The Southern California Pharmaceutical Discussion Group (SCPDG) Announces our January 23, 2025, Meeting:
Challenges in Developing High Drug Loaded Redispersible Amorphous Nanoparticle Formulations of BCS IV Compound
Presented By
Miki Yu
AbbVie Inc.
North Chicago, IL
Abstract: Amorphous solid dispersion (ASD) is an enabling approach utilized to deliver poorly soluble compounds. ASDs can spontaneously generate drug-rich amorphous nanoparticles upon dissolution, which can act as a reservoir for maintaining supersaturation during oral absorption. But, conventional ASDs are often limited in drug loadings to < 20 %. For indications where the dose is high, this can translate into a significant pill burden. The aim of this research was to develop a high drug loading (DL) amorphous nanoparticle (ANP) formulation that can release the drug-rich nanoparticles into solution upon contact with aqueous environment. Nanoparticles were directly engineered using solvent/anti-solvent precipitation. The obtained nanoparticle suspension was then concentrated followed by solidification to a 45% drug loaded re-dispersible amorphous powder by freeze drying (FD). An oral suspension of this FD powder demonstrated promising pharmacokinetics in dogs when compared with a suspension from 10% drug loaded ASD. This preclinical data enabled a human proof-of-concept assessment opportunity. Challenges manifested during scale-up from 50g (lab scale) to 280g (for clinical supply). Given the preclinical data, formulation change was restricted, therefore, process modifications were implemented. Cold collection after precipitation prevented particle growth but resulted in 75 nm particles at clinical scale (CS), compared to 150 nm at laboratory scale (LS). This size decrease rendered stabilizer amounts suboptimal for FD operation. Consequently, when FD powder was resuspended in water a smaller fraction of particles was below 450 nm (by filtration), ~65% for CS compared to ~85% for LS. Formulation was stable for > 6 months, evaluated by monitoring moisture content, assay, powder X-ray diffraction (PXRD), and redispersion time. Despite ~65% re-dispersibility, this 45% DL formulation oral suspension in humans had higher Cmax and AUC ~73% and ~46% respectively in fasted-state, and under fed-state it met bioequivalence criteria for AUC but Cmax was 20% lower compared to reference (10% DL ASD tablets) demonstrating advantage of ANP strategy over ASD approach.
Biography: Miki Yu is a Senior Scientist at AbbVie, in small molecule drug product design and development, with a focus on formulation development in early stage. Miki obtained her Bachelor as well as PhD degree in chemical engineering. Her thesis was in mixing and segregation of granular materials. After her PhD work, she joined AbbVie as a postdoc working on amorphous nanoparticles, aiming to develop formulation/process that achieve similar bioavailability to ASD at a high drug loading (>45% w/w).
Date: Thursday, January 23, 2025
Agenda: 4:00-4:30 PM PT, Check-In, Networking and Refreshments, 4:30-5:30 PM PT, Presentation and Discussion.
Location: Waters Office, 3540 Howard Way, Suite 100, Costa Mesa, CA 92626 or join us on-line. You must register to attend live or receive the link to attend virtually. General admission is $20.00 (to cover the cost of refreshments), Students with ID and Retirees are $5.00.
Registration: Please register by Noon, Tuesday, January 21, using the link below or copy and type into your browser: https://www.eventbrite.com/e/scpdg-january-discussion-group-meeting-tickets-1131363501689?aff=oddtdtcreator
Note: Must register to receive Zoom Link.
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Ke Wu Ph.D.
Associate Director
Abbvie
Irvine CA
[email protected]Disclaimer: Opinions expressed are solely my own and do not express the views or opinions of my employer.
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