Cationic Cyclodextrin-Based Carriers for Drug and Nucleic Acid Delivery

Cyclodextrins can serve as carriers for various payloads, utilizing their capacity to form unique host–guest inclusion complexes within their cavity and their versatile surface functionalization. Recently, cationic cyclodextrins have gained considerable attention, as they can improve drug permeabili...

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Main Authors: Adila Nazli, Milo Malanga, Tamás Sohajda, Szabolcs Béni
Format: Article
Language:English
Published: MDPI AG 2025-01-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/17/1/81
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author Adila Nazli
Milo Malanga
Tamás Sohajda
Szabolcs Béni
author_facet Adila Nazli
Milo Malanga
Tamás Sohajda
Szabolcs Béni
author_sort Adila Nazli
collection DOAJ
description Cyclodextrins can serve as carriers for various payloads, utilizing their capacity to form unique host–guest inclusion complexes within their cavity and their versatile surface functionalization. Recently, cationic cyclodextrins have gained considerable attention, as they can improve drug permeability across negatively charged cell membranes and efficiently condense negatively charged nucleic acid due to electrostatic interactions. This review focuses on state-of-the-art and recent advances in the construction of cationic cyclodextrin-based delivery systems. First, we identified different cationic moieties that are commonly employed in the design of cyclodextrins with enhanced complexation ability. Subsequently, a wide range of cationic cyclodextrin-based drug delivery systems were analyzed with emphasis on chemistry, drug release profiles, and therapeutic outcomes. The evaluation of the delivery platforms was also based on the four major types of drugs, such as anticancer, anti-inflammatory, antibacterial, and antidiabetic agents. The delivery systems for nucleic acids were also summarized while focusing on their condensation ability, transfection efficiency, and biocompatibility in comparison to commercially available vectors such as PEI 25 kDa and lipofectamine 2000. Furthermore, we highlighted the potential of cationic cyclodextrins in constructing multimodal delivery systems for the simultaneous encapsulation of both drugs and nucleic acids. Finally, the challenges and limitations associated with cationic cyclodextrin setups were discussed.
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series Pharmaceutics
spelling doaj-art-760d0271611b4f5583c938a86eb90dcf2025-01-24T13:45:52ZengMDPI AGPharmaceutics1999-49232025-01-011718110.3390/pharmaceutics17010081Cationic Cyclodextrin-Based Carriers for Drug and Nucleic Acid DeliveryAdila Nazli0Milo Malanga1Tamás Sohajda2Szabolcs Béni3Department of Pharmacognosy, Semmelweis University, 1085 Budapest, HungaryCarboHyde Zrt., Berlini u. 47-49, 1045 Budapest, HungaryCarboHyde Zrt., Berlini u. 47-49, 1045 Budapest, HungaryIntegrative Health and Environmental Analysis Research Laboratory, Department of Analytical Chemistry, Institute of Chemistry, Eötvös Loránd University, 1117 Budapest, HungaryCyclodextrins can serve as carriers for various payloads, utilizing their capacity to form unique host–guest inclusion complexes within their cavity and their versatile surface functionalization. Recently, cationic cyclodextrins have gained considerable attention, as they can improve drug permeability across negatively charged cell membranes and efficiently condense negatively charged nucleic acid due to electrostatic interactions. This review focuses on state-of-the-art and recent advances in the construction of cationic cyclodextrin-based delivery systems. First, we identified different cationic moieties that are commonly employed in the design of cyclodextrins with enhanced complexation ability. Subsequently, a wide range of cationic cyclodextrin-based drug delivery systems were analyzed with emphasis on chemistry, drug release profiles, and therapeutic outcomes. The evaluation of the delivery platforms was also based on the four major types of drugs, such as anticancer, anti-inflammatory, antibacterial, and antidiabetic agents. The delivery systems for nucleic acids were also summarized while focusing on their condensation ability, transfection efficiency, and biocompatibility in comparison to commercially available vectors such as PEI 25 kDa and lipofectamine 2000. Furthermore, we highlighted the potential of cationic cyclodextrins in constructing multimodal delivery systems for the simultaneous encapsulation of both drugs and nucleic acids. Finally, the challenges and limitations associated with cationic cyclodextrin setups were discussed.https://www.mdpi.com/1999-4923/17/1/81targeted drug releasetransfection efficiencyinclusion complexplasmid DNAmicroRNAsmall interfering RNA
spellingShingle Adila Nazli
Milo Malanga
Tamás Sohajda
Szabolcs Béni
Cationic Cyclodextrin-Based Carriers for Drug and Nucleic Acid Delivery
Pharmaceutics
targeted drug release
transfection efficiency
inclusion complex
plasmid DNA
microRNA
small interfering RNA
title Cationic Cyclodextrin-Based Carriers for Drug and Nucleic Acid Delivery
title_full Cationic Cyclodextrin-Based Carriers for Drug and Nucleic Acid Delivery
title_fullStr Cationic Cyclodextrin-Based Carriers for Drug and Nucleic Acid Delivery
title_full_unstemmed Cationic Cyclodextrin-Based Carriers for Drug and Nucleic Acid Delivery
title_short Cationic Cyclodextrin-Based Carriers for Drug and Nucleic Acid Delivery
title_sort cationic cyclodextrin based carriers for drug and nucleic acid delivery
topic targeted drug release
transfection efficiency
inclusion complex
plasmid DNA
microRNA
small interfering RNA
url https://www.mdpi.com/1999-4923/17/1/81
work_keys_str_mv AT adilanazli cationiccyclodextrinbasedcarriersfordrugandnucleicaciddelivery
AT milomalanga cationiccyclodextrinbasedcarriersfordrugandnucleicaciddelivery
AT tamassohajda cationiccyclodextrinbasedcarriersfordrugandnucleicaciddelivery
AT szabolcsbeni cationiccyclodextrinbasedcarriersfordrugandnucleicaciddelivery