TY - JOUR
T1 - Comparative test of midazolam hydrochloride stability in different storage and temperature container
AU - Endaryanto, Anang
AU - Miatmoko, Andang
AU - Wulandari, Mela Dwi
AU - Aryanti, Novi
N1 - Publisher Copyright:
© 2020, Institute of Medico-Legal Publications. All rights reserved.
PY - 2020/10/1
Y1 - 2020/10/1
N2 - Background: Midazolam hydrochloride is an injection form of benzodiazepines and included in the high alert category in the Dr. Soetomo Teaching Hospital Intensive Care Unit (ICU), Surabaya, Indonesia. Nowadays, the technical preparation of midazolam drugs in the ICU room by doctors and nurses was performed by reconstituting drugs in the injection syringes to be stored for a while in the room. Objectives: To evaluate the preparation process for midazolam hydrochloride injection which has been analyzed in Dr. Soetomo Teaching Hospital. Methods: Physical, chemical, and microbiological stability of 1 mg/mL midazolam hydrochloride in aqua pro injection solvents have been evaluated at points 0, 8, 12, and 24 hours after preparation, as well as a comparison of stability in storage conditions at room temperature compared to refrigerator temperatures. Results: The results showed all the preparations were no foreign particles in the sample container. The midazolam did not experience precipitation in both room and refrigerator temperatures. The pH of midazolam solution during storage proved that the preparation was relatively stable (pH 4.3–4.5). There were no significant differences of midazolam levels in both storages which was in range of 95%. The Miccrobiology Stability Test showed negative germ growth after 24 hours incubation in both storage. Conclusion: This study showed no changes in physical, chemical, or microbiological stability in the midazolam injection samples up to 24 hours after the manufacturing process.
AB - Background: Midazolam hydrochloride is an injection form of benzodiazepines and included in the high alert category in the Dr. Soetomo Teaching Hospital Intensive Care Unit (ICU), Surabaya, Indonesia. Nowadays, the technical preparation of midazolam drugs in the ICU room by doctors and nurses was performed by reconstituting drugs in the injection syringes to be stored for a while in the room. Objectives: To evaluate the preparation process for midazolam hydrochloride injection which has been analyzed in Dr. Soetomo Teaching Hospital. Methods: Physical, chemical, and microbiological stability of 1 mg/mL midazolam hydrochloride in aqua pro injection solvents have been evaluated at points 0, 8, 12, and 24 hours after preparation, as well as a comparison of stability in storage conditions at room temperature compared to refrigerator temperatures. Results: The results showed all the preparations were no foreign particles in the sample container. The midazolam did not experience precipitation in both room and refrigerator temperatures. The pH of midazolam solution during storage proved that the preparation was relatively stable (pH 4.3–4.5). There were no significant differences of midazolam levels in both storages which was in range of 95%. The Miccrobiology Stability Test showed negative germ growth after 24 hours incubation in both storage. Conclusion: This study showed no changes in physical, chemical, or microbiological stability in the midazolam injection samples up to 24 hours after the manufacturing process.
KW - Aseptic Technique
KW - Injection Preparation
KW - Midazolam Hydrochloride
KW - Stability Test
UR - http://www.scopus.com/inward/record.url?scp=85100169778&partnerID=8YFLogxK
U2 - 10.37506/ijfmt.v14i4.11624
DO - 10.37506/ijfmt.v14i4.11624
M3 - Article
AN - SCOPUS:85100169778
SN - 0973-9122
VL - 14
SP - 986
EP - 991
JO - Indian Journal of Forensic Medicine and Toxicology
JF - Indian Journal of Forensic Medicine and Toxicology
IS - 4
ER -