Lipid nanoparticles for brain targeting III. Long-term stability and in vivo toxicity

被引:45
作者
Blasi, Paolo [1 ]
Schoubben, Aurelie [1 ]
Traina, Giovanna [2 ]
Manfroni, Giuseppe [1 ]
Barberini, Lanfranco [3 ]
Alberti, Paolo Francesco [4 ]
Cirotto, Carlo [3 ]
Ricci, Maurizio [1 ]
机构
[1] Univ Perugia, Dipartimento Chim & Tecnol Farm, I-06123 Perugia, Italy
[2] Univ Perugia, Dipartimento Sci Econ Estimat & Alimenti, I-06126 Perugia, Italy
[3] Univ Perugia, Dipartimento Biol Cellulare & Ambientale, I-06123 Perugia, Italy
[4] Univ Perugia, Dipartimento Med Sperimentale & Sci Biochim, I-06126 Perugia, Italy
关键词
Nanoparticles (NPs); Solid lipid nanoparticles (SLN); Long-term stability; Chorioallantoic membrane (CAM) assay; Acute toxicity; CHICK CHORIOALLANTOIC MEMBRANE; BARRIER; VITRO; CARRIERS;
D O I
10.1016/j.ijpharm.2013.06.037
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Purpose: The aim of the work was to assess the long-term stability and the safety of lipid nanoparticles intended for brain drug delivery. Methods: Lipid nanoparticles, prepared by high pressure homogenization, were stored at room temperature and 4 degrees C and monitored for their mean hydrodynamic diameter and Gaussian distribution width over time. Cetylpalmitate and polysorbate (R) 80 chemical integrity were investigated by nuclear magnetic resonance on diagnostic signals. Nanoparticle toxicity was assessed in chicken embryos by chorioallantoic membrane assay and in rodents,by brain histological evaluation. Results: Data showed nanoparticle stability at 4 degrees C over a period of time of 4 years with only a limited particle size increase while at room temperature destabilization was observed after 9 months. Nuclear magnetic resonance investigation confirmed the absence (<5%) of chemical degradation of the lipid matrix and the surfactant after 4 years of storage at 4 degrees C. Chorioallantoic membrane assay and rat brain histology showed the absence of acute toxicity corroborating previously published data. Conclusions: Cetylpalmitate nanoparticle long-term physical and chemical stability, together with the in vivo safety, corroborate the existing evidences of the high value of colloidal lipids as parenteral formulations and carriers for brain drug delivery. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:316 / 323
页数:8
相关论文
共 39 条
[1]
The blood-brain barrier: an overview - Structure, regulation, and clinical implications [J].
Ballabh, P ;
Braun, A ;
Nedergaard, M .
NEUROBIOLOGY OF DISEASE, 2004, 16 (01) :1-13
[2]
Beccari N., 1966, Manuale di Tecnica Microscopica
[3]
Blasi P., 2012, CRS NEWSLETTER, V29, P20
[4]
Blasi P., 2011, CRS IT CHAPT WORKSH
[5]
Blasi P., 2007, NANOMATERIALS LIFE S, pSolid
[6]
Solid lipid nanoparticles for targeted brain drug delivery [J].
Blasi, Paolo ;
Glovagnoli, Stefano ;
Schoubben, Aurelie ;
Ricci, Maurizio ;
Rossi, Carlo .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (06) :454-477
[7]
Blasi P, 2009, EUR J PHARM SCI, V38, P25
[8]
Lipid nanoparticles for brain targeting I. Formulation optimization [J].
Blasi, Paolo ;
Giovagnoli, Stefano ;
Schoubben, Aurelie ;
Puglia, Carmelo ;
Bonina, Francesco ;
Rossi, Carlo ;
Ricci, Maurizio .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2011, 419 (1-2) :287-295
[9]
Budai P., 2004, Communications in Agricultural and Applied Biological Sciences, V69, P807
[10]
Factors governing partial coalescence in oil-in-water emulsions [J].
Fredrick, Eveline ;
Walstra, Pieter ;
Dewettinck, Koen .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 2010, 153 (1-2) :30-42