Functional response of novel bioprotective poloxamer-structured vesicles on inflamed skin

被引:13
作者
Caddeo, Carla [1 ]
Manca, Maria Letizia [1 ]
Matos, Maria [2 ]
Gutierrez, Gemma [2 ]
Diez-Sales, Octavio [3 ,4 ]
Esteban Peris, Jose [3 ]
Usach, Iris [3 ]
Fernandez-Busquets, Xavier [5 ,6 ]
Fadda, Anna Maria [1 ]
Manconi, Maria [1 ]
机构
[1] Univ Cagliari, Dept Sci Vita & Ambiente, Cagliari, Italy
[2] Univ Oviedo, Dept Ingn Quim & Tecnol Medio Ambiente, Oviedo, Spain
[3] Univ Valencia, Dept Pharm & Pharmaceut Technol, Valencia, Spain
[4] Univ Valencia, Ctr Mixto Univ Politecn Valencia, Inst Reconocimiento Mol & Desarrollo Tecnol, Valencia, Spain
[5] Inst Bioengn Catalonia IBEC, Nanomalaria Grp, Barcelona, Spain
[6] Univ Barcelona, Hosp Clin, Barcelona Ctr Int Hlth Res, CRESIB,Barcelona Inst Global Hlth,ISGlobal, Barcelona, Spain
关键词
Phospholipid vesicle; Phenol; Poloxamer; Fibroblasts; Mice; Skin inflammation; TRANSDERMAL DRUG-DELIVERY; IN-VITRO CHARACTERIZATION; TRIBLOCK COPOLYMERS; PENETRATION; QUERCETIN; LIPOSOMES; TRANSFERSOMES; NANOPARTICLES; GLYCEROSOMES; PERMEATION;
D O I
10.1016/j.nano.2016.12.017
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Resveratrol and gallic acid, a lipophilic and a hydrophilic phenol, were co-loaded in innovative, biocompatible nanovesicles conceived for ensuring the protection of the skin from oxidative-and inflammatory-related affections. The basic vesicles, liposomes and glycerosomes, were produced by a simple, one-step method involving the dispersion of phospholipid and phenols in water or water/glycerol blend, respectively. Liposomes and glycerosomes were modified by the addition of poloxamer, a stabilizer and viscosity enhancer, thus obtaining viscous or semisolid dispersions of structured vesicles. The vesicles were spherical, unilamellar and small in size (similar to 70 nm in diameter). The superior ability of the poloxamer-structured vesicles to promote the accumulation of both phenols in the skin was demonstrated, as well as their low toxicity and great ability to protect fibroblasts from chemically-induced oxidative damage. The in vivo administration of the vesicular phenols on TPA (phorbol ester)-exposed skin led to a significant reduction of oedema and leukocyte infiltration. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:1127 / 1136
页数:10
相关论文
共 32 条
[1]   Factorial design formulation optimization and in vitro characterization of curcumin-loaded PLGA nanoparticles for colon delivery [J].
Akl, Mohamed A. ;
Kartal-Hodzic, Alma ;
Oksanen, Timo ;
Ismael, Hatem R. ;
Afouna, Mohsen M. ;
Yliperttula, Marjo ;
Samy, Ahmed M. ;
Viitala, Tapani .
JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2016, 32 :10-20
[2]   Topical drug delivery by a polymeric nanosphere gel: Formulation optimization and in vitro and in vivo skin distribution studies [J].
Batheja, Priya ;
Sheihet, Larisa ;
Kohn, Joachim ;
Singer, Adam J. ;
Michniak-Kohn, Bozena .
JOURNAL OF CONTROLLED RELEASE, 2011, 149 (02) :159-167
[3]   Fabrication of quercetin and curcumin bionanovesicles for the prevention and rapid regeneration of full-thickness skin defects on mice [J].
Castangia, Ines ;
Nacher, Amparo ;
Caddeo, Carla ;
Valenti, Donatella ;
Fadda, Anna Maria ;
Diez-Sales, Octavio ;
Ruiz-Sauri, Amparo ;
Manconi, Maria .
ACTA BIOMATERIALIA, 2014, 10 (03) :1292-1300
[4]   Effect of diclofenac and glycol intercalation on structural assembly of phospholipid lamellar vesicles [J].
Castangia, Ines ;
Manca, Maria Letizia ;
Matricardi, Pietro ;
Sinico, Chiara ;
Lampis, Sandrina ;
Fernandez-Busquets, Xavier ;
Fadda, Anna Maria ;
Manconi, Maria .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2013, 456 (01) :1-9
[5]   Turbiscan Lab® Expert analysis of the stability of ethosomes® and ultradeformable liposomes containing a bilayer fluidizing agent [J].
Celia, Christian ;
Trapasso, Elena ;
Cosco, Donato ;
Paolino, Donatella ;
Fresta, Massimo .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2009, 72 (01) :155-160
[6]   Ultraflexible vesicles, transfersomes, have an extremely low pore penetration resistance and transport therapeutic amounts of insulin across the intact mammalian skin [J].
Cevc, G ;
Gebauer, D ;
Stieber, J ;
Schätzlein, A ;
Blume, G .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1998, 1368 (02) :201-215
[7]   Transfersomes, liposomes and other lipid suspensions on the skin: Permeation enhancement, vesicle penetration, and transdermal drug delivery [J].
Cevc, G .
CRITICAL REVIEWS IN THERAPEUTIC DRUG CARRIER SYSTEMS, 1996, 13 (3-4) :257-388
[8]   Nanotechnology and the transdermal route A state of the art review and critical appraisal [J].
Cevc, Gregor ;
Vierl, Ulrich .
JOURNAL OF CONTROLLED RELEASE, 2010, 141 (03) :277-299
[9]   Interaction and Complexation of Phospholipid Vesicles and Triblock Copolymers [J].
Chieng, Yu Yuan ;
Chen, Shing Bor .
JOURNAL OF PHYSICAL CHEMISTRY B, 2009, 113 (45) :14934-14942
[10]   Characterization of gelation process and drug release profile of thermosensitive liquid lecithin/poloxamer 407 based gels as carriers for percutaneous delivery of ibuprofen [J].
Djekic, Ljiljana ;
Krajisnik, Danina ;
Martinovic, Martina ;
Djordjevic, Dragana ;
Primorac, Marija .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2015, 490 (1-2) :180-189