John Garner

Block-copolymers from PolySciTech used in development of Adapalene-nanoparticle delivery system to cross the blood-brain-barrier

Blog Post created by John Garner on Apr 18, 2019

Medina, 2019 adapalene polymer polyscitech.jpg

“Drugs don’t deliver themselves” is a statement which has multiple meanings depending on who you are talking to. For retinoid molecules, drug-delivery to brain tissue is not a simple task as these highly-effective therapeutics are also highly water insoluble. Furthermore, the brain has extremely selective uptake of molecules across the ‘blood-brain-barrier’ which means any attempt to deliver a medicinal molecule to the brain will require getting the molecule across this barrier so that it can have therapeutic efficacy. Recently, researchers at Barrow Neurological Institute and University of Texas Health Science Center at Houston used PCL (AP108) and mPEG-PLA (AK054) from PolySciTech (www.polyscitech.com) to create adapalene loaded nanoparticles for brain-delivery. This research holds promise to provide for improved therapy against a variety of neurological diseases. Read more: Medina, David X., Eugene P. Chung, Robert Bowser, and Rachael W. Sirianni. "Lipid and polymer blended polyester nanoparticles loaded with adapalene for activation of retinoid signaling in the CNS following intravenous administration." Journal of Drug Delivery Science and Technology (2019). https://www.sciencedirect.com/science/article/pii/S1773224719300358

 

“Abstract: Small molecule retinoids are potential therapeutics for a variety of neurological diseases. However, most retinoids are poorly water soluble and difficult to deliver in vivo, which prevents further study of their utility to treat disease. Here, we focus on adapalene, an FDA approved drug that is a specific agonist for the retinoic acid receptor β (RARβ). We sought to develop nanoparticle delivery systems that would enable effective drug delivery to the CNS. We developed strategies to produce nanoparticles based on the hypothesis that incorporation of hydrophobic molecules into a polyester base would improve adapalene loading. In the first scheme, poly (lactic acid)-poly (ethylene glycol) (PLA-PEG) was blended with low molecular weight poly (lactic acid) (PLA) or poly (caprolactone) (PCL). In the second scheme, poly (lactic-co-glycolic acid) (PLGA) was blended with 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[amino (polyethylene glycol) (DSPE-PEG). Our data demonstrate that blending low molecular weight polyesters or DSPE-PEG into the primary nanoparticle base improves encapsulation of adapalene, presumably by enhancing adapalene solubility in the nanoparticle. Peripheral administration of these nanoparticles activated retinoid signaling in the brain and spinal cord of healthy mice. These studies provide new approaches for nanoparticle fabrication and establish proof of principle that systemically administered, adapalene-loaded nanoparticles activate retinoid signaling in the CNS.”

 

- Biotech, Pharma, Cancer, Research (BPCR) is a free, 1-day scientific networking conference hosted by Akina, Inc. on Aug 28, 2019. See more and register to attend at www.bpcrconference.com

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