Literature DB >> 26246294

Compatibility of butorphanol with granisetron in 0.9% sodium chloride injection packaged in glass bottles or polyolefin bags.

Fu-Chao Chen1, Hui Xiong2, Hui-Min Liu2, Bao-Xia Fang2, Peng Li2.   

Abstract

PURPOSE: The stability of admixtures containing butorphanol and granisetron in polyolefin bags and glass bottles stored at 4 and 25 °C was studied.
METHODS: Commercial solutions of butorphanol tartrate and granisetron hydrochloride were combined and further diluted with 0.9% sodium chloride injection to final concentrations of butorphanol tartrate 0.08 mg/mL and granisetron 0.03 or 0.06 mg/mL; the resulting mixtures were packaged in polyolefin bags and glass bottles. The admixtures were assessed for periods of up to 48 hours after storage at 25 °C without protection from room light and up to 14 days at 4 °C with protection from room light. The chemical stability of the admixtures was evaluated by a validated high-performance liquid chromatography (HPLC) method and by measurement of pH values. Solution appearance and color were assessed by observing the samples against room light and dark backgrounds.
RESULTS: HPLC analysis demonstrated that the percentages of the initial concentrations of butorphanol and granisetron in the various solutions remained above 97% during the testing period. No changes in color or turbidity were observed in any of the prepared solutions. Throughout this period, pH values remained stable.
CONCLUSION: Admixtures of butorphanol tartrate 0.08 mg/mL and granisetron 0.03 or 0.06 mg/mL in 0.9% sodium chloride injection in polyolefin bags or glass bottles remained stable for 48 hours when stored at 25 °C exposed to room light and for 14 days when stored at 4 °C protected from room light.
Copyright © 2015 by the American Society of Health-System Pharmacists, Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2015        PMID: 26246294     DOI: 10.2146/ajhp140824

Source DB:  PubMed          Journal:  Am J Health Syst Pharm        ISSN: 1079-2082            Impact factor:   2.637


  5 in total

1.  Physicochemical stability of ternary admixtures of butorphanol, ketamine, and droperidol in polyolefin bags for patient-controlled analgesia use.

Authors:  Baoxia Fang; Linhai Wang; Junfeng Gu; Fuchao Chen; Xiao-Ya Shi
Journal:  Drug Des Devel Ther       Date:  2016-11-24       Impact factor: 4.162

2.  Simultaneous Determination of Dexamethasone, Ondansetron, Granisetron, Tropisetron, and Azasetron in Infusion Samples by HPLC with DAD Detection.

Authors:  Fu-Chao Chen; Lin-Hai Wang; Jun Guo; Xiao-Ya Shi; Bao-Xia Fang
Journal:  J Anal Methods Chem       Date:  2017-01-11       Impact factor: 2.193

3.  A Comprehensive Strategy to Evaluate Compatible Stability of Chinese Medicine Injection and Infusion Solutions Based on Chemical Analysis and Bioactivity Assay.

Authors:  Jian-Ping Li; Yang Liu; Jian-Ming Guo; Er-Xin Shang; Zhen-Hua Zhu; Kevin Y Zhu; Yu-Ping Tang; Bu-Chang Zhao; Zhi-Shu Tang; Jin-Ao Duan
Journal:  Front Pharmacol       Date:  2017-11-15       Impact factor: 5.810

4.  A Fast and Validated HPLC Method for the Simultaneous Analysis of Five 5-HT3 Receptor Antagonists via the Quantitative Analysis of Multicomponents by a Single Marker.

Authors:  Fuchao Chen; Baoxia Fang; Peng Li; Sicen Wang
Journal:  Int J Anal Chem       Date:  2021-06-26       Impact factor: 1.885

5.  Incompatibilities of lornoxicam with 4 antiemetic medications in polyolefin bags during simulated intravenous administration.

Authors:  Bao-Xia Fang; Peng Li; Xiao-Ya Shi; Fu-Chao Chen; Lin-Hai Wang
Journal:  Medicine (Baltimore)       Date:  2016-06       Impact factor: 1.889

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.