Ultra-High Purity Methanol for mRNA & Gene-Therapy Formulations: Why It Matters

Ultra-High Purity Methanol for mRNA & Gene-Therapy Formulations: Why It Matters

Methanol is one of the most widely used polar solvents in pharmaceutical and biopharmaceutical manufacturing. In recent years, its role has become even more important as the industry shifts towards advanced modalities such as mRNA vaccines, lipid nanoparticle (LNP) systems, viral vectors, and gene-therapy formulations. These products are extremely sensitive to impurities, meaning the quality […]

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Acetone in Nanoparticle / Lipid-Based Formulations (LNPs) — From Precipitation to Solvent Removal

Acetone in Nanoparticle / Lipid-Based Formulations (LNPs) — From Precipitation to Solvent Removal

Nanoparticle and lipid-based formulations (LNPs) have become essential in modern drug delivery, especially for mRNA vaccines, gene therapy products, and targeted therapeutics. These delivery systems allow sensitive molecules to reach their target safely and efficiently. While lipids and polymers form the structure of these nanoparticles, solvents such as acetone play a key role in their […]

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Trace Impurity Monitoring in IPA: Detecting & Preventing Benzene or Other Contaminants

Trace Impurity Monitoring in IPA: Detecting & Preventing Benzene or Other Contaminants

Isopropyl Alcohol (IPA) plays a far more central role in pharmaceutical manufacturing than just cleaning and disinfection; it is deeply integrated into processes that define the quality, appearance, stability, and performance of oral solid dosage (OSD) forms, especially tablet coating and solid dose formation. Because IPA comes into direct contact with excipients, coating polymers, pigments, […]

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MDC in Continuous Pharmaceutical Manufacturing — Feasibility, Challenges & Best Practices

MDC in Continuous Pharmaceutical Manufacturing — Feasibility, Challenges & Best Practices

Continuous pharmaceutical manufacturing is transforming the way medicines are produced. Instead of traditional batch methods, continuous processing allows raw materials to move through each step without interruption. This approach offers improvements in efficiency, consistency, safety, and cost. However, when solvents such as Methylene Dichloride (MDC) — also known as Dichloromethane are used in these systems, […]

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Understanding and Mitigating Residue Risks from IPA Wipes in Critical Cleanrooms

Understanding and Mitigating Residue Risks from IPA Wipes in Critical Cleanrooms

In pharmaceutical, biotechnology, and healthcare industries, cleanrooms are the backbone of contamination control. Maintaining sterile and particle-free surfaces is essential to ensure product quality and patient safety. Isopropyl Alcohol (IPA) wipes are one of the most commonly used tools for surface cleaning and disinfection in these critical environments. However, not all wipes are created equal, […]

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Balancing MDC Toxicity Concerns with its Irreplaceable Efficiency in Drug Synthesis

Balancing MDC Toxicity Concerns with its Irreplaceable Efficiency in Drug Synthesis

Methylene Dichloride (MDC), also known as dichloromethane, has long been a trusted solvent in the pharmaceutical industry. Its unmatched solvency power, versatility, and performance in chemical synthesis make it indispensable in various drug manufacturing processes. However, MDC also comes with toxicity concerns that demand careful management and adherence to safety and environmental standards. This article […]

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Navigating the Grade Selection of Acetone for Non-Critical vs. Critical Pharma Applications

Navigating the Grade Selection of Acetone for Non-Critical vs. Critical Pharma Applications

Acetone is one of the most versatile solvents in the pharmaceutical industry used across research, production, formulation, and analytical testing. However, not all acetone is the same. The grade of acetone you choose can make a significant difference in safety, performance, and compliance especially when distinguishing between critical and non-critical pharmaceutical applications. In this article, […]

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The Role of MDC in Controlled Extraction of Bioactive Compounds

The Role of MDC in Controlled Extraction of Bioactive Compounds

In pharmaceutical and biotechnology industries, the extraction of bioactive compounds is a crucial step in developing high-value products such as active pharmaceutical ingredients (APIs), alkaloids, vitamins, and natural therapeutics. Achieving high purity and yield from complex biological materials requires solvents that can deliver selective, efficient, and controlled extraction. Methylene Dichloride (MDC), also known as Dichloromethane, […]

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Role of Methanol in Lyophilisation and Freeze-Drying Processes

Role of Methanol in Lyophilisation and Freeze-Drying Processes

Freeze-drying, also known as lyophilisation, is one of the most valuable techniques in modern pharmaceutical development. It enables the preservation of heat-sensitive drugs, biologics, and vaccines without compromising their structural integrity or efficacy. While the process seems straightforward on the surface, the choice of reagents and solvents used in lyophilisation plays a significant role in […]

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Role of MDC in Extraction of High-Value Pharmaceutical Alkaloids

Role of MDC in Extraction of High-Value Pharmaceutical Alkaloids

The pharmaceutical industry has long relied on natural products as a foundation for drug discovery and development. Among these, alkaloids occupy a unique space. Derived mainly from plants, alkaloids such as morphine, quinine, vincristine, and reserpine have shaped modern medicine. They offer therapeutic effects ranging from pain relief to cancer treatment. Yet, extracting these valuable […]

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IPA Usage Guidelines in Injectable Drug Manufacturing Units

IPA Usage Guidelines in Injectable Drug Manufacturing Units

Injectable drugs represent some of the most critical and sensitive formulations in modern medicine. Since they are delivered directly into the body, bypassing natural barriers like the gastrointestinal tract, every component of their production must meet the highest possible standards. Among the many materials used in injectable drug manufacturing, Isopropyl Alcohol (IPA) holds a central […]

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How Solvent Selection Impacts the Stability of Biologics and Injectables

How Solvent Selection Impacts the Stability of Biologics and Injectables

The rise of biologics and injectable therapies has changed modern medicine. Monoclonal antibodies, cell-based therapies, and advanced vaccines now stand at the forefront of treatments for cancer, autoimmune disorders, and infectious diseases. These products are highly complex, delicate, and sensitive to their environment. Unlike small molecules, biologics are vulnerable to degradation from heat, light, pH […]

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Methanol as a Reagent in Vaccine Stabiliser Formulations

Methanol as a Reagent in Vaccine Stabiliser Formulations

The development of stable, effective vaccines is a cornerstone of modern public health. From temperature-sensitive mRNA-based platforms to more traditional live attenuated formulations, stability determines shelf life, distribution range, and ultimately, real-world efficacy. One compound playing a quiet but essential role in some vaccine stabiliser formulations is methanol. In pharmaceutical manufacturing, methanol is more than […]

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