3D cyclodextrin-based metal-organic frameworks (CD-MOFs) have emerged as a biocompatible alternative to conventional MOFs, as they are synthesized using safer, nontoxic, or lower-toxicity components, thereby eliminating the need for potentially hazardous metals and organic linkers commonly employed in traditional MOF synthesis. In CD-MOFs, cyclodextrin molecules serve as organic linkers, while metal sources, such as KOH, NaOH, and KCl, provide the necessary metal ions for framework formation. CD-MOFs form body-centered cubic structures by binding to one of the alkali metal cations through coordination of the secondary face hydroxyl groups on the alternate d-glucopyranosyl residues. Beyond the intrinsic advantages of traditional MOFs, CD-MOFs offer additional benefits, particularly in drug delivery applications, where biocompatibility is a crucial factor. These CD-MOFs can be synthesized through various techniques, and multiple strategies can be employed for drug loading. This review comprehensively examines the synthesis of 3D CD-MOFs, their drug loading methodologies, comparative analysis of these methods in terms of advantages and limitations, and the potential of 3D CD-MOFs as drug delivery systems.
Reference:
Edisan Ş, Mutlu-Ağardan NB. Exploring Cyclodextrin-Based MOFs for Drug Delivery: Synthesis, Applications, and Future Perspectives. ACS Omega. 2026 Jan 22;11(4):4940-4956. doi: 10.1021/acsomega.5c10791.
See also:
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