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Tag: dissolution variability

Managing Calibration Failures in Dissolution Testing Equipment for Coated Tablets

Posted on May 31, 2025 By Admin

Managing Calibration Failures in Dissolution Testing Equipment for Coated Tablets Managing Calibration Failures in Dissolution Testing Equipment for Coated Tablets Introduction: Dissolution testing is a critical quality control measure in the pharmaceutical industry, especially for coated tablets. It ensures that the drug releases its active ingredients at the intended rate and extent. However, calibration failures…

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Solid Dosage form, Tablets

Poor reproducibility in dissolution testing results for capsules stored under stressed conditions.

Posted on May 3, 2025 By Admin

Poor reproducibility in dissolution testing results for capsules stored under stressed conditions. Poor reproducibility in dissolution testing results for capsules stored under stressed conditions. Introduction: Dissolution testing is a critical quality control procedure in the pharmaceutical industry, especially for solid oral dosage forms such as capsules. It ensures that the drug releases at the intended…

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Capsules (Hard & Soft Gelatin), Solid Oral Dosage Forms

Poor reproducibility in dissolution profiles for lipid-based capsules.

Posted on April 24, 2025 By Admin

Poor reproducibility in dissolution profiles for lipid-based capsules. Poor reproducibility in dissolution profiles for lipid-based capsules. Introduction: Lipid-based capsules, encompassing both hard and soft gelatin varieties, are critical in the delivery of poorly water-soluble drugs. These formulations improve bioavailability, allowing for efficient drug release and absorption. However, achieving consistent dissolution profiles in lipid-based capsules poses…

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Capsules (Hard & Soft Gelatin), Solid Oral Dosage Forms

Poor reproducibility in validation data for modified-release capsules.

Posted on April 17, 2025 By Admin

Poor reproducibility in validation data for modified-release capsules. Poor reproducibility in validation data for modified-release capsules. Introduction: Modified-release capsules are pivotal in modern therapeutics, offering controlled drug delivery that improves patient compliance and therapeutic outcomes. However, ensuring the reproducibility of validation data for these formulations is crucial in maintaining their efficacy and safety. Inconsistent validation…

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Capsules (Hard & Soft Gelatin), Solid Oral Dosage Forms

Problems with maintaining consistent dissolution profiles over the product’s shelf life.

Posted on April 13, 2025 By Admin

Problems with maintaining consistent dissolution profiles over the product’s shelf life. Problems with maintaining consistent dissolution profiles over the product’s shelf life. Introduction: The dissolution profile of a pharmaceutical product is a critical parameter that impacts its efficacy and safety. Consistency in dissolution profiles over the product’s shelf life ensures that the drug is released…

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Capsules (Hard & Soft Gelatin), Solid Oral Dosage Forms

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

Managing Variability in Dissolution Testing for Immediate Release Tablets

Posted on March 16, 2025 By Admin

Managing Variability in Dissolution Testing for Immediate Release Tablets Managing Variability in Dissolution Testing for Immediate Release Tablets Introduction: Dissolution testing is a critical quality control measure in the pharmaceutical industry, particularly for immediate release tablets. This test ensures that the tablet releases its active ingredients at the desired rate and extent, which is crucial…

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Solid Dosage form, Tablets

Troubleshooting Variability in Dissolution Profiles During Stability Studies

Posted on March 14, 2025 By Admin

Troubleshooting Variability in Dissolution Profiles During Stability Studies Troubleshooting Variability in Dissolution Profiles During Stability Studies Introduction: Dissolution testing is a critical aspect of pharmaceutical development, acting as a quality control measure to ensure that tablets release their active ingredients at the intended rate and extent. During stability studies, the variability in dissolution profiles can…

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Solid Dosage form, Tablets

Common Dissolution Failures in Immediate Release Tablets

Posted on March 9, 2025 By Admin

Common Dissolution Failures in Immediate Release Tablets Common Dissolution Failures in Immediate Release Tablets Introduction: Immediate release tablets are a cornerstone of oral pharmaceutical dosage forms, designed to disintegrate and release their active ingredients promptly upon ingestion. The dissolution process plays a critical role in ensuring the therapeutic efficacy and bioavailability of these tablets. However,…

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Solid Dosage form, Tablets
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