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Solubility and Dissolution Properties of Generic Rifampicin Raw Materials

Drug development and industrial pharmacy, 2000-01, Vol.26 (4), p.403-408

2000

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Identification of the Mebendazole Polymorphic Form Present in Raw Materials and Tablets Available in South Africa

Drug development and industrial pharmacy, 1998-01, Vol.24 (5), p.485-488

1998

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Application of differential scanning calorimetry and high performance liquid chromatography to determine the effects of mixture composition and preparation during the evaluation of niclosamide-excipient compatibility

Journal of pharmaceutical and biomedical analysis, 1997, Vol.15 (4), p.549-557

1997

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A Study of the Changes During Heating of Paracetamol

Drug development and industrial pharmacy, 1998-01, Vol.24 (5), p.447-453

1998

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Correlation between in vitro release from topical delivery vehicles and microbicidal activity of triclosan

Pharmazie, 2006-01, Vol.61 (1), p.35-40

2006

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The Effect of Polymorphism on Powder Compaction and Dissolution Properties of Chemically Equivalent Oxytetracycline Hydrochloride Powders

Drug development and industrial pharmacy, 1999-01, Vol.25 (9), p.1027-1033

1999

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Physicochemical Properties and X-ray Structural Studies of the Trigonal Polymorph of Carbamazepine

Journal of pharmaceutical sciences, 1987-09, Vol.76 (9), p.744-752

1987

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Evaluation of Compatibility of Tablet Excipients with Albendazole and Closantel Using DSC and HPLC

Drug development and industrial pharmacy, 1997, Vol.23 (6), p.533-537

1997

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Preformulation stability screening of ivermectin with non-ionic emulsion excipients

Pharmazie, 1999-05, Vol.54 (5), p.372-376

1999

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Characterization of Zopiclone Crystal Forms Found Among Generic Raw Materials

Drug development and industrial pharmacy, 2000-01, Vol.26 (5), p.531-537

2000

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Kinetics and mechanism of degradation of the heterocyclic cage compound NGP1-01 in aqueous solution

Pharmazie, 1996-04, Vol.51 (4), p.223-227

1996

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Solid-phase extraction and HPLC determination of levamisole hydrochloride in sheep plasma

Onderstepoort journal of veterinary research, 1996-09, Vol.63 (3), p.209

1996

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Kinetic study of the solid-state photolytic degradation of two polymorphic forms of furosemide

International journal of pharmaceutics, 1992-12, Vol.88 (1), p.275-283

1992

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Characterization of the Solubility and Dissolution Properties of Several New Rifampicin Polymorphs, Solvates, and Hydrates

Drug development and industrial pharmacy, 2001-01, Vol.27 (10), p.1017-1030

2001

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LC-MS Identification of the Degradates of NGP1-01 and Subsequent Development of a Routine Stability-Indicating Method of Analysis

Drug development and industrial pharmacy, 1996, Vol.22 (12), p.1249-1252

1996

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Correlation Between Physico-Chemical Properties and Cohesive Behavior of Furosemide Crystal Modifications

Drug development and industrial pharmacy, 1995, Vol.21 (17), p.1975-1988

1995

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Identification and Prevention of Insoluble Reaction Products Forming after Dissolution of Effervescent Multi-Vitamin Tablets

Drug development and industrial pharmacy, 1995, Vol.21 (17), p.1989-1998

1995

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Polymorphs of nitrofurantoin. I: Preparation and X-ray crystal structures of two monohydrated forms of nitrofurantoin

Journal of Crystallographic and Spectroscopic Research, 1993-09, Vol.23 (9), p.739-744

1993

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Structures of two conformational polymorphs of the cholesterol-lowering drug probucol

Journal of Crystallographic and Spectroscopic Research, 1993-11, Vol.23 (11), p.863-869

1993

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Polymorphs of nitrofurantoin. 2. Preparation and X-ray crystal structures of two anhydrous forms of nitrofurantoin

Journal of Crystallographic and Spectroscopic Research, 1993-10, Vol.23 (10), p.785-790

1993

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Physical characterisation of three pseudopolymorphs of cyclopenthiazide

International journal of pharmaceutics, 1991-03, Vol.69 (3), p.265-268

1991

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Compatibility Study Between Propranolol Hydrochloride and Tablet Excipients Using Differential Scanning Calorimetry

Drug development and industrial pharmacy, 1993, Vol.19 (5), p.623-629

1993

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Determination of the position of the ester bond in a micellar prodrug of phenytoin

International journal of pharmaceutics, 1994-02, Vol.102 (1), p.109-116

1994

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Physical characterisation of solid forms of cyclopenthiazide

International journal of pharmaceutics, 1991-07, Vol.73 (2), p.137-145

1991

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The determination of the amphiphilic properties of a prodrug (DDMS) of phenytoin in aqueous media

International journal of pharmaceutics, 1992-10, Vol.86 (2), p.175-186

1992

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Solubility and Dissolution Properties of Generic Rifampicin Raw Materials

Identification of the Mebendazole Polymorphic Form Present in Raw Materials and Tablets Available in South Africa

Application of differential scanning calorimetry and high performance liquid chromatography to determine the effects of mixture composition and preparation during the evaluation of niclosamide-excipient compatibility

A Study of the Changes During Heating of Paracetamol

Correlation between in vitro release from topical delivery vehicles and microbicidal activity of triclosan

The Effect of Polymorphism on Powder Compaction and Dissolution Properties of Chemically Equivalent Oxytetracycline Hydrochloride Powders

Physicochemical Properties and X-ray Structural Studies of the Trigonal Polymorph of Carbamazepine

Evaluation of Compatibility of Tablet Excipients with Albendazole and Closantel Using DSC and HPLC

Preformulation stability screening of ivermectin with non-ionic emulsion excipients

Characterization of Zopiclone Crystal Forms Found Among Generic Raw Materials

Kinetics and mechanism of degradation of the heterocyclic cage compound NGP1-01 in aqueous solution

Solid-phase extraction and HPLC determination of levamisole hydrochloride in sheep plasma

Kinetic study of the solid-state photolytic degradation of two polymorphic forms of furosemide

Characterization of the Solubility and Dissolution Properties of Several New Rifampicin Polymorphs, Solvates, and Hydrates

LC-MS Identification of the Degradates of NGP1-01 and Subsequent Development of a Routine Stability-Indicating Method of Analysis

Correlation Between Physico-Chemical Properties and Cohesive Behavior of Furosemide Crystal Modifications

Identification and Prevention of Insoluble Reaction Products Forming after Dissolution of Effervescent Multi-Vitamin Tablets

Polymorphs of nitrofurantoin. I: Preparation and X-ray crystal structures of two monohydrated forms of nitrofurantoin

Structures of two conformational polymorphs of the cholesterol-lowering drug probucol

Polymorphs of nitrofurantoin. 2. Preparation and X-ray crystal structures of two anhydrous forms of nitrofurantoin

Physical characterisation of three pseudopolymorphs of cyclopenthiazide

Compatibility Study Between Propranolol Hydrochloride and Tablet Excipients Using Differential Scanning Calorimetry

Determination of the position of the ester bond in a micellar prodrug of phenytoin

Physical characterisation of solid forms of cyclopenthiazide

The determination of the amphiphilic properties of a prodrug (DDMS) of phenytoin in aqueous media

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