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Facile hydrolytic cleavage of N,O-diheptafluorobutyryl derivatives of thyroidal amino acids

Journal of Chromatography A, 1982-02, Vol.236 (2), p.493-495

1982

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A simple HPLC method for the dissolution studies on levothyroxine sodium tablets

International journal of pharmaceutics, 1982-01, Vol.12 (4), p.285-294

1982

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Reversed-Phase High-Performance Liquid Chromatographic Analysis of Liothyronine Sodium and Levothyroxine Sodium in Tablet Formulations: Preliminary Studies on Dissolution and Content Uniformity

Journal of pharmaceutical sciences, 1981-02, Vol.70 (2), p.131-134

1981

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Phenotypic differences in dextromethorphan metabolism

Pharmaceutical research, 1989, Vol.6 (1), p.13-19

1989

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Simple and selective high-performance liquid chromatographic method for the determination of hydrochlorothiazide in urine

Journal of chromatography, 1986, Vol.377, p.430-435

1986

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Influence of tablet dissolution on furosemide bioavailability: a bioequivalence study

Pharmaceutical research, 1987-04, Vol.4 (2), p.150-153

1987

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Bioavailability of Hydrochlorothiazide from Tablets and Suspensions

Journal of pharmaceutical sciences, 1984-03, Vol.73 (3), p.359-361

1984

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The effect of food on the absorption of controlled-release theophylline in mini-swine

Pharmaceutical research, 1988, Vol.5 (1), p.48-52

1988

Volltextzugriff (PDF)

Capillary gas chromatographic (GC) analysis of nitroglycerin and its denitration products in plasma

Pharmaceutical research, 1988-02, Vol.5 (2), p.99-102

1988

Volltextzugriff (PDF)

Thiazides XII: A Simple HPLC Method for Determination of Thiazides in Urine

Analytical letters, 1982-01, Vol.15 (6), p.529-536

1982

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Phenytoin II: In Vitro-In Vivo Bioequivalence Standard for 100-mg Phenytoin Sodium Capsules

Journal of pharmaceutical sciences, 1983-03, Vol.72 (3), p.309-310

1983

Volltextzugriff (PDF)

Improved method for the analysis of furosemide in plasma by high-performance liquid chromatography

Journal of chromatography, 1982-02, Vol.227 (2), p.463-469

1982

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Analytical methodology applicable in dissolution testing of norethindrone-mestranol tablets

International journal of pharmaceutics, 1982-01, Vol.11 (3), p.181-186

1982

Volltextzugriff (PDF)

Bioavailability of Hydrocortisone From Commercial 20-mg Tablets

Journal of pharmaceutical sciences, 1984-07, Vol.73 (7), p.964-966

1984

Volltextzugriff (PDF)

Oral Hydrocortisone Pharmacokinetics: A Comparison of Fluorescence and Ultraviolet High-Pressure Liquid Chromatographic Assays for Hydrocortisone in Plasma

Journal of pharmaceutical sciences, 1982-05, Vol.71 (5), p.573-576

1982

Volltextzugriff (PDF)

Thiazides IV: Comparison of Dissolution with Bioavailability of Chlorothiazide Tablets

Journal of pharmaceutical sciences, 1982-07, Vol.71 (7), p.822-824

1982

Volltextzugriff (PDF)

Studies of the dissolution characteristics of norethindrone-mestranol tablets

International journal of pharmaceutics, 1983-01, Vol.15 (2), p.115-123

1983

Volltextzugriff (PDF)

Thiazides VIII: Dissolution Survey of Marketed Hydrochlorothiazide Tablets

Journal of pharmaceutical sciences, 1983-08, Vol.72 (8), p.876-881

1983

Volltextzugriff (PDF)

Fluorometric High-pressure Liquid Chromatographic determination of Hydrocortisone in Human Plasma

Journal of pharmaceutical sciences, 1979-11, Vol.68 (11), p.1374-1376

1979

Volltextzugriff (PDF)

Importance of media selection in establishment of in vitro-in vivo relationships for quinidine gluconate

International journal of pharmaceutics, 1982, Vol.13 (1), p.1-8

1982

Volltextzugriff (PDF)

Dissolution medium—a critical parameter to identify bioavailability problems of furosemide tablets

International journal of pharmaceutics, 1982-01, Vol.11 (1), p.81-90

1982

Volltextzugriff (PDF)

Analysis of Thyroidal Amino Acids in Pharmaceutical Preparations. I - Reverse Phase High Pressure Liquid Chromatography Analysis of Sodium Liothyronine from Tablets

Analytical letters, 1979-01, Vol.12 (11), p.1201-1215

1979

Volltextzugriff (PDF)

Comparison of plasma and urine analyses for thiazides in bioavailability/bioequivalence study

Journal of pharmaceutical sciences, 1981-07, Vol.70 (7), p.833-835

1981

Volltextzugriff (PDF)

Evaluation of Basket and Paddle Dissolution Methods Using Different Performance Standards

Journal of pharmaceutical sciences, 1983-01, Vol.72 (1), p.42-44

1983

Volltextzugriff (PDF)

Thiazides I. Limitations of Bratton-Marshall Colorimetric Assay Method and Its Modifications in the Determination of Chlorothiazide in Bioequivalency Studies

Analytical letters, 1980-01, Vol.13 (2), p.135-148

1980

Volltextzugriff (PDF)

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Facile hydrolytic cleavage of N,O-diheptafluorobutyryl derivatives of thyroidal amino acids

A simple HPLC method for the dissolution studies on levothyroxine sodium tablets

Reversed-Phase High-Performance Liquid Chromatographic Analysis of Liothyronine Sodium and Levothyroxine Sodium in Tablet Formulations: Preliminary Studies on Dissolution and Content Uniformity

Phenotypic differences in dextromethorphan metabolism

Simple and selective high-performance liquid chromatographic method for the determination of hydrochlorothiazide in urine

Influence of tablet dissolution on furosemide bioavailability: a bioequivalence study

Bioavailability of Hydrochlorothiazide from Tablets and Suspensions

The effect of food on the absorption of controlled-release theophylline in mini-swine

Capillary gas chromatographic (GC) analysis of nitroglycerin and its denitration products in plasma

Thiazides XII: A Simple HPLC Method for Determination of Thiazides in Urine

Phenytoin II: In Vitro-In Vivo Bioequivalence Standard for 100-mg Phenytoin Sodium Capsules

Improved method for the analysis of furosemide in plasma by high-performance liquid chromatography

Analytical methodology applicable in dissolution testing of norethindrone-mestranol tablets

Bioavailability of Hydrocortisone From Commercial 20-mg Tablets

Oral Hydrocortisone Pharmacokinetics: A Comparison of Fluorescence and Ultraviolet High-Pressure Liquid Chromatographic Assays for Hydrocortisone in Plasma

Thiazides IV: Comparison of Dissolution with Bioavailability of Chlorothiazide Tablets

Studies of the dissolution characteristics of norethindrone-mestranol tablets

Thiazides VIII: Dissolution Survey of Marketed Hydrochlorothiazide Tablets

Fluorometric High-pressure Liquid Chromatographic determination of Hydrocortisone in Human Plasma

Importance of media selection in establishment of in vitro-in vivo relationships for quinidine gluconate

Dissolution medium—a critical parameter to identify bioavailability problems of furosemide tablets

Analysis of Thyroidal Amino Acids in Pharmaceutical Preparations. I - Reverse Phase High Pressure Liquid Chromatography Analysis of Sodium Liothyronine from Tablets

Comparison of plasma and urine analyses for thiazides in bioavailability/bioequivalence study

Evaluation of Basket and Paddle Dissolution Methods Using Different Performance Standards

Thiazides I. Limitations of Bratton-Marshall Colorimetric Assay Method and Its Modifications in the Determination of Chlorothiazide in Bioequivalency Studies

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