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Tag: tablet disintegration

Resolving Brittleness in Immediate Release Tablets During Long-Term Storage

Posted on May 26, 2025 By Admin

Resolving Brittleness in Immediate Release Tablets During Long-Term Storage Resolving Brittleness in Immediate Release Tablets During Long-Term Storage Introduction: Immediate release tablets are a cornerstone of pharmaceutical dosage forms, designed to disintegrate promptly after administration to ensure rapid drug release. However, maintaining their integrity during long-term storage poses significant challenges. One of the most critical…

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Solid Dosage form, Tablets

Ensuring Robustness in Disintegration Time During Validation Testing

Posted on May 24, 2025 By Admin

Ensuring Robustness in Disintegration Time During Validation Testing Ensuring Robustness in Disintegration Time During Validation Testing Introduction: In the pharmaceutical industry, the disintegration time of tablets is a critical quality attribute that directly impacts drug release and bioavailability. Ensuring robustness in disintegration time during validation testing is essential to maintain consistency in therapeutic efficacy and…

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Solid Dosage form, Tablets

Troubleshooting Brittleness in High-Dose Tablets During Compression Validation

Posted on May 17, 2025 By Admin

Troubleshooting Brittleness in High-Dose Tablets During Compression Validation Troubleshooting Brittleness in High-Dose Tablets During Compression Validation Introduction: In the pharmaceutical industry, tablet formulation and manufacturing represent critical processes that significantly impact the quality, efficacy, and safety of the final product. High-dose tablets are particularly challenging to develop due to the increased risks of brittleness, which…

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Solid Dosage form, Tablets

Ensuring Consistency in Disintegration Time During Long-Term Stability Studies

Posted on May 3, 2025 By Admin

Ensuring Consistency in Disintegration Time During Long-Term Stability Studies Ensuring Consistency in Disintegration Time During Long-Term Stability Studies Introduction: In the realm of pharmaceuticals, ensuring consistency in the disintegration time of tablets during long-term stability studies is pivotal for guaranteeing a drug’s efficacy, safety, and patient compliance. Disintegration time is a critical quality attribute that…

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Solid Dosage form, Tablets

Investigating Non-Uniform Dissolution in Enteric-Coated Tablets During Testing

Posted on April 30, 2025 By Admin

Investigating Non-Uniform Dissolution in Enteric-Coated Tablets During Testing Investigating Non-Uniform Dissolution in Enteric-Coated Tablets During Testing Introduction: The pharmaceutical industry constantly strives to develop effective drug delivery mechanisms, with enteric-coated tablets serving as a crucial form of solid dosage. These tablets are designed to resist the acidic environment of the stomach, releasing their active ingredients…

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Solid Dosage form, Tablets

Troubleshooting Dissolution Failures in Enteric-Coated Tablets

Posted on March 24, 2025 By Admin

Troubleshooting Dissolution Failures in Enteric-Coated Tablets Troubleshooting Dissolution Failures in Enteric-Coated Tablets Introduction: Enteric-coated tablets are a sophisticated pharmaceutical dosage form designed to bypass the acidic environment of the stomach and dissolve in the more neutral pH of the intestines. This coating is crucial for drugs that can be degraded by stomach acid or can…

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Solid Dosage form, Tablets

Troubleshooting Brittleness Failures in Immediate Release Tablets

Posted on March 21, 2025 By Admin

Troubleshooting Brittleness Failures in Immediate Release Tablets Troubleshooting Brittleness Failures in Immediate Release Tablets Introduction: Immediate release tablets represent a significant portion of the pharmaceutical market due to their convenience and effectiveness in delivering medication rapidly. However, brittleness failures in these tablets can pose substantial challenges, affecting their integrity and therapeutic efficacy. Brittleness, often resulting…

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Solid Dosage form, Tablets

Identifying Root Causes of Poor Disintegration in Film-Coated Tablets

Posted on March 21, 2025 By Admin

Identifying Root Causes of Poor Disintegration in Film-Coated Tablets Identifying Root Causes of Poor Disintegration in Film-Coated Tablets Introduction: Film-coated tablets are a popular solid dosage form in the pharmaceutical industry due to their enhanced stability, ease of ingestion, and ability to mask unpleasant tastes. However, one critical quality attribute for these tablets is their…

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Solid Dosage form, Tablets

Managing Tablet Core Erosion in Enteric-Coated Tablets

Posted on March 21, 2025 By Admin

Managing Tablet Core Erosion in Enteric-Coated Tablets Managing Tablet Core Erosion in Enteric-Coated Tablets Introduction: Enteric-coated tablets represent a sophisticated drug delivery system designed to bypass the acidic environment of the stomach and to release their active ingredients in the more neutral pH of the intestines. This method of delivery is essential for drugs that…

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Solid Dosage form, Tablets

Preventing Brittleness in Coated Tablets During High-Speed Compression

Posted on March 20, 2025 By Admin

Preventing Brittleness in Coated Tablets During High-Speed Compression Preventing Brittleness in Coated Tablets During High-Speed Compression Introduction: In the pharmaceutical industry, the production of coated tablets is a complex process that requires meticulous attention to detail. Coated tablets are favored for their ability to mask unpleasant tastes, protect the drug from the stomach environment, and…

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Solid Dosage form, Tablets

Resolving Failures in Moisture Content Tests for Sugar-Coated Tablets

Posted on March 14, 2025 By Admin

Resolving Failures in Moisture Content Tests for Sugar-Coated Tablets Resolving Failures in Moisture Content Tests for Sugar-Coated Tablets Introduction: In the pharmaceutical industry, sugar-coated tablets are a popular dosage form due to their aesthetic appeal and ability to mask unpleasant tastes. However, maintaining the correct moisture content in these tablets is crucial, as it affects…

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Solid Dosage form, Tablets

Resolving Over-Lubrication Issues in Immediate Release Tablets

Posted on March 14, 2025 By Admin

Resolving Over-Lubrication Issues in Immediate Release Tablets Resolving Over-Lubrication Issues in Immediate Release Tablets Introduction: Immediate release tablets are a mainstay in the pharmaceutical industry, offering quick onset of action and ease of administration. However, the formulation and manufacturing of these tablets present unique challenges, particularly with lubrication. Over-lubrication can compromise tablet quality, affecting disintegration…

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Solid Dosage form, Tablets

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  • Aerosol Formulations
  • Capsules (Hard & Soft Gelatin)
  • Drug Discovery
  • External Preparations
  • GLP Guidelines
  • GMP Guidelines
  • Medical Devices
  • Parenteral Drug Manufacturing
  • Pharma Quality Control
  • Pharma Research
  • Schedule M
  • Solid Dosage form
  • Solid Oral Dosage Forms
  • Tablets
  • Tablets

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