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Related Concept Videos

Site-Targeted Drug Delivery Systems: Polymeric Carriers01:24

Site-Targeted Drug Delivery Systems: Polymeric Carriers

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Polymeric carriers enhance targeted drug delivery by increasing efficacy while minimizing off-target effects. These carriers comprise a biodegradable polymeric backbone integrated with functional elements that enable targeting, improve physicochemical properties, and regulate drug release.Targeting MechanismsThe targeting ability of polymeric carriers is mediated by a homing device, which is a molecular recognition component designed to selectively bind to specific tissues or cells. Monoclonal...
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Modified-Release Drug Delivery Systems: Rate-Programmed II01:19

Modified-Release Drug Delivery Systems: Rate-Programmed II

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Rate-programmed drug delivery systems release drugs in a controlled manner to maintain therapeutic levels. Three main designs include reservoir, matrix, and hybrid systems.Reservoir systems consist of a drug core enclosed within a membrane that controls drug release. In non-swelling reservoir systems, polymers like ethyl cellulose or polymethacrylates are used. These do not hydrate in aqueous media and control release through membrane thickness, porosity, or insolubility. This type includes...
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Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence01:27

Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence

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Changes in polymorphic forms can significantly influence the bioavailability of poorly soluble drugs. Although the FDA defines pharmaceutical equivalence based on having the same active ingredient, dosage form, and route of administration, it does not automatically disqualify products with different polymorphic forms. This means two products with different polymorphs can still be deemed pharmaceutically equivalent. However, polymorphic differences can affect properties like wettability,...
214
Factors Influencing Drug Absorption: Pharmaceutical Parameters01:28

Factors Influencing Drug Absorption: Pharmaceutical Parameters

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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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Factors Affecting Dissolution: Particle Size and Effective Surface Area01:23

Factors Affecting Dissolution: Particle Size and Effective Surface Area

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Dissolution kinetics, an essential aspect of oral drug delivery, is significantly influenced by the drug's particle size. According to the Noyes-Whitney dissolution model, the dissolution rate correlates directly with the drug's surface area. The larger the surface area, the higher the drug's solubility in water, leading to a faster drug dissolution rate. Reducing particle size increases the effective surface area, enhancing the dissolution process. Micronization and nanosizing are...
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Bioavailability Enhancement: Drug Stability Enhancement and GI Retention01:05

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Improving a drug's stability in the gastrointestinal (GI) tract is paramount for enhancing its bioavailability and therapeutic effectiveness. Various strategies are employed to protect the drug from the harsh gastric milieu and to ensure its release and absorption at the desired site within the GI tract.Polymer coatings are one such method used to shield drugs from the stomach's acidic environment. By preventing premature drug release, these coatings improve the bioavailability of unstable...
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Related Experiment Video

Updated: Mar 25, 2026

Preparation and Characterization of Individual and Multi-drug Loaded Physically Entrapped Polymeric Micelles
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Polymer Particulates in Drug Delivery.

Harmeet Kaur, Virender Kumar, Krishan Kumar

  • 1Room No. 9, IGVB-South Block, College of Pharmacy, University of Health Sciences, Rohtak- 124001, India. jasbirsinghsekhon@yahoo.co.in.

Current Pharmaceutical Design
|February 23, 2016
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Summary

Polymeric microparticles and nanoparticles offer advanced drug delivery solutions. Engineering polymer properties enhances drug loading, release, and targeting for improved therapeutic outcomes.

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Area of Science:

  • Polymer science and materials engineering
  • Pharmaceutical sciences
  • Biomedical engineering

Background:

  • Conventional drug delivery methods face limitations in efficacy and targeting.
  • Polymer particulates (micro- and nanoparticles) present novel solutions for drug delivery.
  • Tailoring polymer properties allows for optimization of drug loading, release kinetics, and pharmacokinetics.

Purpose of the Study:

  • To review the application of polymeric microparticles, nanoparticles, and copolymer micelles in drug and biomolecule delivery.
  • To discuss the formulation methods for polymer particulates.
  • To cover well-established polymers in pharmaceutical history for drug delivery applications.

Main Methods:

  • Review of existing literature on polymeric drug delivery systems.
  • Analysis of polymer engineering strategies for enhanced drug delivery.
  • Discussion of formulation techniques for micro- and nanoparticles.

Main Results:

  • Polymeric particles can be engineered to improve drug loading, control release rates, and enhance pharmacokinetics.
  • Ligand modification of polymer end-groups enables cell-specific targeting and improved intracellular delivery.
  • Various polymeric materials and formulation methods are suitable for diverse drug delivery applications.

Conclusions:

  • Polymer particulates are versatile platforms for developing effective drug delivery systems.
  • Precise engineering of polymers and their formulations is key to overcoming conventional delivery challenges.
  • This review highlights the potential of polymeric systems for advanced drug and biomolecule delivery.