Pickering emulsions: challenges and opportunities in topical delivery

被引:103
作者
Marto, Joana [1 ]
Ascenso, Andreia [1 ]
Simoes, Sandra [1 ]
Almeida, Antonio J. [1 ]
Ribeiro, Helena M. [1 ]
机构
[1] Univ Lisbon, Fac Pharm, Res Inst Med iMed ULisboa, Lisbon, Portugal
关键词
Cyclodextrins; dermal delivery; pickering emulsions; silica; starch; titanium dioxide; TRANSDERMAL DRUG-DELIVERY; QUINOA STARCH GRANULES; DERMAL DELIVERY; IN-VITRO; SKIN PENETRATION; WATER EMULSIONS; QBD APPROACH; PARTICLES; NANOPARTICLES; SURFACE;
D O I
10.1080/17425247.2016.1182489
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Topical drug delivery is a challenging area with many advantages such as avoidance of first passage effect, stabilization of blood concentrations and attainment of local therapeutic effect with fewer side effects. Despite all these advantages, topical drug delivery remains limited to few molecules, since skin acts as a barrier to the delivery of many therapeutic molecules. To overcome this obstacle, a favored strategy relies on selecting suitable vehicles for dermatologic therapy, such as emulsions, gels and, more recently, nanoparticulate systems. Areas covered: Particle-stabilized emulsions, also known as Pickering emulsions, have garnered interest in recent years. Although most of the investigation on Pickering emulsions has been based on model systems with inorganic or organic solid particles, recent advances have been made regarding the application of nanocarriers, protein-based particles or cyclodextrins for this purpose. This review reports the latest advances in Pickering emulsions technical challenges, and discusses the potential benefits and drawbacks of using these formulations for topical pharmaceutical and cosmetic applications as an alternative to conventional surfactant-based systems. Expert opinion: Pickering emulsions appear as a multifunctional dosage form with endless advantages. A great deal of progress is expected in this area, which might represent a renewed vision for the pharmaceutical and cosmetic industry.
引用
收藏
页码:1093 / 1107
页数:15
相关论文
共 103 条
[1]  
Ai Y, 2014, STARCH, V67, P213
[2]   Solid lipid nanoparticles as a drug delivery system for peptides and proteins [J].
Almeida, Antonio J. ;
Souto, Eliana .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (06) :478-490
[3]  
[Anonymous], 2015, ANDREWS DIS SKIN CLI
[4]   In vitro and in vivo topical delivery studies of tretinoin-loaded ultradeformable vesicles [J].
Ascenso, Andreia ;
Salgado, Ana ;
Euleterio, Carla ;
Praca, Fabiola Garcia ;
Lopes Badra Bentley, Maria Vitoria ;
Marques, Helena C. ;
Oliveira, Helena ;
Santos, Conceicao ;
Simoes, Sandra .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2014, 88 (01) :48-55
[5]   Novel tretinoin formulations: a drug-in-cyclodextrin-in-liposome approach [J].
Ascenso, Andreia ;
Cruz, Mariana ;
Euleterio, Carla ;
Carvalho, Filomena A. ;
Santos, Nuno C. ;
Marques, Helena C. ;
Simoes, Sandra .
JOURNAL OF LIPOSOME RESEARCH, 2013, 23 (03) :211-219
[6]   Topical Delivery of Antioxidants [J].
Ascenso, Andreia ;
Ribeiro, Helena Margarida ;
Marques, Helena Cabral ;
Simoes, Sandra .
CURRENT DRUG DELIVERY, 2011, 8 (06) :640-660
[7]   Complexation and Full Characterization of the Tretinoin and Dimethyl-βeta-Cyclodextrin Complex [J].
Ascenso, Andreia ;
Guedes, Rita ;
Bernardino, Raul ;
Diogo, Herminio ;
Carvalho, Filomena A. ;
Santos, Nuno C. ;
Silva, Aida M. ;
Marques, Helena Cabral .
AAPS PHARMSCITECH, 2011, 12 (02) :553-563
[8]   Formulation studies on a topical gel of tretinoin-dimethyl-beta-cyclodextrin complex [J].
Ascenso, Andreia ;
Duarte, Aida ;
Silva, Alexandra ;
Salgado, Ana ;
Marques, Helena Cabral .
JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY, 2011, 69 (3-4) :339-343
[9]   Emulsions stabilised solely by colloidal particles [J].
Aveyard, R ;
Binks, BP ;
Clint, JH .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 2003, 100 :503-546
[10]   Surface tension and wettability in transdermal delivery: a study on the in-vitro permeation of haloperidol with cyclodextrin across human epidermis [J].
Azarbayjani, Anahita Fathi ;
Lin, Haishu ;
Yap, Chun Wei ;
Chan, Yew Weng ;
Chan, Sui Yung .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2010, 62 (06) :770-778