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A T Serajuddin

Showing results (21-30 of 27) with videos related to

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Journal of Pharmaceutical Sciences|May 1, 1986
Preformulation study of a poorly water-soluble drug, alpha-pentyl-3-(2-quinolinylmethoxy)benzenemethanol: selection of the base for dosage form designA T Serajuddin, P C Sheen, D Mufson, et al.
Journal of Pharmaceutical Sciences|April 1, 1988
Physicochemical basis of increased bioavailability of a poorly water-soluble drug following oral administration as organic solutionsA T Serajuddin, P C Sheen, D Mufson, et al.
Journal of Pharmaceutical Sciences|May 1, 1988
Effect of vehicle amphiphilicity on the dissolution and bioavailability of a poorly water-soluble drug from solid dispersionsA T Serajuddin, P C Sheen, D Mufson, et al.
Journal of Pharmaceutical and Biomedical Analysis|November 1, 1993
Solid-state NMR and IR for the analysis of pharmaceutical solids: polymorphs of fosinopril sodiumH G Brittain, K R Morris, D E Bugay, et al.
Journal of Pharmaceutical Sciences|September 1, 1991
Optimization of cosolvent concentration and excipient composition in a topical corticosteroid solutionS A Varia, M M Faustino, A B Thakur, et al.
PDA Journal of Pharmaceutical Science and Technology|May 24, 2000
Moisture sorption behavior of selected bulking agents used in lyophilized productsM G Fakes, M V Dali, T A Haby, et al.
Journal of Pharmaceutical Sciences|July 7, 1999
Selection of solid dosage form composition through drug-excipient compatibility testingA T Serajuddin, A B Thakur, R N Ghoshal, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Journal of Pharmaceutical Sciences|May 1, 1986
Preformulation study of a poorly water-soluble drug, alpha-pentyl-3-(2-quinolinylmethoxy)benzenemethanol: selection of the base for dosage form designA T Serajuddin, P C Sheen, D Mufson, et al.
Journal of Pharmaceutical Sciences|April 1, 1988
Physicochemical basis of increased bioavailability of a poorly water-soluble drug following oral administration as organic solutionsA T Serajuddin, P C Sheen, D Mufson, et al.
Journal of Pharmaceutical Sciences|May 1, 1988
Effect of vehicle amphiphilicity on the dissolution and bioavailability of a poorly water-soluble drug from solid dispersionsA T Serajuddin, P C Sheen, D Mufson, et al.
Journal of Pharmaceutical and Biomedical Analysis|November 1, 1993
Solid-state NMR and IR for the analysis of pharmaceutical solids: polymorphs of fosinopril sodiumH G Brittain, K R Morris, D E Bugay, et al.
Journal of Pharmaceutical Sciences|September 1, 1991
Optimization of cosolvent concentration and excipient composition in a topical corticosteroid solutionS A Varia, M M Faustino, A B Thakur, et al.
PDA Journal of Pharmaceutical Science and Technology|May 24, 2000
Moisture sorption behavior of selected bulking agents used in lyophilized productsM G Fakes, M V Dali, T A Haby, et al.
Journal of Pharmaceutical Sciences|July 7, 1999
Selection of solid dosage form composition through drug-excipient compatibility testingA T Serajuddin, A B Thakur, R N Ghoshal, et al.
Pageof 3