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Updated: Jul 10, 2026

Porous Silicon Microparticles for Delivery of siRNA Therapeutics
Published on: January 15, 2015
Silica-based mesoporous materials as drug delivery system for methotrexate release
Ida Stefania Carino1, Luigi Pasqua, Flaviano Testa
1Dipartimento di Ingegneria Chimica e dei Materiali, Università della Calabria, Rende, Italia.
Mesoporous alumina-silica materials effectively loaded and released antineoplastic methotrexate, mimicking oral administration. Drug loading and release rates depended on the pore size of these novel drug delivery systems.
Area of Science:
- Materials Science
- Nanotechnology
- Pharmaceutical Sciences
Background:
- Mesoporous silica materials offer tunable properties for drug delivery.
- Antineoplastic drugs like methotrexate require effective delivery systems for oral administration.
- Controlling pore size is crucial for optimizing drug loading and release.
Purpose of the Study:
- To synthesize and characterize mesoporous alumina-silica materials.
- To investigate the loading and in vitro release of methotrexate using these materials.
- To establish the relationship between material pore size and drug delivery performance.
Main Methods:
- Self-assembly synthesis of mesoporous materials using cationic surfactants with varying alkyl chain lengths (C16, C12, C10).
- Preparation of pure silica and alumina-silica samples.
- Drug loading of methotrexate via soaking procedures.
- In vitro release studies mimicking oral administration.
Main Results:
- Alumina-silica mesoporous materials successfully loaded methotrexate, unlike pure silica.
- Drug loading capacity and in vitro release kinetics were significantly influenced by the pore diameter of the materials.
- The pore size directly correlated with the amount of drug loaded and its release profile.
Conclusions:
- Mesoporous alumina-silica materials are promising carriers for antineoplastic drug delivery.
- Tailoring pore size through controlled synthesis is essential for optimizing methotrexate loading and release kinetics.
- These materials demonstrate potential for developing effective oral drug delivery systems.
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Modified-Release Drug Delivery Systems: Rate-Programmed II
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