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Träfflista för sökning "WFRF:(Preto J.) "

Search: WFRF:(Preto J.)

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  • Han, T., et al. (author)
  • Emerging Drone Trends for Blockchain-Based 5G Networks: Open Issues and Future Perspectives
  • 2021
  • In: Ieee Network. - : Institute of Electrical and Electronics Engineers (IEEE). - 0890-8044 .- 1558-156X. ; 35:1, s. 38-43
  • Journal article (peer-reviewed)abstract
    • Unmanned aerial vehicles, commonly known as drones, are receiving growing research interest due to their ability to carry a multitude of sensors and to connect to mobile networks. They are also able to move freely across the air, which enables the creation of numerous applications that were until now considered impracticable. However, such applications may require high computational resources, reliable connection, and high data transmission rates to accomplish different tasks. Therefore, in this work, first, we discuss 5G communication networks and mobile edge computing (MEC) as promising technologies that can provide several benefits to drone-enabled environments and solve some of the presented issues. We also comment on 5G and MEC approaches, presenting the state of the art and seeking to solve each of the latter issues presented. Afterward, we introduce new security concerns of drone communication networks, given their recent popularity. These concerns are related to the possibility of malicious users taking advantage of this brand new technology, which has made many governments ban drones due to public safety. Next, blockchain technology is brought in as a novel solution to the security issues due to its decentralized nature, making it inherently safe. This article also surveys contributions that make use of each of the technologies mentioned to improve the emerging drone industry. Subsequently, we discuss open issues and future perspectives.
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3.
  • Loureiro, A., et al. (author)
  • Size controlled protein nanoemulsions for active targeting of folate receptor positive cells
  • 2015
  • In: Colloids and Surfaces B. - : Elsevier. - 0927-7765 .- 1873-4367. ; 135, s. 90-98
  • Journal article (peer-reviewed)abstract
    • Bovine serum albumin (BSA) nanoemulsions were produced by high pressure homogenization with a tri-block copolymer (Poloxamer 407), which presents a central hydrophobic chain of polyoxypropylene (PPO) and two identical lateral hydrophilic chains of polyethylene glycol (PEG). We observed a linear correlation between tri-block copolymer concentration and size - the use of 5. mg/mL of Poloxamer 407 yields nanoemulsions smaller than 100. nm. Molecular dynamics and fluorescent tagging of the tri-block copolymer highlight their mechanistic role on the size of emulsions. This novel method enables the fabrication of highly stable albumin emulsions in the nano-size range, highly desirable for controlled drug delivery. Folic Acid (FA)-tagged protein nanoemulsions were shown to promote specific folate receptor (FR)-mediated targeting in FR positive cells. The novel strategy presented here enables the construction of size controlled, functionalized protein-based nanoemulsions with excellent characteristics for active targeting in cancer therapy.
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4.
  • Nogueira, Eugenia, et al. (author)
  • Peptide Anchor for Folate-Targeted Liposomal Delivery
  • 2015
  • In: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 16:9, s. 2904-2910
  • Journal article (peer-reviewed)abstract
    • Specific folate receptors are abundantly overexpressed in chronically activated macrophages and in most cancer cells. Directed folate receptor targeting using liposomes is usually achieved using folate linked to a phospholipid or cholesterol anchor. This link is formed using a large spacer like polyethylene glycol. Here, we report an innovative strategy for targeted liposome delivery that uses a hydrophobic fragment of surfactant protein D linked to folate. Our proposed spacer is a small 4 amino acid residue linker. The peptide conjugate inserts deeply into the lipid bilayer without affecting liposomal integrity, with high stability and specificity. To compare the drug delivery potential of both liposomal targeting systems, we encapsulated the nuclear dye Hoechst 34580. The eventual increase in blue fluorescence would only be detectable upon liposome disruption, leading to specific binding of this dye to DNA. Our delivery system was proven to be more efficient (2-fold) in Caco-2 cells than classic systems where the folate moiety is linked to liposomes by polyethylene glycol.
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