Quantumzyme Expands AI Enzyme Platform to Transform Pharmaceutical Manufacturing

By Advos

TL;DR

Quantumzyme's expanded AI enzyme platform offers pharmaceutical companies a competitive edge through sustainable API manufacturing with improved cost efficiency and reduced environmental impact.

Quantumzyme's platform uses AI-driven computational modeling, in silico directed evolution, and high-throughput validation to design optimized biocatalysts that replace traditional chemical reaction steps.

This technology advances green pharmaceutical manufacturing by reducing hazardous waste, toxic solvent use, and carbon emissions, creating a cleaner environment for future generations.

Quantumzyme is expanding its AI enzyme platform beyond ibuprofen to target high-volume APIs like phenylephrine using computational biology for greener drug manufacturing.

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Quantumzyme Expands AI Enzyme Platform to Transform Pharmaceutical Manufacturing

Quantumzyme Corp. has announced the expansion of its proprietary AI-powered enzyme design platform to target additional high-volume Active Pharmaceutical Ingredients beyond ibuprofen, marking a significant advancement in green pharmaceutical manufacturing. This strategic initiative aims to reduce hazardous waste, toxic solvent use, and carbon emissions at scale while addressing the environmental challenges of traditional API production methods.

The expanded program leverages Quantumzyme's enzyme families, machine learning predictive models, and in silico design workflows to develop sustainable pathways for other APIs with substantial global environmental impact. The company's enzyme engineering platform integrates advanced AI-driven computational modeling, in silico directed evolution, mechanistic simulation, and high-throughput validation to deliver optimized biocatalysts that replace traditional energy-intensive chemical reaction steps.

According to CEO Naveen Kulkarni, the global API market is projected to exceed $300 billion by 2030, with generic drugs representing the majority of production volume. Much of this manufacturing currently occurs overseas using legacy chemistries that generate heavy waste streams and carry high solvent and carbon intensity. The expanded R&D pipeline includes multiple high-volume APIs, including chiral intermediates such as phenylephrine and related compounds accessible via ketoreductases, which are widely used in the global generics sector.

Quantumzyme's biocatalysis-first approach offers a sustainable alternative that delivers reduced chemical waste and solvent usage, lower carbon footprint, elimination of toxic reagents, and improved cost and yield efficiency. The company's platform also supports domestic API manufacturing and aligns with U.S. supply chain resilience and sustainability goals. For more information, visit https://www.quantumzymecorp.com and the company's profile at https://www.otcmarkets.com/stock/QTZM.

This expansion highlights the scalability of Quantumzyme's digital biology architecture and its ability to rapidly adapt and redeploy enzyme systems across diverse synthesis targets. Kulkarni emphasized that the company's vision is to redefine chemical manufacturing through sustainable innovation, advancing greener chemistry while supporting supply chain resiliency. The move toward enzyme-driven production could potentially become the industry standard for high-volume APIs, representing a fundamental shift in how pharmaceuticals are manufactured globally.

Curated from NewMediaWire

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