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Related Concept Videos

Factors Influencing Drug Absorption: Pharmaceutical Parameters01:28

Factors Influencing Drug Absorption: Pharmaceutical Parameters

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...
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 II

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, maintaining...
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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Evaluation of roll compaction as a preparation method for hydroxypropyl cellulose-based matrix tablets.

Imjak Jeon1, Tiziana Gilli, Gabriele Betz

  • 1Department of Pharmaceutical Sciences, Industrial Pharmacy Lab, University of Basel, Klingelbergstrasse 50, 4056 Basel, Switzerland.

Journal of Pharmacy & Bioallied Sciences
|June 21, 2011
PubMed
Summary

Roll compaction improves hydroxypropyl cellulose (HPC) matrix tablets, offering better dosage uniformity and faster drug release compared to direct compression. Process parameters like roll pressure and milling speed are key to optimizing tablet properties.

Keywords:
Dry granulationhydroxypropyl cellulosematrix tabletroll compactionsustained release

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Area of Science:

  • Pharmaceutical Technology
  • Materials Science

Background:

  • Hydroxypropyl cellulose (HPC) is utilized in sustained-release matrix tablets.
  • Traditional tablet manufacturing methods may present challenges with certain excipients like HPC.

Purpose of the Study:

  • To evaluate roll compaction as a granulation method for hydroxypropyl cellulose (HPC)-based sustained-release matrix tablets.
  • To compare the properties of roll-compacted tablets with directly compacted tablets.

Main Methods:

  • Roll compaction was employed for the preparation of HPC-based matrix tablets.
  • Key process parameters investigated included HPC viscosity grade, roll pressure, and milling speed.
  • Tablet properties such as dosage uniformity and drug release rate were assessed.

Main Results:

  • Roll-compacted matrix tablets demonstrated superior dosage uniformity compared to direct-compacted tablets.
  • Faster drug release profiles were observed in matrix tablets prepared via roll compaction.
  • HPC viscosity grade, roll pressure, and milling speed significantly influenced the final tablet characteristics.

Conclusions:

  • Roll compaction is an effective and adequate granulation technique for producing HPC-based sustained-release matrix tablets.
  • The method offers advantages in process simplicity, handling of tacky HPC, and particle size control.
  • Optimization of plastic excipient ratios and starting material particle size is crucial for successful roll compaction.