Liposome Encapsulation of the Palmitoyl–KTTKS Peptide: Structural and Functional Characterization

Author:

Vitali Alberto1ORCID,Paolicelli Patrizia2ORCID,Bigi Barbara2ORCID,Trilli Jordan2,Di Muzio Laura2,Carriero Vito Cosimo2ORCID,Casadei Maria Antonietta2ORCID,Petralito Stefania2

Affiliation:

1. Istituto di Scienze e Tecnologie Chimiche “Giulio Natta”, National Research Council of Italy, Largo Francesco Vito 1, 00168 Rome, Italy

2. Department of Drug Chemistry and Technologies, Sapienza University of Rome, Piazzale Aldo Moro 5, 00185 Rome, Italy

Abstract

In this study, the amphiphilic N-palmitoyl–KTTKS peptide was integrated in the bilayer of egg-derived phosphatidylcholine (PC) vesicles using two different preparation methods, namely thin-film evaporation (TLE) and reverse-phase evaporation (REV). Both the REV and TLE methods allowed for the formation of homogeneous liposome dispersions (PdI < 0.20) with mean hydrodynamic diameters of <100 nm and <200 nm, respectively, a net negative surface charge and a percentage of structured phospholipids higher than 90%. The inclusion of the amphiphilic N-palmitoyl–KTTKS peptide within phospholipid-based vesicles could improve peptide stability and skin delivery. Therefore, the obtained liposomes were evaluated via experiments assessing the synthesis of collagen and the ECM in 3T3-NIH fibroblasts. The obtained results showed that, when delivered with PC liposomes, pal-KTTKS stimulated collagen production more than free pentapeptide and 1 mM ascorbic acid, used as a positive control.

Publisher

MDPI AG

Subject

Pharmaceutical Science

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