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Surface-modified solid lipid nanoparticles for oral delivery of docetaxel: enhanced intestinal absorption and lymphatic uptake
by
Cho, Hyun-Jong
, Yoon, In-Soo
, Kim, Dae-Duk
, Park, Jin Woo
in
Administration, Oral
/ Animals
/ Antineoplastic Agents - administration & dosage
/ Antineoplastic Agents - pharmacokinetics
/ bioavailability
/ Complications and side effects
/ Docetaxel
/ Dosage and administration
/ Drug Delivery Systems
/ Drugs
/ Intestinal Absorption
/ Lipids - chemistry
/ Lymphatic System - metabolism
/ lymphatic uptake
/ Male
/ Nanomedicine
/ Nanoparticles
/ Nanoparticles - administration & dosage
/ Nanoparticles - chemistry
/ Original Research
/ Polyethylene Glycols
/ Polysorbates
/ Properties
/ Rats
/ Rats, Sprague-Dawley
/ solid lipid nanoparticles
/ Surface Properties
/ Taxoids - administration & dosage
/ Taxoids - pharmacokinetics
/ toxicity
/ Triglycerides - chemistry
/ Vehicles
/ Vitamin E - analogs & derivatives
/ vitamin E TPGS
2014
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Surface-modified solid lipid nanoparticles for oral delivery of docetaxel: enhanced intestinal absorption and lymphatic uptake
by
Cho, Hyun-Jong
, Yoon, In-Soo
, Kim, Dae-Duk
, Park, Jin Woo
in
Administration, Oral
/ Animals
/ Antineoplastic Agents - administration & dosage
/ Antineoplastic Agents - pharmacokinetics
/ bioavailability
/ Complications and side effects
/ Docetaxel
/ Dosage and administration
/ Drug Delivery Systems
/ Drugs
/ Intestinal Absorption
/ Lipids - chemistry
/ Lymphatic System - metabolism
/ lymphatic uptake
/ Male
/ Nanomedicine
/ Nanoparticles
/ Nanoparticles - administration & dosage
/ Nanoparticles - chemistry
/ Original Research
/ Polyethylene Glycols
/ Polysorbates
/ Properties
/ Rats
/ Rats, Sprague-Dawley
/ solid lipid nanoparticles
/ Surface Properties
/ Taxoids - administration & dosage
/ Taxoids - pharmacokinetics
/ toxicity
/ Triglycerides - chemistry
/ Vehicles
/ Vitamin E - analogs & derivatives
/ vitamin E TPGS
2014
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Surface-modified solid lipid nanoparticles for oral delivery of docetaxel: enhanced intestinal absorption and lymphatic uptake
by
Cho, Hyun-Jong
, Yoon, In-Soo
, Kim, Dae-Duk
, Park, Jin Woo
in
Administration, Oral
/ Animals
/ Antineoplastic Agents - administration & dosage
/ Antineoplastic Agents - pharmacokinetics
/ bioavailability
/ Complications and side effects
/ Docetaxel
/ Dosage and administration
/ Drug Delivery Systems
/ Drugs
/ Intestinal Absorption
/ Lipids - chemistry
/ Lymphatic System - metabolism
/ lymphatic uptake
/ Male
/ Nanomedicine
/ Nanoparticles
/ Nanoparticles - administration & dosage
/ Nanoparticles - chemistry
/ Original Research
/ Polyethylene Glycols
/ Polysorbates
/ Properties
/ Rats
/ Rats, Sprague-Dawley
/ solid lipid nanoparticles
/ Surface Properties
/ Taxoids - administration & dosage
/ Taxoids - pharmacokinetics
/ toxicity
/ Triglycerides - chemistry
/ Vehicles
/ Vitamin E - analogs & derivatives
/ vitamin E TPGS
2014
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Surface-modified solid lipid nanoparticles for oral delivery of docetaxel: enhanced intestinal absorption and lymphatic uptake
Journal Article
Surface-modified solid lipid nanoparticles for oral delivery of docetaxel: enhanced intestinal absorption and lymphatic uptake
2014
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Overview
Docetaxel is a potent anticancer drug, but development of an oral formulation has been hindered mainly due to its poor oral bioavailability. In this study, solid lipid nanoparticles (SLNs) surface-modified by Tween 80 or D-alpha-tocopheryl poly(ethylene glycol 1000) succinate (TPGS 1000) were prepared and evaluated in terms of their feasibility as oral delivery systems for docetaxel. Tween 80-emulsified and TPGS 1000-emulsified tristearin-based lipidic nanoparticles were prepared by a solvent-diffusion method, and their particle size distribution, zeta potential, drug loading, and particle morphology were characterized. An in vitro release study showed a sustained-release profile of docetaxel from the SLNs compared with an intravenous docetaxel formulation (Taxotere®). Tween 80-emulsified SLNs showed enhanced intestinal absorption, lymphatic uptake, and relative oral bioavailability of docetaxel compared with Taxotere in rats. These results may be attributable to the absorption-enhancing effects of the tristearin nanoparticle. Moreover, compared with Tween 80-emulsified SLNs, the intestinal absorption and relative oral bioavailability of docetaxel in rats were further improved in TPGS 1000-emulsified SLNs, probably due to better inhibition of drug efflux by TPGS 1000, along with intestinal lymphatic uptake. Taken together, it is worth noting that these surface-modified SLNs may serve as efficient oral delivery systems for docetaxel.
Publisher
Dove Medical Press Limited,Dove Press,Dove Medical Press
Subject
/ Animals
/ Antineoplastic Agents - administration & dosage
/ Antineoplastic Agents - pharmacokinetics
/ Complications and side effects
/ Drugs
/ Lymphatic System - metabolism
/ Male
/ Nanoparticles - administration & dosage
/ Rats
/ Taxoids - administration & dosage
/ toxicity
/ Vehicles
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