Influence of Surfactant and Lipid Type on the Physicochemical Properties and Biocompatibility of Solid Lipid Nanoparticles

被引:59
作者
Dal Pizzol, Carine [1 ]
Filippin-Monteiro, Fabiola Branco [1 ]
Sierra Restrepo, Jelver Alexander [2 ]
Pittella, Frederico [3 ]
Silva, Adny Henrique [1 ]
de Souza, Paula Alves [1 ]
de Campos, Angela Machado [1 ]
Creczynski-Pasa, Tania Beatriz [1 ]
机构
[1] Univ Fed Santa Catarina, Dept Ciencias Farmaceut, Programa Posgrad Farm, BR-88040900 Florianopolis, SC, Brazil
[2] Univ Fed Santa Catarina, Progama Posgrad Engn Mat, BR-88040900 Florianopolis, SC, Brazil
[3] Univ Fed Juiz de Fora, Dept Anal Clin, BR-36036900 Juiz De Fora, MG, Brazil
关键词
solid lipid nanoparticles; cytotoxicity; surfactant; lipid; biocompatibility; STEARIC-ACID; DELIVERY; TOXICITY; CARRIERS; SYSTEMS; SLN; CYTOTOXICITY; FORMULATION; STABILITY; APOPTOSIS;
D O I
10.3390/ijerph110808581
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Nine types of solid lipid nanoparticle (SLN) formulations were produced using tripalmitin (TPM), glyceryl monostearate (GM) or stearic acid (SA), stabilized with lecithin S75 and polysorbate 80. Formulations were prepared presenting PI values within 0.25 to 0.30, and the physicochemical properties, stability upon storage and biocompatibility were evaluated. The average particle size ranged from 116 to 306 nm, with a negative surface charge around -11 mV. SLN presented good stability up to 60 days. The SLN manufactured using SA could not be measured by DLS due to the reflective feature of this formulation. However, TEM images revealed that SA nanoparticles presented square/rod shapes with an approximate size of 100 nm. Regarding biocompatibility aspects, SA nanoparticles showed toxicity in fibroblasts, causing cell death, and produced high hemolytic rates, indicating toxicity to red blood cells. This finding might be related to lipid type, as well as, the shape of the nanoparticles. No morphological alterations and hemolytic effects were observed in cells incubated with SLN containing TPM and GM. The SLN containing TPM and GM showed long-term stability, suggesting good shelf-life. The results indicate high toxicity of SLN prepared with SA, and strongly suggest that the components of the formulation should be analyzed in combination rather than separately to avoid misinterpretation of the results.
引用
收藏
页码:8581 / 8596
页数:16
相关论文
共 36 条
[1]   Geometry and surface characteristics of gold nanoparticles influence their biodistribution and uptake by macrophages [J].
Arnida ;
Janat-Amsbury, M. M. ;
Ray, A. ;
Peterson, C. M. ;
Ghandehari, H. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2011, 77 (03) :417-423
[2]  
Bae DH, 2009, B KOREAN CHEM SOC, V30, P339
[3]   Influence of shape, adhesion and simulated lung mechanics on amorphous silica nanoparticle toxicity [J].
Brown, Scott C. ;
Kamal, Mohammed ;
Nasreen, Najmunnisa ;
Baumuratov, Aidos ;
Sharma, Parvesh ;
Antony, Veena B. ;
Moudgil, Brij M. .
ADVANCED POWDER TECHNOLOGY, 2007, 18 (01) :69-79
[4]   Biodistribution, pharmacokinetics, and blood compatibility of native and PEGylated tobacco mosaic virus nano-rods and -spheres in mice [J].
Bruckman, Michael A. ;
Randolph, Lauren N. ;
VanMeter, Allen ;
Hern, Stephen ;
Shoffstall, Andrew J. ;
Taurog, Rebecca E. ;
Steinmetz, Nicole F. .
VIROLOGY, 2014, 449 :163-173
[5]  
COHEN JJ, 1993, IMMUNOL TODAY, V14, P126, DOI 10.1016/0167-5699(93)90214-6
[6]   EFFECT OF SURFACTANTS ON CRYSTAL-STRUCTURE MODIFICATION OF STEARIC-ACID [J].
GARTI, N ;
WELLNER, E ;
SARIG, S .
JOURNAL OF CRYSTAL GROWTH, 1982, 57 (03) :577-584
[7]   Melatonin-loaded lecithin/chitosan nanoparticles: Physicochemical characterisation and permeability through Caco-2 cell monolayers [J].
Hafner, Anita ;
Lovric, Jasmina ;
Voinovich, Dario ;
Filipovic-Grcic, Jelena .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2009, 381 (02) :205-213
[8]   Physico-chemical stability of colloidal lipid particles [J].
Heurtault, B ;
Saulnier, P ;
Pech, B ;
Proust, JE ;
Benoit, JP .
BIOMATERIALS, 2003, 24 (23) :4283-4300
[9]   Design and in vivo pharmacodynamic evaluation of nanostructured lipid carriers for parenteral delivery of artemether: Nanoject [J].
Joshi, Medha ;
Pathak, Sulabha ;
Sharma, Shobhona ;
Patravale, Vandana .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2008, 364 (01) :119-126
[10]   Lipid nanoparticles for parenteral delivery of actives [J].
Joshi, Medha D. ;
Mueller, Rainer H. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2009, 71 (02) :161-172