Zobrazeno 1 - 10
of 59
pro vyhledávání: '"VOBALABOINA, Venkateswarlu"'
Autor:
Meka, Lingam *, Kesavan, Bhaskar, Kalamata, Venkatasimhadri Naidu, Eaga, Chandra Mohan, Bandari, Suresh, Vobalaboina, Venkateswarlu, Yamsani, Madhusudan Rao
Publikováno v:
In Journal of Pharmaceutical Sciences June 2009 98(6):2122-2132
Autor:
Vobalaboina Venkateswarlu, Srinivas Arutla, Surya Prakash Sola, Annarapu Malleswara Reddy, Hitesh A. Jogia, Lovleen Kumar Garg
Publikováno v:
Dissolution Technologies. 21:45-48
Biorelevant dissolution media were designed and proposed based on physiological and physicochemical properties of the small intestine luminal contents in the fastedand fed-state conditions. Biorelevant dissolution media have proved to be an excellent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a78ace240e90fff36c2e32dec9fc52d1
https://doi.org/10.14227/dt210114p45
https://doi.org/10.14227/dt210114p45
Autor:
Veerareddy, Prabhakar Reddy1 (AUTHOR) vpreddyindia@yahoo.com, Vobalaboina, Venkateswarlu1 (AUTHOR), Ali, Nahid2 (AUTHOR)
Publikováno v:
Journal of Drug Targeting. Feb2009, Vol. 17 Issue 2, p140-147. 8p. 2 Charts, 4 Graphs.
Autor:
Patlolla, Ram Reddy1 (AUTHOR), Vobalaboina, Venkateswarlu1 (AUTHOR) vobala@yahoo.com
Publikováno v:
Journal of Drug Targeting. May2008, Vol. 16 Issue 4, p269-275. 7p. 1 Color Photograph, 1 Chart, 4 Graphs.
Autor:
Hotha Kishore Kumar, Yarramu Narasimha Reddy, Dasari Vijaya Bharathi, Kandibedala Thriveni, Vobalaboina Venkateswarlu
Publikováno v:
American Journal of Analytical Chemistry. :559-569
The aim of the proposed research work was to develop and validate a simple, selective high sensitive and high-throughput assay for the simultaneous estimation of Atorvastatin and Glimepiride in human plasma using liquid chromatography tandem mass spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd5c77454f8d1c4b0aad471e2e9a1bed
https://doi.org/10.4236/ajac.2012.38074
https://doi.org/10.4236/ajac.2012.38074
Autor:
Vobalaboina Venkateswarlu, Vakati Venkata Arvind, Rajesh Kaza, Durgumahanthi Sai Meera, R Nagaraju
Publikováno v:
Current Drug Discovery Technologies. 6:299-305
The core-in-cup matrix tablets of Metoprolol succinate were prepared by wet granulation technique. Of all the investigated formulations, the optimized formulation of MS-09 followed zero-order kinetics of drug release. Trail on MS-09 was formulated us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99d4a0678baf6cafec75a2e4a1137088
https://doi.org/10.2174/157016309789869029
https://doi.org/10.2174/157016309789869029
Autor:
Vobalaboina Venkateswarlu, Veerareddy Prabhakar Reddy, Kesavan Bhaskar, Meka Lingam, Yamsani Madhusudan Rao, Chinnala Krishna Mohan
Publikováno v:
Drug Development and Industrial Pharmacy. 34:719-725
The aim of the investigation is to develop solid lipid nanoparticles (SLN) and nano-structured lipid carrier (NLC) as carriers for topical delivery of nitrendipine (NDP). NDP-loaded SLN and NLC were prepared by hot homogenization technique followed b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dfedf551da38ccce667059694708024
https://doi.org/10.1080/03639040701842485
https://doi.org/10.1080/03639040701842485
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 16:2134-2138
In continuation of our investigations of unsymmetrical bisquaternary monooximes, we synthesized four new series of compounds bridged by hexyl, heptyl, octyl and nonyl groups. All eight monooximes viz., dibromides of 1-(4-hydroxyiminomethylpyridinium)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::980af66cb16a6adf49bf14915f750c47
https://doi.org/10.1016/j.bmcl.2006.01.065
https://doi.org/10.1016/j.bmcl.2006.01.065
Publikováno v:
Journal of Drug Targeting. 14:13-19
The high level of expression of transferrin receptors (Tf-R) on the surface of endothelial cells of the blood-brain-barrier (BBB) had been widely utilized to deliver drugs to the brain. The primary aim of this study was to use transferrin receptor me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24b9738c97d65d9f4bb71fc250063e0a
https://doi.org/10.1080/10611860600613241
https://doi.org/10.1080/10611860600613241
Publikováno v:
Journal of Drug Targeting. 14:632-645
The aim of this research was to study whether the bioavailability of nitrendipine (NDP) could be improved by administering nitrendipine solid lipid nanoparticles (SLN) duodenally to rats.Nitrendipine was incorporated into SLN prepared by hot homogeni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::101337a3bb0eed3a1d3c72815ca66626
https://doi.org/10.1080/10611860600888850
https://doi.org/10.1080/10611860600888850