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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...
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Alternative drug dissolution methods include the rotating bottle, intrinsic dissolution test, peristalsis, and the Franz diffusion cell method. The rotating bottle method involves meticulously rotating tightly capped controlled-release beads in a temperature-controlled bath. Periodic decanting of samples allows for residue assay, followed by refilling with fresh medium and testing at various pH levels to emulate the gastrointestinal tract conditions.In contrast, the intrinsic dissolution test...
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After oral administration, poor permeability often limits the rate at which drugs are absorbed through the intestinal epithelium. Enhancing drug permeability is crucial for effective therapy, and several strategies have been developed to overcome this challenge.One effective strategy involves the use of lipid-based formulations. These formulations enhance dissolution and solubility, targeting physiological mechanisms to increase drug absorption. This includes stimulating bile salt secretion,...
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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, maintaining...
Bioavailability Enhancement: Drug Solubility Enhancement01:16

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Bioavailability is a critical factor in determining a drug's effectiveness. It refers to the proportion of a drug that enters the circulation when introduced into the body and is, as a result, able to have an active effect. Enhancing bioavailability is essential for drugs with poor solubility, as it can significantly impact their therapeutic efficacy. Various methods are employed to increase the solubility of drugs, thereby enhancing their bioavailability.Micronization and nanonization are...
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Bioavailability is a critical pharmacological concept that measures the extent and rate at which an active drug ingredient or therapeutic moiety enters the systemic circulation, remaining unchanged. It's a pivotal factor in determining a drug's efficacy and safety.The Biopharmaceutics Classification System (BCS) plays an essential role in drug development by categorizing drugs into four classes based on their solubility and permeability. This classification aids in understanding drug absorption...

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Frugal Imaging Technique of Capillary Flow Through Three-Dimensional Polymeric Printing Powders
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Practical methods for improving flow properties of active pharmaceutical ingredients.

Kalyana C Pingali1, Kostas Saranteas, Reza Foroughi

  • 1Department of Chemical and Biochemical Engineering, Rutgers University, Piscataway, NJ 09954, USA.

Drug Development and Industrial Pharmacy
|November 26, 2009
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Summary

Formulation additives significantly improve active pharmaceutical ingredient (API) powder flow without altering particle characteristics. Electrical properties like impedance correlate with powder cohesiveness and flowability, suggesting a common mechanism for flow improvement.

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Area of Science:

  • Pharmaceutical Sciences
  • Materials Science

Background:

  • Powder flow is critical for pharmaceutical manufacturing processes.
  • Particle size and shape modifications are common but complex methods to improve powder flow.

Purpose of the Study:

  • To develop formulation strategies for enhancing active pharmaceutical ingredient (API) powder flow properties.
  • To investigate additive effects on flow without modifying particle size or shape.

Main Methods:

  • A formulation approach was employed using three distinct APIs: acetaminophen, levalbuterol tartrate, and didesmethylsibutramine tartrate.
  • Small quantities of lubricants, glidants, and other additives were individually and combinedly mixed with APIs using a V-blender.
  • Flow index, dilation, and electrical impedance were measured for 24 different blends.

Main Results:

  • All tested APIs demonstrated improved flow properties upon additive incorporation.
  • The combination of SiO2, MgSt, and talc significantly reduced cohesiveness and enhanced powder flowability.
  • A strong correlation was observed between flow index, dilation, and electrical impedance across all APIs.

Conclusions:

  • Improved powder flow in APIs is associated with low dilation and low electrical impedance values.
  • Electrical properties play a significant role in API powder cohesivity.
  • A unified mechanism underlies the development and mitigation of cohesive phenomena in pharmaceutical powders.