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Related Concept Videos

Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence01:27

Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence

Changes in polymorphic forms can significantly influence the bioavailability of poorly soluble drugs. Although the FDA defines pharmaceutical equivalence based on having the same active ingredient, dosage form, and route of administration, it does not automatically disqualify products with different polymorphic forms. This means two products with different polymorphs can still be deemed pharmaceutically equivalent. However, polymorphic differences can affect properties like wettability,...
Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism01:21

Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism

Polymorphism refers to the existence of a drug substance in multiple crystalline forms, known as polymorphs. Recently, this term has been expanded to include solvates (forms containing a solvent), amorphous forms (non-crystalline forms), and desolvated solvates (forms from which the solvent has been removed).
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
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Antipsychotic Drugs: Typical and Atypical Agents

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Psychosis: Goals of Pharmacotherapy

Antipsychotic drugs are a crucial treatment method for acute and chronic psychoses, bipolar illness, and behavioral disorders. The selection of these drugs depends on several factors, including the state of the disease, clinical judgment, possible drug interactions, and the patient's sensitivity to adverse effects. In immediate scenarios, such as delirium and dementia, short-term treatment with low doses of high-potency typical or atypical agents can effectively manage symptom exacerbation. For...
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Calculating drug dosage and accumulation in multiple-dose regimens is crucial for achieving therapeutic efficacy while avoiding toxicity. This involves determining the plasma drug concentrations over time to optimize dosing schedules. The principle of superposition is fundamental in this process, allowing for the prediction of drug concentration in plasma following multiple doses based on single-dose data.The principle of superposition asserts that the plasma concentration-time curves from...

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Related Experiment Video

Updated: May 27, 2026

Behavioral Characterization of Pentylenetetrazole-induced Seizures: Moving Beyond the Racine Scale
07:35

Behavioral Characterization of Pentylenetetrazole-induced Seizures: Moving Beyond the Racine Scale

Published on: July 8, 2025

Polymorphic form IV of olanzapine.

Ranjit Thakuria1, Ashwini Nangia

  • 1School of Chemistry, University of Hyderabad, Hyderabad 500 046, India.

Acta Crystallographica. Section C, Crystal Structure Communications
|November 5, 2011
PubMed
Summary

A new crystal form (Form IV) of olanzapine, a psychotropic drug, was discovered. This thienobenzodiazepine exhibits unique dimer arrangements stabilized by specific molecular interactions.

Area of Science:

  • Crystallography
  • Solid-state chemistry
  • Pharmacology

Background:

  • Olanzapine (2-Methyl-4-(4-methylpiperazin-1-yl)-10H-thieno[2,3-b][1,5]benzodiazepine) is a key psychotropic agent in the thienobenzodiazepine class.
  • Understanding olanzapine's solid-state forms is crucial for its pharmaceutical development and efficacy.

Purpose of the Study:

  • To investigate the formation and structural characteristics of a novel polymorph of olanzapine.
  • To elucidate the intermolecular interactions governing the crystal packing of this new form.

Main Methods:

  • Attempted cocrystallization of olanzapine with nicotinamide in an ethyl acetate solution.
  • Single-crystal X-ray diffraction analysis to determine the crystal structure.

Main Results:

Related Experiment Videos

Last Updated: May 27, 2026

Behavioral Characterization of Pentylenetetrazole-induced Seizures: Moving Beyond the Racine Scale
07:35

Behavioral Characterization of Pentylenetetrazole-induced Seizures: Moving Beyond the Racine Scale

Published on: July 8, 2025

  • A new polymorph, designated Form IV, was successfully obtained.
  • Form IV features centrosymmetric dimers of olanzapine molecules stabilized by C-H···π interactions.
  • The crystal structure of Form IV exhibits a herringbone arrangement of these dimers, distinct from the parallel arrangement in Form II.
  • Both forms are stabilized by N-H···N hydrogen bonds.

Conclusions:

  • The study successfully identified and characterized a new polymorph (Form IV) of olanzapine.
  • The findings highlight the role of weak interactions (C-H···π) and hydrogen bonding in dictating the crystal architecture of thienobenzodiazepines.
  • This research contributes to the understanding of olanzapine's solid-state properties, potentially impacting formulation and drug delivery.