Literature DB >> 32296509

Physicochemical stability of nefopam and nefopam/droperidol solutions in polypropylene syringes for intensive care units.

Elise D'Huart1, Jean Vigneron1, Igor Clarot2, Béatrice Demoré1,3.   

Abstract

Introduction: Nefopam has been reported to be effective in postoperative pain control with an opioid-sparing effect, but the use of nefopam can lead to nausea and vomiting. To prevent these side effects, droperidol can be mixed with nefopam. In intensive care units, high concentrations of nefopam and droperidol in syringes can be used with a continuous flow.
Objectives: The first objective of this work was to study the physicochemical stability of a nefopam solution 2.5 mg/mL diluted in NaCl 0.9% in polypropylene syringes immediately after preparation and after 6, 24 and 48 hours at room temperature. The second objective was to study the physicochemical stability of mixtures of nefopam 2.5 mg/mL and droperidol 52 µg/mL diluted in NaCl 0.9% in polypropylene syringes at room temperature over 48 hours. Materials and methods: Three syringes for each condition were prepared. For each time of analysis, three samples for each syringe were prepared and analysed by high performance liquid chromatography coupled to photodiode array detection. The method was validated according to the International Conference on Harmonisation Q2(R1). Physical stability was evaluated by visual and subvisual inspection (turbidimetry by UV spectrophotometry). pH values were measured at each time of analysis.
Results: Solutions of nefopam at 2.5 mg/mL and the mixture of nefopam 2.5 mg/mL with droperidol 52 µg/mL, diluted in NaCl 0.9%, without protection from light, retained more than 90% of the initial concentration after 48 hours storage at 20-25°C. No modification in visual or subvisual evaluation and pH values were observed.
Conclusion: Nefopam solutions at 2.5 mg/mL and the mixture of nefopam 2.5 mg/mL with droperidol 52 µg/mL diluted in NaCl 0.9% were stable over a period of 48 hours at room temperature. These stability data provide additional knowledge to assist intensive care services in daily practice. © European Association of Hospital Pharmacists 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  HPLC; droperidol; intensive care unit; nefopam; stability

Mesh:

Substances:

Year:  2019        PMID: 32296509      PMCID: PMC7147557          DOI: 10.1136/ejhpharm-2019-001856

Source DB:  PubMed          Journal:  Eur J Hosp Pharm        ISSN: 2047-9956


  10 in total

Review 1.  Nefopam analgesia and its role in multimodal analgesia: A review of preclinical and clinical studies.

Authors:  Philippe Girard; Marcel Chauvin; Marc Verleye
Journal:  Clin Exp Pharmacol Physiol       Date:  2016-01       Impact factor: 2.557

2.  Physicochemical stability of norepinephrine bitartrate in polypropylene syringes at high concentrations for intensive care units.

Authors:  E D'Huart; J Vigneron; I Clarot; B Demore
Journal:  Ann Pharm Fr       Date:  2019-02-22

3.  Compatibility and stability of binary mixtures of acetaminophen, nefopam, ketoprofen and ketamine in infusion solutions.

Authors:  Moufida Hamdi; Claude Lentschener; Christophe Bazin; Yves Ozier; Laurent Havard
Journal:  Eur J Anaesthesiol       Date:  2009-01       Impact factor: 4.330

4.  Effect of nefopam- versus fentanyl-based patient-controlled analgesia on postoperative nausea and vomiting in patients undergoing gynecological laparoscopic surgery: a prospective double-blind randomized controlled trial.

Authors:  Chung-Sik Oh; Eugene Jung; Sun Joo Lee; Seong-Hyop Kim
Journal:  Curr Med Res Opin       Date:  2015-07-09       Impact factor: 2.580

5.  Guidelines for the practical stability studies of anticancer drugs: a European consensus conference.

Authors:  C Bardin; A Astier; A Vulto; G Sewell; J Vigneron; R Trittler; M Daouphars; M Paul; M Trojniak; F Pinguet
Journal:  Ann Pharm Fr       Date:  2011-08-03

6.  Degradation mechanism of nefopam in solution under stressed storage conditions.

Authors:  D P Wang; Y H Tu; L V Allen; F C Cheng
Journal:  Acta Pharm Nord       Date:  1990

Review 7.  Nefopam: a review of its pharmacological properties and therapeutic efficacy.

Authors:  R C Heel; R N Brogden; G E Pakes; T M Speight; G S Avery
Journal:  Drugs       Date:  1980-04       Impact factor: 9.546

8.  Long-term stability of tramadol hydrochloride and droperidol mixture in 5% dextrose infusion polyolefin bags at 5+/-3 degrees C.

Authors:  M Lebitasy; J-D Hecq; D Vanbeckbergen; J Jamart; L Galanti
Journal:  Ann Pharm Fr       Date:  2009-04-22

9.  Compatibility of butorphanol and droperidol in 0.9% sodium chloride injection.

Authors:  Fu-Chao Chen; Bao-Xia Fang; Peng Li; Jin-Guo Yang; Ben-Hong Zhou
Journal:  Am J Health Syst Pharm       Date:  2013-03-15       Impact factor: 2.637

10.  Stability of Droperidol 0.625 mg/mL Diluted with 0.9% Sodium Chloride Injection and Stored in Polypropylene Syringes.

Authors:  Susan V McClusky; Jenna K Lovely
Journal:  Int J Pharm Compd       Date:  2011 Mar-Apr
  10 in total

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