β-cyclodextrin dendritic derivatives as permeation mediators to enhance the in vitro albendazole cysticidal activity by the improvement of the diffusion component

• Published in: RSC advances Vol. 12; no. 36; pp. 23153 - 23161
• Main Authors: López-Méndez, Luis José, Palomares-Alonso, Francisca, González-Hernández, Iliana, Jung-Cook, Helgi, Cabrera-Quiñones, Neyra Citlali, Guadarrama, Patricia
• Format: Journal Article
• Language: English
• Published: Cambridge Royal Society of Chemistry 16.08.2022; The Royal Society of Chemistry
• Subjects: Chemistry; Cyclodextrins; Dendritic structure; Diffusion; Inclusion complexes; Membranes; NMR; Nuclear magnetic resonance; Penetration; Production costs
• ISSN: 2046-2069; 2046-2069
• DOI: 10.1039/d2ra03314c

The improvement of permeation of drugs across parasites' membranes to promote their diffusion component represents a challenge to achieve better therapeutic effects, including the avoidance of drug resistance. In the context of medicinal chemistry, suitable structural modifications can be made, either on a drug or a nanocarrier, to trigger different mechanisms that promote the influx across membranes. This study aimed to demonstrate the potential of a set of dendritic derivatives of β-cyclodextrin (m2G, h2G, and m3G) as nanocarriers, based on their physicochemical and biological behavior in terms of (i) stability, monitored by 1 H NMR at pH 7 for seven days, (ii) ability to complex, and subsequently release around 50–80% of the cargo molecule (albendazole) in a biphasic medium and (iii) the absence of in vitro cysticidal effect in cysticercus cultures. The albendazole/nanocarrier inclusion complexes (ICs) were proved in the T. crassiceps model. According to the EC 50 values related to the cysticidal activity of albendazole, either free or complexed, the potency of this drug in the ICs experienced a significant increase, which may be attributed to the enhancement of its solubility but also to a better permeation mediated by the amphiphilic dendritic moieties, which ultimately positively impacts the diffusion of this drug through the tegument of the cysticerci. Additional considerations akin to synthetic ease of the dendritic nanocarriers, and production cost, along with the obtained outcomes, allowed us to place m2G followed by m3G as the best options to be considered for further in vivo assays.