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Showing 1-19 of 19 results for "700001p" within Papers
Keni Yang et al.
Acta biomaterialia, 106, 314-327 (2020-02-23)
Nano-sized objects such as liposomes are modified by adsorption of biomolecules in biological fluids. The resulting corona critically changes nanoparticle behavior at cellular level. A better control of corona composition could allow to modulate uptake by cells. Within this context
Design of novel proliposome formulation for antioxidant peptide, glutathione with enhanced oral bioavailability and stability
Byeon JC, et al.
Drug delivery, 26(1), 216?225-216?225 (2019)
Cationic liposome (DC-Chol/DOPE= 1: 2) and a modified ethanol injection method to prepare liposomes, increased gene expression
Maitani Y, et al
International Journal of Pharmaceutics, 342(1-2), 33-39 (2007)
Keishi Suga et al.
Langmuir : the ACS journal of surfaces and colloids, 33(15), 3831-3838 (2017-03-09)
We investigated the effect of organic acids such as mandelic acid (MA) and tartaric acid (TA) on the adsorption behavior of both histidine (His) and propranolol (PPL) onto liposomes. A cationic and heterogeneous liposome prepared using 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC)/sphingomyelin (SM)/3β-[N-(N',N'-dimethylaminoethane)carbamoyl]cholesterol (DC-Ch)
Jinju Lee et al.
Journal of controlled release : official journal of the Controlled Release Society, 321, 184-197 (2020-02-09)
Despite the promising anticancer effects of kinesin spindle protein (KSP) inhibition, functional plasticity of kinesins induced resistance against KSP inhibitors in a variety of cancers, leading to clinical failure. Additionally, paclitaxel is a widely used anticancer agent, but drug resistance
Yoshie Maitani et al.
International journal of pharmaceutics, 356(1-2), 69-75 (2008-02-06)
Cationic lipid-based gene delivery systems have shown promise in transfecting cells in vitro and in vivo. However, liposome/DNA complexes tend to form aggregates after preparation. Lyophilization of these systems, therefore, has become of increasing interest. In this study, we investigated
PLGA/liposome hybrid nanoparticles for short-chain ceramide delivery
Zou P, et al.
Pharmaceutical Research, 31(3), 684-693 (2014)
Novel cholesterol-based cationic lipids as transfecting agents of DNA for efficient gene delivery
Ju J, et al.
International Journal of Molecular Sciences, 16(3), 5666-5681 (2015)
Ultrasound microbubble-mediated CRISPR/Cas9 knockout of C-erbB-2 in HEC-1A cells
Cai J, et al.
The Journal of International Medical Research, 47(5), 2199-2206 (2019)
Pharmaceutical Chemistry ? I, 142-142 (2003)
Milda Naciute et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 152, 183-192 (2020-05-08)
The aim of this study was to develop an oral vaccine that could be used to treat colorectal cancer. Oral vaccines are technically challenging to develop due to the harsh gastric environment but have numerous benefits including high patient acceptability
Cationic nanoliposomes meet mRNA: efficient delivery of modified mRNA using hemocompatible and stable vectors for therapeutic applications
Michel T, et al.
Molecular Therapy, 8, 459-468 (2017)
Cabazitaxel-Loaded Nanocarriers for Cancer Therapy with Reduced Side Effects
Kommineni N, et al.
Pharmaceutics, 11(3) (2019)
A mechanistic explanation of the inhibitory role of the protein corona on liposomal gene expression.
Sara Palchetti et al.
Biochimica et biophysica acta. Biomembranes, 1862(3), 183159-183159 (2019-12-21)
The past three decades have witnessed fast advances in the use of cationic liposome-DNA complexes (lipoplexes) for gene delivery applications. However, no lipoplex formulation has reached into the clinical practice so far. The primary drawback limiting clinical use of lipoplexes
Cationic cage-like complexes formed by DC-cholesterol, Quil-A, and phospholipid
Lendemans DG, et al.
Journal of Pharmaceutical Sciences, 94(8), 1794-1807 (2005)
Yoshie Maitani et al.
International journal of pharmaceutics, 342(1-2), 33-39 (2007-06-15)
Cationic liposomes composed of 3beta-[N-(N',N'-dimethylaminoethane)-carbamoyl] cholesterol (DC-Chol) and dioleoylphosphatidylethanolamine (DOPE) (DC-Chol/DOPE liposome, molar ratio, 1:1 or 3:2) prepared by the dry-film method have been often used as non-viral gene delivery vectors. The formulation and preparation of DC-Chol/DOPE liposomes, as well
Modulation of yeast hexokinase on bio-inspired membranes
Umakoshi H and Nishida A
Biochemical Engineering Journal, 69(5), 138-143 (2012)
C Colonna et al.
International journal of pharmaceutics, 364(1), 108-118 (2008-09-09)
The aim of this work was to investigate lipid-based dried powders as transfection competent carriers capable of promoting the expression of therapeutic genes. The lipid-based vectors were prepared by combining different cationic lipids 1,2-dioleoyl-3-trimethylammoniumpropane chloride (DOTAP), 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE), 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC)
ADP-ribosylation reactions, 948-948 (2001)
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