Human parathyroid hormone medicine composition
A technology of parathyroid hormone and composition, which is applied in the direction of drug combination, drug delivery, and pharmaceutical formulation, and can solve problems such as instability
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Embodiment 1
[0043] 0.1 mg rhPTH(1-34) (SEQ ID NO: 2), 50 mg mannitol, 2.5 mg m-cresol, 0.52 mg acetic acid and 0.12 mg sodium acetate were mixed in 1 ml distilled water.
Embodiment 2
[0045] 0.25 mg rhPTH(1-34) (SEQ ID NO: 2), 45.4 mg mannitol, 3 mg m-cresol, 0.41 mg acetic acid and 0.1 mg sodium acetate were mixed in 1 ml distilled water.
[0046] The formulations of Examples 1 and 2 according to the invention were compared to solutions without stabilizers, 0.9% NaCl, 20 mM acetate and 10 mM acetate as primary stabilizers. Stability was determined by determining the percentage of the amount of rhPTH(1-34) (SEQ ID NO: 2) that remained over time. Assay by HPLC. The results are shown in Tables 1 and 2.
[0047] water
[0048] 20mM acetate
Embodiment 3
[0050] The following experiments were performed to show that lyophilized powder formulations prepared from the stabilizing solutions of the present invention were more stable than controls prepared with PTH(1-34) and mannitol alone.
[0051] The control solution and sample A to O solutions were prepared as described above, and their components and contents are shown in Table 3. The solution was then lyophilized and the resulting lyophilized powder formulation was stored at 40°C for one month. Then, the content of PTH(1-34) retained in each sample was determined by HPLC. The results are shown in Table 3.
[0052] sample
[0053] * Stability was 96% at 2 months.
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