高效液相色谱法检测肺炎克雷伯菌产生的β-内酰胺酶

Rika Narashima, Yuya Hasunuma, Yoshikazu Tokuoka
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引用次数: 0

摘要

为了建立一种检测β-内酰胺酶的新方法,采用高效液相色谱法测定产β-内酰胺酶的肺炎克雷伯菌对β-内酰胺类抗生素氨苄西林钠(ABPC)和头孢噻肟钠(CTX)的降解。采用高效液相色谱法,以ODS柱和磷酸缓冲液和甲醇为洗脱液,在10 min内检测出ABPC和CTX。经肺炎克雷伯菌培养后,ABPC和CTX降解。与峰面积率相对应的降解率随McFarland号的增加而增加。细菌悬浮液和培养时间。在McFarland No. 3.0培养条件下,培养90 min,肺炎克雷伯菌对ABPC和CTX的降解率分别为52.6和70.8%,而敏感菌对ABPC和CTX的降解率均小于10%。因此,这些结果证实了ABPC-和ctx -耐药菌产生的β-内酰胺酶可以在大约120 min内通过HPLC检测到。
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[Detection of β-Lactamase Produced by Klebsiella pneumoniae Using High Performance Liquid Chromatography].

In order to develop a new method to detect β-lactamase, we determined degradation of β-lactam antibiotics, ampicillin sodium (ABPC) and cefotaxime sodium (CTX), by β-lactamase-producing Klebsiella pneumoniae (K. pneumoniae) in terms of high performance liquid chromatography (HPLC). Using HPLC with an ODS column and an eluent composed of phosphate buffer and methanol, we could detect ABPC and CTX within 10 min. After cultured with K. pneumoniae, ABPC and CTX were degraded. The degradation rate corresponding to the rate of peak area incubated with and without bacteria increased with increasing McFarland No. of bacterial suspension and incubation time. Under the culture condition of McFarland No. 3.0 and 90-min incubation, the degradation rate of ABPC and CTX was 52.6 and 70.8% by K. pneumoniae, whereas it was less than 10% by susceptible bacteria. Consequently, these results confirmed that β-lactamase produced by ABPC- and CTX-resistant bacteria could be detected within about 120 min through HPLC measurement.

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