Search Results - "DALI, Mandar"
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Preclinical and Early Clinical Development of PTC596, a Novel Small-Molecule Tubulin-Binding Agent
Published in Molecular cancer therapeutics (01-10-2021)“…PTC596 is an investigational small-molecule tubulin-binding agent. Unlike other tubulin-binding agents, PTC596 is orally bioavailable and is not a…”
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Effect of pepsin on maintaining the supersaturation of the HCl salt of a weakly basic drug: a case study
Published in Pharmaceutical development and technology (02-04-2016)“…The impact of pepsin on the maintenance of supersaturated solution of the HCl salt of a weakly basic drug was evaluated in simulated gastric fluid by…”
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The effect of the physical states of binders on high-shear wet granulation and granule properties: a mechanistic approach towards understanding high-shear wet granulation process. Part I. Physical characterization of binders
Published in Journal of pharmaceutical sciences (01-01-2011)“…In this study, the objective is to investigate the effect of the physical state of a binder on wet granulation and granule properties using a binary model…”
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Phase 1 Study of Safety, Tolerability, and Pharmacokinetics of PTC299, an Inhibitor of Stress-Regulated Protein Translation
Published in Clinical pharmacology in drug development (01-07-2016)“…PTC299 is a novel small molecule that specifically blocks the production of protein from selected mRNAs that under certain conditions use noncanonical…”
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Phosphonooxymethyl prodrugs of the broad spectrum antifungal azole, ravuconazole: Synthesis and biological properties
Published in Bioorganic & medicinal chemistry letters (03-11-2003)“…Synthesis of phosphonooxymethyl derivatives of ravuconazole, 2 (BMS-379224) and 3 (BMS-315801) and their biological evaluation as potential water-soluble…”
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First‐in‐Human Studies of Pharmacokinetics and Safety of Utreloxastat (PTC857), a Novel 15‐Lipooxygenase Inhibitor for the Treatment of Amyotrophic Lateral Sclerosis
Published in Clinical pharmacology in drug development (01-02-2023)“…Utreloxastat (PTC857) is a 15‐lipoxygenase inhibitor being developed to treat amyotrophic lateral sclerosis. This first‐in‐human study investigated the safety…”
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Particle Size Distributions in Mesh Cuts and Microscopically Estimated Volumetric Shape Factors
Published in Drug development and industrial pharmacy (01-01-1999)“…When particle size distribution parameters are calculated from sieve analysis, it is generally assumed that the distribution within the particle cut is either…”
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The effect of the physical states of binders on high-shear wet granulation and granule properties: a mechanistic approach toward understanding high-shear wet granulation process. Part II. Granulation and granule properties
Published in Journal of pharmaceutical sciences (01-01-2011)“…The objective is to provide mechanistic understanding of a preferred wet granulation process that a binder is added in a dry state. Blends of CaCO(3) and…”
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Understanding drug-excipient compatibility: Oxidation of compound A in a solid dosage form
Published in Pharmaceutical development and technology (01-10-2009)“…Drug-excipient compatibility studies lay the foundation for designing a chemically stable formulation for clinical and commercial development. This article…”
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Effect of change in shape factor of a single crystal on its dissolution behavior
Published in Pharmaceutical research (1996)“…To study the effect of change in the shape factor of real crystals on their dissolution behavior using a potassium dichromate crystal as a model for…”
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Determination of Mass Transfer Dissolution Rate Constants from Critical Time of Dissolution of a Powder Sample
Published in Pharmaceutical development and technology (1999)“…ABSTRACT This article presents a method for obtaining mass transfer dissolution rate constants of polydisperse, particulate solids under given hydrodynamic…”
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Particle Size Distributions from Multiparticulate Dissolution
Published in Drug development and industrial pharmacy (01-01-1998)“…Abstract It has been demonstrated theoretically that the particle size distribution of particles in a given sieve fraction of a powder may be assessed by means…”
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Powder dissolution as a tool to estimate particle size and shape parameters of crystalline solids
Published 01-01-1997“…A parallelepiped geometry has been considered to mimic real particles, instead of a spherical approximation. A model that describes the dissolution of a single…”
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Dissertation -
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Calculation of Intensified Sampling Plans in Blending Validation
Published in Pharmaceutical development and technology (1997)Get full text
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Blending validation of low drug content dosage forms
Published in Pharmaceutical development and technology (1996)Get more information
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