Keywords: خود تحریک کننده سیستم های تحویل دارویی; ALT; alanine aminotransferase; ANOVA; analysis of variance; CCl4; carbon tetrachloride; COX-2; cyclooxygenase-2; DLS; dynamic light scattering; ESI; electrospray ionization; GI; gastrointestinal; 6G; 6-gingerol; 8G; 8-gingerol; GE; ginger extract; HPMC; h
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Keywords: خود تحریک کننده سیستم های تحویل دارویی; Self-emulsifying drug delivery systems; Zeta potential changing systems; Mucus barrier; Intestinal alkaline phosphatase;
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Self-emulsifying drug delivery systems; Peptide drugs; Nanoparticles; Liposomes; Mucus permeation; Water movement; Desmopressin;
Keywords: خود تحریک کننده سیستم های تحویل دارویی; C; chitosan; CCMV; cowpea chlorotic mottle virus; CPMV; cowpea mosaic virus; CF; cystic fibrosis; LC; long chain; MC; medium chain; NAC; N-acetylcysteine; NL; no lipids; PLGA; poly(lactic-co-glycolic acid); PCL; periciliary layer; PGA; 6 phosphoglucuronic
Keywords: خود تحریک کننده سیستم های تحویل دارویی; BCA; bicinchoninic acid; BRO; bromelain; CYS; cysteine; DNA; deoxyribonucleic acid; EDAC; ethyl-dimethylaminopropyl-carbodiimide; LMWH; low molecular weight heparin; MCS; mucolytic carrier system; MECS; mucolytic enzyme decorated carrier systems; NHS; N-h
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Drug delivery; Lipid carrier; Nanotechnology; Nanocarrier; Controlled release; NEMS; Nano electromechanical systems; MEMS; Micro-electromechanical systems; NE; Nanoemulsions; NPs; Nanoparticles; QD; Quantum dots; PLA; Polylactic acid; PGA; Polyglycolic ac
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Leuprorelin; Insulin; Desmopressin; Self-emulsifying drug delivery systems; Hydrophobic ion paring; Peptide delivery;
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Monoacyl phosphatidylcholine; Self-emulsifying drug delivery systems; In vitro lipolysis; Colloidal structures; Small-angle X-ray scattering; Cryogenic transmission electron microscopy;
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Cationic surfactant; Intestinal alkaline phosphatase; Phosphatidic acid; Self-emulsifying drug delivery systems; Mucus permeation; Zeta potential changing systems
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Functional foods; Nutraceuticals; Nano-carrier system; Nanoliposomes; Nanoemulsions; Self-emulsifying drug delivery systems; Solid lipid nanoparticles; Nanostructured lipid carriers; Nanosuspensions; Polymeric nanoparticles; Inclusion complex; Protein-bas
Design and evaluation of SEDDS exhibiting high emulsifying properties
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Self-emulsifying drug delivery systems; SEDDS; Emulsifying properties; Log D SEDDS/Water; Emulsification time;
Impact of different hydrophobic ion pairs of octreotide on its oral bioavailability in pigs
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Self-emulsifying drug delivery systems; Octreotide; Lipase stability; In-vivo study; Drug release;
Do drug release studies from SEDDS make any sense?
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Self-emulsifying drug delivery systems; SEDDS; Drug release; Partition coefficient;
Oral Delivery of Highly Lipophilic, Poorly Water-Soluble Drugs: Self-Emulsifying Drug Delivery Systems to Improve Oral Absorption and Enable High-Dose Toxicology Studies of a Cholesteryl Ester Transfer Protein Inhibitor in Preclinical Species
Keywords: خود تحریک کننده سیستم های تحویل دارویی; solubility; absorption; bioavailability; lipid-based formulations; self-emulsifying; preclinical species; AUC; area under the curve; GI tract; gastrointestinal tract; ND; not determined; IV; intravenous; SEDDS; self-emulsifying drug delivery systems; SMED
In vitro and in vivo performance of monoacyl phospholipid-based self-emulsifying drug delivery systems
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Self-emulsifying drug delivery systems; Monoacyl phospholipid; Emulsification; Small-angle X-ray scattering; Wide-angle X-ray scattering; In vitro lipolysis; Pharmacokinetics;
Development of solid SEDDS, VI: Effect of precoating of Neusilin® US2 with PVP on drug release from adsorbed self-emulsifying lipid-based formulations
Keywords: خود تحریک کننده سیستم های تحویل دارویی; SEDDS; Solid dosage forms; Silicates; Lipid based formulations; PVP; Pore size distribution; NCE's; new chemical entities; GI; gastro-intestinal; SEDDS; self-emulsifying drug delivery systems; SMEDDS; self-microemulsifying drug delivery systems;
Development of solid SEDDS, VII: Effect of pore size of silica on drug release from adsorbed self-emulsifying lipid-based formulations
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Self-emulsifying drug delivery systems; Macroporous silicas; Silica synthesis; Pore size distribution; Drug release; PVP coating; Solid dosage forms;
Development and in vitro characterisation of an oral self-emulsifying delivery system for daptomycin
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Oral peptide delivery; Self-emulsifying drug delivery systems; Payload; Mucus permeation; Pancreatic lipase; α-Chymotrypsin
50Â years of oral lipid-based formulations: Provenance, progress and future perspectives
Keywords: خود تحریک کننده سیستم های تحویل دارویی; AP; Aqueous phase; API; Active pharmaceutical ingredient; b-r-o-5; Beyond rule-of-five; BS; Bile salt; DG; Diglyceride; FA; Fatty acid; GIT; Gastrointestinal tract; IL; Ionic liquid; LBF; Lipid based formulation; LCT; Long chain triglyceride; LFCS; Lipid
Lipid-Based Formulations Solidified Via Adsorption onto the Mesoporous Carrier Neusilin® US2: Effect of Drug Type and Formulation Composition on In Vitro Pharmaceutical Performance
Keywords: خود تحریک کننده سیستم های تحویل دارویی; poorly water-soluble drugs; lipids; self-emulsifying; adsorption; lipid-based formulations; self-emulsifying drug delivery systems; neusilin®; adsorbents;
Novel semisolid SNEDDS based on PEG-30-dipolyhydroxystearate: Development and characterization
Keywords: خود تحریک کننده سیستم های تحویل دارویی; %T; percentage transmittance; 1H NMR; proton nuclear magnetic resonance; aN; hyperfine coupling constant; D2O; deuterium oxide; dB; decibel; d-DMSO; deuterated dimethyl sulfoxide; DLS; dynamic light scattering; DPHS; Cithrol® DPHS; DSC; differential scan
Introduction of diffusing wave spectroscopy to study self-emulsifying drug delivery systems with respect to liquid filling of capsules
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Diffusing wave spectroscopy; Microrheology; Visco-elastic; Self-emulsifying drug delivery systems; Capsules; Quality by design;
Impact of emulsion-based drug delivery systems on intestinal permeability and drug release kinetics
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Oil-in-water emulsions; Effect of formulation parameters; Self-emulsifying drug delivery systems; SEDDS; Experimental design
ESR studies on the influence of physiological dissolution and digestion media on the lipid phase characteristics of SEDDS and SEDDS pellets
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Self-emulsifying drug delivery systems; ESR; In vitro digestion; Poorly water soluble drugs; Pellets; Oral delivery system
Development and characterization of oral lipid-based Amphotericin B formulations with enhanced drug solubility, stability and antifungal activity in rats infected with Aspergillus fumigatus or Candida albicans
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Amphotericin B; Lipid-based drug delivery; Self-emulsifying drug delivery systems; Oral formulation; Lipid excipients; Antifungal activity; Aspergillus fumigatus; Candida albicans
Design of Lipid-Based Formulations for Oral Administration of Poorly Water-Soluble Drugs: Precipitation of Drug after Dispersion of Formulations in Aqueous Solution
Keywords: خود تحریک کننده سیستم های تحویل دارویی; lipid formulation classification system; self-emulsifying systems; self-emulsifying drug delivery systems; SEDDS; SMEDDS; drug precipitation; oral drug delivery;
In vitro–in vivo correlations of self-emulsifying drug delivery systems combining the dynamic lipolysis model and neuro-fuzzy networks
Keywords: خود تحریک کننده سیستم های تحویل دارویی; In vitro–in vivo correlations (IVIVC); In vitro dynamic lipolysis model; Self-emulsifying drug delivery systems; Mathematical modelling; Neuron-fuzzy networks
Formulation of lipid-based delivery systems for oral administration: Materials, methods and strategies
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Lipid-based formulations; Self-emulsifying drug delivery systems; Excipients, Lipid Formulation Classification System; Formulation strategies; Surfactants; Self-dispersion
Enhancing intestinal drug solubilisation using lipid-based delivery systems
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Drug absorption; Lipid-based delivery systems; Self-emulsifying drug delivery systems; In vitro lipolysis; Solubilisation
Preparation and characterization of a self-emulsifying pellet formulation
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Pellets; Extrusion/spheronization; Self-emulsifying drug delivery systems; Poorly water soluble drugs; Oral delivery system; ESR
Lipid Formulation Strategies for Enhancing Intestinal Transport and Absorption of P-Glycoprotein (P-gp) Substrate Drugs: In vitro/In vivo Case Studies
Keywords: خود تحریک کننده سیستم های تحویل دارویی; biopharmaceutics; drug transport; P-glycoprotein inhibition; active compounds; surfactants; lipid formulations; self-emulsifying drug delivery systems; poorly soluble drugs; case studies;
Formulation of poorly water-soluble drugs for oral administration: Physicochemical and physiological issues and the lipid formulation classification system
Keywords: خود تحریک کننده سیستم های تحویل دارویی; Poorly soluble drugs; Bioavailability; Lipid systems; Self-emulsifying drug delivery systems; Digestion; Solubilization; Lipid formulation classification system (LFCS)