1999
DOI: 10.1006/meth.1999.0786
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Antisense Oligonucleotide Delivery with Polyhexylcyanoacrylate Nanoparticles as Carriers

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Cited by 49 publications
(13 citation statements)
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“…Aqueous acidic médium DEAE dextran -Vero cells, mouse Protection from degradation, significantly enhanced cellular uptake, improved antisense treatments for tumour and antiviral therapy, liver targeting [114] *Pharmacological availability/bioavailability determined based on the extent of hypoglycaemic/hypocalcemic response relative to subcutaneous injection of insulin or salmon calcitonin, respectively. [117] PEG-/PS80-…”
Section: Odnsmentioning
confidence: 99%
“…Aqueous acidic médium DEAE dextran -Vero cells, mouse Protection from degradation, significantly enhanced cellular uptake, improved antisense treatments for tumour and antiviral therapy, liver targeting [114] *Pharmacological availability/bioavailability determined based on the extent of hypoglycaemic/hypocalcemic response relative to subcutaneous injection of insulin or salmon calcitonin, respectively. [117] PEG-/PS80-…”
Section: Odnsmentioning
confidence: 99%
“…The most common treatments for cancer are a) surgery, b) chemotherapy, c) radiation therapy, and d) targeted therapy. antisense therapeutic research [9][10][11][12][13][14][15][16][17][18][19][20][21][22]. Currently, over a hundred oligonucleotides are in clinical trials from 30 different pharmaceutical companies [23].…”
Section: Editorialmentioning
confidence: 99%
“…In vivo, the biodistribution of the oligonucleotide nanoparticle complex resulted in targeting of oligonucleotides to the liver. Improvements in antisense treatments with nanoparticles were demonstrated for tumor therapy as well as for antiviral applications (Zimmer, 1999). Sineerat et al (2008) investigated a water insoluble complex of cationic propranolol HCl with anionic sodium lauryl sulfate.…”
Section: Miscellaneousmentioning
confidence: 99%