Готові списки джерел за темами / Rosuvastatin calcium

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Добірка наукової літератури з теми "Rosuvastatin calcium"

Автор: Grafiati

Опубліковано: 3 червня 2025

Оновлено: 31 липня 2025

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Статті в журналах з теми "Rosuvastatin calcium"

Cada, Dennis J., Terri Levien, and Danial E. Baker. "Rosuvastatin Calcium." Hospital Pharmacy 39, no. 1 (2004): 52–68. http://dx.doi.org/10.1177/001857870403900107.

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Quirk, Jeremy, Mark Thornton, and Peter Kirkpatrick. "Rosuvastatin calcium." Nature Reviews Drug Discovery 2, no. 10 (2003): 769–70. http://dx.doi.org/10.1038/nrd1205.

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Pawar, Prajakta Arun, Vivek Ranjan Sinha, and Ashok Kumar Yadav. "Compatibility Study and Solid Dose Formulation of Rosuvastatin Calcium." Journal of Modern Pharmacology and Pathology 2 (June 6, 2024): 5. http://dx.doi.org/10.53964/jmpp.2024005.

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Objective: The goal of present study is to recognize acceptable excipients to increase performance and stability of oral solid formulations of rosuvastatin calcium by estimating compatibility study of rosuvastatin calcium and used excipients. Methods: Analytical instruments like fourier transform infrared spectroscopy Spectrum RX 1, [differential scanning calorimetry-Q20, TA], Bruker Advance Neo 500MHz NMR spectrometer, thin layer chromatography] were utilized. Excipients and rosuvastatin calcium were got from Loba chemie and Biocon, respectively. USP1-type dissolution apparatus, and Auto Dock

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Sutiswa, Shandra Isasi, Yeyet Cahyati, and Diky Mudhakir. "PENINGKATAN DISOLUSI ROSUVASTATIN CALSIUM DARI SEDIAAN TABLET DENGAN TEKNIK LIQUISOLID DAN PEMBENTUKAN KOMPLEKS INKLUSI." Jurnal Riset Kefarmasian Indonesia 1, no. 2 (2019): 93–102. http://dx.doi.org/10.33759/jrki.v1i2.21.

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Rosuvastatin calcium is a salt form of rosuvastatin with antilipidemia activity. Rosuvastatin Calcium classified in class two of Biopharmaceutics Clasification System (BCS) has low solubility in water (17.96 mg / L) and high permeability. Based on this, rosuvastatin calcium needs to be formulated appropriately in order to produce high bioavailability and maximum therapeutic effect. The bioavailability of BCS 2 drug is determined by the dissolution rate of the drug in gastrointestinal fluid so that a technique is needed in formulating the drug. This study aims to develop a formulation technique

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Rahul, Rajan R. S.1* Anitha Thomas2. "Simultaneous Estimation Of Rosuvastatin Calcium And Ezetimibe In Their Combined Tablet Dosage Form By Absorbance Ratio Method." International Journal in Pharmaceutical Sciences 2, no. 9 (2024): 180–86. https://doi.org/10.5281/zenodo.13646983.

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A simple, accurate, precise, and economical Q-absorbance ratio UV-spectrophotometric method was developed and validated for simultaneous estimating Rosuvastatin Calcium and Ezetimibe in combined tablet dosage form. The solvent used was a 1:1 t mixture of Isopropyl alcohol and distilled water. Two wavelengths 244nm (λmax of Rosuvastatin Calcium) and 240nm (Isoabsorptive point) were selected to estimate Rosuvastatin Calcium and Ezetimibe for the Q-Absorbance ratio method. The drug concentration was determined using the ratio of absorbance at the iso-absorptive point (λ1 = 240 nm) a

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Vishal, Sambhaji Sutar1* Nitin Anandrao Kamble2. "Phytochemical Screening And Gc-Ms Analysis Of Ocimum Sanctum, Amaranthus Viridis, And Cystone." International Journal in Pharmaceutical Sciences 2, no. 9 (2024): 258–70. https://doi.org/10.5281/zenodo.13694788.

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Brijesh, Kumar Rajesh Kumar* Ashutosh Kumar Rikesh Patel. "SIMULTANEOUS RP-HPLC METHOD DEVELOPMENT AND VALIDATION OF FENOFIBRATE AND ROSUVASTATIN CALCIUM IN BULK AND TABLET DOSAGE FORM." Indo American Journal of Pharmaceutical Sciences 04, no. 11 (2017): 4288–97. https://doi.org/10.5281/zenodo.1057885.

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Анотація:

An isocratic reversed-phase liquid chromatograpic assay method was developed for the quantitative determination of fenofibrate and rosuvastatin calcium in bulk and tablet dosage form. A Lichrosphere Select-B C8 (250x4.6mm & 5.0μm) column with a mobile phase containing Solution A (Milli-Q water has pH3.0 made by orthophosphoric acid): Methanol (20:80). The flow rate was 1.0 mL min−1: 1.5 ml/min and the detection of fenofibrate and rosuvastatin calcium was carried out on absorbance detector at 254nm.The retention times was 12 min (rosuvastatin- 3.40, fenofibrate-7.75). A linear response r2 &

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Pimpale, Awdhut, and Rajendra Kakde. "Development and Validation of Stability-Indicating Assay Method by RP-HPLC for Simultaneous Estimation of Rosuvastatin Calcium and Fenofibrate in Pharmaceutical Dosage Form." Journal of Drug Delivery and Therapeutics 10, no. 4 (2020): 79–86. http://dx.doi.org/10.22270/jddt.v10i4.4203.

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A Simple, precise, and accurate stability-indicating reversed-phase high-performance liquid chromatography method has been established for the simultaneous estimation of rosuvastatin calcium and fenofibrate in combined bulk and tablet formulation. The chromatographic separation was performed on reverse phase Princeton (C18) (250 mm x 4.6 mm, 5µ) column with mobile phase as a mixture of water (pH adjusted to 3.0 with orthophosphoric acid) and acetonitrile in the ratio (40:60) v/v at the flow rate 1.0 ml/min. Detection was carried out at wavelength 240 nm. The retention time under the optimized

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Jana, Kallol, and Beduin Mahanti. "An Improved Efficient Chromatographic Development and Validation for Quantitative Determination of Rosuvastatin Calcium and Cholecalciferol in Solid Pharmaceutical Tablets Dosage Forms." INTERNATIONAL JOURNAL OF PHARMACEUTICAL QUALITY ASSURANCE 13, no. 04 (2022): 433–40. http://dx.doi.org/10.25258/ijpqa.13.4.15.

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The simple, reliable, sensitive and isocratic analytical chromatography was developed for the estimation, separation and validation of both the drugs rosuvastatin calcium and cholecalciferol in tablets dosage forms. Chromatographic elution was attained by C18 thermo, 250 x 4.6 mm column, with particle size 5 μm and 1.5 mL per minute flow rate using mobile phase as methanol : acetonitrile : triethanolamine (55:45:0.4%). Detection of both drugs were monitored at 265 nm. The retention time of rosuvastatin calcium and cholecalciferol were 1.336 and 6.031 minutes, respectively and overall chromatog

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Kansara, Devansh, Usmangani K. Chhalotiya, Hetaben M. Kachhiya, and Ishita Patel. "Development of TLC method for simultaneous estimation of novel combination of amlodipine besylate, rosuvastatin calcium, and fimasartan potassium in synthetic mixture." Journal of Chemical Metrology 14, no. 2 (2020): 142–52. http://dx.doi.org/10.25135/jcm.45.20.07.1744.

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An accurate, sensitive, robust and precise high performance thin layer liquid chromatography method was developed based on ICH Q2 (R1) guidelines for estimation of novel combination of Amlodipine besylate, Rosuvastatin calcium and Fimasartan potassium in bulk and its synthetic mixture. Pre-coated silica gel aluminum plate 60 F254 was selected as the stationary phase and n-hexane, n-butanol, methanol, and Glacial Acetic Acid (5.7:2:2.3:0.1, v/v/v/v) was selected as mobile phase. All three drugs showing appreciable absorbance at the common wavelength of 242 nm were selected for quantification of

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Більше джерел

Дисертації з теми "Rosuvastatin calcium"

Tetila, Amanda Feba. "Utilização de plasma rico em plaquetas e rosuvastatina no processo cicatricial de feridas de coelhos: estudo longitudinal." Universidade do Oeste Paulista, 2018. http://bdtd.unoeste.br:8080/jspui/handle/jspui/1126.

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Submitted by Michele Mologni (mologni@unoeste.br) on 2019-02-06T16:42:48Z No. of bitstreams: 1 Amanda Feba Tetila.pdf: 624432 bytes, checksum: 02fdc1e6bd21bfbcd706448afe017b9c (MD5) Made available in DSpace on 2019-02-06T16:42:49Z (GMT). No. of bitstreams: 1 Amanda Feba Tetila.pdf: 624432 bytes, checksum: 02fdc1e6bd21bfbcd706448afe017b9c (MD5) Previous issue date: 2018-09-28 Tissue engineering, as well as regenerative medicine, are fields that have been growing in recent years, aiming to repair, regenerate or replace damaged tissues and organs. PRP has been extensively studied in the a

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Lin, Chia-yu, and 林佳諭. "Development of Rosuvastatin calcium oral tablet bioequivalent with Crestatinâ -Investigate the degradation of this product by a Stability- Indicating LC Method." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/38793410768564788803.

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碩士 大仁科技大學 製藥科技研究所 100 Rosuvastatin calcium, bis [(E)-7 [4-(4-fluorophenyl)-6 isopropyl- 2-[methyl (methyl-sulphonyl) amino] pyrimidin-5-yl] (3R, 5S) -3,5-dihydroxyhept-6-enoic acid] calcium salt, was approved by the US FDA in August 2003 to reduce cholesterol levels in patients with hypercholesterolaemia. This agent is a selective, potent and competitive inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase catalizing the conversion of HMG-CoA to mevalonate, which is an early and rate-limiting step in cholesterol biosynthesis. In the literature, the Rosuvastatin ca

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Частини книг з теми "Rosuvastatin calcium"

"Rosuvastatin Calcium." In Hale’s Medications & Mothers’ Milk™ 2019. Springer Publishing Company, 2018. http://dx.doi.org/10.1891/9780826150356.0914.

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"Risedronate sodium to Rosuvastatin calcium." In Pharmaceutical Substances, edited by Axel Kleemann, Jürgen Engel, Bernhard Kutscher, and Dietmar Reichert. Georg Thieme Verlag, 2009. http://dx.doi.org/10.1055/b-0035-108711.

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Тези доповідей конференцій з теми "Rosuvastatin calcium"

Kulkarni, N. S., S. N. Dhole, and N. S. Ranpise. "Development and evaluation of Self Micro-emulsifying drug delivery for rosuvastatin calcium." In 2013 International Conference on Advanced Nanomaterials and Emerging Engineering Technologies (ICANMEET). IEEE, 2013. http://dx.doi.org/10.1109/icanmeet.2013.6609263.

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Nhu-Trang, Tran-Thi, Hoang-Nguyen Nguyen, Thi-Xong Thach, Hoang-Nguyen Nguyen, Cong-Hau Nguyen, and Minh Huy Do. "A simple electrochemical method for determination of rosuvastatin calcium in cholesterol-lowering medical products." In II INTERNATIONAL SCIENTIFIC FORUM ON COMPUTER AND ENERGY SCIENCES (WFCES-II 2021). AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0099661.

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