New amphiphilic derivatives of poly(ethylene glycol) (PEG) as surface modifiers of colloidal drug carriers. III. Lipoamino acid conjugates with carboxy- and amino-PEG(5000) polymers

作者：Pignatello Rosario^*; Impallomeni Giuseppe; Pistara Venerando; Cupri Sarha; Graziano Adriana C E; Cardile Venera; Ballistreri Alberto

来源：Materials Science & Engineering C-Materials for Biological Applications, 2015, 46: 470-481.

DOI：10.1016/j.msec.2014.10.054

• PEG
• Lipoamino acid
• Stealth drug carriers
• Polymeric conjugates
• DSC
• MTT test

Within a research directed to developing new polymeric materials, suitable for decorating the surface of colloidal drug carriers, PEG(5000) polymers containing a free carboxyl or amine group at one end were conjugated to an alpha-lipoamino moiety (LAA). The conjugates were characterized by FT-IR,H-1-NMR, and MALDI-TOF mass spectrometry. They showed the same profile of solubility as the parent PEGs in water and in some polar and apolar solvents of pharmaceutical use. Representative terms showed to be well tolerated when incubated with Caco-2 or L929 cell cultures.
Dedicated differential scanning calorimetry (DSC) studies were performed to prove the interaction of increasing molar fractions of the PEG(5000)-LAA conjugates with dipalmitoylphosphatidylcholine (DPPC) bilayers, to gain information about their possible incorporation in drug nanocarriers. While the parent PEGs affected only the superficial structure of bilayers, the amphiphilic PEG-LAA conjugates induced a perturbing effect on the thermotropic behavior of DPPC liposomes, according to the structure of the linked LAA residue. A molar concentration of these PEG-LAA between 5 and 10% was individuated as the most suitable to produce stable vesicles.

• 出版日期2015-1-1