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The level of particles in parenteral pharmaceutical formulations is a critical quality attribute. This is no surprise; the clinical consequence of their presence can be very severe, including fatality. In the major pharmacopeia, from the US, Europe, and Japan, there is a specified limit for particles in the final parenteral formulation. Moreover, these pharmacopeia specify two methods for measurement – light obscuration (LO) and microscopic particle count (MPC).
For the analysis of drug product, LO is the primary method and, MPC should be used only if LO is not adequate or not possible. However, for the analysis of components, both MCP and LO are recommended. MCP is more effective at detecting particles >25µm in diameter. Additionally, MCP allows for the use of surfactant in the extraction, which improves the ability to rinse particles from the component surface. However, LO can be used effectively for the analysis of sub-visible particulate on components, if used appropriately. The principle behind LO is simple. The sample solution is drawn into an illuminated flow cell path; particles in the sample solution obscure light. The degree of obscuration is dependent upon the size of the particles. Data are compared to that for standard polystyrene beads; an equivalent spherical diameter of particles is calculated. With today’s technology, it is more efficient and requires less labor.But – are the results from LO accurate and reflective of the actual quality of the samples tested? To ensure the answer is yes, the following conditions are necessary:
a) robust pre-rinse protocol – to avoid any effects of disturbance
b) appropriate dilution – a solution too concentrated may cause coincidence of particles
c) test solution free of bubbles
d) particle-free test environment
e) sufficient difference in refractive index difference between particles and test solution
Take an in-depth look at the science behind containment & delivery of injectable medicines in the West Knowledge Center.