Showing 141 - 160 results of 5,484 for search '"Pharmaceutical"', query time: 0.06s Refine Results
  1. 141

    Utility of σ and π-Acceptors for the Spectrophotometric Determination of Gemifloxacin Mesylate in Pharmaceutical Formulations by Marothu Vamsi Krishna, Dannana Gowri Sankar

    Published 2008-01-01
    “…The proposed methods were applied successfully to the determination of GFX in pharmaceutical formulations with good accuracy and precision.…”
    Get full text
    Article
  2. 142
  3. 143
  4. 144

    Simple UV Spectrophotometric Method for the Determination of Fluvastatin Sodium in Bulk and Pharmaceutical Formulations by J. Saminathan, A. S. Sankar, K. Anandakumar, T. Vetrichelvan

    Published 2009-01-01
    “…The proposed method was successfully applied to the determination of FVS in pharmaceutical formulations without any interference from common excipients. …”
    Get full text
    Article
  5. 145
  6. 146

    Spectrophotometric Determination of Antidepressant Drug Duloxetine in Pharmaceutical Preparations using π-Acceptors by Sidika Ertürk Toker, Armagan Önal

    Published 2012-01-01
    “…The proposed methods have been successfully applied to the pharmaceutical analysis without any interference from excipients. …”
    Get full text
    Article
  7. 147
  8. 148

    Application of a nucleophilic substitution reaction for spectrofluorimetric quantification of ketamine in pharmaceutical and plasma matrices by Reem M. Alnemari, Maram H. Abduljabbar, Yusuf S. Althobaiti, Farooq M. Almutairi, Muneef M. Aldhafeeri, Atiah H. Almalki, Sherif Ramzy

    Published 2024-12-01
    “…The method demonstrated exceptional sensitivity with detection and quantitation limits of 2.37 ng/mL and 7.18 ng/mL, respectively, allowing for the detection of ketamine in both pharmaceutical and plasma samples. The method was precise (%RSD < 1) accurate (%R = 99.74%) and robust (% R ± SD from 98.00 ± 1.11 to 99.97 ± 0.75). …”
    Get full text
    Article
  9. 149

    Advancements in electron paramagnetic resonance (EPR) spectroscopy: A comprehensive tool for pharmaceutical research by Bešić Erim, Rajić Zrinka, Šakić Davor

    Published 2024-12-01
    “…Despite its extensive utility in these areas, EPR spectroscopy’s application within pharmaceutical science has historically been constrained, primarily due to factors such as high equipment costs, a steep learning curve, complex spectral deconvolution and analysis, and a traditional lack of emphasis on single-electron chemistry in pharmaceutical research. …”
    Get full text
    Article
  10. 150

    Development and Validation of LC Method for the Determination of Famciclovir in Pharmaceutical Formulation Using an Experimental Design by Srinivas Vishnumulaka, Narasimha Rao Medicherla, Allam Appa Rao, G. Edela Srinubabu

    Published 2008-01-01
    “…A rapid and sensitive RP-HPLC method with UV detection (242 nm) for routine analysis of famciclovir in pharmaceutical formulations was developed. Chromatography was performed with mobile phase containing a mixture of methanol and phosphate buffer (50:50, v/v) with flow rate 1.0 mL min−1. …”
    Get full text
    Article
  11. 151
  12. 152

    Lean Approach of Pharmaceutical Installations At Hospital ABC Purbalingga to Increase Pharmacy Service Efficiency by Rani Aulia Imran

    Published 2022-07-01
    “…A good pharmacy quality services are intended to the pharmaceutical product which is well prepared, stored, distributed, dispensed and discarded. …”
    Get full text
    Article
  13. 153
  14. 154

    Chemometric-Assisted Spectrophotometric Method for the Simultaneous Determination of Ciprofloxacin and Doxycycline Hyclate in Pharmaceutical Formulations by Tadele Eticha, Getu Kahsay, Fitsum Asefa, Teklebrhan Hailu, Hailekiros Gebretsadik, Tesfamichael Gebretsadikan, Boovizhikannan Thangabalan

    Published 2018-01-01
    “…Two chemometrics methods—principal component regression and partial least squares—were developed for simultaneous spectrophotometric estimation of ciprofloxacin and doxycycline hyclate in pharmaceutical dosage forms without any pretreatment. …”
    Get full text
    Article
  15. 155

    Reform of economic evaluation of medicines in Spain: proposals from the Advisory Committee for Pharmaceutical Financing by Marta Trapero-Bertran, Jaume Puig-Junoy, Emilio J. Alegre-del-Rey, Ana Clopés, Félix Lobo, Ana Ortega

    Published 2025-01-01
    “…This paper describes the reforms recommended by the Advisory Committee on the Financing of Pharmaceuticals (CAPF) for the National Health System (NHS) of Spain from 2019 to 2024 for the drug pricing and reimbursement process, to integrate economic evaluations and improve efficiency and sustainability. …”
    Get full text
    Article
  16. 156

    Electrochemical Analysis of Antichemotherapeutic Drug Zanosar in Pharmaceutical and Biological Samples by Differential Pulse Polarography by Chennupalle Nageswara Reddy, Puthalapattu ReddyPrasad, NeelamYughandhar Sreedhar

    Published 2013-01-01
    “…Excipients did not interfere with the determination of zanosar in pharmaceutical formulation and spiked urine samples. Precision and accuracy of the developed method were checked by recovery studies in pharmaceutical formulation and spiked human urine samples.…”
    Get full text
    Article
  17. 157

    New Spectrophotometric Method for the Determination of Bosentan - An Anti-Hypertensive Agent in Pharmaceutical Dosage Forms by A. Narendra, D. Deepika, M. Mathrusri Annapurna

    Published 2012-01-01
    “…A new, simple and sensitive spectrophotometric method in ultraviolet region has been developed for the determination of Bosentan in bulk and in pharmaceutical formulations. Bosentan exhibits absorption maxima at 273 nm with apparent molar absorptivity of 1.3293×104 L/mol.cm in methanol and octane 1-sulfonic acid solvent mixture. …”
    Get full text
    Article
  18. 158

    A Simple and Sensitive HPLC Method for Simultaneous Analysis of Nabumetone and Paracetamol in Pharmaceutical Formulations by Prafulla Kumar Sahu, M. Mathrusri Annapurna, Dillipkumar Sahoo

    Published 2011-01-01
    “…The method has been successively applied to pharmaceutical formulation. No chromatographic interference from the tablet excipients was found. …”
    Get full text
    Article
  19. 159
  20. 160