Guilfoyle D E, Roos R, Carito S L
Food and Drug Administration, Department of Health and Human Services, Brooklyn, New York.
J Parenter Sci Technol. 1990 Nov-Dec;44(6):314-9.
Pharmaceutical drug products often contain antimicrobial agents as a preservative in their formulation. These excipients are required to destroy or impede the growth of microorganisms that inadvertently enter the product during manufacturing. Unfortunately, these preservatives may also interfere with microbiological assays used to determine product sterility or bioburden levels. The extent of interference by these preservatives can be quite significant, but varies depending on the method used. The most frequently used method for testing parenteral drug products is the membrane filtration technique. Membrane filters are composed of a wide variety of materials such as cellulose, polycarbonate, acrylic polypropylene, Teflon, and nylon. This study evaluated the adsorption characteristics that nylon filters, obtained from five different manufacturers, had on the filtration of solutions of four different antimicrobial compounds (phenol, methylparaben, propylparaben, and benzalkonium chloride). The adsorption properties were determined using both HPLC and microbiological assay techniques. The data revealed that there was a wide range in the amounts of antimicrobial agent (2.3 to 94.1%) bound to the membrane filters when direct product filtration was used without a subsequent rinse step. However, when a rinse step is included, only propylparaben showed any significant "true" adsorption (less than 1 to 33.3%), but showed only marginal bacterial inhibition. Interestingly, the microbiological assays indicated that with a saline rinse step, only benzalkonium chloride was lethal for the two challenge organisms even though the percent adsorbed as measured by HPLC was below 1%. This discrepancy is significant because it demonstrates the analytical limitation when using HPLC to detect minimal concentrations of benzalkonium chloride that may be deleterious to microorganisms.(ABSTRACT TRUNCATED AT 250 WORDS)
药物制剂通常在配方中含有抗菌剂作为防腐剂。这些辅料用于破坏或抑制在生产过程中意外进入产品的微生物的生长。不幸的是,这些防腐剂也可能干扰用于确定产品无菌性或生物负荷水平的微生物检测。这些防腐剂的干扰程度可能相当大,但因所使用的方法而异。检测注射用药品最常用的方法是膜过滤技术。膜过滤器由多种材料制成,如纤维素、聚碳酸酯、丙烯酸聚丙烯、聚四氟乙烯和尼龙。本研究评估了从五个不同制造商获得的尼龙过滤器对四种不同抗菌化合物(苯酚、对羟基苯甲酸甲酯、对羟基苯甲酸丙酯和苯扎氯铵)溶液过滤的吸附特性。使用高效液相色谱法(HPLC)和微生物检测技术测定吸附特性。数据显示,在不进行后续冲洗步骤直接进行产品过滤时,与膜过滤器结合的抗菌剂数量范围很广(2.3%至94.1%)。然而,当包含冲洗步骤时,只有对羟基苯甲酸丙酯显示出任何显著的“真实”吸附(小于1%至33.3%),但仅表现出轻微的细菌抑制作用。有趣的是,微生物检测表明,即使通过HPLC测量的吸附百分比低于1%,在进行盐水冲洗步骤时,只有苯扎氯铵对两种挑战微生物具有致死性。这种差异很显著,因为它证明了使用HPLC检测可能对微生物有害的最低浓度苯扎氯铵时的分析局限性。(摘要截选至250字)