Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Sudharshan Hariharan"'
Autor:
Thomas R. Fleming, Christine E. Garnett, Laurie S. Conklin, Solange Corriol-Rohou, Sudharshan Hariharan, Daphne Hsu, Guenther Mueller-Velten, Yeruk Mulugeta, Ronald Portman, Mark D. Rothmann, Norman L. Stockbridge, Simon Wandel, Jialu Zhang, Lynne Yao
Publikováno v:
Therapeutic innovationregulatory science. 57(1)
Even with recent substantive improvements in health care in pediatric populations, considerable need remains for additional safe and effective interventions for the prevention and treatment of diseases in children. The approval of prescription drugs
Publikováno v:
Ophthalmology and Eye Diseases, Vol 2009, Iss 1, Pp 21-31 (2009)
Objective: To delineate the plasma pharmacokinetics and determine the corneal uptake of valine based stereoisomeric dipeptide prodrugs of acyclovir (ACV) in rats. Methods: Male Sprague-Dawley rats were used for the study. Pharmacokinetics of ACV, L-v
Externí odkaz:
https://doaj.org/article/68eef9ebbed647cd9c51195d698f1c50
Autor:
Gowraganahalli Jagadeesh, Mohan K. Sapru, Tzu-Yun McDowell, Ququan Liu, Norman Stockbridge, Sudharshan Hariharan, Venkateswaran C Pillai, Martin Rose, Fortunato Senatore, Mary Ross Southworth
Publikováno v:
American Journal of Cardiovascular Drugs. 19:11-20
Distributive shock is a subset of shock marked by decreased systemic vascular resistance, organ hypoperfusion and altered oxygen extraction. Despite the use of intravenous fluids and either higher dose of catecholamines or other additional exogenous
Autor:
R. Angelo de Claro, Richard Pazdur, Nicholas Richardson, Chao Liu, Gregory H. Reaman, Margret Merino, Anusha Ande, Simbarashe Zvada, Sudharshan Hariharan, Ann T. Farrell
Publikováno v:
Pediatric bloodcancerREFERENCES. 67(12)
On May 16, 2019, the U.S. Food and Drug Administration (FDA) approved dalteparin sodium for the treatment of symptomatic venous thromboembolism (VTE) to reduce the risk of recurrence in pediatric patients 1 month of age and older. Approval was primar
Publikováno v:
The Journal of Clinical Pharmacology. 54:884-888
Publikováno v:
AAPS PharmSciTech. 15:1454-1467
The purpose of this study was to develop a clear aqueous mixed nanomicellar formulation (MNF) of dexamethasone utilizing both D-α-tocopherol polyethylene glycol-1000 succinate (Vit E TPGS) and octoxynol-40 (Oc-40). In this study, Vit E TPGS and Oc-4
Autor:
Jwala Jwala, Sudharshan Hariharan, Sai H.S. Boddu, Ashim K. Mitra, Ravinder Earla, Kishore Cholkar
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 52:525-533
A sensitive, selective, accurate and robust LC-MS/MS method was developed and validated for the quantitative determination of glucocorticoids in rabbit ocular tissues. Samples were processed by a simple liquid- liquid extraction procedure. Chromatogr
Publikováno v:
Clinical Research and Regulatory Affairs. 26:65-72
The objective of this work was to study the disposition kinetics of valine-valine-acyclovir (VVACV), a dipeptide ester prodrug of acyclovir following intravenous and oral administrations in rat. A validated LC-MS/MS analytical method was developed fo
Publikováno v:
Pharmaceutical Research. 26:1270-1282
The objectives were (i) to test in vivo functional activity of MRP2 on rabbit corneal epithelium and (ii) to evaluate modulation of P-gp and MRP2 mediated efflux of erythromycin when co-administered with corticosteroids.Cultured rabbit primary cornea
Publikováno v:
International Journal of Pharmaceutics. 362:93-101
In vivo systemic absorption of the amino acid prodrugs of acyclovir (ACV) after oral administration was evaluated in rats. Stability of the prodrugs, l -alanine-ACV (AACV), l -serine-ACV (SACV), l -isoleucine-ACV (IACV), γ-glutamate-ACV (EACV) and l