TY - JOUR
T1 - Stability of octreotide acetate decreases in a sodium bisulfate concentration-dependent manner
T2 - Compatibility study with morphine and metoclopramide injections
AU - Tanabe, Kouichi
AU - Wada, Junko
AU - Ohkubo, Jun
AU - Nitta, Atsumi
AU - Ikezaki, Tomoaki
AU - Takeuchi, Miyako
AU - Handa, Aya
AU - Tanaka, Mai
AU - Murakami, Nozomu
AU - Kashii, Tatsuhiko
AU - Kitazawa, Hidenori
N1 - Funding Information:
This registry was sponsored by the Korean Society of Interventional Cardiology.
PY - 2015/5
Y1 - 2015/5
N2 - Purpose: Sodium bisulfate is known to affect the stability of octreotide. However, the critical concentration of sodium bisulfate is not known. Therefore, we assessed the critical concentration of sodium bisulfate needed to preserve the stability of octreotide using actual drugs containing sodium bisulfate. Methods: Although morphine and metoclopramide preparations are considered to be compatible with octreotide, some of their products are known to contain sodium bisulfate. Thus, octreotide was mixed with preparations of sodium bisulfate solutions at serial concentrations and morphine and metoclopramide preparations containing sodium bisulfate, and octreotide stability was then evaluated using high performance liquid chromatography. Results: Octreotide concentrations decreased significantly at a sodium bisulfate concentration of 0.1 mg/mL or higher after 10 days when octreotide was mixed with sodium bisulfate solutions at various concentrations. A significant decrease in octreotide concentrations also occurred when it was mixed with morphine and metoclopramide preparations containing sodium bisulfate and stored for 10 days; however, slight decreases were observed in the mixture with both preparations and were within the clinically acceptable range for morphine preparations. Conclusions: These results indicate that the residual rate of octreotide decreases with time in a sodium bisulfate concentration-dependent manner when octreotide was mixed with morphine or metoclopramide. However, this incompatibility may be clinically acceptable when the final sodium bisulfate concentration is lower than 0.1 mg/mL and the mixed solution is used within 7 days.
AB - Purpose: Sodium bisulfate is known to affect the stability of octreotide. However, the critical concentration of sodium bisulfate is not known. Therefore, we assessed the critical concentration of sodium bisulfate needed to preserve the stability of octreotide using actual drugs containing sodium bisulfate. Methods: Although morphine and metoclopramide preparations are considered to be compatible with octreotide, some of their products are known to contain sodium bisulfate. Thus, octreotide was mixed with preparations of sodium bisulfate solutions at serial concentrations and morphine and metoclopramide preparations containing sodium bisulfate, and octreotide stability was then evaluated using high performance liquid chromatography. Results: Octreotide concentrations decreased significantly at a sodium bisulfate concentration of 0.1 mg/mL or higher after 10 days when octreotide was mixed with sodium bisulfate solutions at various concentrations. A significant decrease in octreotide concentrations also occurred when it was mixed with morphine and metoclopramide preparations containing sodium bisulfate and stored for 10 days; however, slight decreases were observed in the mixture with both preparations and were within the clinically acceptable range for morphine preparations. Conclusions: These results indicate that the residual rate of octreotide decreases with time in a sodium bisulfate concentration-dependent manner when octreotide was mixed with morphine or metoclopramide. However, this incompatibility may be clinically acceptable when the final sodium bisulfate concentration is lower than 0.1 mg/mL and the mixed solution is used within 7 days.
UR - http://www.scopus.com/inward/record.url?scp=84929457596&partnerID=8YFLogxK
U2 - 10.1136/ejhpharm-2014-000555
DO - 10.1136/ejhpharm-2014-000555
M3 - 学術論文
C2 - 25984298
AN - SCOPUS:84929457596
SN - 2047-9956
VL - 22
SP - 171
EP - 175
JO - European Journal of Hospital Pharmacy
JF - European Journal of Hospital Pharmacy
IS - 3
ER -