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Related Concept Videos

Factors Influencing Drug Absorption: Pharmaceutical Parameters01:28

Factors Influencing Drug Absorption: Pharmaceutical Parameters

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Solid dosage forms such as tablets and capsules undergo rigorous manufacturing processes to ensure stability and effectiveness. Their dissolution and absorption properties are influenced significantly by the choice of excipients (inactive ingredients that serve various roles in the formulation), and the methodology applied during production. The manufacturing parameters, such as compression force and granulation techniques, significantly affect dissolution rates. Elevated compression forces...
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Formulation and Manufacturing Process: Physical Attributes of Generic Tablets and Capsules01:18

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Bioequivalence in generic drugs, such as tablets and capsules, refers to their pharmaceutical equivalence to the brand-name counterparts. However, for therapeutic equivalence, manufacturers must also consider physical attributes like size, shape, and weight (FDA Guidance for Industry, December 2003). Discrepancies in these aspects could impact patient compliance and cause medication errors. For instance, swallowing difficulties, often experienced with larger tablets or capsules, can lead to...
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In Vitro Drug Dissolution: Compendial Testing Models II01:09

In Vitro Drug Dissolution: Compendial Testing Models II

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Various dissolution methods are utilized to assess a drug’s dissolution rate, including the flow-through cell, paddle-over-disk, cylinder, and reciprocating disk methods.The flow-through cell apparatus (USP (United States Pharmacopeia) method 4) comprises a reservoir for the dissolution medium and a pump that propels the medium through the cell containing the test sample. This method is crucial for assessing modified-release dosage forms with minimally soluble active ingredients,...
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In Vitro Drug Dissolution: Compendial Testing Models I01:13

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Compendial dissolution methods are standardized procedures defined by pharmacopeias to evaluate the rate at which a drug dissolves in a specific medium. These methods ensure batch-to-batch consistency, enable quality control, and support the prediction of drug bioavailability. They are critical for both immediate and modified-release drug products.The apparatuses used for dissolution testing differ in their design and mechanical function, but all aim to simulate the physiological environment of...
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Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence01:27

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

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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,...
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Compacting Factor test01:22

Compacting Factor test

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The compacting factor test is a method used to assess the workability of concrete. It is  especially suitable for concrete mixes containing aggregates up to one and a half inches in size. This test involves specialized equipment consisting of two truncated cone-shaped hoppers and a cylinder, all with polished interior surfaces to minimize friction.
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Related Experiment Video

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Numerical study for tableting process in consideration of compression speed.

Shuji Ohsaki1, Kazune Kushida1, Yu Matsuda1

  • 1Department of Chemical Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Naka-ku, Sakai, Osaka 599-8531, Japan.

International Journal of Pharmaceutics
|December 18, 2019
PubMed
Summary
This summary is machine-generated.

A new visco-plastic model combining Drucker-Prager Cap (DPC) and Perzyna models accurately simulates powder compaction during tableting. This novel approach accounts for compression speed, improving predictions of tablet strength and preventing failures.

Keywords:
Compression speedDrucker-Prager cap modelFinite element methodPerzyna modelTableting process

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Area of Science:

  • Pharmaceutical Engineering
  • Materials Science
  • Computational Mechanics

Background:

  • Tableting process simulation is crucial for understanding tablet structural changes and failure mechanisms like capping and lamination.
  • The widely used Drucker-Prager Cap (DPC) model in pharmaceuticals lacks the ability to incorporate compaction speed, a critical factor in tablet strength.

Purpose of the Study:

  • To develop and validate a novel computational model for powder tableting that incorporates visco-plastic behavior and considers compression speed.
  • To enhance the accuracy of numerical simulations in predicting tablet mechanical properties and failure modes.

Main Methods:

  • A combined Drucker-Prager Cap (DPC) and Perzyna model was developed to simulate powder compaction with visco-plasticity.
  • Numerical simulations were performed using cellulose, lactose, and acetaminophen as model powders.
  • Model parameters were calibrated using experimental data from compaction, unconfined compression, and tension tests.

Main Results:

  • The proposed DPC-Perzyna model accurately reproduced experimental loading curves across various compaction speeds.
  • Simulations demonstrated that higher compression speeds lead to reduced plastic deformation and increased residual stress in tablets.
  • The model effectively captured the influence of compression speed on tablet mechanical behavior.

Conclusions:

  • The developed DPC-Perzyna model offers a significant advancement for analyzing the tableting process by incorporating compression speed.
  • This model provides a more realistic simulation of powder behavior, aiding in the optimization of tablet manufacturing and the prevention of defects.