The adsorption/release behaviour of oligodeoxynucleotides (ODNs) on double functional core-shell polymethylmethacrylate nanospheres, with a narrow size distribution, is described. The outer shell consists of alkyl or glycolic chains containing permanently-charged quaternary ammonium groups. Ion pair formation between negatively-charged ODN phosphate groups and positively-charged groups, present on the nanosphere surface, is the main mechanism of interaction. The amount of adsorbed ODN depends on both the ODN concentration and the nanosphere surface charge density. An adsorption-induced swelling mechanism is proposed in which a modification of the charged diffuse layer around the nanospheres increases the ODN binding site accessibility with ...
Antisense oligodeoxynucleotides can selectively inhibit individual gene expression provided they rem...
A drug delivery system designed specifically for oligonucleotide therapeutics can ameliorate the pro...
The aim of this study was to compare two methods to encapsulate a 25-mer-phosphorothioate oligonucle...
The adsorption/release behaviour of oligodeoxynucleotides (ODNs) on double functional core-shell pol...
The adsorption/release behavior of oligodeoxynucleotides (ODNs) on new PEGylated core-shell polymeth...
Polymthyl methacrylate-based stealth and functional nanospheres, specifically designed for the rever...
Antisense technology is a novel drug discovery method, which provides an essential tool for directly...
Two polymethylmethacrylate functional nanosphere series, specifically designed for the reversible ad...
Antisense oligonucleotides, and particularly those with phosphorothioate backbones, have emerged as ...
The efficacy of antisense oligodeoxynucleotides (AsODNs) is compromised by their poor stability in b...
A drug delivery system designed specifically for oligonucleotide therapeutics can ameliorate the pro...
Antisense oligonucleotides provide a promising therapeutic approach for several disorders including ...
For more than two decades, antisense oligonucleotides (ODNs) have been used to modulate gene express...
Antisense oligonucleotide (ASO)-conjugated-?-tocopherol succinate (TCS)-loaded-poly(lactic acid)-g-p...
A multifunctional envelope-type nano device (MEND) was developed for use as an efficient non-viral s...
Antisense oligodeoxynucleotides can selectively inhibit individual gene expression provided they rem...
A drug delivery system designed specifically for oligonucleotide therapeutics can ameliorate the pro...
The aim of this study was to compare two methods to encapsulate a 25-mer-phosphorothioate oligonucle...
The adsorption/release behaviour of oligodeoxynucleotides (ODNs) on double functional core-shell pol...
The adsorption/release behavior of oligodeoxynucleotides (ODNs) on new PEGylated core-shell polymeth...
Polymthyl methacrylate-based stealth and functional nanospheres, specifically designed for the rever...
Antisense technology is a novel drug discovery method, which provides an essential tool for directly...
Two polymethylmethacrylate functional nanosphere series, specifically designed for the reversible ad...
Antisense oligonucleotides, and particularly those with phosphorothioate backbones, have emerged as ...
The efficacy of antisense oligodeoxynucleotides (AsODNs) is compromised by their poor stability in b...
A drug delivery system designed specifically for oligonucleotide therapeutics can ameliorate the pro...
Antisense oligonucleotides provide a promising therapeutic approach for several disorders including ...
For more than two decades, antisense oligonucleotides (ODNs) have been used to modulate gene express...
Antisense oligonucleotide (ASO)-conjugated-?-tocopherol succinate (TCS)-loaded-poly(lactic acid)-g-p...
A multifunctional envelope-type nano device (MEND) was developed for use as an efficient non-viral s...
Antisense oligodeoxynucleotides can selectively inhibit individual gene expression provided they rem...
A drug delivery system designed specifically for oligonucleotide therapeutics can ameliorate the pro...
The aim of this study was to compare two methods to encapsulate a 25-mer-phosphorothioate oligonucle...