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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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Synthesis and Characterization of Functionalized Metal-organic Frameworks
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Silane-Functionalized Metal-Organic Frameworks for Stimuli-Responsive Drug Delivery Systems: A New Universal

Xingkun Luan1, Zehong Xiang2, Jiangtao Dong1

  • 1Key Laboratory of Mesoscopic Chemistry (Ministry of Education), State Key Laboratory of Coordination Chemistry, and School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, People's Republic of China.

ACS Applied Materials & Interfaces
|May 29, 2023
PubMed
Summary

A novel silanization strategy enables versatile functionalization of metal-organic frameworks (MOFs). This method creates responsive nanovalves for targeted drug delivery, showing significant tumor inhibition with minimal toxicity.

Keywords:
chemotherapycontrolled drug releasemetal−organic frameworksilane functionalizationsupramolecular nanovalve

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Area of Science:

  • Materials Science
  • Nanotechnology
  • Chemical Engineering

Background:

  • Metal-organic frameworks (MOFs) offer tunable properties for diverse applications.
  • Functionalization of MOFs is crucial for enhancing their performance and expanding their utility.
  • Existing MOF modification methods often lack universality and efficiency.

Purpose of the Study:

  • To develop a universal strategy for silane functionalization of MOFs.
  • To construct supramolecular nanovalves on MOF surfaces for controlled drug delivery.
  • To evaluate the therapeutic efficacy and safety of the developed nanovalves.

Main Methods:

  • Hydrolysis of silanes followed by condensation reactions with MOF hydroxyl groups to form metal-O-Si bonds.
  • Surface silanization of nanoscale MOFs (NMOFs) with benzimidazole stalks.
  • Assembly of cyclodextrin polymer (CDP) onto silanized NMOFs to create multivalent nanovalves.

Main Results:

  • A universal silanization method was established, enabling covalent coupling of silanes to MOFs via metal-O-Si bonds.
  • CDP-valved NMOFs demonstrated stimuli-responsive controlled release of drugs at low pH and in the presence of α-amylase.
  • In vitro and in vivo studies confirmed significant tumor growth inhibition and negligible toxicity to normal tissues.

Conclusions:

  • The developed silanization strategy is a versatile approach for MOF functionalization.
  • CDP-valved NMOFs show great promise as intelligent drug delivery systems for cancer therapy.
  • This work opens new avenues for MOF applications in drug delivery, catalysis, and materials science.