Hybrid nanoparticles as a new technological approach to enhance the delivery of cholesterol into the brain

被引:27
作者
Daniela, Belletti [1 ]
Martin, Grabrucker Andreas [2 ,3 ,5 ]
Francesca, Pederzoli [1 ]
Isabel, Menrath [4 ]
Angela, Vandelli Maria [1 ]
Giovanni, Tosi [1 ]
Jason, Duskey Thomas [1 ]
Flavio, Forni [1 ]
Barbara, Ruozi [1 ]
机构
[1] Univ Modena & Reggio Emilia, Dept Life Sci, Via Campi 103, Modena, Italy
[2] Univ Limerick, Dept Biol Sci, Limerick, Ireland
[3] Univ Limerick, Bernal Inst, Limerick, Ireland
[4] Ulm Univ, Inst Anat & Cell Biol, Ulm, Germany
[5] Univ Limerick, HRI, Limerick, Ireland
关键词
Nanoparticles; Cholesterol; PLGA; Blood brain barrier; CENTRAL-NERVOUS-SYSTEM; HUNTINGTONS-DISEASE; DRUG-DELIVERY; MECHANISMS; PLGA; MICE;
D O I
10.1016/j.ijpharm.2018.03.061
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Restoration of the Choi homeostasis in the Central Nervous System (CNS) could be beneficial for the treatment of Huntington's Disease (HD), a progressive, fatal, adult-onset, neurodegenerative disorder. Unfortunately, Chol is unable to cross the blood-brain barrier (BBB), thus a novel strategy for a targeted delivery of Chol into the brain is highly desired. This article aims to investigate the production of hybrid nanoparticles composed by Chol and PLGA (MIX-NPs) modified with g7 ligand for BBB crossing. We described the impact of ratio between components (Chol and PLGA) and formulation process (nanoprecipitation or single emulsion process) on physico-chemical and structural characteristics, we tested MIX-NPs in vitro using primary hippocampal cell cultures evaluating possible toxicity, uptake, and the ability to influence excitatory synaptic receptors. Our results elucidated that both formulation processes produce MIX-NPs with a Chol content higher that 40%, meaning that Chol is a structural particle component and active compound at the same time. The formulation strategy impacted the architecture and reorganization of components leading to some differences in Chol availability between the two types of g7 MIX-NPs. Our results identified that both kinds of MIX-NPs are efficiently taken up by neurons, able to escape lysosomes and release Chol into the cells resulting in an efficient modification in expression of synaptic receptors that could be beneficial in HD.
引用
收藏
页码:300 / 310
页数:11
相关论文
共 33 条
[1]   Phospholipid/cholesterol model membranes: formation of cholesterol crystallites [J].
Bach, D ;
Wachtel, E .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2003, 1610 (02) :187-197
[2]   EXPLOITING THE VERSATILITY OF CHOLESTEROL IN NANOPARTICLES FORMULATION [J].
Belletti, D. ;
Grabrucker, A. M. ;
Pederzoli, F. ;
Menrath, I. ;
Cappello, V. ;
Vandelli, M. A. ;
Forni, F. ;
Tosi, G. ;
Ruozi, B. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2016, 511 (01) :331-340
[3]   DISSOLUTION PROPERTIES OF NAPROXEN IN COMBINATIONS WITH POLYVINYLPYRROLIDONE [J].
BETTINETTI, G ;
MURA, P .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1994, 20 (08) :1353-1366
[4]   The hippocampus and memory: insights from spatial processing [J].
Bird, Chris M. ;
Burgess, Neil .
NATURE REVIEWS NEUROSCIENCE, 2008, 9 (03) :182-194
[5]   Altered cholesterol and fatty acid metabolism in Huntington disease [J].
Block, Robert C. ;
Dorsey, E. Ray ;
Beck, Christopher A. ;
Brenna, J. Thomas ;
Shoulson, Ira .
JOURNAL OF CLINICAL LIPIDOLOGY, 2010, 4 (01) :17-23
[6]   PHARMACEUTICAL APPLICATIONS OF SOLID DISPERSION SYSTEMS [J].
CHIOU, WL ;
RIEGELMAN, S .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1971, 60 (09) :1281-+
[7]   Cholesterol metabolism in the central nervous system during early development and in the mature animal [J].
Dietschy, JM ;
Turley, SD .
JOURNAL OF LIPID RESEARCH, 2004, 45 (08) :1375-1397
[8]   Polylactide-co-glycolide nanoparticles for controlled delivery of anticancer agents [J].
Dinarvand, R. ;
Sepehri, N. ;
Manoochehri, S. ;
Rouhani, H. ;
Atyabi, F. .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2011, 6 :877-895
[9]  
Egerton, 2005, PHYS PRINCIPLES ELEC, DOI DOI 10.1016/S1369-7021(05)71290-6
[10]   Progress and perspectives on targeting nanoparticles for brain drug delivery [J].
Gao, Huile .
ACTA PHARMACEUTICA SINICA B, 2016, 6 (04) :268-286