Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Ramesh Panchagnula"'
Publikováno v:
Arzneimittelforschung. 55:198-204
The transdermal route provides an attractive alternative to the presently used peroral therapy with tricyclic antidepressants due to the avoidance of first-pass metabolism and the associated side effects. In this investigation an earlier developed tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77ce66d347613bf4c8a6176e75385d2d
https://doi.org/10.1055/s-0031-1296845
https://doi.org/10.1055/s-0031-1296845
Autor:
V. Bhardwaj, Ramesh Panchagnula
Publikováno v:
Drug Development and Industrial Pharmacy. 34:642-649
Rifampicin, one of the main first line anti-TB drugs, shows variable bioavailability in different marketed preparations and reasons cited include physiological, degradation, manufacturing/ processing, solid state, and bioavailability assessment proce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a9cc628a6488ceda8bfc26adcf07f94
https://doi.org/10.1080/03639040701842451
https://doi.org/10.1080/03639040701842451
Autor:
Manthena V.S. Varma, Gunjan Kohli, Kanwal Jit Kaur, Singh I, Shrutidevi Agrawal, Shantaram R Bhade, Yasvanth Ashokraj, Ramesh Panchagnula
Publikováno v:
Clinical Research and Regulatory Affairs. 25:1-12
The current recommended treatment for tuberculosis (TB) is a cocktail of anti-TB drugs, preferably in fixed dose combinations (FDC). Rifampicin, one of the important anti-TB drugs, was reported to exhibit variable bioavailability and is classified as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aad57d594cd07b6d41578efb3a3649ce
https://doi.org/10.1080/10601330701885041
https://doi.org/10.1080/10601330701885041
Publikováno v:
Clinical Research and Regulatory Affairs. 24:61-76
The purpose of this investigation was to develop the dissolution methodology for evaluation of rifampicin-containing fixed-dose combinations of antituberculosis (anti-TB) drugs using BCS-based approach. In this investigation, dissolution studies were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88e24309c0f38b5157e21b0e93cbaadf
https://doi.org/10.1080/10601330701683305
https://doi.org/10.1080/10601330701683305
Publikováno v:
Analytica Chimica Acta. 570:41-45
An accurate, sensitive and specific reversed phase high performance liquid chromatographic method (RP-HPLC) for the simultaneous quantitative determination of the nucleoside reverse transcriptase inhibitors lamivudine, stavudine with the non-nucleosi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0930f674d11ec3ccd7d925c796315b11
https://doi.org/10.1016/j.aca.2006.03.107
https://doi.org/10.1016/j.aca.2006.03.107
Autor:
Singh I, Kaur Kj, Shantaram Ramdos Bade, Jitendra Parmar, Ramesh Panchagnula, Yasvanth Ashokraj
Publikováno v:
International Journal of Pharmaceutics. 313:5-13
Tuberculosis is one of the microbial diseases having a long history of its occurrence and yet to be eradicated from the world. Due to the development of bacterial resistance, treatment has changed from monotherapy to combotherapy to fixed dose combin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79c0035f0c65fe738bb98ab9cc5f95a0
https://doi.org/10.1016/j.ijpharm.2005.12.049
https://doi.org/10.1016/j.ijpharm.2005.12.049
Publikováno v:
Clinical Research and Regulatory Affairs. 23:53-70
The use of fixed dose combinations (FDCs) of anti-TB (Tuberculosis) drugs is recommended by World Health Organization (WHO) and International Union Against Tuberculosis and Lung Disease (IUATLD) to ensure proper treatment of tuberculosis. FDCs have t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b7d43324d79014e29f87726d44c2e62
https://doi.org/10.1080/10601330600718913
https://doi.org/10.1080/10601330600718913
Publikováno v:
Clinical Research and Regulatory Affairs. 23:71-83
The objective of this investigation was to study the effect of contact of rifampicin physical form with the dissolution medium. Solid-state characterization of the residues obtained from powder dissolution studies were conducted and found that rifamp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc1d2fb081bd7c48037c64e45fd49d38
https://doi.org/10.1080/10601330600718939
https://doi.org/10.1080/10601330600718939
Publikováno v:
Journal of Pharmaceutical Sciences. 94:2632-2643
The purpose of this investigation is to evaluate the quantitative contribution of pH-dependent passive permeability on the functional activity of P-glycoprotein (P-gp) in limiting intestinal absorption of weakly basic drugs, in order to include this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3da52f09eb5065684505b3b77c99692f
https://doi.org/10.1002/jps.20489
https://doi.org/10.1002/jps.20489
Autor:
Neeraj Kumar, Alf Lamprecht, V. Bhardwaj, Ramesh Panchagnula, I. Bala, M. N. V. Ravi Kumar, S. Hariharan
Publikováno v:
Journal of Biomedical Nanotechnology. 1:235-258
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2a6b7aa488231fb724198e4695e8639
https://doi.org/10.1166/jbn.2005.033
https://doi.org/10.1166/jbn.2005.033