Zobrazeno 1 - 10
of 84
pro vyhledávání: '"J.K. Lalla"'
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 11:385-388
An HPLC method is described for the determination of drotaverine in plasma; papaverine is used as the internal standard. The lower limit of quantitation is 50 ng ml −1 with an inter-assay precision (RSD) of below 4%. The method has been validated a
Publikováno v:
Journal of ethnopharmacology. 78(1)
Oral and externally used dermatological preparation for acne vulgaris employing herbal extracts have been developed and standardized, the herbal extracts used here were of the plants described in ayurvedic treatise like Bhavprakasha Nighantu and Char
Autor:
Michael P. Schön, B. Rama, J.K. Lalla, S.M. Al-Saidan, F. Höche, B. Jayaram, M.P. Schön, Johannes Wohlrab, Claudia Drewniok, Charles Martin Heard, O. Pillai, S. Mac-Mary, Patrice Muret, Yellela S.R. Krishnaiah, N. Leveque, P. Humbert, P. Bhaskar, K. Abdulmajed, Christopher McGuigan, T. Klapperstück, J.-P. Kantelip, M. Gloor, W.J. Pugh, S. Makki, R. Panchagnula, D.V. Chandrasekhar
Publikováno v:
Skin Pharmacology and Physiology. 17:323-324
Autor:
J.-P. Kantelip, B. Rama, Christopher McGuigan, M.P. Schön, J.K. Lalla, Patrice Muret, P. Bhaskar, N. Leveque, P. Humbert, B. Jayaram, Charles Martin Heard, K. Abdulmajed, W.J. Pugh, Michael P. Schön, S.M. Al-Saidan, Claudia Drewniok, T. Klapperstück, Yellela S.R. Krishnaiah, S. Mac-Mary, M. Gloor, S. Makki, O. Pillai, R. Panchagnula, F. Höche, Johannes Wohlrab, D.V. Chandrasekhar
Publikováno v:
Skin Pharmacology and Physiology. 17:325-326
Autor:
J.K. Lalla, Shruti U. Bhat
Publikováno v:
Journal of pharmaceutical sciences. 82(12)
Design and evaluation of 8-h controlled-release isosorbide dinitrate capsules representing 20.0 and 40.0 mg of the drug are described. The formulation conforms to the total drug incorporated in the dosage form. In vitro dissolution studies indicate t
Publikováno v:
Journal of pharmaceutical sciences. 82(12)
Isosorbide dinitrate (ISDN) capsules containing 20.0 and 40.0 mg of the drug (reported earlier in Part I of this series) were evaluated in vivo in eight healthy volunteers in a double-blind study with marketed sustained-release preparations containin
Autor:
S.M. Al-Saidan, Y.S.R. Krishnaiah, D.V. Chandrasekhar, J.K. Lalla, B. Rama, B. Jayaram, P. Bhaskar
Publikováno v:
Skin Pharmacology & Physiology; Nov2004, Vol. 17 Issue 6, p310-320, 11p
Publikováno v:
Journal of Controlled Release. 9:43-55
Formulation and evaluation of controlled release nitroglycerin capsules are being reported. The formulation aspects include evaluation of polymer membranes for drug diffusion, coating of sugar beads with drug followed by rate-controlling membrane, an
Publikováno v:
Journal of Controlled Release. 8:211-222
A solid dispersion of indomethocin in PEG 6000 was incorporated in an Eudragit matrix and compressed into tablets, each containing 35 mg of drug in controlled release dosage form. The tablets were investigated before and after acetone treatment for p
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