-71.

  • Logoyda L. S., Vronsky L. V., Groshovuy T. A. Study of the influence of excipients on the basic parameters of pills containing herbal extracts and glycine // Current issues of pharmaceutical and medical science and practice. – 2011. – № 3. – P. 52-55.

  • Vasenda M. M., Vronsky L. V., Logoyda L. S., Mykhalkiv M. M. Development of methods of quantitative determination of glycine in tablets containing magnesium asparahinat, glycine and thiotriasolin // Pharmaceutical Journal. – 2011. – № 4. – P. 73-76.

  • Logoyda L. S., Vronsky L., Nagirnuy J. P. Market Research sedative medicines from valerian // Pharmaceutical Journal. – 2010. – № 3. – P. 62-65.

  • Logoyda L. S. Vronsky L., Demid A. E., Mykhalkiv M. M. Spectrophotometric determination of glycine in tablets containing glycine and some plant extracts // Pharmaceutical Journal. – 2010. – № 4. – P. 50-54.

  • Logoyda L., Vronska L. Research and selection of extraction of getting extracts of the herb Melissa officinalis // Pharmaceutical Journal. – 2009. – № 3. – P. 56-59.