4.7 Article Proceedings Paper

Structural analysis of nanoparticulate carriers for encapsulation of macromolecular drugs

期刊

JOURNAL OF MOLECULAR LIQUIDS
卷 235, 期 -, 页码 83-89

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.molliq.2016.11.064

关键词

Self-assembled nanocarriers; Liquid crystalline phase transitions; Cationic lipids; Macromolecular drugs; CRISPR/Cas9 therapeutics; Synchrotron SAXS

资金

  1. European Regional Development Fund [CZ.02.1.01/0.0/0.0/15_008/0000162]
  2. BIMF (Bayreuth Institute of Macromolecular Research)
  3. BZKG (Bayreuth Center for Colloids and Interfaces)

向作者/读者索取更多资源

Recently developed macromolecular drugs display strong potential to cure diseases involving genetic components, e.g. Rheumatoid arthritis, diabetes, Alzheimer's disease, Huntington's disease, Duchenne muscular dystrophy, Retinitis pigmentosa, and several types of cancers. Bioavailability and enhanced drug specificity necessitate the preparation of efficient carrier systems for the macromolecular therapeutics. We employ synchrotron small angle X-ray scattering (SAXS) and cryogenic transmission electron microscopy (Cryo-TEM) to study the nano structure formation, macromolecular drug upload, and the topological transformations occurring upon complexation of supercoiled plasmid DNA (encoding for the therapeutic protein brain-derived neurotrophic factor, BDNF) with cationic lipid nanocarrier assemblies. Understanding of the liquid crystalline nanostructure formation (hexosomes, cubosomes, inverted hexagonal and intermediate mesophases, or onion-type complexes) enabling efficient delivery of new generation sequencing systems is expected to contribute to the progress in precision nanomedicine and the treatment of various severe diseases. (C) 2016 Elsevier B.V. All rights reserved.

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