TY - JOUR
T1 - Development of oil-based gels as versatile drug delivery systems for pediatric applications
AU - Kirtane, Ameya R.
AU - Karavasili, Christina
AU - Wahane, Aniket
AU - Freitas, Dylan
AU - Booz, Katelyn
AU - Thi Hong Le, Dao
AU - Hua, Tiffany
AU - Scala, Stephen
AU - Lopes, Aaron
AU - Hess, Kaitlyn
AU - Collins, Joy
AU - Tamang, Siddartha
AU - Ishida, Keiko
AU - Kuosmanen, Johannes L.P.
AU - Rajesh, Netra Unni
AU - Phan, Nhi V.
AU - Li, Junwei
AU - Krogmann, Annlyse
AU - Lennerz, Jochen K.
AU - Hayward, Alison
AU - Langer, Robert
AU - Traverso, Giovanni
N1 - Publisher Copyright:
Copyright © 2022 The Authors, some rights reserved.
PY - 2022/5
Y1 - 2022/5
N2 - Administering medicines to 0- to 5-year-old children in a resource-limited environment requires dosage forms that circumvent swallowing solids, avoid on-field reconstitution, and are thermostable, cheap, versatile, and taste masking. We present a strategy that stands to solve this multifaceted problem. As many drugs lack adequate water solubility, our formulations used oils, whose textures could be modified with gelling agents to form “oleogels.” In a clinical study, we showed that the oleogels can be formulated to be as fluid as thickened beverages and as stiff as yogurt puddings. In swine, oleogels could deliver four drugs ranging three orders of magnitude in their water solubilities and two orders of magnitude in their partition coefficients. Oleogels could be stabilized at 40°C for prolonged durations and used without redispersion. Last, we developed a macrofluidic system enabling fixed and metered dosing. We anticipate that this platform could be adopted for pediatric dosing, palliative care, and gastrointestinal disease applications.
AB - Administering medicines to 0- to 5-year-old children in a resource-limited environment requires dosage forms that circumvent swallowing solids, avoid on-field reconstitution, and are thermostable, cheap, versatile, and taste masking. We present a strategy that stands to solve this multifaceted problem. As many drugs lack adequate water solubility, our formulations used oils, whose textures could be modified with gelling agents to form “oleogels.” In a clinical study, we showed that the oleogels can be formulated to be as fluid as thickened beverages and as stiff as yogurt puddings. In swine, oleogels could deliver four drugs ranging three orders of magnitude in their water solubilities and two orders of magnitude in their partition coefficients. Oleogels could be stabilized at 40°C for prolonged durations and used without redispersion. Last, we developed a macrofluidic system enabling fixed and metered dosing. We anticipate that this platform could be adopted for pediatric dosing, palliative care, and gastrointestinal disease applications.
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U2 - 10.1126/sciadv.abm8478
DO - 10.1126/sciadv.abm8478
M3 - Article
C2 - 35622910
AN - SCOPUS:85131108618
SN - 2375-2548
VL - 8
JO - Science Advances
JF - Science Advances
IS - 21
M1 - eabm8478
ER -