Nanoformulation of a poorly water soluble API for enhanced oral bioavailability and dose reduction strategy

Potential pharmacological development of an InnoForm nanomaterial of API ‘X’ and an equivalent aqueous preparation using (A) an in vitro transwell model and (B) a pre clinical in vivo model, following a single oral dose. (C) Dose reduction strategy following multiple-doses in a pre clinical in vivo model. Examples of the methods employed and results for different APIs are described in McDonald et al., 2014; Giardiello et al 2016 and Savage et al., 2019.

Nanoformulation of a poorly water soluble API for Long Acting parenteral delivery
Potential pharmacological development of an InnoForm nanomaterial of API ‘Y’ for long-acting parenteral (subcutaneous or intramuscular) delivery. (A) in vitro release rate of API ‘Y’ performed in biologically relevant simulating buffers (B) plasma exposure of API ‘Y’ in a pre-clinical in vivo model, following a single parenteral injection. Examples of the methods employed and results for different APIs are described in Bakshi et al., 2018; Tatham et al., 2019 and Hobson et al., 2019.

Nanoformulation of a poorly water soluble agrochemical for improved herbicidal and fungicidal activity
Potential glasshouse/field trial of an InnoForm nanomaterial of Agrochemical ‘Z’ following spray application. Previous studies have shown improved biocidal activity of InnoForm prepared agrochemicals and biocides and the potential for reduced dose or application rate.