Related Experiment Video
Updated: Jan 27, 2026

Practical Use of RNA Interference: Oral Delivery of Double-stranded RNA in Liposome Carriers for Cockroaches
Published on: May 1, 2018
Double-headed nanosystems for oral drug delivery
1Department of Pharmaceutical Sciences, Irma Lerma Rangel College of Pharmacy, Texas A&M University, TAMU Mailstop 1114, College Station, Texas 77843, USA. mnvrkumar@tamhsc.edu.
We developed double-headed nanosystems to improve curcumin bioavailability. Higher ligand density on these nanoparticles enhances drug delivery and absorption in vivo.
Area of Science:
- Biomedical Engineering
- Materials Science
- Nanotechnology
Background:
- Curcumin exhibits poor bioavailability, limiting its therapeutic potential.
- Developing effective drug delivery systems is crucial for enhancing curcumin's efficacy.
- Nanoparticle-based systems offer promise for improving drug solubility and absorption.
Purpose of the Study:
- To engineer novel double-headed nanosystems for enhanced curcumin delivery.
- To investigate the relationship between ligand density and curcumin bioavailability.
- To evaluate the in vivo performance of the developed nanosystems.
Main Methods:
- Chemical modification of carboxyl terminal polyester with a tripodal ligand linker.
- Fabrication of double-headed nanosystems with varying ligand densities.
- In vivo assessment of encapsulated curcumin bioavailability.
- Correlation analysis between ligand density and bioavailability.
Main Results:
- Successfully engineered double-headed nanosystems with tripodal ligand arrangements.
- Demonstrated that in vivo curcumin bioavailability is proportional to ligand density.
- Established a direct correlation between nanoparticle surface ligand density and drug absorption.
Conclusions:
- The novel double-headed nanosystems effectively enhance curcumin bioavailability.
- Ligand density is a critical factor in optimizing nanoparticle-mediated drug delivery.
- This strategy holds potential for improving the therapeutic efficacy of poorly bioavailable drugs.
More Related Videos
Related Concept Videos
Non-Oral Extravascular Drug Absorption Routes
Lipophilic drugs that are stable at salivary pH (6) and exhibit minimal binding to the oral mucosa are absorbed more...
Drug Delivery: Overview
Enteral delivery involves administering drugs directly through swallowing, sublingual placement, or buccal application. Orally administered drugs predominantly navigate the...
Drug Delivery: Enteral Route
Drug Delivery: Parenteral Route
There are three primary parenteral routes: intravenous (IV), intramuscular (IM), and subcutaneous (SC). The IV route introduces the drug directly into the bloodstream, ensuring immediate action. The IM route...
Drug Delivery: Miscellaneous Routes
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...
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...

