六种静脉混合液用于术后多模式镇痛的相容性及理化稳定性。

IF 5.1 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-09-09 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S543730
Carmen Lopez-Cabezas, Judith Baguena, Mireia Marcé Briansó, Gemma Gotor, Susana Ceamanos, Tomas Cuñat, Francesc Broto-Puig, Dolors Soy
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引用次数: 0

摘要

目的:评价6种用于术后静脉多模式镇痛的药物组合在不同储存条件和不同容器下的理化相容性。方法:采用曲马多、氯胺酮与右酮洛芬或酮乐酸的三元或四元复合镇痛药,部分配伍加美沙酮,均用生理盐水稀释。在制备后48小时(室温)和30天后(2°-8°C)对聚烯烃袋中的混合物进行物理相容性、pH值和药物浓度(超高效液相色谱(UHPLC-DAD))测定,在室温下对有机硅和聚异戊二烯弹性体中的混合物进行14天后的测定。结果:未观察到物理变化,pH值在整个研究过程中保持稳定。5种药物在聚烯烃袋中的回收率均在95 ~ 105%范围内。在弹性体中制备的混合物中,曲马多和右酮洛芬的回收率在95-105%之间,而美沙酮的回收率小于40%。随后的甲醇萃取证明了美沙酮在容器壁上的吸附,在硅胶中比在聚异戊二烯储层中更明显。结论:曲马多、氯胺酮与佐剂(右酮洛芬或酮乐酸,加或不加美沙酮)的镇痛合剂在室温下具有48小时的物理化学稳定性,在聚烯烃袋中2°-8°C下具有30天的物理化学稳定性。然而,曲马多、右酮洛芬和美沙酮的组合在两种测试的弹性体装置中由于美沙酮的吸附而不稳定,不适合临床使用。这些发现强调了容器材料在药物稳定性中的关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Compatibility and Physico-Chemical Stability of Six Intravenous Mixtures for Postoperative Multimodal Analgesia.

Compatibility and Physico-Chemical Stability of Six Intravenous Mixtures for Postoperative Multimodal Analgesia.

Compatibility and Physico-Chemical Stability of Six Intravenous Mixtures for Postoperative Multimodal Analgesia.

Purpose: To evaluate the physical-chemical compatibility of six drug combinations used in intravenous multimodal postoperative analgesia under differing storage conditions and different containers.

Methods: The analgesic mixtures studied were ternary and quaternary combinations of tramadol and ketamine with dexketoprofen or ketorolac, plus methadone in some mixtures, all diluted in saline solution. Physical compatibility, pH and concentration of drugs (ultra high performance liquid chromatography (UHPLC-DAD)) were determined 48 hours post-preparation (room temperature) and after 30 days (2°-8°C) for the mixtures in polyolefin bags, and after 14 days at room temperature for those mixtures in silicone and polyisoprene elastomers.

Results: No physical changes were observed, and pH remained stable throughout the study. For all five drugs in polyolefin bags the recovery percentage remained within the range 95-105%. Regarding mixtures prepared in elastomers, the recovery percentage for tramadol and dexketoprofen stayed within the range 95-105%, while for methadone it was less than 40%. A subsequent extraction with methanol demonstrated the methadone adsorption on the container walls, more pronounced in the silicone than in the polyisoprene reservoirs.

Conclusion: Analgesic mixtures of tramadol and ketamine with adjuvants (dexketoprofen or ketorolac, with or without methadone) showed physicochemical stability for 48 hours at room temperature and up to 30 days at 2°-8°C in polyolefin bags. However, the combination of tramadol, dexketoprofen, and methadone was unstable in both tested elastomeric devices due to methadone adsorption, making it unsuitable for clinical use. These findings underscore the critical role of container material in drug stability.

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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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