Yissum - Research Development Company of the Hebrew University

Pro-Nano Lipospheres as Oral Delivery Platform for Lipophilic Drugs

Posted by Yissum - Research Development Company of the Hebrew UniversityResponsive · Innovative Products and Technologies · Israel

Summary of the technology

Cluster9
oral dispersible concentrate preparation for improving the bioavailability and distribution of lipidic drugs that are substrates of
first pass intestinal metabolism and/or are substrates of Pgp efflux. Thus, the formulation elevates the amount of drug that reach the systemic blood circulation and
reduces the variability in the oral absorption properties.


Project ID : 6-2008-2126

Yissum - Research Development Company of the Hebrew University
Yissum - Research Development Company of the Hebrew University
Yissum - Research Development Company of the Hebrew University
Yissum - Research Development Company of the Hebrew University

Description of the technology

Categories:

Life Science & Biotechnology

Technology Keywords:

Formulation, drug delivery, increased bioavailability

Development Stage:

POC in animal

Our Innovation

The PNL formulation composed of GRAS materials enabling co-administration of lipophilic drugs and bio-enhancers for improved bioavailability.

The PNL vehicle serves as a platform for the successful oral delivery of lipophilic drugs separately or together with natural absorption enhancers such as piperine (black pepper component).

Our work centered in application of the PNL for Δ9-tetrahydrocannabinol (THC) and cannabidiol (CBD) which are the primarily investigated compounds of the cannabis plant. These molecules have great therapeutic potential but their oral administration is hindered by poor solubility and extensive metabolism.

Advantages

  • GRAS (Generally Regarded as Safe)based materials
  • Dissolves lipophilic drugs and absorption enhancers found in foods such as piperine, resveratrol etc.
  • The drug is co-administrated with absorption enhancer, allowing it to perform its inhibitory effects on first pass metabolism
  • The formulation self emulsifies in the GI milieu forming an O/W nano emulsion with particle size of 50nm and less
  • The formulation overcomes absorption obstacles of lipophilic drugs
  • Increase in oral bioavailability leads a lower inter and intra subject variability

Technology

The poorly absorbed drug is dissolved in the oily formulation with the absorption enhancer. Upon contact with water, the formulation forms nano particles. Theses nano particles trap the lipophilic components in their lipid core. This allows the lipophilic drug and absorption enhancer to be solubilized in the aqueous environment of the GI.

Development Milestones

Pre-clinical studies in male Wistar rats showed a 6 fold increase in the relative oral bioavailability of THC given in PNL (Figure 1) and an additional 1.5 fold increase with piperine-PNL. Similarly, there was a 3 fold increase in the relative oral bioavailability of CBD-PNL and an additional 2 fold increase with piperine-PNL (Figure 2).

A two-way crossover, single administration clinical study with 9 healthy volunteers was conducted. The volunteers received a THC-CBD piperine-PNL capsule and the oromucosal spray Sativex® with a washout period in between formulations. Single oral administration of the cannabinoids in piperine-PNL formulation resulted in a 3-fold increase in Cmax and a 1.5-fold increase in AUC for THC compared to Sativex®. A 4-fold increase in Cmax and a 2.2-fold increase in AUC for CBD compared to Sativex® were observed (Figure 3 and 4)

Figure 1: Pro-NanoLipospheres (PNL) and piperine-PNL enhance THC bioavailability. Plasma THC concentration–time plot (mean ± S.E.M.) following PO administration of dispersed THC PNL (20mg/kg)and THC-piperine-PNL ( THC 20mg/kg, piperine 10mg/kg) (n=6 for each group).

Figure 2: Pro-NanoLipospheres (PNL) and piperine-PNL enhance CBD bioavailability. Plasma CBD concentration–time plot (mean ± S.E.M.) following PO administration of dispersed CBD PNL (15mg/kg) and CBD-piperine-PNL (CBD 15mg/kg, piperine 10mg/kg) (n=6 for each group).

Figure 3: Plasma THC concentration vs. time plot (mean ± SEM) following oral administration of THC-CBD-piperine-PNL and buccal administration of Sativex®at a dose of 10.8 mg (n = 9 for each group)

Figure 4: Plasma CBD concentration vs. time plot (mean ± SEM) following oral administration of THC-CBD-piperine-PNL and buccal

The Opportunity

Many of today’s leading compounds and drugs in pipeline fail to reach clinical stages due to poor oral bioavailability. This formulation presents an ideal, simple solution for the optimal oral delivery of these compounds and a direct to clinic development.

Project manager

Mel Larrosa
VP Business Development Healthcare

Project researchers

Amnon Hoffman
HUJI, School of Medicine - IMRIC
School of Pharmacy- Institute for Drug Research

Abraham Domb
HUJI, School of Medicine - IMRIC
School of Pharmacy- Institute for Drug Research

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About Yissum - Research Development Company of the Hebrew University

Technology Transfer Office from Israel

Yissum Research Development Company of the Hebrew University of Jerusalem Ltd. Founded in 1964 to protect and commercialize the Hebrew University’s intellectual property. Ranked among the top technology transfer companies, Yissum has registered over 8,900 patents covering 2,500 inventions; has licensed out 800 technologies and has spun-off 90 companies. Products that are based on Hebrew University technologies and were commercialized by Yissum generate today over $2 Billion in annual sales.

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