The trusted partner who provides a flexible approach to nanotechnology formulation solutions
Nanotechnology Development Services
LLS Health is a leader in the field of nanotechnology for pharmaceuticals. We don’t take a one-size-fits-all approach; we design programs based on each individual molecule and overall end goals of the drug product.
Our scientists have extensive experience in developing and scaling up nanoparticulate suspensions. When it comes to solubility enhancement, we are the leaders in the use of nanomilling, employing both commercial milling equipment and our own proprietary mills (SteriMill™).
This flexibility in formulation and process design combined with access to cutting edge technologies ensures the best possible outcome for your drug product.
Broad offerings, deep expertise
LLS Health employs several nanotechnology approaches during formulation selection. This allows us to consider different options to achieve your technical and commercial goals. Once we develop a formulation, we have the facilities and equipment to produce clinical and commercial-scale materials for all phases of drug development.
From improving bioavailability or stability, formulating higher doses, improving safety and patient compliance, managing toxicity, controlling release rates, or protecting unstable APIs from degradation, we can create a viable formulation that is scalable and effective.
Our expertise includes the following technologies:
- High energy media milling and micronization
- Spray drying
- Tangential flow filtration (TFF)
We have experience in developing and manufacturing nanoparticulate suspensions for a wide variety of projects involving new chemical entities (NCEs) and 505(b)(2)s. Our deep expertise in complex formulations and breadth of technologies make us ideally suited to take on unique challenges.
Decades of experience
We were one of the first companies to scale and commercialize a nanoparticle with our work on zinc oxide (Z-Cote®) for skincare products in 1990s. Over the years, our scientists have worked on hundreds of nanoparticulate projects, including highly potent APIs and controlled substances.
Expert in nanomilling
We are experts in the development of nanoparticulate suspensions to achieve solubility enhancement and long-acting drug release. Our team has strong relationships with leading equipment manufacturers for nanomilling production and processing.
Aseptic and sterile capabilities
We are the only CDMO that can perform nanomilling under aseptic conditions, including commercial production, and our cleanroom facilities are equipped with processing space that can accommodate even the most complex production lines.
LLS Health is a leader in nanomilling—an efficient, reproducible, and scalable approach for improving the rate of dissolution and bioavailability of BCS Class II and IV compounds. In just 8 weeks, our Nanomilling Feasibility Program (NFP) allows us to:
- Develop a target product profile and screen your API for nanomilling with GRAS excipients
- Generate particle size distribution and short-term stability data for each formulation
- Identify promising formulation(s) and provide material for small animal pharmacokinetic (PK) studies.
Nanomilling is a proven, commercially-validated process for formulating just about any poorly water-soluble API. Numerous BCS class II and IV APIs have benefited from this technology and 10+ nanomilled drug products have gained FDA approval since 2000, including both solid and liquid dosage forms. The key to nanomilling is particle size reduction, which increases the surface area of an API and improves dissolution rate.
LLS Health has decades of experience developing nanoparticulate suspensions, and we are the only CDMO capable of performing nanomilling under aseptic conditions. If you choose to move forward with your nanomilling project, we have the personnel, facilities, and equipment to produce clinical and commercial scale nanomilled formulations. If you have an insoluble API, contact us today to learn how nanomilling can help to solve your formulation challenges, and let us take your product from concept to commercial.
LLS Health is a flexible, full-service CDMO, offering formulation development, drug product manufacturing with supporting analytical services and quality oversight as well as professional project management. We can help you every step of the way from concept through commercialization.
Our formulation team employs a data-driven approach to find solutions for even the most challenging APIs employing a range of technologies to maximize bioavailability, control release rate, and enhance stability. Our scientists work on projects from early-stage development through scale-up and transition to our clinical and commercial manufacturing teams.
We offer GMP manufacturing for many dosage forms, and our integrated approach creates a smooth transition from pre-clinical activities through clinical validation. We have GMP manufacturing space that is supported by in-house analytical services, bioanalytical services, physicochemical characterization, and ICH-compliant stability programs.
Our purpose-built commercial manufacturing facility is ideally suited to sterile and complex drug products, including those with small batch sizes and sterility requirements. We have GMP manufacturing space that features a well-equipped processing room as well as Grade A filling and lyophilization suites.