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Modified-Release Drug Delivery Systems: Rate-Programmed II01:19

Modified-Release Drug Delivery Systems: Rate-Programmed II

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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Rate-programmed drug delivery systems (DDS) are designed to release drugs at specific, controlled rates to maintain consistent therapeutic levels. These systems are categorized based on their release mechanisms, including dissolution-controlled DDS, diffusion-controlled DDS, and combined dissolution-diffusion-controlled DDS.In dissolution-controlled DDS, the release rate depends on the slow dissolution of the drug itself or the surrounding matrix. Drugs with inherently slow dissolution rates,...
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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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Stimuli-activated drug delivery systems are designed to release drugs in response to specific physical, chemical, or biological stimuli. These systems often utilize hydrogels—three-dimensional, hydrophilic polymer networks capable of swelling in aqueous environments and retaining significant fluid volumes. Upon exposure to particular stimuli, these hydrogels undergo structural transitions that allow the embedded drug to be released. Due to this adaptive behavior, such systems are also called...
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Delayed-release drug delivery systems are specialized pharmaceutical formulations designed to postpone the release of active compounds until the drug reaches a specific region of the gastrointestinal (GI) tract, typically the intestine. These systems are essential for drugs that may cause gastric irritation, are unstable in acidic environments, or need to exert therapeutic effects locally in the intestinal or colonic regions.The core feature of delayed-release systems is the use of enteric...
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Poly (lactic-co-glycolic acid) as a controlled release delivery device.

Tee Yong Lim1, Chye Khoon Poh, W Wang

  • 1Department of Orthopaedic Surgery, National University of Singapore, Kent Ridge, Singapore, Singapore. doslty@nus.edu.sg

Journal of Materials Science. Materials in Medicine
|March 14, 2009
PubMed
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Researchers developed a novel method to coat unmodified Poly (lactic-co-glycolic acid) (PLGA) with angiogenic factors. This technique enables controlled release of vascular endothelial growth factor (VEGF) to promote stem cell differentiation for tissue engineering applications.

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Area of Science:

  • Biomaterials Science
  • Tissue Engineering
  • Regenerative Medicine

Background:

  • Poly (lactic-co-glycolic acid) (PLGA) is a widely used biodegradable polymer in resorbable sutures and tissue engineering due to its tunable degradation rate and mechanical properties.
  • Functionalizing PLGA with bioactive molecules often requires chemical modifications that can compromise material integrity and molecule efficacy.
  • Developing methods to incorporate bioactive factors into PLGA without compromising its properties is crucial for advanced biomedical applications.

Purpose of the Study:

  • To investigate a method for coating unmodified PLGA suture substrates with an angiogenic factor.
  • To assess the potential of this coating to induce differentiation of human mesenchymal stem cells (hMSCs) into endothelial cells (ECs).
  • To explore the utility of this approach for creating functional, controlled-release PLGA-based delivery devices.

Main Methods:

  • Coating of unmodified PLGA suture substrates with vascular endothelial growth factor (VEGF).
  • Assessing the gradual release of VEGF from the PLGA surface into solution.
  • Evaluating the differentiation of human mesenchymal stem cells (hMSCs) into endothelial cells (ECs) induced by the released VEGF.

Main Results:

  • The developed coating method successfully anchored VEGF onto the PLGA surface.
  • Gradual release of VEGF from the PLGA substrate was observed.
  • The released VEGF effectively induced the differentiation of hMSCs into ECs.

Conclusions:

  • A novel, non-chemical modification method enables the functionalization of PLGA with angiogenic factors.
  • This technique facilitates controlled release of VEGF, promoting stem cell differentiation for tissue regeneration.
  • The approach holds promise for creating advanced PLGA materials, such as sutures, meshes, and scaffolds, as effective controlled-release delivery systems for various bioactive molecules.