Goodwin Biotechnology offers a Single Source Solution™ that starts with cellline development and extends through Process Development and cGMP
manufacturing.
We have collaborative partners for molecular biology and cell line
development activities with whom we work to develop your cell line. Working
with our partners, we can develop cell lines from cDNA or gene sequences that
you provide for antibodies, hybridomas, or recombination proteins and to
engineer highly productive and stable cell lines in HEK-293, BHK, CHO, NS0,
SP2/0 cells or proprietary third-party systems like PER.C6®, ACE, GS, and UCOE.
Our partners offer their own proprietary vectors to develop cell lines
that can routinely produce up to 4g/L in CHO cell lines. If you have an
existing vector, we can start the cell line development from that. If you do
not, we will do gene synthesis where we do vector design and construction.
We adopt a risk-based, Quality by Design (QbD) approach for all projects,
and specifically Cell Line Development. Before we start a project, we created a
cell line development project plan (Design Input Plan). Our clients review the
plan and we only start on the project after it is approved.
Once transfection of the cell has been done, screening amplification and
subcloning will be performed, which is then followed by the adaptation of cell
lines to suspension culture in media that is serum-free and chemically-defined.
If you so desire, we will have a stable pool of transfectants generated and
characterized for you before we generate a high-producing single stable clone.
We identify between 3 and 5 high-producing single stable clones and we
will create 10 liquid nitrogen vials of each of the clones. There is a shake
flask stage of the cell line development process where you can get a small
sample of the harvest and purify it for initial protein structural
characterization (quaternary, tertiary, secondary, or primary). You can also do
binding characteristics through such methods as binding kinetics, mass
spectrometry, amino acid analysis, glycosylation, and potency. This, coupled
with productivity and generational stability data, helps in the selection of
the best cell line for your Research Cell Bank (RCB).
Our team also performs generational stability studies during the cell
line development process. We do this for up to 50 generations. We
evaluate such things as cell growth productivity and cell growth kinetics for
every five generations. We will produce up to 40 vials of the RCB and we will have
it tested for such things as adventitious viruses, mycoplasma, and sterility. We
will develop a final cell line development report which you get to review and
approve before we ship the product to you.
The final product is then ready for process development work and for GMP
MCB creation. Our Process Development team is led by Dr. Legmann who has over
10 years of experience in the production and characterization of clones to
fully active mammalian and bacterial recombinant protein expression products.
She and her team have vast experience in mammalian cell culture bioreactor
optimization which makes it possible for us to develop a robust and reproducible cell culture
process for the production of complex therapeutic protein drug candidates.
At Goodwin Biotechnology we also provide expert
Regulatory support to our clients to assist them in quickly and effectively
moving their drug candidates through the regulatory application and review
process. Goodwin Biotechnology provides full regulatory support services for
projects beginning with process development initiatives in support of
toxicology study materials through the preparation of Chemistry, Manufacturing
& Controls (CMC) information for IND filings and amendments. Our staff
provides regulatory assistance in all aspects of client projects including
meeting with regulatory agencies to discuss manufacturing and testing issues.
Our staff is knowledgeable in US, Canadian, and European requirements, as well
as guidelines for products produced using novel platforms. Please contact us…
No comments:
Post a Comment