Light- and temperature-responsive liposomes incorporating cinnamoyl Pluronic F127.

International journal of pharmaceutics (2014-04-09)
MinHui Wang, Jin-Chul Kim
RESUMO

Light- and temperature-responsive liposomes were prepared by immobilizing cinnamoyl Pluronic F127 (CP F127) on the surface of egg phosphatidylcholine liposomes. CP F127 was prepared by a condensation reaction, and the molar ratio of cinnamoyl group to Pluronic F127 was calculated to be 1:1.4 on (1)H NMR spectrum. The cinnamoyl group of CP F127 was readily dimerized under the irradiation of a UV light (254 nm, 6 W). CP F127 decreased the absolute value of the zeta potential of liposome possibly because it can shift the hydrodynamic plane away from the liposome surface. The size of liposome decorated with CP F127, measured on a dynamic light scattering machine and observed on a TEM, was larger than that of bare liposome. The liposome bearing CP F127 seemed to fuse and aggregate each other. The liposome released calcein, a fluorescence dye, in response to a UV irradiation, possibly because the photo-dimerization of cinnamoyl group perturbs the liposomal membrane. Moreover, the liposome released the dye in response to a temperature change, possible due to the phase transition of Pluronic F127 layer on the liposomal surface or the hydrophobic interaction of the polymer with liposomal membrane.

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Triethylamine, ≥99.5%
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Triethylamine, ≥99%
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Triethylamine, puriss. p.a., ≥99.5% (GC)
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Triethylamine, BioUltra, ≥99.5% (GC)
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Calcein, Used for the fluorometric determination of calcium and EDTA titration of calcium in the presence of magnesium.
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Cinnamoyl chloride, 98%
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Triethylamine, analytical standard
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Triethylamine, for amino acid analysis, ≥99.5% (GC)
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Triethylamine, for protein sequence analysis, ampule, ≥99.5% (GC)
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