β-CD is a cyclic polysaccharide molecule with a hollow cylindrical structure that encapsulates certain compounds to form an inclusion complex. This encapsulation is based on the interaction between the hydrophobicity inside and the hydrophilicity outside of the hollow structure of β-CD, thus "encapsulating" small molecule compounds. Based on this property, β-CD is used in a wide range of applications, including drug formulation, separation and purification, environmental protection, etc. CD BioGlyco is focusing on the research on GlycoCLICK™-based Drug Delivery to provide the most professional services, which includes β-CD-based drug delivery service. There are a variety of drug delivery systems that can be constructed using β-CD, and our offerings encompass but are not restricted to the subsequent services.
In the drug delivery system composed of β-CD and non-covalent attached micelles (NCCMs), β-CD as a host molecule binds to drug molecules through non-covalent interactions to form a stable micelle structure. According to the properties and requirements of the drug, we select suitable β-CD molecules to form clathrates with the drug molecules. Subsequently, we interact the clathrates with other surfactants or adjuvants to form micellar structures so that these surfactants form non-covalent connections with β-CD-drug clathrates. We use click chemistry to modify the surface of nanogels to introduce specific functional groups for binding to drug molecules or other targeted ligands for targeted delivery. Finally, the properties including drug loading, release rate, stability, and biocompatibility of NCCMs are evaluated.
We first covalently link β-CD with polyethylene glycol (PEG)-modified phospholipids to form a modified molecule with a cyclic structure. Then, β-CD-PEG-lipid is added to the lipid solution for sonication, high-pressure homogenization, etc., so that the β-CD-modified molecules interact with the surface of the lipids to form β-CD-based lipid nanoparticles (β-CD-LNPs). We modify the function or surface of β-CD-LNPs and the molecules of interest are further modified or conjugated, such as targeting ligands, imaging agents, or stimulus-response parts, by introducing reactive functional groups on the surface of β-CD-LNPs. This enhances the specificity, versatility, and functionality of β-CD-LNPs in drug delivery applications. After routine nanoparticle characterization, the prepared β-CD-LNPs are subjected to in vitro or in vivo drug delivery experiments to evaluate their drug delivery effect and biosafety.
Fig.1 Technologies for β-CD-based drug delivery. (CD BioGlyco)
Technology: NMR, FTIR, UV-vis, and cytotoxicity test
Journal: Macromolecular Bioscience
IF: 5.859
Published: 2020
Results: This paper presents a cell membrane-targeted drug delivery system based on choline phosphate functionalized β-CD (CP-β-CD). The researchers loaded fluorescein isothiocyanate-labeled amantadine (FITC-AMD) into CP-β-CD and used it as an indicator. The experimental results showed that the CP-β-CD@FITC-AMD drug delivery system could rapidly enter cells within 4 hours, showing strong cell targeting ability. In addition, the researchers evaluated the inhibitory effect of CP-β-CD@Apatinib on human umbilical vein endothelial cells (HUVECs). The results showed that the antiangiogenic activity of CP-β-CD@Apatinib was higher than that of β-CD@Apatinib and free Apatinib, and the inhibitory effect was stronger with the increase of drug concentration. Overall, the CP-β-CD drug delivery system can improve the anti-angiogenic activity of Apatinib and has good cell targeting ability.
Fig.2 Schematic illustration of cell membrane adhesion and penetration of CP-β-CD@Apatinib. (Feng, et al., 2020)
With our extensive experience and knowledge in the field of drug delivery, specifically utilizing β-CD, CD BioGlyco is confident in our ability to provide you with a highly satisfactory service. Our expertise in drug delivery allows us to design and develop innovative solutions. For further details, please don't hesitate to
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