Industry Information

Urofollitropin Instructions and Ulinastatin Manufacturing

  Urofollitropin (r-hGH) is a recombinant human growth hormone that is used to treat patients with short stature due to growth hormone deficiency (GHD) or Turner syndrome. It is a recombinant form of human growth hormone that is produced in a cell culture using genetically modified bacteria. Ulinastatin is a protein inhibitor that is used to treat high creatinine levels in patients with kidney failure. It is produced through recombinant DNA technology using eukaryotic cells.

Urofollitropin Instructions and Ulinastatin Manufacturing

  Urofollitropin Instructions:

  Use of r-hGH requires careful follow-up and monitoring by a healthcare professional. Before starting r-hGH treatment, it is important to assess the patient's GHD diagnosis, severity of short stature, and current medical conditions. The patient's height, weight, and other relevant medical information should be recorded before starting treatment. The patient should be observed for any adverse reactions to r-hGH, such as increased muscle mass, increased thirst, or increased hunger. The healthcare professional should monitor the patient's creatinine levels and adjust the r-hGH dosage as needed.

  Ulinastatin Manufacturing:

  Ulinastatin is produced through recombinant DNA technology using eukaryotic cells. The process involves the transfection of human ovary cells with a plasmid encoding for ulinastatin cDNA. The transfected cells are then cultured and the ulinastatin protein is purified from the supernatant. The purified ulinastatin is then tested for purity, potency, and stability. The final product is stored at controlled temperatures to ensure stability and prevent degradation.

  Conclusion:

  Urofollitropin and ulinastatin are important recombinant proteins produced through recombinant DNA technology. Both drugs are used in the treatment of various medical conditions, but require careful monitoring and titration by healthcare professionals. The development and production of these drugs represents a significant advance in the field of protein therapy and provides hope for patients with limited options for treatment.