Format

Send to

Choose Destination
J Pharm Sci. 2015 Mar;104(3):988-94. doi: 10.1002/jps.24300. Epub 2014 Dec 27.

Engineering of recombinant spider silk proteins allows defined uptake and release of substances.

Author information

1
Thomas Scheibel, Lehrstuhl Biomaterialien, Fakultät für Ingenieurwissenschaften, Universität Bayreuth, Bayreuth, 95440, Germany.

Abstract

Drug delivery carriers stabilize drugs and control their release, expanding the therapeutic window, and avoiding side effects of otherwise freely diffusing drugs in the human body. Materials used as carrier vehicles have to be biocompatible, biodegradable, nontoxic, and nonimmunogenic. Previously, particles made of the recombinant spider silk protein eADF4(C16) could be effectively loaded with positively and neutrally charged model substances. Here, a new positively charged variant thereof, named eADF4(κ16), has been engineered. Its particle formation is indistinguishable to that of polyanionic eADF4(C16), but in contrast polycationic eADF4(κ16) allows incorporation of negatively charged substances. Both high-molecular-weight substances, such as nucleic acids, and low-molecular-weight substances could be efficiently loaded onto eADF4(κ16) particles, and release of nucleic acids was shown to be well controlled.

KEYWORDS:

DNA/oligonucleotide delivery; biodegradable polymers; biomaterials; biotechnology; drug delivery system

PMID:
25546241
DOI:
10.1002/jps.24300
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Elsevier Science
Loading ...
Support Center