Development of oil-based gels as versatile drug delivery systems for pediatric applications

Author:

Kirtane Ameya R.12ORCID,Karavasili Christina1ORCID,Wahane Aniket1ORCID,Freitas Dylan2ORCID,Booz Katelyn3ORCID,Le Dao Thi Hong14,Hua Tiffany1,Scala Stephen15ORCID,Lopes Aaron12,Hess Kaitlyn1,Collins Joy12,Tamang Siddartha1ORCID,Ishida Keiko1ORCID,Kuosmanen Johannes L. P.1,Rajesh Netra Unni16ORCID,Phan Nhi V.1ORCID,Li Junwei12ORCID,Krogmann Annlyse3ORCID,Lennerz Jochen K.7ORCID,Hayward Alison128ORCID,Langer Robert19ORCID,Traverso Giovanni129ORCID

Affiliation:

1. David H. Koch Institute for Integrative Cancer Research and Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

2. Division of Gastroenterology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA 02115, USA.

3. Sensory Spectrum Inc., New Providence, NJ 07974, USA.

4. Swiss Federal Institute of Technology (ETH), Zurich 8092, Switzerland.

5. Stonehill College, North Easton, MA 02357, USA.

6. University of Toronto, Toronto, ON, Canada.

7. Department of Pathology, Center for Integrated Diagnostics, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.

8. Division of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

9. Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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