2008
DOI: 10.1080/01932690701815762
|View full text |Cite
|
Sign up to set email alerts
|

Bioconjugation of Interferon-alpha Molecules to Lysine-Capped Gold Nanoparticles for Further Drug Delivery Applications

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
11
0

Year Published

2010
2010
2020
2020

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 13 publications
(11 citation statements)
references
References 28 publications
0
11
0
Order By: Relevance
“…EDAC forms an unstable intermediate complex with carboxylic groups, which is susceptible to amide bond formation if it reacts with a primary amine. A recent example of EDAC use in bioconjugation can be found in the work of Aghdam and coworkers, who immobilized the N-terminus of lysine on gold nanoparticles and proceeded to bind interferons to the free C-termini [12].…”
Section: Introductionmentioning
confidence: 99%
“…EDAC forms an unstable intermediate complex with carboxylic groups, which is susceptible to amide bond formation if it reacts with a primary amine. A recent example of EDAC use in bioconjugation can be found in the work of Aghdam and coworkers, who immobilized the N-terminus of lysine on gold nanoparticles and proceeded to bind interferons to the free C-termini [12].…”
Section: Introductionmentioning
confidence: 99%
“…'AuNPs' is the area of research interest due to their unique properties such as tunable surface plasmon resonance (SPR), surface-enhanced Raman scattering, electrical, magnetic, thermal conductivity, antibacterial activity, chemical and biostability [7][8][9][10][11][12][13]. Besides this, the use of AuNPs as potential materials in the field of drug delivery and DNA delivery systems is noteworthy [14,15]. Most of the available methods for the synthesis of AuNPs involve photochemical reduction, chemical reduction, and electrochemical reduction [16][17][18].…”
Section: Introductionmentioning
confidence: 99%
“…The use of amine-terminating ligands for binding with GNPs is well established [68][69][70][71] although not very popular with glycans yet. Indeed, the direct conjugation of amino-functionalized antigenic glycans with pre-formed GNPs has not earlier been reported to the best our knowledge although simple amines, amino acids and peptides [68][69][70][71][72][73][74][75][76][77][78], as well as diethylaminoethyl-dextran [79] and chitosan [80] have been reported to bind to GNPs in pH-dependent manner as the energy of Au-N interaction is intermediate between those of Au-S and Au-O [81] (the affinity of different functional groups to the GNPs's surface decreases in the series Au-S>Au-NH2>Au-COOH [82]) thus making exchange of citrate ligands with amines possible. The amine-capped GNPs are stable enough to be used as targeting agents for drug delivery applications [75], antigens for generation of antibodies [77] or antimicrobial agents [78].…”
Section: Tuberculosis (Tb) Which Is Caused By the Pathogenic Bacterimentioning
confidence: 99%