Zobrazeno 1 - 10
of 17
pro vyhledávání: '"T. E. G. K. Murthy"'
Publikováno v:
Journal of Advanced Pharmaceutical Technology & Research, Vol 6, Iss 3, Pp 118-124 (2015)
A new, simple and accurate liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for simultaneous determination of rosuvastatin (ROS) and metformin (MET) in human plasma was developed. The assay procedure involved simple protein precipitat
Externí odkaz:
https://doaj.org/article/2be8dd8c925547b9af57b7bf524f9a9d
Publikováno v:
Toxicology International. :239-256
The present study aimed to determine the acute toxicity and screening of central analgesic activity of various extracts of Rhizophora apiculata leaves. The animals (Mice) were divided into control (no drug) and extract-treated groups (n=5), which wer
Publikováno v:
International Research Journal Of Pharmacy. 10:85-91
Autor:
B. Praveen Kumar, Suryadevara Vidyadhara, R. L. C. Sasidhar, V. Sri Krishna, T. E. G. K. Murthy
Publikováno v:
Eurasian Journal of Analytical Chemistry. 12:459-468
Autor:
P PavanKumara, T E G K Murthy
Publikováno v:
Journal of Young Pharmacists. 6:44-49
Background:The dried blood spot (DBS) technique is a convenient alternative sample collection method to venipuncture. The use of DBS was first widely introduced in the 1960’s by Dr Guthrie to measure levels of phenylalanine in newborns for the diag
Publikováno v:
Scopus-Elsevier
A simple, precise, accurate, reproducible, robust reverse phase high-performance liquid chromatographic method was developed for the simultaneous estimation of frovatriptan, almotriptan and zolmitriptan in bulk and pharmaceutical dosage forms. The me
Publikováno v:
INDIAN DRUGS. 49:39-46
Compatibility studies are essential for preformulation studies of formulation development. Acetazolamideis a carbonic anhydrase inhibitor used in the treatment and management of cardiac oedema, glaucomaand other conditions. The objective of this stud
Autor:
T. E. G. K. Murthy, G Sailesh
Publikováno v:
INDIAN DRUGS. 49:47-51
Telmisartan is used in the treatment of hypertension. It exhibits poor water solubility. It belongs to class II of Biopharmaceutical Classification system (BCS). It needs enhancement in dissolution and hence bioavailability. The dissolution of drug w
Publikováno v:
Dissolution Technologies. 19:38-42
In vitro release studies were performed for three commercial, modified-release brands of the anti-diabetic drug gliclazide at 30-mg strength. Dissolution media such as 0.1 N HCl (pH 1.2), acetate buffer (pH 4.5), distilled water (pH 7.0), and phospha
Publikováno v:
International Journal of Pharmaceutical Investigation
Background: The aim of the present study was to formulate and optimize the self-emulsifying drug delivery systems (SEDDS) of nevirapine (NVP) by use of 22 factorial designs to enhance the oral absorption of NVP by improving its solubility, dissolutio