Viability of selected microorganisms in parenteral preparations for novel systemic anti-cancer therapy.

IF 1.3 4区 医学 Q4 ONCOLOGY
Journal of Oncology Pharmacy Practice Pub Date : 2024-06-01 Epub Date: 2023-06-04 DOI:10.1177/10781552231179185
Jannik Almasi, Laura Knoll, Judith Thiesen, Irene Krämer
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引用次数: 0

Abstract

Background: Risk factors for aseptic preparation of parenteral medicines encompass the growth-promoting nature of the preparation. Although many aqueous parenteral preparations do not have growth-promoting properties, inadvertently introduced microorganisms may remain viable. Knowledge about the viability of microorganisms in parenteral preparations can add useful information for assigning shelf life to preparations used to treat cancer patients.

Aim: The aim of the study was to assess the viability of four different facultative pathogenic microorganisms in 20 ready-to-administer parenteral preparations aseptically prepared in hospital pharmacies.

Methods: Samples of 20 different biologics and small molecules for systemic anti-cancer therapy were inoculated either with different bacteria (i.e., Staphylococcus aureus, Pseudomonas aeruginosa, Enterococcus faecium) or with Candida albicans suspension. The resulting test concentrations were 104-105 microorganisms per mL. Aliquots of inoculated test solutions were transferred in duplicate to tryptic soy agar plates at the time points 0, 4, 24, 48, 144 h. The plates were incubated for 24 h (bacterial strains) and 72 h (C. albicans) at 37 °C and colony forming units (CFUs) were counted.

Results: In most test solutions, especially in monoclonal antibody solutions, increased CFU counts of P. aeruginosa and unchanged or increased CFU counts of E. faecium and S. aureus were registered. Pronounced nutritive properties of monoclonal antibodies and filgrastim were not registered. Azacitidine, pixantrone and vinflunine containing test solutions revealed species-specific bacteriostatic and even bactericidal activity. All test solutions, except nivolumab and pixantrone containing solutions, showed constant or increasing CFU counts of C. albicans after incubation.

Conclusion: Viability of the selected pathogenic microorganisms was retained in most of the tested biological and small molecule preparations used to treat cancer patients. Therefore, in pharmacy departments strict aseptic conditions should be regarded and the lack of antimicrobial activity should be considered when assigning shelf life to RTA parenteral preparations.

用于新型全身抗癌疗法的肠外制剂中特定微生物的存活率。
背景:无菌制备肠外药物的风险因素包括制剂的促生长特性。尽管许多水性肠外制剂并不具有促进生长的特性,但无意中引入的微生物仍有可能存活。了解肠外制剂中微生物的存活率可为确定用于治疗癌症患者的制剂的保质期提供有用信息。目的:本研究旨在评估医院药房无菌配制的 20 种即用型肠外制剂中四种不同的面致病微生物的存活率:方法:将 20 种不同的生物制剂和用于全身抗癌治疗的小分子药物样品接种到不同的细菌(即金黄色葡萄球菌、铜绿假单胞菌、粪肠球菌)或白色念珠菌悬浮液中。测试浓度为每毫升 104-105 个微生物。在 0、4、24、48 和 144 小时的时间点,将接种的试验溶液一式两份转移到胰蛋白酶大豆琼脂平板上。平板在 37 °C下培养 24 小时(细菌菌株)和 72 小时(白僵菌),并计算菌落形成单位(CFUs):结果:在大多数试验溶液中,尤其是在单克隆抗体溶液中,铜绿假单胞菌的菌落形成单位计数增加,而粪大肠杆菌和金黄色葡萄球菌的菌落形成单位计数不变或增加。单克隆抗体和非格司亭没有明显的营养特性。含有阿扎胞苷、匹泛龙和长春氟宁的试液显示出针对不同物种的抑菌甚至杀菌活性。除含有尼伐单抗和匹杉群的溶液外,所有测试溶液在培养后都显示白僵菌的 CFU 计数不变或增加:结论:在大多数用于治疗癌症患者的受测生物制剂和小分子制剂中,所选病原微生物都有存活能力。因此,药剂部门应注意严格的无菌条件,在确定 RTA 非肠道制剂的保质期时应考虑到其缺乏抗菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.70
自引率
7.70%
发文量
276
期刊介绍: Journal of Oncology Pharmacy Practice is a peer-reviewed scholarly journal dedicated to educating health professionals about providing pharmaceutical care to patients with cancer. It is the official publication of the International Society for Oncology Pharmacy Practitioners (ISOPP). Publishing pertinent case reports and consensus guidelines...
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