Drug ingredients are key to liposomal drug production. The characteristics of active pharmaceutical ingredients (API) also contribute to the drug stability. BOC Sciences has extensive experience in supporting drug development and can help you analyze the identity, purity, and quantity of APIs in liposomal drugs.
What are APIs?
APIs are chemical entities used in the manufacturing of pharmaceuticals or in the pure form of prescription drugs. Due to their intended use, it is important that these APIs meet stringent quality and purity standards.
The quality of an API depends on two basic factors - right chemical and correct potency.
We have the expertise and resources needed to solve market complexity, providing you with reliable and trusted APIs analysis services.
What We Do?
|Identity||Identification of ions and functional groups||Chromatography: HPLC, TLC and GC|
Spectroscopy: IR, UV
|Strength and purity||Chromatographic methods: HPLC, UHPLC, HPTLC and GC, titration|
|Safety||Extreme testing of heavy metals and ions, residual solvents by GC|
We can handle any combination of analytical testing for a single method or a complete distribution package.
- Powerful testing and verification
We can work with your technology or take advantage of our extensive resources in the fields of chemistry and chemical engineering for identity, purity, and quantitative analysis of the APIs. Our protocols are optimized to reduce development time and cost.
- Professional technical support
- High accuracy
- Fast delivery
- Competitive price