AJIPHASE™ Scalable Manufacturing for Oligonucleotides and Peptides

AJIPHASE™ is our proprietary hybrid liquid-phase synthesis technology designed to produce high-purity, scalable peptides, oligonucleotides, and PMOs in a homogeneous reaction mixture. The platform supports programs from development to commercial cGMP manufacturing with reduced environmental impact.

How AJIPHASE™ Works

AJIPHASE™ combines elements of traditional solid-phase and liquid-phase synthesis. It replaces the resin base with a proprietary soluble anchor. This anchor allows a homogeneous single-reactor process with no column and no resin ceiling, enabling up to 200 kg per GMP batch using standard chemical reactors. By combining the best of solid- and liquid-phase chemistry, AJIPHASE™ delivers scalable, high-quality, and environmentally friendly manufacturing for oligonucleotides, peptides, and PMOs.

Why AJIPHASE™ Changes the Scale Equation

AJIPHASE™ enables seamless scale-up from lab to commercial production across 1–8,000 L reactors, supported by commercial-scale manufacturing, 30+ GMP production campaigns, and consistent product quality across scales. By lessening manufacturing waste, AJIPHASE™ supports pharmaceutical companies in achieving sustainability and ESG objectives while enabling efficient large-scale production.

AJIPHASE™ Applications by Molecule Type

Oligonucleotides, PMOs, and peptides — proven capabilities across a range of molecule types and production scales. AJIPHASE™ is validated across each of these programs. Not every molecule fits every platform — here’s how AJIPHASE™ performs by modality.

Oligonucleotides

AJIPHASE™ provides a scalable manufacturing platform for ASOs and siRNAs using the same phosphoramidite chemistry as conventional solid-phase synthesis. Common modifications such as 2′-modifications and phosphorothioate (PS) backbones and conjugations are supported. For siRNA, AJIPHASE™-manufactured or solid-phase-manufactured fragments can be combined with enzymatic ligation, providing a cost-effective route to higher product quality and enhanced scalability. GMP manufacturing are available, supported by extensive manufacturing experience and CMC support expertise.

PMO

AJIPHASE™ provides a highly scalable manufacturing platform for PMOs, particularly for programs requiring quantities above 100 g through commercial supply. The platform enables seamless scale-up, robust process control, and cost-efficient manufacturing using standard chemical reactors. Both GMP and non-GMP manufacturing are supported by extensive manufacturing experience and integrated CMC expertise from development through commercial supply.

Peptides

AJIPHASE™ provides a scalable manufacturing platform for peptides, particularly high-volume therapeutics such as GLP-1 analogs and complex structure such as multi-cyclic peptides. The liquid-phase process enables efficient large-scale production with reduced amino acid, reagent, and solvent consumption while utilizing standard chemical manufacturing equipment. Both GMP and non-GMP manufacturing are available, supported by extensive manufacturing experience and integrated CMC expertise from development through commercial supply.

A More Sustainable Path to Scale and Reliability

As oligonucleotide and peptide therapies advance toward larger patient populations, manufacturing processes must deliver not only scalability and reliability, but also improved sustainability. AJIPHASE™ addresses these challenges through highly efficient liquid-phase chemistry that enables large-scale production while reducing resource consumption.
Compared with traditional solid-phase synthesis, AJIPHASE™ reduces the consumption of solvents, reagents, and raw materials, helping to lower process mass intensity. These efficiencies can reduce environmental impact while also improving manufacturing economics, making sustainability and cost efficiency complementary, rather than competing objectives.

From Research to Commercial: One Platform Throughout

AJIPHASE™ supports oligonucleotide and peptide programs from development through commercial supply on a single scalable platform. For programs developed using conventional synthesis methods, Ajinomoto Bio-Pharma Services can help evaluate and implement a transition to AJIPHASE™ while minimizing development risk. Backed by integrated process development, analytical, regulatory, and manufacturing expertise, we help customers realize the benefits of scalable, efficient, and cost-effective manufacturing throughout the product lifecycle.

Let’s Discuss AJIPHASE™ for Your Program

Whether starting a new program or transitioning from an existing synthesis process, AJIPHASE™ provides a practical path to scalable manufacturing.

Frequently Asked Questions

What is AJIPHASE™ and how does it differ from solid-phase synthesis?

AJIPHASE™ is Ajinomoto Bio-Pharma Services’ proprietary liquid-phase synthesis technology for oligonucleotides and peptides. Instead of the resin used in solid-phase synthesis, AJIPHASE™ uses a proprietary soluble anchor, enabling highly efficient reactions, simpler scale-up, and robust process control.

What is the maximum scale for AJIPHASE™ synthesis under cGMP?

AJIPHASE™ synthesis is highly scalable — up to 200 kg per batch for oligonucleotides and exceeding 100 kg per batch for peptides — in one reactor with no additional specialized equipment, providing cost-effective and pure oligonucleotides and peptides with fewer waste byproducts. AJIPHASE™ allows for optimized time, cost, and value when scaling your products to commercial quantities.

Does AJIPHASE™ produce equivalent purity to traditional solid-phase synthesis?

Quality and purity profiles show no difference between AJIPHASE™ and traditional solid-phase synthesis

Does AJIPHASE™ offer cost advantages over traditional solid-phase at large scale?

Because AJIPHASE™ requires less solvent and reagents than solid-phase synthesis for large-scale production, it provides increased sustainability and cost-effective manufacturing advantages.