Natural lipids-based NLC containing lidocaine: from pre-formulation to in vivo studies

被引:71
作者
Ribeiro, Ligia N. M. [1 ]
Breitkreitz, Marcia C. [2 ]
Guilherme, Viviane A. [1 ]
da Silva, Gustavo H. R. [1 ]
Couto, Veronica M. [1 ]
Castro, Simone R. [1 ]
de Paula, Barbara O. [1 ]
Machado, Daisy [1 ]
de Paula, Eneida [1 ]
机构
[1] Univ Estadual Campinas, UNICAMP, Inst Biol, Dept Biochem & Tissue Biol, Rua Monteiro Lobato 255 Cidade Univ Zeferino Vaz, BR-13083862 Campinas, SP, Brazil
[2] Univ Estadual Campinas, Inst Chem, Dept Analyt Chem, Campinas, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Beeswax; Nanostructured lipid carriers; Vegetable fats; Vegetable oils; OF-THE-ART; DRUG-DELIVERY; NANOPARTICLES SLN; SYSTEMS; PRILOCAINE; ZEBRAFISH; OIL; CARRIERS; RELEASE; DESIGN;
D O I
10.1016/j.ejps.2017.05.060
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In a nanotechnological approach we have investigated the use of natural lipids in the preparation of nanostructured lipid carriers (NLC). Three different NLC composed of copaiba oil and beeswax, sweet almond oil and shea butter, and sesame oil and cocoa butter as structural matrices were optimized using factorial analysis; Pluronic (R) 68 and lidocaine (LDC) were used as the colloidal stabilizer and model encapsulated drug, respectively. The optimal formulations were characterized by different techniques (IR-ATR, DSC, and TEM), and their safety and efficacy were also tested. These nanocarriers were able to upload high amounts of the anesthetic with a sustained in vitro release profile for 24 h. The physicochemical stability in terms of size (nm), PDI, zeta potential (mV), pH, nanoparticle concentration (particles/mL), and visual inspection was followed during 12 months of storage at 25 degrees C. The formulations exhibited excellent structural properties and stability. They proved to be nontoxic in vitro (cell viability tests with Balb/c 3T3 fibroblasts) and significantly improved the in vivo effects of LDC, over the heart rate of zebra fish larvae and in the blockage of sciatic nerve in mice. The results from this study support that the proper combination of natural excipients is promising in DDS, taking advantage of the biocompatibility, low cost, and diversity of lipids.
引用
收藏
页码:102 / 112
页数:11
相关论文
共 55 条
[1]  
Ali H.H., 2015, EUR J LIPID SCI TECH, V117, P1
[2]   Optimization and physicochemical characterization of a triamcinolone acetonide-loaded NLC for ocular antiangiogenic applications [J].
Araujo, J. ;
Gonzalez-Mira, E. ;
Egea, M. A. ;
Garcia, M. L. ;
Souto, E. B. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2010, 393 (1-2) :167-175
[3]   Further characterization of theobroma oil-beeswax admixtures as lipid matrices for improved drug delivery systems [J].
Attama, A. A. ;
Schicke, B. C. ;
Mueller-Goymann, C. C. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2006, 64 (03) :294-306
[4]   Effect of beeswax modification on the lipid matrix and solid lipid nanoparticle crystallinity [J].
Attama, Anthony A. ;
Mueller-Goymann, Christel C. .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2008, 315 (1-3) :189-195
[5]   Use of various vegetable oils in designing photoprotective nanostructured formulations for UV protection and antioxidant activity [J].
Badea, Gabriela ;
Lacatusu, Ioana ;
Badea, Nicoleta ;
Ott, Cristina ;
Meghea, Aurelia .
INDUSTRIAL CROPS AND PRODUCTS, 2015, 67 :18-24
[6]   Lipid nanoparticles: state of the art, new preparation methods and challenges in drug delivery [J].
Battaglia, Luigi ;
Gallarate, Marina .
EXPERT OPINION ON DRUG DELIVERY, 2012, 9 (05) :497-508
[7]  
Berridge J.C., 2004, ICH Q8 PHARM DEV
[8]   DLS and zeta potential - What they are and what they are not? [J].
Bhattacharjee, Sourav .
JOURNAL OF CONTROLLED RELEASE, 2016, 235 :337-351
[9]   Calcium, ATP, and ROS: a mitochondrial love-hate triangle [J].
Brookes, PS ;
Yoon, YS ;
Robotham, JL ;
Anders, MW ;
Sheu, SS .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2004, 287 (04) :C817-C833
[10]   Development of cataplasmic transdermal drug delivery system containing eutectic mixture of lidocaine and prilocaine [J].
Chun M.-K. ;
Hossain K. ;
Choi S.-H. ;
Ban S.-J. ;
Moon H. ;
Choi H.-K. .
Journal of Pharmaceutical Investigation, 2012, 42 (3) :139-146