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Related Concept Videos

Bioavailability Enhancement: Drug Stability Enhancement and GI Retention01:05

Bioavailability Enhancement: Drug Stability Enhancement and GI Retention

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Body: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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Drug Delivery: Overview01:16

Drug Delivery: Overview

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The selection of a drug's delivery route depends upon its physicochemical properties, including lipid or water solubility and ionization, as well as the therapeutic requirement, such as immediate or sustained effect. These routes can be divided into three primary categories: enteral, parenteral, and topical.
Enteral delivery involves administering drugs directly through swallowing, sublingual placement, or buccal application. Orally administered drugs predominantly navigate the...
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Bioavailability Enhancement: Drug Permeability Enhancement01:27

Bioavailability Enhancement: Drug Permeability Enhancement

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Body: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...
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Drug Delivery: Enteral Route01:18

Drug Delivery: Enteral Route

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The enteral drug administration involves three primary routes: oral, sublingual, and buccal. Oral ingestion is the most prevalent, safe, economical, and convenient method for drug administration. However, it has certain drawbacks, including limited absorption due to the drug's low water solubility or poor membrane permeability, possible emesis from GI mucosa irritation, destruction of drugs by digestive enzymes or low gastric pH, and irregular absorption along with food or other drugs.
991
Drug Delivery: Miscellaneous Routes01:22

Drug Delivery: Miscellaneous Routes

578
Drug delivery methods like oral inhalation, nasal sprays, transdermal patches, eye drops, intravitreal injection,  and rectal administration provide localized effects with reduced toxicity.
Oral inhalation and nasal sprays swiftly transfer drugs across the respiratory epithelium's mucosal layer. Inhaled glucocorticoids and bronchodilators directly target lung conditions such as asthma, while fluticasone nasal spray mitigates allergic rhinitis.
Transdermal patches transport drugs...
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Bioavailability Enhancement: Determination and Conceptual Approaches in Overcoming Bioavailability Problems01:22

Bioavailability Enhancement: Determination and Conceptual Approaches in Overcoming Bioavailability Problems

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Body: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...
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Updated: Nov 3, 2025

Alternating Magnetic Field-Responsive Hybrid Gelatin Microgels for Controlled Drug Release
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Bioactive glass: A multifunctional delivery system.

Smriti Gupta1, Shreyasi Majumdar1, Sairam Krishnamurthy1

  • 1Neurotherapeutics Laboratory, Department of Pharmaceutical Engineering and Technology, Indian Institute of Technology (Banaras Hindu University), Varanasi 221005, India.

Journal of Controlled Release : Official Journal of the Controlled Release Society
|June 4, 2021
PubMed
Summary
This summary is machine-generated.

Bioactive glasses (BAGs) are versatile drug delivery systems, offering controlled release of therapeutics for conditions like osteoporosis and cancer. Further research is needed to bridge the gap between laboratory findings and clinical application.

Keywords:
Bioactive glassDopant ionsDrug-delivery systemsGene delivery vectorOsteogenesisPhytopharmaceuticals

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Area of Science:

  • Biomaterials Science
  • Materials Chemistry
  • Drug Delivery Systems

Background:

  • Bioactive glasses (BAGs) have a 50-year history in orthopedic and dental applications.
  • Recent research has focused on BAGs as advanced delivery systems for diverse therapeutics, including ions, drugs, and macromolecules.
  • The unique properties of BAGs facilitate therapeutic molecule entrapment and controlled release kinetics.

Purpose of the Study:

  • To review the evolution of bioactive glasses from melt-quenched to mesoporous sol-gel formulations.
  • To summarize scientific advancements in using BAGs for delivering various therapeutic agents.
  • To identify challenges hindering the clinical translation of BAG-based therapies.

Main Methods:

  • Literature review of bioactive glass development and applications.
  • Analysis of therapeutic molecule loading and release mechanisms.
  • Evaluation of BAGs' biological activity and dissolution products.

Main Results:

  • BAGs offer tailorable controlled release kinetics for targeted delivery.
  • Dissolution products of BAGs exhibit beneficial biological activity in conditions like osteoporosis, cancer, infection, and inflammation.
  • Significant research has explored BAGs for delivering therapeutic ions, small molecules, and macromolecules.

Conclusions:

  • Bioactive glasses represent a promising platform for advanced drug delivery due to their tunable properties and therapeutic potential.
  • Addressing current research gaps is crucial for successful clinical translation of BAG-based therapies.
  • Future directions include optimizing BAG formulations for specific pathological conditions and enhancing their bench-to-bedside transition.