- Cell Biology
- Product Type
- Research Area
- New Products
- About Tocris
- Contact Us
Cell and gene therapies are new treatment modalities that are rapidly advancing from the lab into the clinic. With the clinical phases of development being highly regulated, there is a need for superior grade ancillary reagents (also known as raw materials) in the manufacture of cell therapies to ensure the safety and suitability of the final product. At Tocris we are known for our commitment to quality, and now we are supporting the development of new cell therapies with our range of enhanced quality ancillary reagents. Manufactured in our ISO 9001 certified facilities using strictly controlled processes, and with rigorous quality management systems, our GMP and Ancillary Material Grade compounds are intended for use in the manufacture of cell and gene therapies.
Find out more about Bio-techne's GMP Capabilities and how we can support your Cell and Gene Therapy development program by visiting bio-techne.com.
Ancillary Materials are essential components required for the manufacture of cell and gene therapies or tissue-engineered therapies, but they are not intended to be part of the final product. This includes reagents such as small molecules and proteins as well as cell culture media. Although ancillary materials are not meant to be found in the final product, they can impact the safety, purity and thus suitability of the final cell product for clinical use.
Small molecules offer several advantages when compared to other ancillary materials for cell therapy manufacture:
The quality of cell and gene therapies relies on the quality and safety of raw materials, so it is important to assess the source, purity, identity, safety and suitability of your ancillary materials. If using an ancillary reagent in the development of a cell therapy where these factors are unknown, extensive qualification studies may be required by medicines regulators to ensure that the material used is suitable and will not compromise the safety of the final cell therapy product.
Working in partnership with cell and gene therapy manufacturers, Tocris has developed two enhanced quality small molecule ranges, GMP and Ancillary Material (AM)-Grade. These have been developed for cell and gene therapy manufacture, for example in regenerative medicine or immune cell therapy. They are produced with a higher level of scrutiny, documentation and quality control than our standard catalog products.
|Standard Catalog||Ancillary Material Grade||GMP|
|Controlled Manufacturing Zone||✔||✔|
|TSE and BSE Certification||✔||✔|
|Risk-based Approach to Manufacturing||✔|
The production of our Ancillary Material Grade compounds is in accordance with ISO TS 20399 guidelines. The synthesis of Ancillary Material Grade small molecules is based on that of the equivalent standard catalog or research use only (RUO) products. Using established synthetic procedures allows a wider range of products to be brought to the superior AM-grade than just focusing of the highly risk assessed and time consuming GMP process. The key differences compared with RUO products include enhanced QC testing, a more detailed QA review and accompanying documentation. AM-grade products are manufactured to provide:
Our GMP (Good Manufacturing Practice) small molecules are produced according to Current Good Manufacturing Practice guidelines. In addition to the controls listed above the following also apply to our GMP compounds:
Our protocol snapshots highlight how small molecules may be used in the stem cell workflow for maintenance, reprogramming and differentiation.Browse Protocols
Stem cell therapies have the potential to treat several diseases, and these therapies are now entering clinical trials and approaching the clinic. This blog discusses small molecules as an ancillary material (AMs) for stem cell therapy manufacture, including their advantages over other types of AMs.Read Now!
Small molecules are increasingly being used alone, or in combination with growth factors, to modulate stem cells. They can be used at all stages of the stem cell workflow, i.e. in reprogramming, maintenance, storage and differentiation protocols. This blog post outlines the advantages of using small molecules.Read Now!
Tocris offers the following scientific literature for GMP & Ancillary Material Grade Small Molecules to showcase our products. We invite you to request* your copy today!
*Please note that Tocris will only send literature to established scientific business / institute addresses.
Written by Kirsty E. Clarke, Victoria B. Christie, Andy Whiting and Stefan A. Przyborski, this review provides an overview of the use of small molecules in the control of stem cell growth and differentiation. Key signaling pathways are highlighted, and the regulation of ES cell self-renewal and somatic cell reprogramming is discussed. Compounds available from Tocris are listed.
Stem cells have potential as a source of cells and tissues for research and treatment of disease. This poster summarizes some key protocols demonstrating the use of small molecules across the stem cell workflow, from reprogramming, through self-renewal, storage and differentiation to verification. Advantages of using small molecules are also highlighted.