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  1. Article: Chitosan coated nanostructured lipid carriers for brain delivery of proteins by intranasal administration

    Gartziandia, Oihane / Enara Herran / Eva Carro / Jose Luis Pedraz / Manoli Igartua / Rosa Maria Hernandez

    Colloids and Surfaces B: Biointerfaces. 2015 Oct. 01, v. 134

    2015  

    Abstract: The remarkable increase in the prevalence of neurodegenerative diseases has become a serious public health problem. Considering the lack of effective treatments to address these diseases and the difficulties in accessing the brain due to the blood– ... ...

    Abstract The remarkable increase in the prevalence of neurodegenerative diseases has become a serious public health problem. Considering the lack of effective treatments to address these diseases and the difficulties in accessing the brain due to the blood–brain barrier (BBB), to attain a successful strategy to improve drug delivery to the brain, the administration route becomes a point of interest. The intranasal route provides a non-invasive method to bypass the BBB. Moreover, the development of new technologies for the protection and delivery of peptides is an interesting approach to consider. Thus, in this work, a suitable chitosan coated nanostructured lipid carrier (CS-NLC) formulation with the capacity to reach the brain after being intranasally administered was successfully developed and optimized. The optimal formulation displayed a particle size of 114nm with a positive surface charge of +28mV. The in vitro assays demonstrated the biocompatibility of the nanocarrier and its cellular uptake by 16HBE14o- cells. Furthermore, no haemagglutination or haemolysis processes were observed when the particles were incubated with erythrocytes, and no toxicity signals appeared in the nasal mucosa of mice after the administration of CS-NLCs. Finally, the biodistribution study of CS-NLC-DiR demonstrated an efficient brain delivery of the particles after intranasal administration. In conclusion, CS-NLC can be considered to be a safe and effective nanocarrier for nose-to-brain drug delivery; however, to obtain a higher concentration of the drug in the brain following intranasal administration, further modifications are warranted in the CS-NLC formulation.
    Keywords biocompatibility ; blood-brain barrier ; brain ; chitosan ; colloids ; drugs ; erythrocytes ; hemagglutination ; hemolysis ; in vitro studies ; intranasal administration ; lipids ; mice ; nanocarriers ; nasal mucosa ; neurodegenerative diseases ; particle size ; peptides ; proteins ; public health ; toxicity
    Language English
    Dates of publication 2015-1001
    Size p. 304-313.
    Publishing place Elsevier B.V.
    Document type Article
    ZDB-ID 1500523-9
    ISSN 1873-4367 ; 0927-7765
    ISSN (online) 1873-4367
    ISSN 0927-7765
    DOI 10.1016/j.colsurfb.2015.06.054
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: Generation of one iPSC line (IMEDEAi006-A) from an early-onset familial Alzheimer's Disease (fAD) patient carrying the E280A mutation in the PSEN1 gene

    Sara Vallejo-Diez / Aarne Fleischer / Jose María Martín-Fernández / Almudena Sánchez-Gilabert / Mónica Castresana / David Aguillón / Andrés Villegas / Claudio A. Mastronardi / Lady G. Espinosa / Mauricio Arcos-Burgos / Ángel del Pozo / Enara Herrán / Eusebio Gainza / Mario Isaza-Ruget / Francisco Lopera / Daniel Bachiller

    Stem Cell Research, Vol 37, Iss , Pp - (2019)

    2019  

    Abstract: The mutation E280A in PSEN1 (presenilin-1) is the most common cause of early-onset familial Alzheimer's Disease (fAD). It presents autosomal dominant inheritance and frequently leads to the manifestation of the disease in relatively young individuals. ... ...

    Abstract The mutation E280A in PSEN1 (presenilin-1) is the most common cause of early-onset familial Alzheimer's Disease (fAD). It presents autosomal dominant inheritance and frequently leads to the manifestation of the disease in relatively young individuals. Here we report the generation of one PSEN1 E280A iPSC line derived from an early-onset patient. OriP/EBNA1-based episomal plasmids containing OCT3/4, SOX2, KLF4, L-MYC, LIN28, BCL-xL and shp53 were used to reprogram oral mucosa fibroblasts. The iPSC line generated has normal karyotype, carry the E280A mutation, is free of plasmid integration, express high levels of pluripotency markers and can differentiate into all three germ layers.
    Keywords Biology (General) ; QH301-705.5
    Language English
    Publishing date 2019-05-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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