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Mesoporous Silica Container Particles: New Approaches and New Opportunities

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Abstract

The review analyzes the general trends of the studies devoted to the encapsulation of various functional compounds (from drugs to corrosion inhibitors) in silica mesoporous container particles (MCPs). The main focus is on discussing new approaches to creating such structures. Primarily, they are approaches that allow one to combine the stages of the synthesis of MCPs and their loading with one or several targeted substances. The data available from the literature have been used to show the advantages and promises of such one-stage approaches to solving problems relevant to providing MCPs with high content of encapsulated substances and controlling the rate of their release.

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Notes

  1. Relatively recently, surfactant vesicles have begun to be used for this purpose. This method yields particles having the structure of capsules [28, 29].

  2. An interested reader may turn to [33, 34, 37–41].

  3. This scenario is of interest for the limited cases (e.g., for the treatment of acute inflammations), while, in most cases, it is necessary that the release of the targeted substance be more uniform and prolonged.

  4. It should, however, be taken into account that, in this case, there is no substantial difference between healthy and tumor cells. As a consequence, additional efforts are required for the targeted delivery of particles into a tumor.

  5. This mechanism is due to an “imperfectness” of blood and lymphatic vessels in tumor tissues [62, 63].

  6. Analysis of published data (see, e.g., [34]) has indicated that the incorporation of magnetic particles (e.g., Fe3O4) into a SiO2 matrix also leads to the selective accumulation of MCPs in a tumor under the action of a magnetic field. However, the discussing of this problem is beyond the scope of this review.

  7. The authors of [88] are of the opinion that this effect is due to the protonation of amino groups.

  8. Note that according to FDA, silica itself is nontoxic [105].

  9. To be more exact, oxygen atoms in −CH2−CH2−O− groups.

  10. In particular, these factors are the coefficient of hydrophobic compound distribution between water and a micellar phase and the solubilization capacity of micelles.

  11. Note that the long-term exposure of MCPs in deionized water may result in some “pitting” of their surface [159]; however, the porous structure of the particles, as a whole, remains preserved.

  12. Catamine AB is a mixture of n-alkyldimethylbenzylammonium chlorides, which are characterized by the general formula [R(CH3)2(CH2C6H5)N]+Cl–, where R = C10H21−C18H37.

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ACKNOWLEDGMENTS

I am sincerely grateful to V.M. Rudoy (Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences) for valuable advises regarding this review.

Funding

This work was performed in accordance with the order of the Ministry of Science and Higher Education of the Russian Federation and partially supported by the Russian Foundation for Basic Research, project no. 19-03-00703.

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  1. Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, 119071, Moscow, Russia

    O. V. Dement’eva

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Translated by A. Kirilin

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Dement’eva, O.V. Mesoporous Silica Container Particles: New Approaches and New Opportunities. Colloid J 82, 479–501 (2020). https://doi.org/10.1134/S1061933X20050038

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