Strontium Chloride Sr-89

Strontium Chloride Sr-89

Cat Number
API14119107
CAS Number
14119-10-7

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CAS Number
14119-10-7
Synonyms
Metastron;Strontium-89 chloride
Molecular Formula
Cl2Sr
Molecular Weight
159.81
Smiles
[Cl-].[Cl-].[89Sr+2]
General Description
Strontium Chloride Sr-89 is the strontium-89 radioactive isotope salt of strontium chloride. Strontium-89 is a beta-emitting radionuclide with a physical half-life of 50.5 days and a maximum beta emission energy of 1.46 MeV. Due to its chemical similarity to calcium, strontium is selectively incorporated into bone mineral.
Mechanism of Action
Following administration, Sr-89 ions are incorporated into the hydroxyapatite crystal matrix of bone through ion exchange with calcium, concentrating preferentially in areas of increased osteoblastic activity. The emitted beta radiation induces local radiotherapy effects in adjacent tumor cells and bone marrow within a few millimeters of the Sr-89 deposition site.
Application
Indicated for the palliative treatment of bone pain in patients with skeletal metastases from advanced cancer. Strontium Chloride Sr-89 is a beta-emitting radiopharmaceutical that selectively concentrates in bone through calcium-like incorporation into hydroxyapatite, providing localized radiation therapy to metastatic bone lesions.

Strontium-89 chloride is a calcium analogue that selectively accumulates at sites of osteoblastic bone metastases through incorporation into newly synthesized collagen during bone formation. The biological mechanism of pain palliation involves both direct and indirect radiation-induced effects.
Direct radiotoxic effects of 89SrCl2 on prostate carcinoma PC-3 cells were comparable to an equivalent dose of 2 Gy X-rays. Indirect effects were investigated using MC3T3-E1 pre-osteoblast cells. Exposure to 89SrCl2 resulted in a concentration-dependent increase in prostaglandin E2 production by MC3T3-E1 cells, reaching approximately 175 percent of control levels at the highest concentration tested. This PGE2 response was not observed with X-ray exposure either in the presence or absence of stable strontium chloride. Interleukin-6 was subsequently produced by MC3T3-E1 cells in response to 89SrCl2 exposure via a PGE2-mediated pathway. These findings demonstrate that 89SrCl2 induces the release of potent biochemical modifiers of bone turnover, suggesting that pain palliation results from a complex interaction of direct tumor cell radiotoxicity and indirect radiation-induced effects on bone cell populations.

Fig. 1 Interleukin 6 (IL-6) production by the MC3T3-E1 cells upon exposure to 89SrCl2/SrCl2. (Davis J, Pither R J. 2001) Fig. 1 Interleukin 6 (IL-6) production by the MC3T3-E1 cells upon exposure to 89SrCl2/SrCl2. (Davis J, Pither R J. 2001)

References

  1. Davis J, Pither R J. Biochemical responses in cultured cells following exposure to 89SrCl2: potential relevance to the mechanism of action in pain palliation. European Journal of Cancer, 2001, 37(18): 2464-2469.

Why does Sr-89 selectively target bone metastases?

Strontium chemically resembles calcium, allowing Sr-89 to substitute in hydroxyapatite during bone mineralization, with preferential uptake in areas of high bone turnover typical of metastatic lesions.

What purity grade is available?

Supplied as a high-purity radiopharmaceutical-grade compound meeting quality specifications for R&D and analytical applications.

Can packaging be customized?

Packaging and order quantities can be customized to meet specific R&D and regulatory requirements.

Is international shipping available?

Available to qualified licensed customers in most countries and regions, subject to radiological safety regulations.
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