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Review
. 2021 Jun 29;26(13):3963.
doi: 10.3390/molecules26133963.

Role of Calixarene in Chemotherapy Delivery Strategies

Affiliations
Review

Role of Calixarene in Chemotherapy Delivery Strategies

Rossella Basilotta et al. Molecules. .

Abstract

Since cancer is a multifactorial disease with a high mortality rate, the study of new therapeutic strategies is one of the main objectives in modern research. Numerous chemotherapeutic agents, although widely used, have the disadvantage of being not very soluble in water or selective towards cancerous cells, with consequent side effects. Therefore, in recent years, a greater interest has emerged in innovative drug delivery systems (DDSs) such as calixarene, a third-generation supramolecular compound. Calixarene and its water-soluble derivatives show good biocompatibility and have low cytotoxicity. Thanks to their chemical-physical characteristics, calixarenes can be easily functionalized, and by itself can encapsulate host molecules forming nanostructures capable of releasing drugs in a controlled way. The encapsulation of anticancer drugs in a calixarene derivate improves their bioavailability and efficacy. Thus, the use of calixarenes as carriers of anticancer drugs could reduce their side effects and increase their affinity towards the target. This review summarizes the numerous research advances regarding the development of calixarene nanoparticles capable of encapsulating various anticancer drugs.

Keywords: calixarene; cancer; chemotherapeutic agents; drug delivery system (DDS).

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Schematic representation of functionalized structures of calixarene.
Figure 2
Figure 2
Schematic representation of DOX encapsulated in the calixarene structure.
Figure 3
Figure 3
Schematic representation of the calyxarene structure capable of hosting both CPT and PTX.
Figure 4
Figure 4
Schematic representation of TMZ encapsulated in the p-sulfonatocalix [4] arene macromolecule. The hydrophobic core of p-sulfonatocalix [4] arene interact and protect the methyl group of TMZ.

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