Ionophore-mediated uptake of ciprofloxacin and vincristine into large unilamellar vesicles exhibiting transmembrane ion gradients

• Published in: Biochimica et biophysica acta 1998-11, Vol.1414 (1), p.188-204
• Main Authors: Fenske, David B., Wong, Kim F., Maurer, Elisabeth, Maurer, Norbert, Leenhouts, Johanna M., Boman, Nancy, Amankwa, Lawrence, Cullis, Pieter R.
• Format: Article
• Language: English
• Subjects: A23187; Animals; Blood; Calcimycin - pharmacology; Ciprofloxacin; Ciprofloxacin - chemistry; Ciprofloxacin - pharmacokinetics; Dextrans; Divalent cation; Drug Carriers; Drug loading; Edetic Acid - pharmacology; Gels; Hydrogen-Ion Concentration; Ion Transport; Ionophore; Ionophores - pharmacology; Liposomes - chemistry; Manganese; Manganese - metabolism; Mice; Nigericin; Nigericin - pharmacology; pH gradient; Potassium - metabolism; Vincristine; Vincristine - chemistry; Vincristine - pharmacokinetics
• ISSN: 0005-2736; 0006-3002; 1879-2642
• DOI: 10.1016/S0005-2736(98)00166-7

A new method, based on the ion-translocating properties of the ionophores nigericin and A23187, is described for loading large unilamellar vesicles (LUVs) with the drugs vincristine and ciprofloxacin. LUVs composed of distearoyl-phosphatidylcholine/cholesterol (DSPC/Chol) (55:45 mollmol) or sphingomyelin (SPM)/Chol (55:45 mol/mol) exhibiting a transmembrane salt gradient (for example, internal solution 300 mM MnS04 or K 2SO 4; external solution 300 mM sucrose) are incubated in the presence of drug and, for experiments involving divalent cations, the chelator EDTA. The addition of ionophore couples the outward movement of the entrapped cation to the inward movement of protons, thus acidifying the vesicle interior. External drugs that are weak bases can be taken up in response to this induced transmembrane pH gradient. It is shown that both nigericin and A23187 facilitate the rapid uptake of vincristine and ciprofloxacin, with entrapment levels approaching 100% and excellent retention in vitro. Following drug loading, the ionophores can be removed by gel exclusion chromatography, dialysis, or treatment with biobeads. In vitro leakage assays (addition of 50% mouse serum) and in vivo pharmacokinetic studies (in mice) reveal that the A23187/Mn2+ system exhibits superior drug retention over the nigericin/K + system, and compares favorably with vesicles loaded by the standard ΔpH or amine methods. The unique features of this methodology and possible benefits are discussed.