Microbial Challenge of Stable Compounded Clozapine Suspensions in Plastic Bottles.

Q4 Medicine
Jessica Berzy, Hanif Sachedina, Arif Virji, Jason A Gross, Erica Cull, Scott E Walker
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引用次数: 0

Abstract

Background and rationale: A clozapine oral suspension is not commercially available in Canada and is required for administration to patients who cannot swallow intact tablets. While a stable formula has been described, no studies document the effectiveness of the preservative system used in this formulation to control inadvertent microbial contamination by the user during use of the preparation.

Objective: The objective of this study was to evaluate the antimicrobial effectiveness of 25-mg/mL and 50-mg/mL oral suspension of clozapine after 120-days of storage at 20o-25oC, ensuring a compounded clozapine preparation can be provided to a patient with confidence and supporting the beyond-use-date of the preparation.

Methods: The USP Chapter <51> Preservative Effectiveness Test protocol was followed as described for category 3 products. After storage for 120-days at 20o-25oC in amber glycol-modified polyethylene terephthalate (PET-G), both the 25-mg/mL and 50-mg/mL clozapine suspensions were inoculated with 3 different strains of bacteria and 2 strains of fungi and incubated for 28-days. On days 7, 14 and 28, the bacterial and fungal colony counts determined the antimicrobial effectiveness of the suspension. The suitability of the microbial recovery method was validated prior to completing the challenge test.

Results: The microbial load of the clozapine suspensions declined from an initial CFU count between 105-106 to less than 10-CFU by day 7 for bacteria and less than 30-50 CFU for yeast & fungi. On days 14 and 28, the bacteria showed no changes from counts at day 7th, while the yeast & fungi declined to less than 10 CFU. This indicates effective antimicrobial activity of the clozapine oral suspension.

Conclusions: The 25-mg/mL and 50-mg/mL clozapine suspensions have been demonstrated to effectively control bacterial and fungal contamination, as judged by the USP Chapter <51> Antimicrobial Effectiveness Test. This bracketed formulation has been previously demonstrated to retain more than 95% of its initial active concentration when stored at 4oC or 25oC for 120-days.

稳定复方氯氮平混悬液在塑料瓶中的微生物挑战。
背景和理由:氯氮平口服混悬液在加拿大没有市售,需要给不能吞咽完整片剂的患者。虽然已经描述了一个稳定的配方,但没有研究证明该配方中使用的防腐剂系统在使用制剂期间控制用户无意的微生物污染的有效性。目的:本研究的目的是评价25 mg/mL和50 mg/mL氯氮平口服混悬液在20- 25℃下保存120 d后的抗菌效果,确保复方氯氮平制剂能够放心地提供给患者,并支持制剂的超期使用。方法:按照美国药典第3类产品防腐效果试验规程进行。将25 mg/mL和50 mg/mL氯氮平混悬液分别接种3株不同的细菌和2株不同的真菌,在20 ~ 25℃的琥珀醇改性聚对苯二甲酸乙二醇酯(PET-G)中保存120 d。在第7、14和28天,细菌和真菌菌落计数决定了混悬液的抗菌效果。在完成激射试验之前,对微生物回收方法的适用性进行了验证。结果:氯氮平混悬液的微生物负荷从最初的105-106个CFU计数下降到第7天细菌的小于10个CFU,酵母和真菌的小于30-50个CFU。在第14和28天,细菌的数量与第7天相比没有变化,而酵母和真菌的数量则下降到10 CFU以下。这表明氯氮平口服混悬液具有有效的抗菌活性。结论:25 mg/mL和50 mg/mL氯氮平混悬液可有效控制细菌和真菌污染。先前已证明,当在4℃或25℃下储存120天时,该支架制剂可保留95%以上的初始活性浓度。
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
0.40
自引率
0.00%
发文量
62
期刊介绍: The International Journal of Pharmaceutical Compounding (IJPC) is a bi-monthly, scientific and professional journal emphasizing quality pharmaceutical compounding. IJPC is the only publication that covers pharmaceutical compounding topics relevant and necessary to empower pharmacists to meet the needs of today"s patients. No other publication features hands-on, how-to compounding techniques or the information that contemporary pharmacists need to provide individualized care.
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