稀释后的洗必泰在药物过敏评估中用于皮肤测试的稳定性。

Divya Shah MD , Gabriel Cojuc-Konigsberg BS , Stacy D. Brown PhD , Sergio E. Chiarella MD , Gerald W. Volcheck MD , Hirohito Kita MD , Lene H. Garvey MD, PhD (Professor) , Alexei Gonzalez-Estrada MD
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引用次数: 0

摘要

背景:葡萄糖酸氯己定(CHX)是围手术期过敏性休克的常见原因,经常用于过敏评估中的皮试。虽然已知道 CHX 的最大无刺激浓度,但其稀释液在皮试中的稳定性仍有待探索,尤其是在使用注射用无菌水(SWFI)或生理盐水(NS)作为稀释剂时:我们的目的是评估 CHX 经 SWFI 或 NS 稀释后用于药物过敏皮肤试验时的稳定性和沉淀情况:方法:使用 SWFI 和 NS 制备 CHX 稀释液(5-0.002 mg/mL)。采用高效液相色谱法和紫外可见分光光度法评估 48 小时内的稳定性和沉淀情况。在不同的时间点测量浊度,以监测沉淀情况:高效液相色谱分析显示,CHX-SWFI 和 CHX-NS 稀释液的峰高无明显差异。然而,60 分钟后,在较高浓度(5 毫克/毫升)的 CHX-NS 中观察到明显的沉淀和浊度增加(>100 NTU)。任何浓度的 CHX-SWFI 在 48 小时内均未出现沉淀:结论:对于 CHX 皮肤测试,当浓度高于 0.02 毫克/毫升时,SWFI 是避免沉淀的首选稀释剂。使用 NS 进行 0.02 至 0.002 mg/mL 的最终稀释是可行的,并可减少注射疼痛。除 5 毫克/毫升的 CHX-NS 外,试剂可在检测前 24 小时内配制完成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stability of diluted chlorhexidine for skin testing in drug allergy evaluations

Background

Chlorhexidine gluconate (CHX), a common cause of perioperative anaphylaxis, is frequently used for skin testing in allergy evaluations. Although CHX’s maximal nonirritating concentrations are known, the stability of its dilutions for skin testing remains unexplored, particularly when sterile water for injection (SWFI) or normal saline (NS) are used as diluents.

Objective

Our aim was to evaluate the stability and precipitation of CHX when diluted with SWFI or NS for drug allergy skin testing.

Methods

CHX dilutions (5-0.002 mg/mL) were prepared using SWFI and NS. HPLC and UV-visible spectrophotometry were used to assess stability and precipitation over 48 hours. Turbidity was measured at various time points to monitor precipitation.

Results

HPLC analysis showed no significant differences in peak heights between CHX-SWFI and CHX-NS dilutions. However, visible precipitation and increased turbidity (>100 NTU) were observed in CHX-NS at higher concentrations (5 mg/mL) after 60 minutes. No precipitation occurred in CHX-SWFI at any concentration for 48 hours.

Conclusion

For CHX skin testing, SWFI is the preferred diluent at concentrations higher than 0.02 mg/mL to avoid precipitation. Using NS for the final dilution from 0.02 to 0.002 mg/mL is feasible and reduces injection pain. Except for CHX-NS at 5 mg/mL, reagents can be prepared up to 24 hours before testing.
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来源期刊
The journal of allergy and clinical immunology. Global
The journal of allergy and clinical immunology. Global Immunology, Allergology and Rheumatology
CiteScore
0.70
自引率
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审稿时长
92 days
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