Inclusion Complex between Local Anesthetic/2-hydroxypropyl-β-cyclodextrin in Stealth Liposome

Molecules. 2022 Jun 29;27(13):4170. doi: 10.3390/molecules27134170.

Abstract

The drugs delivery system in the treatment of diseases has advantages such as reduced toxicity, increased availability of the drug, etc. Therefore, studies of the supramolecular interactions between local anesthetics (LAs) butamben (BTB) or ropivacaine (RVC) complexed with 2-hydroxypropyl-β-cyclodextrin (HP-βCD) and carried in Stealth liposomal (SL) are performed. 1H-NMR nuclear magnetic resonance (DOSY and STD) were used as the main tools. The displacements observed in the 1H-NMR presented the complexion between LAs and HP-βCD. The diffusion coefficients of free BTB and RVC were 7.70 × 10-10 m2 s-1 and 4.07 × 10-10 m2 s-1, and in the complex with HP-βCD were 1.90 × 10-10 m2 s-1 and 3.64 × 10-10 m2 s-1, respectively, which indicate a strong interaction between the BTB molecule and HP-βCD (98.3% molar fraction and Ka = 72.279 L/mol). With STD-NMR, the encapsulation of the BTB/HP-βCD and RVC/HP-βCD in SL vesicles was proven. Beyond the saturation transfer to the LAs, there is the magnetization transfer to the hydrogens of HP-βCD. BTB and RVC have already been studied in normal liposome systems; however, little is known of their behavior in SL.

Keywords: 1H-NMR; NMR-STD; butamben; ropivacaine; stealth liposomes.

MeSH terms

  • 2-Hydroxypropyl-beta-cyclodextrin / chemistry
  • Anesthetics, Local*
  • Liposomes
  • Magnetic Resonance Spectroscopy
  • Solubility
  • beta-Cyclodextrins* / chemistry

Substances

  • Anesthetics, Local
  • Liposomes
  • beta-Cyclodextrins
  • 2-Hydroxypropyl-beta-cyclodextrin