TY - JOUR
T1 - Development and characterization of a novel drug nanocarrier for oral delivery, based on self-assembled β-casein micelles
AU - Bachar, Michal
AU - Mandelbaum, Amitai
AU - Portnaya, Irina
AU - Perlstein, Hadas
AU - Even-Chen, Simcha
AU - Barenholz, Yechezkel
AU - Danino, Dganit
PY - 2012/6/10
Y1 - 2012/6/10
N2 - 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.
AB - 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.
KW - Amphiphilic block copolymers
KW - Celecoxib
KW - Drug delivery
KW - Nanomedicine
KW - Protein micelles
UR - http://www.scopus.com/inward/record.url?scp=84861702785&partnerID=8YFLogxK
U2 - 10.1016/j.jconrel.2012.01.004
DO - 10.1016/j.jconrel.2012.01.004
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C2 - 22266050
AN - SCOPUS:84861702785
SN - 0168-3659
VL - 160
SP - 164
EP - 171
JO - Journal of Controlled Release
JF - Journal of Controlled Release
IS - 2
ER -