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Promethazine orally disintegrating tabletGraben, Roger Dale, Parsons, Daniel L. January 2006 (has links)
Dissertation (Ph.D.)--Auburn University, / Abstract. Vita. Includes bibliographic references (p.175-179).
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Studies on carboxymethylcellulose and starch as tablet disintegrantsKennon, Lloyd, January 1953 (has links)
Thesis (M.S.)--University of Wisconsin--Madison, 1953. / Typescript. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 68-69).
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Surface chemical aspects of aqueous polymer film coatingJohnson, Barbara Alice. January 1985 (has links)
Thesis (Ph. D.)--University of Wisconsin--Madison, 1985. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 202-218).
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Viscoelastic properties and compaction behaviour of pharmaceutical particulate materialsTsardaka, Ekaterini D. January 1990 (has links)
No description available.
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Design and characterization of direct compression excipientsPatel, Chaitanya I. January 1986 (has links)
No description available.
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Biopharmaceutical properties of solid dosage formWoo, Wendy Weng Wah January 1968 (has links)
A completely automatic continuous flow dissolution procedure was developed and tested. Pertinent dissolution conditions were investigated and chosen to study the dissolution characteristics of seven brands of phenylbutazone tablets. A pumping system enabled the simulated digestive fluid to flow from the dissolution vessel into the flow cell of a recording spectrophotometer for a continuous recording of the drug concentration in the dissolution medium, which was gradually changed from an acidic medium to a basic one.
From the "in vitrott” data obtained by this test procedure, a T₅₀% value of 120 minutes was chosen as a limit of acceptance for the test products. The "in vivo" characteristics of six of the brands were compared with those observed for a pharmaceutically acceptable product. Of the seven test products, only four were acceptable on the basis of both the "in vitro" and the "in vivo" data. Correlation of the "in vitro" and the "in vivo" data resulted in "least squares" lines with negative slopes. / Pharmaceutical Sciences, Faculty of / Graduate
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An evaluation of directly compressible tablet bases on the performance of ibuprofen tabletsVawda, Naseem 02 February 2001 (has links)
A research report submitted to the Faculty of Health Sciences, University of the Witwatersrand , in partial fulfilment of the requirements for the degree of Master of Science in Medicine (Pharmaceutical affairs) / Ibuprofen is a phenylpropionic acid derivative, which has analgesic, antiinflammatory and antipyretic actions. It is used in the management of mild to moderate pain, inflammatory conditions, peri-articular disorders, musculoskeletal disorders and joint disorders.
Tablets, like ibuprofen, can be manufactured by three different processes viz. wet granulation, dry granulation and direct compression. With direct compression, the directly compressible base, along with the active ingredient (ibuprofen) and other suitable excipients, can be compressed directly. / IT2018
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Evaluation of potential multi-particulate drug delivery systems /Murty, Aruna Mummini. January 2006 (has links)
Thesis (Ph. D.)--University of Rhode Island, 2006. / Typescript. Includes bibliographical references (leaves 210-235).
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In-vitro testing of the influence of ethanol on the release rate of oral extended-release solid dosage formsCook, Rebecca, January 2007 (has links)
Thesis (M.S.)--Rutgers University, 2006. / "Graduate Program in Pharmaceutical Science." Includes bibliographical references (p. 89-93).
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Drug release from matrix tabletsDaly, P. B. January 1984 (has links)
No description available.
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