Biocompatible Drug Delivery System Based on a MOF Platform for a Sustained and Controlled Release of the Poorly

Preety Yadav1, Sarita Kumari1, Anand Yadav1

  • 1Department of Chemistry, School of Basic Sciences, Central University of Haryana, Jant-Pali, Mahendergarh 123031, Haryana, India.

ACS Omega
|August 14, 2023
PubMed

Insights

This study developed a new drug delivery system using metal-organic frameworks (MOFs) to improve norfloxacin (NFX) delivery. The biocompatible NFX@MIL-100(Fe) system enhanced drug loading and controlled release, showing potential for pharmaceutical applications.

Area of Science:

  • Materials Science
  • Nanotechnology
  • Pharmaceutical Science

Background:

  • Norfloxacin (NFX), a fluoroquinolone antibiotic, exhibits poor solubility and permeability (Biopharmaceutics Classification System Class IV).
  • These physicochemical limitations hinder effective drug delivery and pose challenges for pharmaceutical development.
  • Developing novel drug delivery systems (DDSs) is crucial for improving the therapeutic efficacy of poorly soluble drugs like NFX.

Purpose of the Study:

  • To develop a novel DDS for norfloxacin (NFX) using a biocompatible metal-organic framework (MOF), MIL-100(Fe).
  • To characterize the drug-loaded MOF (NFX@MIL-100(Fe)) and evaluate its drug loading capacity and release profile.
  • To assess the biocompatibility and cytotoxicity of the developed DDSs.

Main Methods:

  • Norfloxacin was loaded onto the MIL-100(Fe) MOF platform.
  • Characterization of NFX@MIL-100(Fe) using FTIR, UV-Vis spectroscopy, TGA, and nitrogen adsorption.
  • Controlled release studies and PEGylation of NFX@MIL-100(Fe) to create PEG{NFX@MIL-100(Fe)}.
  • Biocompatibility and cytotoxicity assessment using MTT assay.

Main Results:

  • High drug loading (approximately 20 wt%) of NFX onto MIL-100(Fe) was achieved.
  • The NFX@MIL-100(Fe) system demonstrated sustained drug release.
  • PEGylation of the DDS further controlled norfloxacin release.
  • Toxicity studies confirmed the biocompatibility of both NFX@MIL-100(Fe) and PEG{NFX@MIL-100(Fe)} DDSs with insignificant cytotoxicity.

Conclusions:

  • Metal-organic framework MIL-100(Fe) serves as an effective platform for developing a novel drug delivery system for norfloxacin.
  • The developed DDSs (NFX@MIL-100(Fe) and PEG{NFX@MIL-100(Fe)}) exhibit high drug loading, controlled release, and excellent biocompatibility.
  • This approach offers a promising strategy for enhancing the delivery and therapeutic potential of poorly soluble drugs like norfloxacin.

Related Concept Videos

Drug Delivery: Overview01:16

Drug Delivery: Overview

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...
322
Drug Delivery: Miscellaneous Routes01:22

Drug Delivery: Miscellaneous Routes

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...
381
Drug Distribution: Tissue Binding01:21

Drug Distribution: Tissue Binding

Upon entering the systemic circulation, drugs can distribute into the interstitial and intracellular fluid of various tissue cells. This distribution is facilitated by the binding of drugs to different cellular components within tissues, which may lead to drug accumulation in specific areas. Drugs bound to tissue components serve as reservoirs that release free drugs back into the system, prolonging the drug's overall action. However, this accumulation can also result in local toxicity.
For...
2.7K
Pore Transport and Ion-Pair Transport01:17

Pore Transport and Ion-Pair Transport

Pore transport and ion-pair formation are critical mechanisms for the absorption and distribution of drugs in the body.
Pore transport, also known as convective transport, is a process where small molecules like urea, water, and sugars rapidly cross cell membranes as though there were channels or pores in the membrane. Although direct microscopic evidence is limited  but the concept of pores or channels is widely accepted based on physiological evidence. Despite the lack of direct...
513