Dix Jackie, Weber Robert J, Frye Reginald F, Nolin Thomas D, Mrvos Rita, Krenzelok Edward
Department of Pharmacy & Therapeutics, University of Pittsburgh School of Pharmacy, Pittsburgh, Pennsylvania, USA.
J Toxicol Clin Toxicol. 2003;41(6):771-5. doi: 10.1081/clt-120025341.
Preparedness for chemical terrorism includes the procurement of the appropriate pharmacological antagonists. A large emphasis has been placed on having a sufficient quantity of atropine available to treat patients exposed to acetylcholinesterase inhibitors such as sarin. Severe exposures may necessitate the administration of large amounts of atropine and dictate the need to prepare significant quantities of extemporaneously compounded atropine solution to respond to mass numbers of casualties over the first 24-48 hours postexposure.
The objective of this project was to determine the stability of a 1 mg/mL atropine solution prepared in multidose IV solutions of 0.9% sodium chloride over a 72-hr period stored at varying temperatures.
Atropine sulfate solution 1 mg/mL in 0.9% sodium chloride was prepared from sterile pharmaceutical-grade atropine sulfate powder. Multidose bags of atropine sulfate (100 mL) were stored at controlled temperatures of 4 degrees C to 8 degrees C, 20 degrees C to 25 degrees C, and 32 degrees C to 36 degrees C for 3 days and covered with an amber occlusive cover to minimize exposure to light. Six samples from each bag were drawn at 6, 12, 24, 48, and 72 h after preparation and compared with a time zero control sample. The samples were assayed using United States Pharmacopeia/National Formulary (USP/NF) high-performance liquid chromatography (HPLC) methods for atropine sulfate injection. The USP standard of 95% for atropine sulfate stability was used as the primary endpoint.
Atropine sulfate 1 mg/mL in 0.9% sodium chloride was stable for at least 72hr at 4 degrees C to 8 degrees C (percent initial concentration ranging from 96.5% to 103.4%), 20 degrees C to 25 degrees C (percent initial concentration ranging from 98.7% to 100.2%), and 32 degrees C to 36 degrees C (percent initial concentration ranging from 98.3% to 102.8%). Because the IV bags were protected from light during this study, we recommend this practice after preparing the atropine solution.
The amount of atropine necessary to treat hundreds to thousands of victims of a chemical attack is immense. The extemporaneous preparation of atropine solution from pharmaceutical-grade powder eliminates concerns about the storage of excessive quantities of atropine. A 1 mg/mL solution is stable for at least 3 days, allowing for use during the most critical treatment periods after exposure.
化学恐怖主义的应对准备工作包括采购合适的药理学拮抗剂。大量的重点放在了储备足够数量的阿托品,以治疗接触诸如沙林等乙酰胆碱酯酶抑制剂的患者。严重暴露可能需要大量使用阿托品,并表明有必要准备大量临时配制的阿托品溶液,以应对暴露后最初24至48小时内大量伤亡情况。
本项目的目的是确定在不同温度下储存72小时期间,0.9%氯化钠多剂量静脉输液中配制的1毫克/毫升阿托品溶液的稳定性。
由无菌药用级硫酸阿托品粉末制备0.9%氯化钠中1毫克/毫升的硫酸阿托品溶液。硫酸阿托品多剂量袋(100毫升)在4℃至8℃、20℃至25℃和32℃至36℃的控制温度下储存3天,并用琥珀色遮光罩覆盖,以尽量减少光照。在制备后6、12、24、48和72小时从每个袋子中抽取六个样品,并与零时间对照样品进行比较。使用美国药典/国家处方集(USP/NF)硫酸阿托品注射液的高效液相色谱(HPLC)方法对样品进行分析。以硫酸阿托品稳定性的USP标准95%作为主要终点。
0.9%氯化钠中1毫克/毫升的硫酸阿托品在4℃至8℃(初始浓度百分比范围为96.5%至103.4%)、20℃至25℃(初始浓度百分比范围为98.7%至100.2%)和32℃至36℃(初始浓度百分比范围为98.3%至l02.8%)至少稳定72小时。由于在本研究期间静脉输液袋受到了光照保护,我们建议在配制阿托品溶液后采用这种做法。
治疗数百至数千名化学袭击受害者所需的阿托品数量巨大。从药用级粉末临时配制阿托品溶液消除了对大量储存阿托品的担忧。1毫克/毫升的溶液至少稳定3天,可在暴露后最关键的治疗期间使用。