TY - JOUR
T1 - Electrodeless electrohydrodynamic drop-on-demand encapsulation of drugs into porous polymer films for fabrication of personalized dosage units
AU - Elele, Ezinwa
AU - Shen, Yueyang
AU - Susarla, Ramana
AU - Khusid, Boris
AU - Keyvan, Golshid
AU - Michniak-Kohn, Bozena
N1 - Funding Information:
Authors thank Dr. Mirko Schoenitz, NJIT, for collaboration in DSC and X-ray diffraction analysis and Rajyalakshmi Boppana, NJIT, for collaboration in testing the content uniformity of dosage units. The work was supported by the NSF Engineering Research Center on Structured Organic Particulate Systems, NSF grant EEC-0540855.
PY - 2012/7
Y1 - 2012/7
N2 - Noncontact drop-on-demand (DOD) dosing is a promising strategy for manufacturing of personalized dosage units. However, current DOD methods developed for printing chemically and thermally stable, low-viscosity inks are of limited use for pharmaceuticals due to fundamentally different functional requirements. To overcome their deficiency, we developed a novel electrohydrodynamic (EHD) DOD (Appl, Phys, Lett. 97, 233501, 2010) that operates on fluids of up to 30 Pa·s in viscosity over a wide range of droplet sizes and provides a precise control over the droplet volume. We now evaluate the EHD DOD as a method for fabrication of dosage units by printing drug solutions on porous polymer films prepared by freeze-drying. Experiments were carried out on ibuprofen and griseofulvin, as model poorly water-soluble drugs, polyethylene glycol 400, as a drug carrier, and hydroxypropyl methylcellulose films. The similarities between drug release profiles from different dosage units were assessed by model-independent difference, f1, and similarity, f2, factors. The results presented show that EHD DOD offers a powerful tool for the evolving field of small-scale pharmaceutical technologies for tailoring medicines to individual patient's needs by printing a vast array of predefined amounts of therapeutics arranged in a specific pattern on a porous film.copy; 2012 Wiley Periodicals, Inc.
AB - Noncontact drop-on-demand (DOD) dosing is a promising strategy for manufacturing of personalized dosage units. However, current DOD methods developed for printing chemically and thermally stable, low-viscosity inks are of limited use for pharmaceuticals due to fundamentally different functional requirements. To overcome their deficiency, we developed a novel electrohydrodynamic (EHD) DOD (Appl, Phys, Lett. 97, 233501, 2010) that operates on fluids of up to 30 Pa·s in viscosity over a wide range of droplet sizes and provides a precise control over the droplet volume. We now evaluate the EHD DOD as a method for fabrication of dosage units by printing drug solutions on porous polymer films prepared by freeze-drying. Experiments were carried out on ibuprofen and griseofulvin, as model poorly water-soluble drugs, polyethylene glycol 400, as a drug carrier, and hydroxypropyl methylcellulose films. The similarities between drug release profiles from different dosage units were assessed by model-independent difference, f1, and similarity, f2, factors. The results presented show that EHD DOD offers a powerful tool for the evolving field of small-scale pharmaceutical technologies for tailoring medicines to individual patient's needs by printing a vast array of predefined amounts of therapeutics arranged in a specific pattern on a porous film.copy; 2012 Wiley Periodicals, Inc.
KW - Dissolution rate
KW - Drug delivery systems
KW - Encapsulation
KW - Freeze-drying
KW - Processing
KW - Solid dosage form
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U2 - 10.1002/jps.23165
DO - 10.1002/jps.23165
M3 - Article
C2 - 22527973
AN - SCOPUS:84866269838
SN - 0022-3549
VL - 101
SP - 2523
EP - 2533
JO - Journal of Pharmaceutical Sciences
JF - Journal of Pharmaceutical Sciences
IS - 7
ER -