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Featured researches published by Matthew A. Augustine.


Journal of Pharmacy and Pharmacology | 1987

Common ion effect on solubility and dissolution rate of the sodium salt of an organic acid

Abu T.M. Serajuddin; Pai-Chang Sheen; Matthew A. Augustine

The solubility and the dissolution rate of the sodium salt of an acidic drug (REV 3164; 7‐chloro‐5‐propyl‐1H,4H‐[1,2,4]triazolo[4,3‐a]quinoxaline‐1,4‐dione) decreased by the effect of common ion present in aqueous media. The solubility of the sodium salt of REV 3164 in a buffered medium was much lower than that in an unbuffered medium. Also, the presence of NaCl decreased its solubility in water. The apparent solubility product (Ksp ***of the salt, however, did not remain constant when the concentration of NaCl was changed. A decrease in Ksp value with the increase in NaCl concentration was observed; for example, the Ksp values at 0 and 1 M NaCl were 7ṁ84 times 10−4 and 3ṁ94 times 10−4 M2, respectively. Even when corrected for the effect of ionic strength, the solubility product decreased. This decrease in the solubility product in the presence of NaCl indicated a decrease in the degree of self‐association (increase in activity coefficient) of the drug in aqueous media.


Drug Development and Industrial Pharmacy | 1988

Hygroscopicity of Celiprolol Hydrochloride Polymorphs

Arvind Narurkar; A. Rashid Purkaystha; Pai-Chang Sheen; Matthew A. Augustine

AbstractThe moisture absorption of two crystalline forms (form I and form II) of celiprolol hydrochloride was investigated at different relative humidities. Celiprolol hydrochloride form I was found to be less hygroscopic than celiprolol hydrochloride form II. It was also found that the high melting form I undergoes a transition to a low melting form II at high relative humidity.


Drug Development and Industrial Pharmacy | 1986

Studies on the Light Stability of Flordipine Tablets in Amber Blister Packaging Material

Arvind Narurkar; Pai-Chang Sheen; David F. Bernstein; Matthew A. Augustine

AbstractAccelerated light conditions have been used in the evaluation of light stability of flordipine tablets. The tablets were subjected to exaggerated light exposure in a fadeometer and to 150 foot candles of fluorescent light in a light cabinet. A comparative study was conducted between tile tablets exposed directly to light and to those covered with amber vinyl sheeting. The color change was evaluated by a tristimulus colorimeter using the Hunter L, a, b scale. The b coordinate was selected for the final evaluation of light stability since it corresponded closely to the visual increase in yellowness with time. The data demonstrated that the amber colored vinyl sheeting had an excellent protective effect on the discoloration of flordipine tablets. Data obtained in the fadeometer in six hours as well as results from exposure in the light cabinet for twenty-nine days, facilitate the comparative evaluation of light stability of flordipine tablets. One hours exposure to fade oneter was found to be equal ...


Drug Development and Industrial Pharmacy | 1987

EFFECT OF PARTICLE SIZE ON THE DISSOLUTION CHARACTERISTICS OF CHLORTHALIDONE

Arvind Narurkar; Pai-Chang Sheen; Ernest L. Hurwitz; Matthew A. Augustine

AbstractThe particle size reduction of chlorthalidone by fluid energy milling, Alpine milling and Fitzpatrick milling were evaluated. The desired particle size was achieved by both the fluid energy milling and Alpine milling processes. Alpine mil1ing, however, is a more complex process and is susceptible to product decomposition, whereas fluid energy milling is a simple and efficient process without any risk of product decomposition. The desired particle size cannot be achieved by Fitzmilling because of the low probability of impaction force on particles. The dissolution rate of the chlorthalidone from chlorthalidone/propranolol hydrochloride tablets (25/80 mg) prepared with fluid energy milled chlorthalidone was significantly better than the tablets prepared with Fitzpatrick - milled chlorthalidone. The minimum effective specific surface area of chlorthalidone needed for maximum dissolution in water was found to be around 3.5 m2/g.


Journal of Pharmaceutical Sciences | 1988

Effect of vehicle amphiphilicity on the dissolution and bioavailability of a poorly water-soluble drug from solid dispersions.

Abu T.M. Serajuddin; Daniel Mufson; David F. Bernstein; Pai-Chang Sheen; Matthew A. Augustine


Journal of Pharmaceutical Sciences | 1990

Improved Dissolution of a Poorly Water-Soluble Drug from Solid Dispersions in Polyethylene Glyco1:Polysorbate 80 Mixtures

Abu T.M. Serajuddin; Pai-Chang Sheen; Matthew A. Augustine


Journal of Pharmaceutical Sciences | 1986

Water migration from soft gelatin capsule shell to fill material and its effect on drug solubility

Abu T.M. Serajuddin; Pai-Chang Sheen; Matthew A. Augustine


Journal of Pharmaceutical Sciences | 1988

Physicochemical basis of increased bioavailability of a poorly water-soluble drug following oral administration as organic solutions

Abu T.M. Serajuddin; Pai-Chang Sheen; Daniel Mufson; David F. Bernstein; Matthew A. Augustine


Journal of Pharmaceutical Sciences | 1986

Preformulation Study of a Poorly Water-Soluble Drug, α-Pentyl-3-(2-quinolinylmethoxy)benzenemethanol: Selection of the Base for Dosage Form Design

Abu T.M. Serajuddin; Pai-Chang Sheen; Daniel Mufson; David F. Bernstein; Matthew A. Augustine


Journal of Pharmaceutical Sciences | 1970

Effect of Lipid Polarity and Cell Design on the In Vitro Transport of Salicylic Acid

Matthew A. Augustine; James Swarbrick

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James Swarbrick

University of Connecticut

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Heng Zhang

University of Connecticut

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Jack Gromek

University of Connecticut

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