Development and characterization of a novel drug nanocarrier for oral delivery, based on self-assembled β-casein micelles

β-casein is an amphiphilic protein that self-organizes into well-defined core–shell micelles. We developed these micelles as efficient nanocarriers for oral drug delivery. Our model drug is celecoxib, an anti-inflammatory hydrophobic drug utilized for treatment of rheumatoid arthritis and osteoarthr...

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Veröffentlicht in:Journal of controlled release 2012-06, Vol.160 (2), p.164-171
Hauptverfasser: Bachar, Michal, Mandelbaum, Amitai, Portnaya, Irina, Perlstein, Hadas, Even-Chen, Simcha, Barenholz, Yechezkel, Danino, Dganit
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container_end_page 171
container_issue 2
container_start_page 164
container_title Journal of controlled release
container_volume 160
creator Bachar, Michal
Mandelbaum, Amitai
Portnaya, Irina
Perlstein, Hadas
Even-Chen, Simcha
Barenholz, Yechezkel
Danino, Dganit
description β-casein is an amphiphilic protein that self-organizes into well-defined core–shell micelles. We developed these micelles as efficient nanocarriers for oral drug delivery. Our model drug is celecoxib, an anti-inflammatory hydrophobic drug utilized for treatment of rheumatoid arthritis and osteoarthritis, now also evaluated as a potent anticancer drug. This system is unique as it enables encapsulation loads >100-fold higher than other β-casein/drug formulations, and does not require additives as do other formulations that have high loadings. This is combined with the ability to lyophilize the formulation without a cryoprotectant, long-term physical and chemical stability of the resulting powder, and fully reversible reconstitution of the structures by rehydration. The dry dosage form, in which >95% of the drug is encapsulated, meets the daily dose. Cryo-TEM and DLS prove that drug encapsulation results in micelle swelling, and X-ray diffraction shows that the encapsulated drug is amorphous. Altogether, our novel dosage form is highly advantageous for oral administration. [Display omitted]
doi_str_mv 10.1016/j.jconrel.2012.01.004
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subjects additives
Administration, Oral
Amphiphilic block copolymers
anti-inflammatory activity
Anti-Inflammatory Agents, Non-Steroidal - administration & dosage
Anti-Inflammatory Agents, Non-Steroidal - chemistry
antineoplastic agents
beta-casein
Caseins - chemistry
Celecoxib
Chemistry, Pharmaceutical
Cryoelectron Microscopy
Drug Carriers - chemistry
Drug Compounding
Drug delivery
Drug Design
drug formulations
encapsulation
Freeze Drying
Hydrophobic and Hydrophilic Interactions
hydrophobicity
Micelles
Microscopy, Electron, Transmission
Molecular Structure
nanocarriers
Nanomedicine
Nanoparticles - chemistry
oral administration
osteoarthritis
Protein micelles
Pyrazoles - administration & dosage
Pyrazoles - chemistry
rehydration
rheumatoid arthritis
Solubility
Sulfonamides - administration & dosage
Sulfonamides - chemistry
Surface Properties
Surface-Active Agents - chemistry
X-Ray Diffraction
title Development and characterization of a novel drug nanocarrier for oral delivery, based on self-assembled β-casein micelles
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