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Tag: Pharmaceutical excipients

What are the potential issues with capsule shell disintegration?

Posted on August 6, 2023July 31, 2023 By Admin

Potential Issues with Capsule Shell Disintegration Capsule shell disintegration is a critical factor in the dissolution and release of the active pharmaceutical ingredient (API) from the capsule. Disintegration issues can affect the drug’s bioavailability, therapeutic efficacy, and patient compliance. Several potential issues may arise with capsule shell disintegration, leading to problems with drug release. Here…

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Capsules (Hard & Soft Gelatin)

How are injectable formulations adjusted for better compatibility with patient physiology?

Posted on August 5, 2023August 2, 2023 By Admin

Adjusting Injectable Formulations for Better Compatibility with Patient Physiology Injectable formulations are carefully designed and adjusted to ensure optimal compatibility with patient physiology. The goal is to create formulations that are safe, effective, and well-tolerated when administered to patients. Here are several key considerations and approaches used to adjust injectable formulations for better compatibility with…

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Parenteral Drug Manufacturing

What is the role of excipients in capsule manufacturing?

Posted on August 5, 2023July 31, 2023 By Admin

Role of Excipients in Capsule Manufacturing Excipients play a vital role in capsule manufacturing as they are inactive ingredients used alongside the active pharmaceutical ingredient (API) to facilitate the formulation process, enhance drug delivery, and improve the overall performance of the capsules. Excipients serve several important functions that contribute to the quality, stability, and bioavailability…

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Capsules (Hard & Soft Gelatin)

What are the potential problems with injectable container-closure compatibility?

Posted on August 4, 2023August 2, 2023 By Admin

Potential Problems with Injectable Container-Closure Compatibility Injectable container-closure compatibility is a critical aspect of pharmaceutical packaging to ensure the safety, stability, and efficacy of the injectable product throughout its shelf life. Container-closure systems encompass the vial or ampoule and its associated closure, such as a rubber stopper or a cap. Incompatibility between the injectable formulation…

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Parenteral Drug Manufacturing

How are sustained-release capsules formulated and manufactured?

Posted on August 4, 2023July 31, 2023 By Admin

Formulation and Manufacturing of Sustained-Release Capsules Sustained-release capsules, also known as extended-release or controlled-release capsules, are designed to release the active pharmaceutical ingredient (API) gradually over an extended period, providing a steady and prolonged therapeutic effect. The formulation and manufacturing of sustained-release capsules require specialized techniques and excipients to achieve the desired release profile. Here’s…

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Capsules (Hard & Soft Gelatin)

Explain the role of excipients in injectable formulations.

Posted on August 3, 2023August 2, 2023 By Admin

Role of Excipients in Injectable Formulations Excipients play a crucial role in injectable formulations, which are pharmaceutical products administered directly into the body via intravenous, intramuscular, or subcutaneous routes. Excipients are inactive ingredients added to the formulation alongside the active pharmaceutical ingredient (API) to ensure the safety, stability, and effectiveness of the injectable product. Here’s…

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Parenteral Drug Manufacturing

Explain the process of dry powder filling in capsule production.

Posted on August 3, 2023July 31, 2023 By Admin

Process of Dry Powder Filling in Capsule Production Dry powder filling is a common method used in capsule production to fill capsules with powdered or granulated materials, including active pharmaceutical ingredients (APIs) and excipients. The process involves several steps to ensure accurate and uniform filling of the capsules. Here’s a detailed explanation of the dry…

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Capsules (Hard & Soft Gelatin)

How is the uniformity of fill volume ensured during injectable production?

Posted on August 2, 2023 By Admin

Ensuring Uniformity of Fill Volume During Injectable Production Maintaining the uniformity of fill volume is a critical aspect of injectable production to ensure consistent and accurate dosing of medications. Variability in fill volume can lead to dosing inaccuracies and affect the safety and efficacy of the injectable product. Several measures are taken to ensure the…

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Parenteral Drug Manufacturing

How are capsule formulations optimized for better bioavailability?

Posted on August 2, 2023July 31, 2023 By Admin

Optimizing Capsule Formulations for Better Bioavailability Achieving better bioavailability in capsule formulations is a critical goal in pharmaceutical development. Bioavailability refers to the extent and rate at which the active pharmaceutical ingredient (API) in a capsule is absorbed into the bloodstream and becomes available for therapeutic action. Several strategies can be employed to optimize capsule…

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Capsules (Hard & Soft Gelatin)

How are enteric-coated capsules prepared?

Posted on August 1, 2023July 31, 2023 By Admin

Preparation of Enteric-Coated Capsules Enteric-coated capsules are designed to resist disintegration and dissolution in the acidic environment of the stomach. Instead, they disintegrate and release their contents in the more alkaline environment of the small intestine. The enteric coating helps protect sensitive drugs from degradation in the stomach and allows for targeted drug release. Here’s…

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Capsules (Hard & Soft Gelatin)

What are the guidelines for good manufacturing practices (GMP) for injectables?

Posted on July 28, 2023July 28, 2023 By Admin

Guidelines for Good Manufacturing Practices (GMP) for Injectables Good Manufacturing Practices (GMP) are a set of quality assurance standards and guidelines that pharmaceutical manufacturers must follow to ensure the production of safe, effective, and high-quality injectable products. Compliance with GMP is essential for safeguarding patient health and maintaining the integrity of the pharmaceutical industry. Here’s…

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Parenteral Drug Manufacturing

How are injectables formulated for extended-release profiles?

Posted on July 28, 2023July 28, 2023 By Admin

Formulating Injectable Extended-Release Profiles Injectable extended-release formulations are designed to release the drug over an extended period, providing a sustained therapeutic effect and reducing the frequency of administration. The formulation process involves careful selection of excipients and drug delivery technologies to achieve the desired release profile. Here’s how injectables are formulated for extended-release profiles: 1….

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Parenteral Drug Manufacturing

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  • GLP Guidelines
  • GMP Guidelines
  • Medical Devices
  • Parenteral Drug Manufacturing
  • Pharma Quality Control
  • Pharma Research
  • Schedule M
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  • Solid Oral Dosage Forms
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