Introduction
RoosterBio
is introducing a new product for highly efficient bioreactor expansion of human
Mesenchymal Stem/Stromal Cells (hMSCs) that we are calling RoosterReplenish-MSC. This innovative,
first-in-class stem cell product is a concentrated bioreactor feed that
replaces nutrients and growth factors that have been depleted during
microcarrier expansion of hMSCs and replaces the need for a media exchange,
enabling scalable and efficient fed-batch hMSC bioreactor expansion
processes. This is the first of several
new products that we will launch enabling a cell therapy and tissue engineering
bioprocess revolution that will be the foundation of a sustainable Regenerative
Medicine Industry.
Media Designed for Scale-up
Human
stem cells, characterized by their multi-lineage differentiation potential,
tissue regenerative capacity, and high proliferation rates, are the most critical
raw material in Regenerative Medicine today. Most cell-based therapies require between
50 million and >1 billion cells per patient application, necessitating
efficient expansion (i.e. manufacturing) of starting cell sources. Today, the most
widely used cell expansion platforms for stem cell culture
are planar technologies such as flasks and multi-layer cell factories (Rowley
et. al), but it is generally accepted that lot sizes and COGS generated from these
platforms are insufficient to meet the demand of a widely-used commercial
product (Simaria et al).
MSC
expansion in suspension bioreactors is typically done by growing
cells on adherent substrates, such as microcarriers (Chen et al, Schnitzler et
al, Szczypka et al). Optimization of an efficient
MSC bioreactor culture is central to maximizing yields and recovering healthy,
functional cells at harvest. Another key attribute to efficient manufacturing processes
is cost, and minimizing cost is crucial for building successful business models
around MSC-based regenerative therapies.
Cell culture media is consistently the main cost driver of any stem cell
production process, and it is critical to minimize media usage to keep
production costs to a minimum (Rowley et al). Optimization of MSC-microcarrier
cultures typically involves either full or partial media exchanges to manage
nutrient supply and waste build-up (Goh et. al, Reichmann et al, Nienow et al,
Santos et al, and Heathman et al), which is expensive and impractical at larger
scales of >50L culture. This media exchange mentality is driven by the fact
that commercially-available hMSC media formulations have been designed for
flask-based culture processes and full media exchanges.
Half
media exchanges are the simplest to perform in small scale; however, when spent
medium is only partially replaced with growth medium, the final concentration
of nutrients and growth factors required for optimum cell proliferation are
significantly reduced, resulting in lower cell proliferation rates. In addition,
this procedure is time consuming, and the feasibility at larger scales decreases.
Fed-batch
culture, on the other hand, is more efficient in reducing
processing time, mitigating contamination risk, and reducing costs associated
with waste management such as time, labor, equipment and facility required to
prepare and handle spent media. Hence, a new media design philosophy is
required for suspension-based hMSC culture, and RoosterReplenish-MSC, coupled with RoosterBio’s High Perfromance
Media kit, is the first media system designed specifically for hMSC bioreactor
culture.
RoosterReplenish-MSC,
a concentrated bioreactor feed, replaces nutrients and growth factors that have
been depleted from RoosterBio’s
High Performance Growth Media (KT-001) during extended culture.
The nutrient boost provided by RoosterReplenish-MSC replaces the need for
partial or full media exchanges when using our rich basal media, yielding a
more streamlined culture process for hMSC expansion in bioreactors, and enabling
efficiency in media utilization.
In the next section, we will describe a series of studies performed with RoosterReplenish-MSC in microcarrier suspension culture.
Experimental Methods, Results &
Discusssions