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1.
RECIIS (Online) ; 14(3): 563-579, jul.-set. 2020. ilus
Artigo em Português | LILACS | ID: biblio-1121421

RESUMO

Um dos desafios das mudanças e evoluções das tecnologias de informação e comunicação (TIC) em corporações é a preservação das informações digitais. Entre as corporações com grande geração de informações digitais estão as universidades. Neste artigo, é apresentada uma estratégia para se elaborar uma política de preservação digital no bojo de uma política arquivística direcionada para a manutenção da autenticidade dos documentos de arquivo. O objetivo é expor um modelo para elaboração de políticas de preservação digital de documentos de arquivo por instituições de ensino superior (IES), com os elementos que devem compô-las, a partir da literatura estudada e da política elaborada e aprovada na Universidade Estadual Paulista (Unesp). São apresentados os conceitos relacionados à política arquivística para a preservação digital de documentos de arquivo, sua definição, seus aspectos e elementos. Concluiu-se que o modelo pode ser adaptado para outros objetos digitais, bem como para outras instituições.


One of the challenges of the changes and evolutions of the information and communication technology (ICT) in corporations is the preservation of digital information. The universities are among the corporations with a large generation of digital information. This article presents a strategy for the elaboration of a digital preservation policy, in the context of an archival policy which is aimed at maintaining the authenticity of archival documents. The objective of this article is to present a model so that the higher education institutions could making policies for the digital preservation of their archival documents, showing the elements that must compose each one, based on the studied literature and on the policy elaborated in Unesp and which was officially approved by that institution. Concepts related to archival policy for the digital preservation of archival documents, their definition, aspects and elements are presented here. It was concluded that the model can be adapted for other digital objects, as well as for other institutions.


Uno de los desafíos de los cambios y la evolución de las TIC en las corporaciones es la preservación de informaciones digitales. Entre las corporaciones con una gran generación de información digital se encuentran las universidades. En este artículo, se presenta una estrategia para elaborar una política de preservación digital, en medio de una política de archivo dirigida a mantener la autenticidad de los documentos de archivo. El objetivo del artículo es presentar un modelo para la elaboración de políticas de preservación digital de documentos de archivo por instituciones de enseñanza superior, con los elementos que deben componerlas, basado en la literatura estudiada y en la política desarrollada y aprobada en la Unesp. Se presentan conceptos relacionados con la política de archivo para la preservación digital de documentos de archivo, su definición, aspectos y elementos. Se concluyó que este modelo puede adaptarse para otros objetos digitales, así como para otras instituciones.


Assuntos
Humanos , Registros , Tecnologia da Informação , Políticas , Arquivamento , Cultura Organizacional , Armazenamento e Recuperação da Informação , Administração das Tecnologias da Informação
2.
Eur J Pharm Biopharm ; 142: 449-459, 2019 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-31326581

RESUMO

MicroRNAs (miRNAs) play a key role on gene expression regulation contributing to cell homeostasis, and they are highly dysregulated in cancer. Consequently, miRNA-based therapies are an attractive approach to develop novel anticancer strategies. The main objective of this work was to explore the full potential of protamine nanocapsules (Pr NCs) to develop an anticancer therapy based on the restoration of oncosuppressor miR-145, downregulated in colorectal cancer cells. The composition of Pr NCs was defined based on the selection of surfactants, and protamine that would enable an efficient association and intracellular delivery of miRNA mimics according to the layer-by-layer approach, and the encapsulation of curcumin within the oily core. After exposure of colorectal cancer cells with (i) miR-145 and (ii) curcumin-loaded Pr NCs, a strong increase in the intracellular levels of miR-145, which translated into a decreased cell proliferation rate and migration capacity of the treated cells, was observed. The potential of exploiting Pr NCs for the co-delivery of both biomolecules, miRNAs and curcumin, has also been proved. All together, here we evaluate the possibility to use Pr NCs to efficiently increase the intracellular levels of the oncosuppressor miR-145.


Assuntos
Proliferação de Células/efeitos dos fármacos , Neoplasias Colorretais/tratamento farmacológico , MicroRNAs/genética , Nanocápsulas/química , Protaminas/química , Protaminas/farmacologia , Linhagem Celular Tumoral , Movimento Celular/efeitos dos fármacos , Neoplasias Colorretais/genética , Curcumina/química , Regulação para Baixo/efeitos dos fármacos , Portadores de Fármacos/química , Humanos
3.
Drug Deliv Transl Res ; 6(6): 708-721, 2016 12.
Artigo em Inglês | MEDLINE | ID: mdl-27392604

RESUMO

Corneal injuries are one of the most frequently observed ocular diseases, leading to permanent damage and impaired vision if they are not treated properly. In this sense, adequate wound healing after injury is critical for keeping the integrity and structure of the cornea. The goal of this work was to assess the potential of polymeric nanocapsules, either unloaded or loaded with cyclosporine A or vitamin A, alone or in combination with mitomycin C, for the treatment of corneal injuries induced by photorefractive keratectomy surgery. The biopolymers selected for the formation of the nanocapsules were polyarginine and protamine, which are known for their penetration enhancement effect. The results showed that, following topical instillation to a mouse model of corneal injury, all the nanocapsule formulations, either unloaded or loaded with cyclosporine A or vitamin A, were able to stimulate corneal wound healing. In addition, the healing rate observed for the combination of unloaded protamine nanocapsules with mitomycin C was comparable to the one observed for the positive control Cacicol®, a biopolymer known as a corneal wound healing enhancer. Regarding the corneal opacity, the initial grade of corneal haze (>3) induced by the photorefractive keratectomy was more rapidly reduced in the case of the positive control, Cacicol®, than in corneas treated with the nanocapsules. In conclusion, this work shows that drug-free arginine-rich (polyarginine, protamine) nanocapsules exhibit a positive behavior with regard to their potential use for corneal wound healing.


Assuntos
Portadores de Fármacos/administração & dosagem , Nanocápsulas/administração & dosagem , Peptídeos/administração & dosagem , Protaminas/administração & dosagem , Animais , Córnea/efeitos dos fármacos , Córnea/patologia , Lesões da Córnea/tratamento farmacológico , Lesões da Córnea/patologia , Ciclosporina/administração & dosagem , Ciclosporina/química , Portadores de Fármacos/química , Masculino , Camundongos Endogâmicos C57BL , Microscopia Eletrônica de Transmissão , Mitomicina/administração & dosagem , Mitomicina/química , Nanocápsulas/química , Nanocápsulas/ultraestrutura , Peptídeos/química , Protaminas/química , Coelhos , Vitamina A/administração & dosagem , Vitamina A/química , Cicatrização/efeitos dos fármacos
4.
Colloids Surf B Biointerfaces ; 143: 327-335, 2016 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-27022873

RESUMO

Selective drug delivery to inflamed tissues is of widespread interest for the treatment of inflammatory bowel disease (IBD). Because a lack of physiological lipids has been described in patients suffering IBD, and some lipids present immunomodulatory properties, we hypothesize that the combination of lipids and anti-inflammatory drugs together within a nanocarrier may be a valuable strategy for overcoming IBD. In the present study, we investigated and compared the in vitro and in vivo efficacy of three lipid-based nanocarriers containing curcumin (CC) as an anti-inflammatory drug for treating IBD in a murine DSS-induced colitis model. These nanocarriers included self-nanoemulsifying drug delivery systems (SNEDDS), nanostructured lipid carriers (NLC) and lipid core-shell protamine nanocapsules (NC). In vitro, a 30-fold higher CC permeability across Caco-2 cell monolayers was obtained using NC compared to SNEDDS (NC>SNEDDS>NLC and CC suspension). The CC SNEDDS and CC NLC but not the CC NC or CC suspension significantly reduced TNF-α secretion by LPS-activated macrophages (J774 cells). In vivo, only CC NLC were able to significantly decrease neutrophil infiltration and TNF-α secretion and, thus, colonic inflammation. Our results show that a higher CC permeability does not correlate with a higher efficacy in IBD treatment, which suggests that lipidic nanocarriers exhibiting increased CC retention at the intestinal site, rather than increased CC permeability are efficient treatments of IBD.


Assuntos
Curcumina/farmacologia , Doenças Inflamatórias Intestinais/tratamento farmacológico , Lipídeos/química , Nanopartículas/química , Animais , Anti-Inflamatórios não Esteroides/administração & dosagem , Anti-Inflamatórios não Esteroides/química , Anti-Inflamatórios não Esteroides/farmacologia , Células CACO-2 , Linhagem Celular , Sobrevivência Celular/efeitos dos fármacos , Colite/induzido quimicamente , Colite/tratamento farmacológico , Colite/metabolismo , Curcumina/administração & dosagem , Curcumina/química , Sulfato de Dextrana , Portadores de Fármacos/química , Sistemas de Liberação de Medicamentos/métodos , Feminino , Humanos , Doenças Inflamatórias Intestinais/metabolismo , Macrófagos/citologia , Macrófagos/efeitos dos fármacos , Macrófagos/metabolismo , Camundongos Endogâmicos C57BL , Microscopia Confocal , Fator de Necrose Tumoral alfa/metabolismo
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